Eesti Geenivaramu publikatsioonid 2002-2014 | Tartu Ülikooli genoomika instituut

TÜ üksuste kontaktandmed

humanitaarteaduste ja kunstide valdkond
Faculty phone: 
737 5341
Faculty address: 
Jakobi 2, ruumid 116–121, 51014 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5341
    Faculty address: 
    Jakobi 2, ruumid 116–121, 51005 Tartu
  • ajaloo ja arheoloogia instituut
    Faculty phone: 
    737 5651
    Faculty address: 
    Jakobi 2, 51005 Tartu
  • eesti ja üldkeeleteaduse instituut
    Faculty phone: 
    737 5221
    Faculty address: 
    Jakobi 2, IV korrus, 51005 Tartu
  • filosoofia ja semiootika instituut
    Faculty phone: 
    737 5314
    Faculty address: 
    Jakobi 2, ruumid 309–352, 51005 Tartu
  • kultuuriteaduste instituut
    Faculty phone: 
    737 5223
    Faculty address: 
    Ülikooli 16, 51003 Tartu
  • maailma keelte ja kultuuride kolledž
    Faculty address: 
    Lossi 3, 51003 Tartu
  • usuteaduskond
    Faculty phone: 
    737 5300
    Faculty address: 
    Ülikooli 18-310, 50090 Tartu
  • Viljandi kultuuriakadeemia
    Faculty phone: 
    435 5232
    Faculty address: 
    Posti 1, 71004 Viljandi
sotsiaalteaduste valdkond
Faculty phone: 
737 5957
Faculty address: 
Lossi 36, 51003 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5900
    Faculty address: 
    Lossi 36, 51003 Tartu
  • haridusteaduste instituut
    Faculty phone: 
    737 6440
    Faculty address: 
    Salme 1a–29, 50103 Tartu
  • Johan Skytte poliitikauuringute instituut
    Faculty phone: 
    737 5582
    Faculty address: 
    Lossi 36–301, 51003 Tartu
  • majandusteaduskond
    Faculty phone: 
    737 6310
    Faculty address: 
    J. Liivi 4, 50409 Tartu
  • psühholoogia instituut
    Faculty phone: 
    737 5902
    Faculty address: 
    Näituse 2, 50409 Tartu
  • õigusteaduskond
    Faculty phone: 
    737 5390
    Faculty address: 
    Näituse 20–324, 50409 Tartu
  • ühiskonnateaduste instituut
    Faculty phone: 
    737 5188
    Faculty address: 
    Lossi 36, 51003 Tartu
  • Narva kolledž
    Faculty phone: 
    740 1900
    Faculty address: 
    Raekoja plats 2, 20307 Narva
  • Pärnu kolledž
    Faculty phone: 
    445 0520
    Faculty address: 
    Ringi 35, 80012 Pärnu
meditsiiniteaduste valdkond
Faculty phone: 
737 5326
Faculty address: 
Ravila 19, 50411 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5326
    Faculty address: 
    Ravila 19, 50411 Tartu
  • bio- ja siirdemeditsiini instituut
    Faculty phone: 
    737 4210
    Faculty address: 
    Biomeedikum, Ravila 19, 50411 Tartu
  • farmaatsia instituut
    Faculty phone: 
    737 5286
    Faculty address: 
    Nooruse 1, 50411 Tartu
  • hambaarstiteaduse instituut
    Faculty phone: 
    731 9856
    Faculty address: 
    Raekoja plats 6, 51003 Tartu
  • kliinilise meditsiini instituut
    Faculty phone: 
    737 5323
    Faculty address: 
    L. Puusepa 8, 50406 Tartu
  • peremeditsiini ja rahvatervishoiu instituut
    Faculty phone: 
    737 4190
    Faculty address: 
    Ravila 19, 50411 Tartu
  • sporditeaduste ja füsioteraapia instituut
    Faculty phone: 
    737 5360
    Faculty address: 
    Jakobi 5–205, 51005 Tartu
loodus- ja täppisteaduste valdkond
Faculty phone: 
737 5820
Faculty address: 
Vanemuise 46–208, 51005 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5820
    Faculty address: 
    Vanemuise 46–208, 51005 Tartu
  • arvutiteaduse instituut
    Faculty phone: 
    737 5445
    Faculty address: 
    J. Liivi 2, 50409 Tartu
  • Eesti mereinstituut
    Faculty phone: 
    671 8902
    Faculty address: 
    Mäealuse 14, 12618 Tallinn
  • füüsika instituut
    Faculty address: 
    W. Ostwaldi 1, 50411 Tartu
  • keemia instituut
    Faculty phone: 
    737 5261
    Faculty address: 
    Ravila 14a, 50411 Tartu
  • matemaatika ja statistika instituut
    Faculty phone: 
    737 5860
    Faculty address: 
    J. Liivi 2, 50409 Tartu
  • molekulaar- ja rakubioloogia instituut
    Faculty phone: 
    737 5011
    Faculty address: 
    Riia 23, 23b–134, 51010 Tartu
  • Tartu observatoorium
    Faculty phone: 
    737 4510
    Faculty address: 
    Observatooriumi 1, Tõravere, 61602 Tartumaa
  • tehnoloogiainstituut
    Faculty phone: 
    737 4800
    Faculty address: 
    Nooruse 1, 50411 Tartu
  • ökoloogia ja maateaduste instituut
    Faculty phone: 
    737 5835
    Faculty address: 
    Vanemuise 46, 51003 Tartu
Asutused
  • raamatukogu
    Faculty phone: 
    737 5702
    Faculty address: 
    W. Struve 1, 50091 Tartu
  • teaduskool
    Faculty phone: 
    737 5581
    Faculty address: 
    Uppsala 10, 51003 Tartu
  • genoomika instituut
    Faculty phone: 
    737 4000
    Faculty address: 
    Riia 23b, 51010 Tartu
  • muuseum
    Faculty phone: 
    737 5674
    Faculty address: 
    Lossi 25, 51003 Tartu
  • loodusmuuseum ja botaanikaaed
    Faculty phone: 
    737 6076
    Faculty address: 
    Vanemuise 46, 51003 Tartu
Tugiüksused
  • ettevõtlus- ja innovatsioonikeskus
    Faculty phone: 
    737 6339
    Faculty address: 
    Lossi 3, III korrus, 51003 Tartu
  • grandikeskus
    Faculty phone: 
    737 6215
    Faculty address: 
    Lossi 3, III korrus, 51003 Tartu
  • hankeosakond
    Faculty phone: 
    737 6632
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • infotehnoloogia osakond
    Faculty phone: 
    737 6000, arvutiabi: 737 5500
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • kantselei
    Faculty phone: 
    737 5606
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • kinnisvaraosakond
    Faculty phone: 
    737 5137
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • personaliosakond
    Faculty phone: 
    737 5145
    Faculty address: 
    Ülikooli 18, ruumid 302 ja 304, 50090 Tartu
  • rahandusosakond
    Faculty phone: 
    737 5125
    Faculty address: 
    Jakobi 4, 51005 Tartu
  • rektoraadi büroo
    Faculty phone: 
    737 5600
    Faculty address: 
    Ülikooli 18, 51014 Tartu
  • siseauditi büroo
    Faculty address: 
    Ülikooli 17–103, 51005 Tartu
  • Tallinna esindus
    Faculty phone: 
    737 6600
    Faculty address: 
    Teatri väljak 3, 10143 Tallinn
  • turundus- ja kommunikatsiooniosakond
    Faculty phone: 
    737 5687
    Faculty address: 
    Ülikooli 18, ruumid 102, 104, 209, 210, 50090 Tartu
  • õppeosakond
    Faculty phone: 
    737 5620
    Faculty address: 
    Ülikooli 18, 50090 Tartu
  • üliõpilasesindus
    Faculty phone: 
    737 5400
    Faculty address: 
    Ülikooli 18b, 51005 Tartu
Muud üksused
  • MTÜ Tartu Ülikooli Akadeemiline Spordiklubi
    Faculty phone: 
    737 5371
    Faculty address: 
    Ujula 4, 51008 Tartu
  • MTÜ Tartu Üliõpilasküla
    Faculty phone: 
    740 9959
    Faculty address: 
    Narva mnt 25, 51013 Tartu
  • MTÜ Tartu Üliõpilasmaja
    Faculty phone: 
    730 2400
    Faculty address: 
    Kalevi 24, Tartu
  • OÜ Tartu Ülikooli Kirjastus
    Faculty phone: 
    737 5945
    Faculty address: 
    W. Struve 1, 50091 Tartu
  • SA Tartu Ülikooli Kliinikum
    Faculty phone: 
    731 8111
    Faculty address: 
    L. Puusepa 1a, 50406 Tartu
  • Tartu Ülikooli Sihtasutus
    Faculty phone: 
    737 5852
    Faculty address: 
    Ülikooli 18a–106, Tartu

TÜ üksuste kontaktandmed

humanitaarteaduste ja kunstide valdkond
Faculty phone: 
737 5341
Faculty address: 
Jakobi 2, ruumid 116–121, 51014 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5341
    Faculty address: 
    Jakobi 2, ruumid 116–121, 51005 Tartu
  • ajaloo ja arheoloogia instituut
    Faculty phone: 
    737 5651
    Faculty address: 
    Jakobi 2, 51005 Tartu
  • eesti ja üldkeeleteaduse instituut
    Faculty phone: 
    737 5221
    Faculty address: 
    Jakobi 2, IV korrus, 51005 Tartu
  • filosoofia ja semiootika instituut
    Faculty phone: 
    737 5314
    Faculty address: 
    Jakobi 2, ruumid 309–352, 51005 Tartu
  • kultuuriteaduste instituut
    Faculty phone: 
    737 5223
    Faculty address: 
    Ülikooli 16, 51003 Tartu
  • maailma keelte ja kultuuride kolledž
    Faculty address: 
    Lossi 3, 51003 Tartu
  • usuteaduskond
    Faculty phone: 
    737 5300
    Faculty address: 
    Ülikooli 18-310, 50090 Tartu
  • Viljandi kultuuriakadeemia
    Faculty phone: 
    435 5232
    Faculty address: 
    Posti 1, 71004 Viljandi
sotsiaalteaduste valdkond
Faculty phone: 
737 5957
Faculty address: 
Lossi 36, 51003 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5900
    Faculty address: 
    Lossi 36, 51003 Tartu
  • haridusteaduste instituut
    Faculty phone: 
    737 6440
    Faculty address: 
    Salme 1a–29, 50103 Tartu
  • Johan Skytte poliitikauuringute instituut
    Faculty phone: 
    737 5582
    Faculty address: 
    Lossi 36–301, 51003 Tartu
  • majandusteaduskond
    Faculty phone: 
    737 6310
    Faculty address: 
    J. Liivi 4, 50409 Tartu
  • psühholoogia instituut
    Faculty phone: 
    737 5902
    Faculty address: 
    Näituse 2, 50409 Tartu
  • õigusteaduskond
    Faculty phone: 
    737 5390
    Faculty address: 
    Näituse 20–324, 50409 Tartu
  • ühiskonnateaduste instituut
    Faculty phone: 
    737 5188
    Faculty address: 
    Lossi 36, 51003 Tartu
  • Narva kolledž
    Faculty phone: 
    740 1900
    Faculty address: 
    Raekoja plats 2, 20307 Narva
  • Pärnu kolledž
    Faculty phone: 
    445 0520
    Faculty address: 
    Ringi 35, 80012 Pärnu
meditsiiniteaduste valdkond
Faculty phone: 
737 5326
Faculty address: 
Ravila 19, 50411 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5326
    Faculty address: 
    Ravila 19, 50411 Tartu
  • bio- ja siirdemeditsiini instituut
    Faculty phone: 
    737 4210
    Faculty address: 
    Biomeedikum, Ravila 19, 50411 Tartu
  • farmaatsia instituut
    Faculty phone: 
    737 5286
    Faculty address: 
    Nooruse 1, 50411 Tartu
  • hambaarstiteaduse instituut
    Faculty phone: 
    731 9856
    Faculty address: 
    Raekoja plats 6, 51003 Tartu
  • kliinilise meditsiini instituut
    Faculty phone: 
    737 5323
    Faculty address: 
    L. Puusepa 8, 50406 Tartu
  • peremeditsiini ja rahvatervishoiu instituut
    Faculty phone: 
    737 4190
    Faculty address: 
    Ravila 19, 50411 Tartu
  • sporditeaduste ja füsioteraapia instituut
    Faculty phone: 
    737 5360
    Faculty address: 
    Jakobi 5–205, 51005 Tartu
loodus- ja täppisteaduste valdkond
Faculty phone: 
737 5820
Faculty address: 
Vanemuise 46–208, 51005 Tartu
  • valdkonna dekanaat
    Faculty phone: 
    737 5820
    Faculty address: 
    Vanemuise 46–208, 51005 Tartu
  • arvutiteaduse instituut
    Faculty phone: 
    737 5445
    Faculty address: 
    J. Liivi 2, 50409 Tartu
  • Eesti mereinstituut
    Faculty phone: 
    671 8902
    Faculty address: 
    Mäealuse 14, 12618 Tallinn
  • füüsika instituut
    Faculty address: 
    W. Ostwaldi 1, 50411 Tartu
  • keemia instituut
    Faculty phone: 
    737 5261
    Faculty address: 
    Ravila 14a, 50411 Tartu
  • matemaatika ja statistika instituut
    Faculty phone: 
    737 5860
    Faculty address: 
    J. Liivi 2, 50409 Tartu
  • molekulaar- ja rakubioloogia instituut
    Faculty phone: 
    737 5011
    Faculty address: 
    Riia 23, 23b–134, 51010 Tartu
  • Tartu observatoorium
    Faculty phone: 
    737 4510
    Faculty address: 
    Observatooriumi 1, Tõravere, 61602 Tartumaa
  • tehnoloogiainstituut
    Faculty phone: 
    737 4800
    Faculty address: 
    Nooruse 1, 50411 Tartu
  • ökoloogia ja maateaduste instituut
    Faculty phone: 
    737 5835
    Faculty address: 
    Vanemuise 46, 51003 Tartu
Asutused
  • raamatukogu
    Faculty phone: 
    737 5702
    Faculty address: 
    W. Struve 1, 50091 Tartu
  • teaduskool
    Faculty phone: 
    737 5581
    Faculty address: 
    Uppsala 10, 51003 Tartu
  • genoomika instituut
    Faculty phone: 
    737 4000
    Faculty address: 
    Riia 23b, 51010 Tartu
  • muuseum
    Faculty phone: 
    737 5674
    Faculty address: 
    Lossi 25, 51003 Tartu
  • loodusmuuseum ja botaanikaaed
    Faculty phone: 
    737 6076
    Faculty address: 
    Vanemuise 46, 51003 Tartu
Tugiüksused
  • ettevõtlus- ja innovatsioonikeskus
    Faculty phone: 
    737 6339
    Faculty address: 
    Lossi 3, III korrus, 51003 Tartu
  • grandikeskus
    Faculty phone: 
    737 6215
    Faculty address: 
    Lossi 3, III korrus, 51003 Tartu
  • hankeosakond
    Faculty phone: 
    737 6632
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • infotehnoloogia osakond
    Faculty phone: 
    737 6000, arvutiabi: 737 5500
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • kantselei
    Faculty phone: 
    737 5606
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • kinnisvaraosakond
    Faculty phone: 
    737 5137
    Faculty address: 
    Ülikooli 18a, 51005 Tartu
  • personaliosakond
    Faculty phone: 
    737 5145
    Faculty address: 
    Ülikooli 18, ruumid 302 ja 304, 50090 Tartu
  • rahandusosakond
    Faculty phone: 
    737 5125
    Faculty address: 
    Jakobi 4, 51005 Tartu
  • rektoraadi büroo
    Faculty phone: 
    737 5600
    Faculty address: 
    Ülikooli 18, 51014 Tartu
  • siseauditi büroo
    Faculty address: 
    Ülikooli 17–103, 51005 Tartu
  • Tallinna esindus
    Faculty phone: 
    737 6600
    Faculty address: 
    Teatri väljak 3, 10143 Tallinn
  • turundus- ja kommunikatsiooniosakond
    Faculty phone: 
    737 5687
    Faculty address: 
    Ülikooli 18, ruumid 102, 104, 209, 210, 50090 Tartu
  • õppeosakond
    Faculty phone: 
    737 5620
    Faculty address: 
    Ülikooli 18, 50090 Tartu
  • üliõpilasesindus
    Faculty phone: 
    737 5400
    Faculty address: 
    Ülikooli 18b, 51005 Tartu
Muud üksused
  • MTÜ Tartu Ülikooli Akadeemiline Spordiklubi
    Faculty phone: 
    737 5371
    Faculty address: 
    Ujula 4, 51008 Tartu
  • MTÜ Tartu Üliõpilasküla
    Faculty phone: 
    740 9959
    Faculty address: 
    Narva mnt 25, 51013 Tartu
  • MTÜ Tartu Üliõpilasmaja
    Faculty phone: 
    730 2400
    Faculty address: 
    Kalevi 24, Tartu
  • OÜ Tartu Ülikooli Kirjastus
    Faculty phone: 
    737 5945
    Faculty address: 
    W. Struve 1, 50091 Tartu
  • SA Tartu Ülikooli Kliinikum
    Faculty phone: 
    731 8111
    Faculty address: 
    L. Puusepa 1a, 50406 Tartu
  • Tartu Ülikooli Sihtasutus
    Faculty phone: 
    737 5852
    Faculty address: 
    Ülikooli 18a–106, Tartu

Eesti Geenivaramu publikatsioonid 2002-2014

2017 2016 2015 2014 2013  2012 2011  2010 2009 2008 2007 2005 2004  2002
1. Allebrandt KV, Teder-Laving M, Cusumano P, Frishman G, Levandovski R, Ruepp A, Hidalgo MPL, Costa R, Metspalu A, Roenneberg T, De Pittà C. “Identifying pathways modulating sleep duration: from genomics to transcriptomics”. Scientific Reports, 2017, 7(4555). doi: 10.1038/s41598-017-04027-7.
2. Auffray, C; Sagner, M; Abdelhak, S; Adcock, I; Agusti, A; Amaral, M; Antonarakis, S; … Metspalu, A; …  Uhlen, M; van der Werf, S; Villoslada, P; Vinciguerra, M; Volpert, V; Webb, S; Wouters, E; Sanz, F; Nobrega, F. “Viva Europa, a Land of Excellence in Research and Innovation for Health and Wellbeing”.  Progress in Preventive Medicine, 2017, 2(3), p e006. doi: 10.1097/pp9.0000000000000006
3. Chheda H, Palta P, Pirinen M, McCarthy S, Walter K, Koskinen S, Salomaa V, Daly M, Durbin R, Palotie A, Aittokallio T, Ripatti S. “Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom”. Eur J Hum Genet. 2017 Feb 1. doi: 10.1038/ejhg.2016.205.
4. CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium (…Esko, T; Metspalu, A; Milani, L;  ) “Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.” Nature Genetics, 2017, 49(1):27-35. doi:10.1038/ng.3725
5. Dand N, Mucha S, Tsoi LC3, Mahil SK, Stuart PE, Arnold A, Baurecht H, Burden AD, Callis Duffin K, Chandran V, Curtis CJ, Das S, Ellinghaus D, Ellinghaus E, Enerback C, Esko T, Gladman DD, Griffiths CEM, Gudjonsson JE, Hoffman P, Homuth G, Hüffmeier U, Krueger GG, Laudes M, Lee SH, Lieb W, Lim HW, Löhr S, Mrowietz U, Müller-Nurayid M, Nöthen M, Peters A, Rahman P, Reis A, Reynolds NJ, Rodriguez E, Schmidt CO, Spain SL, Strauch K, Tejasvi T, Voorhees JJ, Warren RB, Weichenthal M, Weidinger S, Zawistowski M, Nair RP, Capon F, Smith CH, Trembath RC, Abecasis GR, Elder JT, Franke A, Simpson MA, Barker JN. “Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signaling”. Human Molecular Genetics, 2017, 26(11): 4301-4313. DOI: 10.1093/hmg/ddx328.
6. Day et al.  (Natalia Pervjakova, Reedik Mägi,  Andres Metspalu, Lili Milani). “Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk”. Nature Genetics, 2017, 49(6): 834-841. DOI:10.1038/ng.3841 Epub 2017 Apr 24
7. Direk, N; Williams, S; ….. Esko, T; ….. Metspalu, A; …Sullivan, P.  “An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype”.  Biological Psychiatry, 2017, 82(5): 322-329. https://doi.org/10.1016/j.biopsych.2016.11.013
8. Duncan L, Yilmaz Z, Gaspar H, Walters R, Goldstein J, Anttila V, Bulik-Sullivan B, Ripke S; Eating Disorders Working Group of the Psychiatric Genomics Consortium (Esko, T, Fischer, K, Männik, K, Metspalu, A.), Thornton L, Hinney A, Daly M, Sullivan PF, Zeggini E, Breen G, Bulik CM. “The American Journal of Psychiatry, 2017, 174(9): 850-858. DOI: https://doi.org/10.1176/appi.ajp.2017.16121402
9. Doucet, Marika; Karl Friedrich Becker, Jens Björkman, Jacques Bonnet, Bruno Clément, Maria-Grazia Daidone, Charles Duyckaerts, Gilles Erb, Helmuth Haslacher, Paul Hofman, Berthold Huppertz, Christophe Junot, Joakim Lundeberg, Andres Metspalu, Marialuisa Lavitrano, Jan-Eric Litton, Helen M. Moore, Manuel Morente, Ben-Youssef Naimi, Uwe Oelmueller, Bill Ollier, Barbara Parodi, Liangliang Ruan, Giorgio Stanta, Paola Turano, Jim Vaught, Peter Watson, H.-Erich Wichmann, Martin Yuille, Myriam Zaomi, Kurt Zatloukal, and Georges Daghe. “Quality Matters: 2016 Annual Conference of the National Infrastructures for Biobanking”. Biopreservation and Biobanking, 2017, 15(3), pp: 270-276. DOI: 10.1089/bio.2016.0053
10. Eichstaedt CA, Pagani L, Antao T, Inchley CE, Cardona A, Mörseburg A, Clemente FJ, Sluckin TJ, Metspalu E, Mitt M, Mägi R, Hudjashov G, Metspalu M, Mormina M, Jacobs GS, Kivisild T. “Evidence of Early-Stage Selection on EPAS1 and GPR126 Genes in Andean High Altitude Populations”.  Scientific Reports, 2017, 7(1):13042. DOI: 10.1038/s41598-017-13382-4.
11. Esko, T; Hirschhorn, J.N; Feldman HA, Hsu YH, Deik AA, Clish CB, Ebbeling CB, Ludwig DS. “Metabolomic profiles as reliable biomarkers of dietary composition”. Am J Clin Nutr. 2017, doi: 10.3945/ajcn.116.144428
12. Graff et al. (Toomas Haller, Reedik Mägi, Markus Perola, Andres Metspalu). “Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults”.   PLOS Genetics, 2017,  13(4): e1006528. DOI:10.1371/journal.pgen.1006528
13. Gorski et al. (Tõnu Esko, Andres Metspalu, Evelin, Mihailov). “1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function”. Sci. Rep. 2017, 7, 45040; doi: 10.1038/srep45040.
14. Guo, Michael H.; Satish K. Nandakumar, Jacob C. Ulirsch, Seyedeh M. Zekavat, Jason D. Buenrostro, Pradeep Natarajan, Rany M. Salem, Roberto Chiarle, Mario Mitt, Mart Kals, Kalle Pärn, Krista Fischer, Lili Milani, Reedik Mägi, Priit Palta, Stacey B. Gabriel, Andres Metspalu, Eric S. Lander, Sekar Kathiresan, Joel N. Hirschhorn, Tõnu Esko, and Vijay G. Sankaran. “Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms”. PNAS, 2017, 114(3), E327-E336, DOI: 10.1073/pnas.1619052114
15. Guha M, Saare M, Maslovskaja J, Kisand K, Liiv I, Haljasorg U, Tasa T, Metspalu A, Milani L, Peterson P. “DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes.” DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes.” The Journal of Biological Chemistry, 2017, M116.764704: 1-25. DOI: 10.1074/jbc.M116.764704.
16. Haller, Toomas; Leitsalu, Liis; Fischer, Krista; Nuotio, Marja-Liisa; Esko, Tonu; Boomsma, Dorothea Irene; Kyvik, Kirsten Ohm; Spector, Tim D; Perola, Markus; Metspalu, Andres. “MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies”. PLOS One; 2017, 12(1), e0170325, DOI:10.1371/journal.pone.0170325
17. Haller-Kikkatalo K, Alnek K, Metspalu A, Mihailov E, Metsküla K, Kisand K, Pisarev H, Salumets A, Uibo R. “Demographic associations for autoantibodies in disease-free individuals of a European population”. Sci Rep. 2017; 7:44846. doi: 10.1038/srep44846.
18. Hulmi JJ, Isola V, Suonpää M, Järvinen NJ, Kokkonen M, Wennerström A, Nyman K, Perola M, Ahtiainen JP, Häkkinen K. “The Effects of Intensive Weight Reduction on Body Composition and Serum Hormones in Female Fitness Competitors”. Front. Physiol. 2017. 7:689. doi: 10.3389/fphys.2016.00689
19. Joshi, PK; Pirastu, N; Kentistou, KA; Fischer, K; … Reedik Mägi, Lili Milani, Andres Metspalu… Esko, T; Kutalik, Z and Wilson JF. “Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity”.  Nature Communications, 2017, 8(1): 910. DOI: 10.1038/s41467-017-00934-5.
20. Justice et al. (Krista Fischer, Natalia Pervjakova, Tõnu Esko, Andres Metspalu, Andrew P. Morris). “Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits”.  Nature Communications, 2017, 8, pp: 14977. DOI:10.1038/ncomms14977
21. Kaakinen M, Mägi R, Fischer K, Heikkinen J, Järvelin MR, Morris AP, Prokopenko I. “MARV: a tool for genome-wide multi-phenotype analysis of rare variants.” BMC Bioinformatics. 2017;18(1):110. doi: 10.1186/s12859-017-1530-2.
22. Kaakinen M, Mägi R, Fischer K, Heikkinen J, Järvelin MR, Morris AP, Prokopenko I. “A rare-variant test for high-dimensional data”.  European Journal of Human Genetics, 2017. 25(8): 988-994. doi: 10.1038/ejhg.2017.90
23. Klaeger, Susan ; Stephanie Heinzlmeir, Mathias Wilhelm, Harald Polzer, Binje Vick, Paul-Albert Koenig, Maria Reinecke, Benjamin Ruprecht, Svenja Petzoldt, Chen Meng, Jana Zecha, Katrin Reiter, Huichao Qiao, Dominic Helm, Heiner Koch, Melanie Schoof, Giulia Canevari, Elena Casale, Stefania Re Depaolini, Annette Feuchtinger, Zhixiang Wu, Tobias Schmidt, Lars Rueckert, Wilhelm Becker, Jan Huenges, Anne-Kathrin Garz, Bjoern-Oliver Gohlke, Daniel Paul Zolg, Gian Kayser, Tonu Vooder, Robert Preissner, Hannes Hahne, Neeme Tõnisson, Karl Kramer, Katharina Götze, Florian Bassermann, Judith Schlegl, Hans-Christian Ehrlich, Stephan Aiche, Axel Walch, Philipp A. Greif, Sabine Schneider, Eduard Rudolf Felder, Juergen Ruland, Guillaume Médard, Irmela Jeremias, Karsten Spiekermann and Bernhard Kuster. “The target landscape of clinical kinase drugs”. Science, 2017:  358 (6367), eaan4368. DOI: 10.1126/science.aan4368
24. Kantojärvi K, Liuhanen J, Saarenpää-Heikkilä O, Satomaa AL, Kylliäinen A, Pölkki P, Jaatela J, Toivola A, Milani L, Himanen SL, Porkka-Heiskanen T, Paavonen J, Paunio T. “Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants.” PLos One 2017, 12(8): e0180652. DOI: 10.1371/journal.pone.0180652
25. Kasela S, Kisand K, Tserel L, Kaleviste E, Remm A, Fischer K, Esko T, Westra HJ, Fairfax BP, Makino S, Knight JC, Franke L, Metspalu A, Peterson P, Milani L. “Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells.” PLoS Genet. 2017;13(3): e1006643. doi: 10.1371/journal.pgen.1006643
26. Kerminen S, Havulinna AS, Hellenthal G, Martin AR, Sarin AP, Perola M, Palotie A, Salomaa V, Daly MJ, Ripatti S, Pirinen M. “Fine-Scale Genetic Structure in Finland”. G3 (Genes/Genomes/Genetics), 2017, 7(10): 3459-3468. DOI: 10.1534/g3.117.300217.
27. Koel, Mariann, Urmo Võsa, Kaarel Krjutškov, Elisabet Einarsdottir, Juha Kere, Juha Tapanainen, Shintaro Katayama, Sulev Ingerpuu, Viljar Jaks, Ulf-Hakan Stenman, Karolina Lundin, Timo Tuuri, Andres Salumets. “Optimizing bone morphogenic protein 4-mediated human embryonic stem cell differentiation into trophoblast-like cells using fibroblast growth factor 2 and transforming growth factor-β/activin/nodal signalling inhibition”. Science Direct. Reproductive BioMedicine Online, 2017, https://doi.org/10.1016/j.rbmo.2017.06.003
28. Kukushkina V, Modhukur V, Suhorutšenko M, Peters M, Mägi R, Rahmioglu N, Velthut-Meikas A, Altmäe S, Esteban FJ, Vilo J, Zondervan K, Salumets A, Laisk-Podar T. “DNA methylation changes in endometrium and correlation with gene expression during the transition from pre-receptive to receptive phase”. Scientific Reports, 2017, 7(3916), doi: 10.1038/s41598-017-03682-0
29. Kõks, G; Fischer, K; Kõks, S. “Smoking-related general and cause-specific mortality in Estonia”. BMC Public Health (2017), 18:34. doi: 10.1186/s12889-017-4590-3 
30. Kääriäinen, H; Muilu, J; Perola, M; Kristiansson, K. “Genetics in an isolated population like Finland: a different basis for genomic medicine?” J Community Genet, 2017, 8(4): 319-326. DOI: 10.1007/s12687-017-0318-4.
31. Leitsalu, L and Metspalu, A. “ From Biobanking to Precision Medicine: The Estonian Experience. “ Genomic and Precision Medicine. Foundations, Translation, and Implementation. Third Editon. Ed. by G.S. Ginsburg, H.F. Willard. Elsever, 2017. ISBN: 978-0-12-800681-8.
32. Lepik, K; Annilo, T; Kukuškina, V; eQTLGen Consortium; Kisand, K; Kutalik, Z; Peterson, P, Peterson, H. “C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis”. PLoS Comput. Biol. 2017, 13(9): e1005766. DOI: 10.1371/journal.pcbi.1005766.
33. Li M, Li Y, Weeks O, Mijatovic V, Teumer A, Huffman JE, Tromp G, Fuchsberger C, Gorski M, ..., Mägi R, Malerba G, Mihailov E…, Esko T, ..., Metspalu A, Mitchell P, Nauck M, Nürnberg P, Orho-Melander M, Parsa A, Pedersen O, Peters A, Peters U, Polasek O, Porteous D, Probst-Hensch NM, Psaty BM, Qi L, Raitakari OT, Reiner AP, Rettig R, Ridker PM, Rivadeneira F, Rossouw JE, Schmidt F, Siscovick D, Soranzo N, Strauch K, Toniolo D, Turner ST, Uitterlinden AG, Ulivi S, Velayutham D, Völker U, Völzke H, Waldenberger M, Wang JJ, Weir DR, Witte D, Kuivaniemi H, Fox CS, Franceschini N, Goessling W, Köttgen A, Chu AY. “SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function”. J Am Soc Nephrol. 2017; 28(3): 981-994. doi: 10.1681/ASN.2016020131
34. Li, Dong; Chang, Xio (… ) Eating Disorders Working Group of the Psychiatric Genomics Consortium (… Tõnu Esko, Krista Fischer, Katrin Männik, Andres Metspalu…). “A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling”. Scientific Reports, 2017,  7(3847), doi: 10.1038/s41598-017-01674-8
35. Liu DJ, Peloso GM, … Tõnu Esko, … Howson JMM, Danesh J, McCarthy MI, Cowan CA, Abecasis G, Deloukas P, Musunuru K, Willer CJ, Kathiresan S.  “Exome-wide association study of plasma lipids in > 300,000 individuals”.  Nature Genetics, 2017, 49(12): 1758-1766. DOI: 10.1038/ng.3977 
36. Lloyd-Jones LR, Holloway A, McRae A, Yang J, Small K, Zhao J, Zeng B, Bakshi A, Metspalu A, Dermitzakis M, Gibson G, Spector T, Montgomery G, Esko T, Visscher PM, Powell JE. “The Genetic Architecture of Gene Expression in Peripheral Blood.” Am J Hum Genet. 2017;100(2):371. doi: 10.1016/j.ajhg.2017.01.026.
37. Lokki, AI; Emma Daly, Michael Triebwasser, Mitja I. Kurki, Elisha D.O. Roberson, Paavo Häppölä, Kirsi Auro, Markus Perola, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Jane E. Salmon, Seppo Meri, Mark Daly, John P. Atkinson, Hannele Laivuori. “Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population”. Hypertension, 2017. 70(2): 365-371. 
38. Loviglio MN, Leleu M, Männik K, Passeggeri M, Giannuzzi G, van der Werf I, Waszak SM, Zazhytska M, Roberts-Caldeira I, Gheldof N, Migliavacca E, Alfaiz AA, Hippolyte L, Maillard AM; 2p15 Consortium; 16p11.2 Consortium (… Andres Metspalu…), Van Dijck A, Kooy RF, Sanlaville D, Rosenfeld JA, Shaffer LG, Andrieux J, Marshall C, Scherer SW, Shen Y, Gusella JF, Thorsteinsdottir U, Thorleifsson G, Dermitzakis ET, Deplancke B, Beckmann JS, Rougemont J, Jacquemont S, Reymond A. “Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes”. Molecular Psychiatry, 2017, 22: 836-849. doi: 10.1038/mp.2016.84
39. Lukowski SW, Lloyd-Jones LR, Holloway A, Kirsten H, Hemani G, Yang J, Small K, Zhao J, Metspalu A, Dermitzakis ET, Gibson G, Spector TD, Thiery J, Scholz M, Montgomery GW, Esko T, Visscher PM, Powell JE. “Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood.” Nature Communications, 2017, 8(1): 483. DOI: 10.1038/s41467-017-00473-z.
40. Läll, Kristi; Mägi, Reedik; Morris, Andrew P; Metspalu, Andres; Fischer, Krista. “Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores”. Genetics in Medicine, 2017, 19(3): 322-329. DOI: 10.1038/gim.2016.103 (Raporteeritud 2016)
41. Mace, A; Tuke, MA; Deelen, P; Kristiansson, K; Mattsson, H; Margit Nõukas, ... Reedik Mägi, Markus Perola, Katrin Männik, Andres Metspalu, ... Reymond, A; Frayling, TM & Kutalik, Z. “CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric trits”.  Nature Communications, 2017, 8(1): 744. DOI: 10.1038/s41467-017-00556-x.
42. Manning A, Highland HM, Gasser J, Sim X, Tukiainen T, Fontanillas P, Grarup N, Rivas MA, Mahajan A, Locke AE, Cingolani P, Pers TH, … Esko T, Mägi R, Milani L, Mihailov E, Metspalu A, …Morris AP, Boehnke M, Altshuler D, McCarthy MI, Gloyn AL, Lindgren CM. “A low-frequency inactivating AKT2 variant enriched in the Finnish population is associated with fasting insulin levels and type 2 diabetes risk. “  Diabetes 2017, 66(7): 2019-2031. https://doi.org/10.2337/db16-1329
43. Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM, Rüeger S, Thorleifsson G, Justice AE, Lamparter D, Stirrups KE, Turcot V, Young KL, Winkler TW, Esko T, ..., Metspalu A, ... EPIC-InterAct Consortium; CHD Exome+ Consortium; ExomeBP Consortium; T2D-Genes Consortium; GoT2D Genes Consortium; Global Lipids Genetics Consortium; ReproGen Consortium; MAGIC Investigators, Rotter JI, Boehnke M, Kathiresan S, McCarthy MI, Willer CJ, Stefansson K, Borecki IB, Liu DJ, North KE, Heard-Costa NL, Pers TH, Lindgren CM, Oxvig C, Kutalik Z, Rivadeneira F, Loos RJ, Frayling TM, Hirschhorn JN, Deloukas P, Lettre G. “Rare and low-frequency coding variants alter human adult height.” Nature. 2017; 542(7640): 186-190. doi: 10.1038/nature21039
44. McLaughlin et al. (Schizophrenia Working Group of the Psychiatric Genomics Consortium: … Andres  Metspalu, Lili Milani, Mari Nelis, Tõnu Esko…). “Genetic correlation between amyotrophic lateral sclerosis and schizophrenia”. Nature Communications, 2017, 8, 14774. doi: 10.1038/ncomms14774
45. Mitt M, Kals M, Pärn K, Gabriel SB, Lander ES, Palotie A, Ripatti S, Morris AP, Metspalu A, Esko T, Mägi R, Palta P. “Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel.” Eur J Hum Genet. 2017 Apr 12. doi: 10.1038/ejhg.2017.51
46. Mägi, Reedik, Yury V. Suleimanov, Geraldine M. Clarke, Marika Kaakinen, Krista Fischer, Inga Prokopenko and Andrew P. Morris. “SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes”.  BMC Bioinformatics, 2017, 18(25). DOI: 10.1186/s12859-016-1437-3
47. Mägi, R;  Horikoshi, M; Sofer, T; Mahajan, A; Kitajima, H; Franceschini, N; McCarthy, MI; Morris, AP. Group Author(s): COGENT- Kidney Consortium ; T2D- GENES Consortium. “Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution”.  Human Molecular Genetics,  2017, 26(18): 3639-3650. DOI: 
48. Mõttus, R; Realo, A; Vainik, U; Allik, J and Esko, T. “Educational Attainment and Personality Are Genetically Intertwined”.  Psychological Science, 2017, 28(11): 1631-1639. https://doi.org/10.1177/0956797617719083
49. NCD Risk Factor Collaboration (NCD-RisC) …Krista Fischer:.. “Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19·1 million participants”. The Lancet. 2017, 389(10065), pp: 37-55. http://dx.doi.org/10.1016/S0140-6736(16)31919-5
50. Nath AP, Ritchie SC, Byars SG, Fearnley LG, Havulinna AS, Joensuu A, Kangas AJ, Soininen P, Wennerström A, Milani L, Metspalu A, Männistö S, Würtz P, Kettunen J, Raitoharju E, Kähönen M1 Juonala M, Palotie A, Ala-Korpela M, Ripatti S, Lehtimäki T, Abraham G, Raitakari O, Salomaa V, Perola M, Inouye M.  “An interaction map of circulating metabolites, immune gene networks, and their genetic regulation”. Genome Biology, 2017, 18:146. DOI: 10.1186/s13059-017-1279-y 
51. Nelson CP, Goel A, Butterworth AS, Kanoni S, Webb TR, Marouli E7,, Zeng L, Ntalla I, Lai FY, Hopewell JC, Giannakopoulou O, Jiang T, Hamby SE, Di Angelantonio E, Assimes TL, Bottinger EP, Chambers JC, Clarke R, Palmer CNA, Cubbon RM, Ellinor P, Ermel R, Evangelou E, Franks PW, Grace C, Gu D, Hingorani AD, Howson JMM, Ingelsson E, Kastrati A, Kessler T, Kyriakou T, Lehtimäki T, Lu X, Lu Y, März W, McPherson R, Metspalu A, Pujades-Rodriguez M, Ruusalepp A, Schadt EE, Schmidt AF, Sweeting MJ, Zalloua PA, AlGhalayini K, Keavney BD, Kooner JS, Loos RJF, Patel RS, Rutter MK, Tomaszewski M, Tzoulaki I, Zeggini E, Erdmann J, Dedoussis G, Björkegren JLM; EPIC-CVD Consortium; CARDIoGRAMplusC4D; UK Biobank CardioMetabolic Consortium CHD working group, Schunkert H, Farrall M, Danesh J, Samani NJ, Watkins H, Deloukas P. “Association analyses based on false discovery rate implicate new loci for coronary artery disease”. Nature Genetics 2017, 49(9); 1385-1391. DOI: 10.1038/ng.3913.
52. Org E, Blum Y, Kasela S, Mehrabian M, Kuusisto J, Kangas AJ, Soininen P, Wang Z, Ala-Korpela M, Hazen SL, Laakso M, Lusis AJ. “Relationships between gut microbiota, plasma metabolites, and metabolic syndrome traits in the METSIM cohort.” Genome Biology 2017, 18:70 pp:1-14.  DOI: 10.1186/s13059-017-1194-2
53. Pappa, L; Kals, M; Kivistik, P-A; Metspalu, A; Paal, A; Nikopensius, T. “Exome analysis in an Estonian multiplex family with neural tube defects—a case report”.  Child’s Nervous System, 2017, 33(9): 1575-1581. doi: 10.1007/s00381-017-3491-1
54. Pirastu N, Joshi PK, de Vries PS, Cornelis MC, McKeigue PM, Keum N, Franceschini N, Colombo M, Giovannucci EL7, Spiliopoulou A, Franke L, North KE, Kraft P, Morrison AC, Esko T, Wilson JF. “GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk”.  Nature Communications, 2017; 8(1): 1584. doi: 10.1038/s41467-017-01490-8.
55. Reisberg, S; Iljasenko, T; Läll, K; Fischer, K; Vilo, J. “Comparing distributions of polygenic risk scores of type 2 diabetes and coronary heart disease within different populations”, PLoS ONE, 2017.  12(7), e0179238. doi: 10.1371/journal.pone.0179238
56. Robinson, MR; … Tõnu Esko, Lili Milani, Reedik Mägi, Andres Metspalu… Visscher, PM.  “Genotype-covariate interaction effects and the heritability of adult body mass index”. Nature Genetics, 2017, 49(8): 1174-1181. doi: 10.1038/ng.3912
57. Schumann G, Liu C, O'Reilly P, Gao H, Song P, Xu B, Ruggeri B, Amin N, Jia T, Preis S, Segura Lepe M, Akira S, Barbieri C, Baumeister S, Cauchi S, Clarke TK, Enroth S, Fischer K, …, Mangelsdorf DJ, Müller CP, Levy D, Elliott P. “KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.” PNAS, 2016. 113(50): 14372-14372. DOI: 10.1073/pnas.1611243113
58. Schormair, B; … Teder-Laving, M; Metspalu, A; ….Perola, M; …Winkelmann, J. “Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis “. Lancet Neurology,  2017, 16(11): 898-907. https://doi.org/10.1016/S1474-4422(17)30327-7
59. Scott RA, Scott LJ, Mägi R, Marullo L, Gaulton KJ, Kaakinen M, Pervjakova N, …, Esko T, Mihailov E, …, Metspalu A, Morris AD, Palmer CN, Hu FB, Thorsteinsdottir U, Stefansson K, Dupuis J, Morris AP, Boehnke M, McCarthy MI, Prokopenko I; DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium. “An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.” Diabetes, 2017,  66(11): 2888-2902. doi: 10.2337/db16-1253 
60. Shungin D, Deng WQ, Varga TV, Luan J, Mihailov E, Metspalu A; GIANT Consortium, Morris AP, Forouhi NG, Lindgren C, Magnusson PKE, Pedersen NL, Hallmans G, Chu AY, Justice AE, Graff M, Winkler TW, Rose LM, Langenberg C, Cupples LA, Ridker PM, Wareham NJ, Ong KK, Loos RJF, Chasman DI, Ingelsson E, Kilpeläinen TO, Scott RA, Mägi R, Paré G, Franks PW. “Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions”. PLoS Genet. 2017, 13(6): e1006812. doi: 10.1371/journal.pgen.1006812
61. Zeng, Biao; Lloyd-Jones, Luke R; Holloway, Alexander; Marigorta, Urko M; Metspalu, Andres; Montgomery, Grant W; Esko, Tõnu; Brigham, Kenneth L; Quyyumi, Arshed A; Idaghdour, Youssef; Yang, Jian; Visscher, Peter M; Powell, Joseph E; Gibson, Greg. “Constraints on eQTL Fine Mapping in the Presence of Multi-site Local Regulation of Gene Expression”. G3: GENES, GENOMES, GENETICS, 2017, doi: 10.1534/g3.117.043752
62. Zillikens, M. C. .. Markus Perola ... et al. “Large meta-analysis of genome-wide association studies identifies five loci for lean body mass”. Nature Communications, 2017, 8:80. doi: 10.1038/s41467-017-00031-7
63. Tamm R, Mägi R, Tremmel R, Winter S, Mihailov E, Smid A, Möricke A, Klein K, Schrappe M, Stanulla M, Houlston R, Weinshilboum R, Mlinarič Raščan I, Metspalu A, Milani L, Schwab M, Schaeffeler E. “Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.” Clin Pharmacol Ther. 2017, 101(5): 684-695. doi: 10.1002/cpt.540
64. Tachmazidou I, Süveges D, Min JL, Ritchie GRS, Steinberg J, Walter K, Iotchkova V, ... SpiroMeta Consortium; GoT2D Consortium, Burton P, Chambers JC, Smith GD, Dedoussis G, Felix JF, Franco OH, Gambaro G, Gasparini P, Hammond CJ, Hofman A, Jaddoe VWV, Kleber M, Kooner JS, Perola M, Relton C, Ring SM, Rivadeneira F, Salomaa V, Spector TD, Stegle O, Toniolo D, Uitterlinden AG; arcOGEN Consortium; Understanding Society Scientific Group; UK10K Consortium, Barroso I, Greenwood CMT, Perry JRB, Walker BR, Butterworth AS, Xue Y, Durbin R, Small KS, Soranzo N, Timpson NJ, Zeggini E. “Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits”.  Am J Hum Genet. 2017, 100(6): 865-884. doi: 10.1016/j.ajhg.2017.04.014
65. Tillmann T, Vaucher J, Okbay A, Pikhart H, Peasey A, Kubinova R, Pajak A, Tamosiunas A, Malyutina S, Hartwig FP, Fischer K, Veronesi G, Palmer T, Bowden J, Davey Smith G, Bobak M, Holmes MV. “Education and coronary heart disease: mendelian randomisation study.” BMJ 2017, 358(j3542): 1-10. DOI: 10.1136/bmj.j3542
66. Urgard, E; Brjalin, A; Langel, Ü; Pooga, M; Rebane, A, and Annilo, T. “Comparison of Peptide- and Lipid-Based Delivery of miR-34a-5p Mimic into PPC-1 Cells”. Nucleic Acid Therapeutics, 2017, 27(5): 295-302. DOI: 10.1089/nat.2017.0670.
67. Urgard, Egon; Reigo, Anu; Reinmaa, Eva; Rebane, Ana; Metspalu, Andres. “Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model.” Cancer Cell Int. 2017; 17:18. doi: 10.1186/s12935-017-0394-x. eCollection 2017.
68. Vals MA, Pajusalu S, Kals M, Mägi R, Õunap K. (2017) The Prevalence of PMM2-CDG in Estonia Based on Population Carrier Frequencies and Diagnosed Patients. In: . JIMD Reports. Springer, Berlin, Heidelberg. pp 1-5. DOI: https://doi.org/10.1007/8904_2017_41
69. Wahl S, Drong A, Lehne B, Loh M, Scott WR, Kunze S, Tsai PC, Ried JS, Zhang W, Yang Y, Tan S, Fiorito G, Franke L, Guarrera S, Kasela S, ... Fischer K, ... Pervjakova N, ... Milani L, van der Harst P, Peters A, Illig T, Relton CL, Waldenberger M, Järvelin MR, Bollati V, Soong R, Spector TD, Scott J, McCarthy MI, Elliott P, Bell JT, Matullo G, Gieger C, Kooner JS, Grallert H, Chambers JC. “Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity”. Nature 2017, 541(7635). 81-86. doi: 10.1038/nature20784
70. Wain LV, Vaez A, Jansen R, Joehanes R, van der Most PJ, Erzurumluoglu AM, O'Reilly PF, Cabrera CP, Warren HR, Rose LM, Verwoert GC, Hottenga JJ, Strawbridge RJ, Esko T, … Metspalu A, Ingelsson E, Boomsma DI, Franco OH, Bochud M, Newton-Cheh C, Munroe PB, Elliott P, Chasman DI, Chakravarti A, Knight J, Morris AP, Levy D, Tobin MD, Snieder H, Caulfield MJ, Ehret GB. “Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney”. Hypertensoin 2017, pii: HYPERTENSIONAHA.117.09438. doi: 10.1161/HYPERTENSIONAHA.117.09438
71. Wang et al. (Tõnu Vooder, Kristjan Välk, Mari Nelis, Andres Metspalu). Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
Nat. Genet. 46, 736–741 (2014); published online 1 June 2014; corrected after print 23 January 2017. doi:10.1038/ng0417-651a
72. Warren HR, Evangelou E, Cabrera CP, Gao H, Ren M, Mifsud B, Ntalla I, Surendran P, Liu C, Cook JP, Kraja AT, Drenos F, Loh M, Verweij N, Marten J, Karaman I, Lepe MP, O'Reilly PF, Knight J, Snieder H, Kato N, He J, Tai ES, Said MA, Porteous D, Alver M, Poulter N, Farrall M, Gansevoort RT, Padmanabhan S, Mägi R, Stanton A, Connell J, Bakker SJ, Metspalu A, Shields DC, Thom S, Brown M, Sever P, Esko T, Hayward C, van der Harst P, Saleheen D, Chowdhury R, Chambers JC, Chasman DI, Chakravarti A, Newton-Cheh C, Lindgren CM, Levy D, Kooner JS, Keavney B, Tomaszewski M, Samani NJ, Howson JM, Tobin MD, Munroe PB, Ehret GB, Wain LV; International Consortium of Blood Pressure (ICBP) 1000G Analyses; BIOS Consortium; Lifelines Cohort Study; Understanding Society Scientific group; CHD Exome+ Consortium; ExomeBP Consortium; T2D-GENES Consortium; GoT2DGenes Consortium; Cohorts for Heart and Ageing Research in Genome Epidemiology (CHARGE) BP Exome Consortium; International Genomics of Blood Pressure (iGEN-BP) Consortium; UK Biobank CardioMetabolic Consortium BP working group. “Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.” Nature Genetics, 2017, 49(3): 403-415. DOI: 10.1038/ng.3768.
73. Webb TR, Erdmann J, Stirrups KE, Stitziel NO, Masca NG, Jansen H, Kanoni S, Nelson CP, ... Esko T, Mihailov E, Escher SA, Alver M, ..., Metspalu A, Palmer CN, Peters A, Rader DJ, Reilly MP, Loos RJ, Reiner AP, Roden DM, Tardif JC, Thompson JR, Wareham NJ, Watkins H, Willer CJ, Samani NJ, Schunkert H, Deloukas P, Kathiresan S; Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators. “Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.” J Am Coll Cardiol. 2017, 69(7): 823-836. doi: 10.1016/j.jacc.2016.11.056.
74. Winsvold BS1, Palta P, Eising E, Page CM; International Headache Genetics Consortium, van den Maagdenberg AM, Palotie A, Zwart JA. “Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study”. Cephalalgia. 2017 Jan 1:333102417690111. doi: 10.1177/0333102417690111. [Epub ahead of print]
75. Xue Y, Mezzavilla M, Haber M, McCarthy S, Chen Y, Narasimhan V, Gilly A, Ayub Q, Colonna V, Southam L, Finan C, Massaia A, Chheda H, Palta P, Ritchie G, Asimit J, Dedoussis G, Gasparini P, Palotie A, Ripatti S, Soranzo N, Toniolo D, Wilson JF, Durbin R, Tyler-Smith C, Zeggini E. “Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations”.  Nature Communications, 2017, 8(15927): 1-7. DOI: 10.1038/ncomms15927.
1. Amin N, Allebrandt KV, van der Spek A, Müller-Myhsok B, Hek K, Teder-Laving M, Hayward C, Esko T, ... Mihailov E, ... Metspalu A, Meitinger T, Franke L, Roenneberg T, van Duijn CM. “Genetic variants in RBFOX3 are associated with sleep latency.”  Eur J Hum Genet. 2016; 24(10): 1488-95.  doi: 10.1038/ejhg.2016.31.
2. Barban N, Jansen R, de Vlaming R, Vaez A, Mandemakers JJ, Tropf FC, Shen X, Wilson JF, ... Esko T, , Mihailov E, Metspalu A, Traglia M, Milani L, Perola M, … Koellinger PD, den Hoed M, Snieder H, Mills MC. “Genome-wide analysis identifies 12 loci influencing human reproductive behavior”.  Nature Genetics 2016, 48(12): 1462-1472. doi: 10.1038/ng.3698
3. Bentham, J; et al. NCD Risk Factor Collaboration (NCD-RisC)(... Krista Fischer, Andres Metspalu, Kairit Mikkel, Mari-Liis Tammesoo...).  “A century of trends in adult human height”. ELIFE, 2016, 5(e13410).  DOI: http://dx.doi.org/10.7554/eLife.13410.001
4. Bigdeli TB, Ripke S, Bacanu SA, Lee SH, Wray NR, Gejman PV, Rietschel M, Cichon S, St Clair D, Corvin A, Kirov G, McQuillin A, Gurling H, Rujescu D, Andreassen OA, Werge T, Blackwood DH, Pato CN, Pato MT, Malhotra AK, O'Donovan MC, Kendler KS, Fanous AH; Schizophrenia Working Group of the Psychiatric Genomics Consortium (… Andres Metspalu, Lili Milani, Tõnu Esko …). “Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.” Am J Med Genet B Neuropsychiatr Genet. 2016; 171(2): 276-289. doi: 10.1002/ajmg.b.32402
5. Cáceres A, Esko T, Pappa I, Gutiérrez A, Lopez-Espinosa MJ, Llop S, Bustamante M, Tiemeier H, Metspalu A, Joshi PK, Wilsonx JF, Reina-Castillón J10, Shin J, Pausova Z, Paus T, Sunyer J, Pérez-Jurado LA, González JR. “Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence.” PLoS One 2016; 11(6): e0157739. doi: 10.1371/journal.pone.0157739
6. Chami N, Chen MH, Slater AJ, Eicher JD, Evangelou E, Tajuddin SM, Love-Gregory L, ... Mihailov E,  Mägi R,, Metspalu A, ... Esko T, Loos RJ, Lange LA, Faraday N, Abumrad NA, Edwards TL, Ganesh SK, Auer PL, Johnson AD, Reiner AP, Lettre G. “Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.” Am J Hum Genet. 2016; 99(1):8-21. doi: 10.1016/j.ajhg.2016.05.007
7. D'Angelo D, Lebon S, Chen Q, Martin-Brevet S, Snyder LG, Hippolyte L, Hanson E, ... Männik K, Metspalu A, ... Reymond A, Jacquemont S, Chung WK; Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study, the 16p11.2 European Consortium, and the Simons Variation in Individuals Project (VIP) Consortium. “Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities”. JAMA Psychiatry, 2016, 73(1):20-30. doi: 10.1001/jamapsychiatry.2015.2123.
8. Degenhardt F, Niklowitz P, Szymczak S, Jacobs G, Lieb W, Menke T, Laudes M, Esko T, Weidinger S, Franke A, Döring F, Onur S. “Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases”. Human Molecular Genetics, 2016. DOI: 10.1093/hmg/ddw134
9. NCD Risk Factor Collaboration (NCD-RisC) (...Krista Fischer, Andres Metspalu, Kairit Mikkel, Mari-Liis Tammesoo... ), Di Cesare M, Bentham J, Stevens GA, Zhou B, Danaei G, Lu Y, Bixby H, Cowan MJ, Riley LM, Hajifathalian K, Fortunato L, Taddei C, Bennett JE, Ikeda N, Khang YH, Kyobutungi C, Laxmaiah A, Li Y, Lin HH, Miranda JJ, Mostafa A, Turley ML, Paciorek CJ, Gunter M, Ezzati M. “Trends in adult body-mass index in 200 countries from 1975 to 2014: a pooled analysis of 1698 population-based measurement studies with 19·2 million participants”. Lancet. 2016; 387(10026): 1377-1396. doi: 10.1016/S0140-6736(16)30054-X.
10. Ehret GB, Ferreira T, Chasman DI, Jackson AU, Schmidt EM, Johnson T, Thorleifsson G, … Esko T, Metspalu A, Perola M, ... Franks PW, Hamsten A, Wichmann HE, Palmer CN, Stefansson K, Ridker PM, Loos RJ, Chakravarti A, Deloukas P, Morris AP, Newton-Cheh C, Munroe PB. “The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.” Nat Genet. 2016 Oct; 48(10):1171-84. doi: 10.1038/ng.3667
11. Eicher JD, Chami N, Kacprowski T, Nomura A, Chen MH, Yanek LR, Tajuddin SM, Schick UM, ... Mihailov E, Mägi R, Hirschhorn J, Metspalu A, Esko T, ... Uitterlinden AG, Franco OH, Dehghan A, Edwards TL, Ganesh SK, Kathiresan S, Faraday N, Auer PL, Reiner AP, Lettre G, Johnson AD. “Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals”. Am J Hum Genet. 2016;99(1):40-55. doi: 10.1016/j.ajhg.2016.05.005.
12. Ellinghaus D, Jostins L, Spain SL, Cortes A, Bethune J, Han B, Park YR, Raychaudhuri S, … Esko T, Metspalu A, … International IBD Genetics Consortium (IIBDGC); International Genetics of Ankylosing Spondylitis Consortium (IGAS); International PSC Study Group (IPSCSG); Genetic Analysis of Psoriasis Consortium (GAPC); Psoriasis Association Genetics Extension (PAGE), Schreiber S, Mrowietz U, Juran BD, Lazaridis KN, Brunak S, Dale AM, Trembath RC, Weidinger S, Weichenthal M, Ellinghaus E, Elder JT, Barker JN, Andreassen OA, McGovern DP, Karlsen TH, Barrett JC, Parkes M, Brown MA, Franke A. “Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.” Nat Genet. 2016; 48(5):510-8. doi: 10.1038/ng.3528.
13. Elosua R, Lluís-Ganella C, Subirana I, Havulinna A, Läll K, Lucas G, Sayols-Baixeras S, Pietilä A, Alver M, Cabrera de León A, Sentí M, Siscovick D, Mellander O, Fischer K, Salomaa V, Marrugat J. “Cardiovascular Risk Factors and Ischemic Heart Disease: Is the Confluence of Risk Factors Greater Than the Parts? A Genetic Approach.”  Circ Cardiovasc Genet. 2016 Jun; 9(3):279-86. doi: 10.1161/CIRCGENETICS.115.001255.
14. Fan Q, Guo X, Tideman JW, Williams KM, Yazar S, Hosseini SM, Howe LD, Pourcain BS, Evans DM, Timpson NJ, McMahon G, Hysi PG, Krapohl E, Wang YX, Jonas JB, Baird PN, Wang JJ, Cheng CY, Teo YY, Wong TY, Ding X, Wojciechowski R, Young TL, Pärssinen O, Oexle K, Pfeiffer N, Bailey-Wilson JE, Paterson AD, Klaver CC, Plomin R, Hammond CJ, Mackey DA, He M, Saw SM, Williams C, Guggenheim JA; CREAM Consortium (…. Andres Metspalu, Evelin Mihailov, Toomas Haller…). “Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium.” Sci Rep. 2016; 6:25853. doi: 10.1038/srep25853.
15. Fan Q, Verhoeven VJ, Wojciechowski R, Barathi VA, Hysi PG, Guggenheim JA, Höhn R, Vitart V, Khawaja AP, Yamashiro K, Hosseini SM, Lehtimäki T, Lu Y, Haller T, ... Mihailov E, ... Metspalu A, ... Farrer L, Zhou X, Chen W, Mizuki N, Meguro A, Mäkelä KM. “Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error”. Nature Communications 7, Article number: 11008 (2016). doi: 10.1038/ncomms11008
16. Franke, B; Stein, JL; Ripke, S; Anttila, V; Hibar, DP; van, Hulzen, KJ; Arias-Vasquez, A; Smoller, JW; Nichols, TE; Neale, MC; McIntosh, AM; Lee, P; McMahon, FJ; Meyer-Lindenberg, A; Mattheisen, M; Andreassen, OA; Gruber, O; Sachdev, PS; Roiz-Santiañez, R; Saykin, AJ; Ehrlich, S; Mather, KA; Turner, JA; Schwarz, E; Thalamuthu, A; Yao, Y; Ho, YY; Martin, NG; Wright, MJ;, Schizophrenia, Working, Group, of, the, Psychiatric, Genomics, Consortium; Psychosis, Endophenotypes, International, Consortium; Wellcome, Trust, Case, Control, Consortium, 2; Enigma, Consortium; O'Donovan, MC; Thompson, PM; Neale, BM; Medland, SE; Sullivan, PF .“Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept”.  Nature Neuroscence 2016; 19(3):420-31. doi: 10.1038/nn.4228. 
17. Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, ...  Esko T, … Milani L, Mihailov E, ... Metspalu A, ... Mägi R, Abecasis G, Florez JC, Scott LJ, Morris AP, Kang HM, Boehnke M, Altshuler D, McCarthy MI. “The genetic architecture of type 2 diabetes.” Nature, 2016, 536(7614):41-47. doi: 10.1038/nature18642. 
18. Ganna A, Genovese G, Howrigan DP, Byrnes A, Kurki MI, Zekavat SM, Whelan CW, Kals M, Nivard MG, Bloemendal A, Bloom JM, Goldstein JI, Poterba T, Seed C, Handsaker RE, Natarajan P, Mägi R, Gage D, Robinson EB, Metspalu A, Salomaa V, Suvisaari J, Purcell SM, Sklar P, Kathiresan S, Daly MJ, McCarroll SA, Sullivan PF, Palotie A, Esko T, Hultman CM, Neale BM. “Ultra-rare disruptive and damaging mutations influence educational attainment in the general population”. Nature Neurosciences 2016, 19(12): 1563-1565. doi: 10.1038/nn.4404
19. Gaulton KJ, Ferreira T, Lee Y, Raimondo A, Mägi R, Reschen ME, Mahajan A, Locke A, Rayner NW, Robertson N, Scott RA, Prokopenko I, Scott LJ, Green T, Sparso T, Thuillier D, Yengo … Esko T, … Mihailov E, … Metspalu A, … Altshuler D, Boehnke M, Teslovich TM, McCarthy MI, Morris AP; DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium. “Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.” Nat Genet. 2015 Dec; 47(12):1415-25. doi: 10.1038/ng.3437.
20. Giani, FC; Fiorini, C; Wakabayashi, A; Ludwig, LS; Salem, RM; Jobaliya, CD; Regan, SN; Ulirsch, JC; Liang, G; Steinberg-Shemer, O; Guo, MH; Esko, T; Tong, W; Brugnara, C; Hirschhorn, JN; Weiss, MJ; Zon, LI; Chou, ST; French, DL; Musunuru, K; Sankaran, VG. “Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells.” Cell Stem Cell. 2016;18(1):73-8. doi: 10.1016/j.stem.2015.09.015.
21. Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, ... Kals M, Mägi R, Pärn K, ... Mihailov E, Milani L, International Headache Genetics Consortium, Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Järvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, Eriksson N, Daly MJ, Neale BM, Olesen J, Chasman DI, Nyholt DR, Palotie A. “Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.” Nat Genet. 2016; 48(8):856-866. doi: 10.1038/ng.3598.
22. Hinney A, Kesselmeier M, Jall S, Volckmar AL, Föcker M, Antel J; GCAN; WTCCC3, Heid IM, Winkler TW; GIANT (…Alavere, H; Esko, T; Mägi, R; Fischer, K; Männik, K; Mihailov, E; Milani, L; Metspalu, A; Nelis, M; Tammesoo, M-L; Metspalu, A.….), Grant SF; EGG, Guo Y, Bergen AW, Kaye W, Berrettini W, Hakonarson H; Price Foundation Collaborative Group; Children’s Hospital of Philadelphia/Price Foundation, Herpertz-Dahlmann B, de Zwaan M, Herzog W, Ehrlich S, Zipfel S, Egberts KM, Adan R, Brandys M, van Elburg A, Boraska Perica V, Franklin CS, Tschöp MH, Zeggini E, Bulik CM, Collier D, Scherag A, Müller TD, Hebebrand J. “Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index”. Mol Psychiatry. 2016 May 17. doi: 10.1038/mp.2016.71
23. Hippolyte L, Maillard AM, Rodriguez-Herreros B, Pain A, Martin-Brevet S, Ferrari C, Conus P, Macé A, Hadjikhani N, Metspalu A, Reigo A, Kolk A, Männik K, Barker M, Isidor B, Le Caignec C, Mignot C, Schneider L, Mottron L, Keren B, David A, Doco-Fenzy M, Gérard M, Bernier R, Goin-Kochel RP, Hanson E, Green Snyder L; 16p11.2 European Consortium, Simons Variation in Individuals Project Consortium, Ramus F, Beckmann JS, Draganski B, Reymond A, Jacquemont S. “The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.” Biol. Psychiatry, 2015 Nov 10. pii: S0006-3223(15)00917-8. doi: 10.1016/j.biopsych.2015.10.021.
24. Homuth G, Wahl S, Müller C, Schurmann C, Mäder U, Blankenberg S, Carstensen M, Dörr M, Endlich K, Englbrecht C, Felix SB, Gieger C, Grallert H, Herder C, Illig T, Kruppa J, Marzi CS, Mayerle J, Meitinger T, Metspalu A, Nauck M, Peters A, Rathmann W, Reinmaa E, Rettig R, Roden M, Schillert A, Schramm K, Steil L, Strauch K, Teumer A, Völzke H, Wallaschofski H, Wild PS, Ziegler A, Völker U, Prokisch H, Zeller T. “Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts”. BMC Med Genomics. 2015 Oct 15;8:65. doi: 10.1186/s12920-015-0141-x.
25. Huan T, Joehanes R, Schurmann C, Schramm K, Pilling LC, Peters MJ, Mägi R, DeMeo D, O'Connor GT, Ferrucci L, Teumer A, Homuth G, Biffar R, Völker U, Herder C, Waldenberger M, Peters A, Zeilinger S, Metspalu A, Hofman A, Uitterlinden AG, Hernandez DG, Singleton AB, Bandinelli S, Munson PJ, Lin H, Benjamin EJ, Esko T, Grabe HJ, Prokisch H, van Meurs JB, Melzer D, Levy D. “A Whole-Blood Transcriptome Meta-Analysis Identifies Gene Expression Signatures of Cigarette Smoking”. Human Molecular Genetics, 2016, online: August 29, pp:
26. Inchley CE, Larbey CD, Shwan NA, Pagani L, Saag L, Antão T, Jacobs G, Hudjashov G, Metspalu E, Mitt M, Eichstaedt CA, Malyarchuk B, Derenko M, Wee J, Abdullah S, Ricaut FX, Mormina M, Mägi R, Villems R, Metspalu M, Jones MK, Armour JA, Kivisild T. “Selective sweep on human amylase genes postdates the split with Neanderthals”. Scientific Reports 2016, 6:37198
27. Ivanov, M; Kals, M; Lauschke V, Barragan I, Ewels P, Käller M, Axelsson T, Lehtiö J, Milani L, Ingelman-Sundberg M. “Single base resolution analysis of 5-hydroxymethylcytosine in 188 human genes: implications for hepatic gene expression.” Nucl. Acids Res. (2016). 44(14): 6756-6769. doi: 10.1093/nar/gkw316.  
28. Jones SE, Tyrrell J, Wood AR, Beaumont RN, Ruth KS, Tuke MA, Yaghootkar H, Hu Y, Teder-Laving M, Hayward C, Roenneberg T, Wilson JF, Del Greco F, Hicks AA, Shin C, Yun CH, Lee SK, Metspalu A, Byrne EM, Gehrman PR, Tiemeier H, Allebrandt KV, Freathy RM, Murray A, Hinds DA, Frayling TM, Weedon MN. “Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.” PLoS Genet. 2016, 12(8):e1006125. doi: 10.1371/journal.pgen.1006125. eCollection 2016.
29. Joshi, Peter K.; Krista Fischer, Katharina E. Schraut, Harry Campbell, Tõnu Esko & James F. Wilson. “Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan”. Nat. Commun. 2016, 7:11174. DOI: 10.1038/ncomms11174. 
30. Kassam I, Lloyd-Jones L, Holloway A, Small KS, Zeng B, Bakshi A, Metspalu A, Gibson G, Spector TD, Esko T, Montgomery GW, Powell JE, Yang J, Visscher PM, McRae AF. “Autosomal genetic control of human gene expression does not differ across the sexes”.  Genome Biology 2016, 17:248. DOI: 10.1186/s13059-016-1111-0
31. Kettunen J, Demirkan A, Würtz P, Draisma HH, Haller T, Rawal R, Vaarhorst A, Kangas AJ, Lyytikäinen LP, Pirinen M, Pool R, Sarin AP, Soininen P, Tukiainen T, Wang Q, Tiainen M, Tynkkynen T, Amin N, Zeller T, Beekman M, Deelen J, van Dijk KW, Esko T, Hottenga JJ, van Leeuwen EM, Lehtimäki T, Mihailov E, Rose RJ, de Craen AJ, Gieger C, Kähönen M, Perola M, Blankenberg S, Savolainen MJ, Verhoeven A, Viikari J, Willemsen G, Boomsma DI, van Duijn CM, Eriksson J, Jula A, Järvelin MR, Kaprio J, Metspalu A, Raitakari O, Salomaa V, Slagboom PE, Waldenberger M, Ripatti S, Ala-Korpela M. “Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.” Nat Commun. 2016;7: 11122. doi: 10.1038/ncomms11122.
32. Kilpeläinen TO, Carli JF, Skowronski AA, Sun Q, Kriebel J, Feitosa MF, Hedman ÅK, Drong AW, ... Perola M, Huupponen RK, Viikari JS, Kähönen M, Lehtimäki T, Raitakari OT, Mellström D, Lorentzon M, Casas JP, Bandinelli S, März W, Isaacs A, van Dijk KW, van Duijn CM, Harris TB, Bouchard C, Allison MA, Chasman DI, Ohlsson C, Lind L, Scott RA, Langenberg C, Wareham NJ, Ferrucci L, Frayling TM, Pramstaller PP, Borecki IB, Waterworth DM, Bergmann S, Waeber G, Vollenweider P, Vestergaard H, Hansen T, Pedersen O, Hu FB, Eline Slagboom P, Grallert H, Spector TD, Jukema JW, Klein RJ, Schadt EE, Franks PW, Lindgren CM, Leibel RL, Loos RJ. “Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels”. Nat Commun. 2016 Feb 1;7:10494. doi:10.1038/ncomms10494.
33. Kööts-Ausmees, L; Schmidt, M; Esko, T. Metspalu, A; Allik, J; Realo, A. “The Role of the Five-factor Personality Traits in General Self-rated Health”. European Journal of Personality, Eur. J. Pers. 30: 492–504 (2016). DOI: 10.1002/per.2058.
34. Leitsalu, Liis; Alavere, Helene; Tammesoo, Mari-Liis; Leego, Erkki; Metspalu, Andres. “Linking a population biobank with national health registries-the Estonian experience.” Journal of personalized medicine, 2016, 5(2): 96-106. DOI: 10.3390/jpm5020096.
35. Leitsalu, L; Alavere, H; Jacquemont, S; Kolk, A; Maillard; AM; Reigo, A; Nõukas, M; Reymond, A; Männik, K; Ng, PC; Metspalu, A. “Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants”. Personalized Medicine, 2016, 13(4): 303-314.  DOI: 10.2217/pme-2016-0009
36. Laisk-Podar T, Lindgren CM, Peters M, Tapanainen JS, Lambalk CB, Salumets A, Mägi R.  “Ovarian Physiology and GWAS: Biobanks, Biology, and Beyond.” Trends in Endocrinology & Metabolism, 2016, 27(7): 516-528. doi:10.1016/j.tem.2016.04.011
37. Lemmelä S, Solovieva S, Shiri R, Benner C, Heliövaara M, Kettunen J, Anttila V, Ripatti S, Perola M, Seppälä I, Juonala M, Kähönen M, Salomaa V, Viikari J, Raitakari OT, Lehtimäki T, Palotie A, Viikari-Juntura E, Husgafvel-Pursiainen K. “Genome-Wide Meta-Analysis of Sciatica in Finnish Population”. PLos One, 2016, 11(10): e0163877, doi: 10.1371/journal.pone.0163877. eCollection 2016
38. Lessard S, Manning AK, Low-Kam C, Auer PL, Giri A, Graff M, Schurmann C, Yaghootkar H, Luan J, Esko T, Karaderi T; NHLBI GO Exome Sequence Project; GOT2D; T2D-GENES; GIANT Consortium, Bottinger EP, Lu Y, Carlson C, Caulfield M, Dubé MP, Jackson RD, Kooperberg C, McKnight B, Mongrain I, Peters U, Reiner AP, Rhainds D, Sotoodehnia N, Hirschhorn JN, Scott RA, Munroe PB, Frayling TM, Loos RJ, North KE, Edwards TL, Tardif JC, Lindgren CM, Lettre G. “Testing the role of predicted gene knockouts in human anthropometric trait variation”. Human Molecular Genetics, 2016; 25(10): 2082-2092. doi: 10.1093/hmg/ddw055.
39. Li M, Li Y, Weeks O, Mijatovic V, Teumer A, Huffman JE, Tromp G, Fuchsberger C, Gorski M, ... Mägi R, Malerba G, Mihailov E, ... Esko T, ... Metspalu A, ... Ulivi S, Velayutham D, Völker U, Völzke H, Waldenberger M, Wang JJ, Weir DR, Witte D, Kuivaniemi H, Fox CS, Franceschini N, Goessling W, Köttgen A, Chu AY. “SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function”.  Journal of the American Society of Nephrology, 2016 Dec 5. pii: ASN.2016020131. [Epub ahead of print]. DOI: 10.1681/ASN.2016020131
40. Limbach M, Saare M, Tserel L, Kisand K, Eglit T, Sauer S, Axelsson T, Syvänen AC, Metspalu A, Milani L, Peterson P. “Epigenetic profiling in CD4+ and CD8+ T cells from Graves' disease patients reveals changes in genes associated with T cell receptor signaling.” J Autoimmun. 2016; 67: 46-56. doi: 10.1016/j.jaut.2015.09.006.
41. Loh PR, Bhatia G, Gusev A, Finucane HK, Bulik-Sullivan BK, Pollack SJ; Schizophrenia Working Group of Psychiatric Genomics Consortium, de Candia TR, Lee SH, Wray NR, Kendler KS, O'Donovan MC, Neale BM, Patterson N, Price AL. “Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.” Nat Genet. 2015 Dec; 47(12):1385-92. doi: 10.1038/ng.3431. Epub 2015 Nov 2.
42. Loley C, Alver M, Assimes TL, Bjonnes A, Goel A, Gustafsson S, Hernesniemi J, Hopewell JC, Kanoni S, Kleber ME, Lau KW, Lu Y, Lyytikäinen LP, Nelson CP, Nikpay M, Qu L, Salfati E, ... Esko T, ... Mihailov E, Morris AP, Nikus K, Pedersen N, Rallidis L, Salomaa V, Shah SH, Stewart AF, Thompson JR, Zalloua PA, Chambers JC, Collins R, Ingelsson E, Iribarren C, Karhunen PJ, Kooner JS, Lehtimäki T, Loos RJ, März W, McPherson R, Metspalu A, Reilly MP, Ripatti S, Sanghera DK, Thiery J, Watkins H, Deloukas P, Kathiresan S, Samani NJ, Schunkert H, Erdmann J, König IR. “No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis.” Scientific Reports 6, Article number: 35278 (2016). doi: 10.1038/srep35278
43. Lu, Y; Day, FR; Gustafsson, S; Buchkovich, ML; Na, J; Bataille, V; Cousminer, DL; Dastani, Z; Drong, AW; Esko, T; ... Mägi, R; ... Perola, M; ... Prokopenko, I; Richards, JB; Schadt, EE; Spector, TD; Widén, E; Willer, CJ; Yang, J; Ingelsson, E; Mohlke, KL; Hirschhorn, JN; Pospisilik, JA; Zillikens, MC; Lindgren, C; Kilpeläinen, TO; Loos, RJ. “New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.” Nat. Commun. 2016, 7:10495. DOI: 10.1038/ncomms10495. 
44. Luyten, Walter; Antal, Peter; Braeckman, Bart P; Bundy, Jake; Cirulli, Francesca; Fang-Yen, Christopher; Fuellen, Georg; Leroi, Armand; Liu, Qingfei; Martorell, Patricia; Metspalu, Andres; Perola, Markus; Ristow, Michael; Saul, Nadine; Schoofs, Liliane; Siems, Karsten; Temmerman, Liesbet; Smets, Tina; Wolk, Alicja; Rattan, Suresh IS. “Ageing with elegans: a research proposal to map healthspan pathways”. Biogerontology, 2016, 17(4): 771-782. http://link.springer.com/article/10.1007%2Fs10522-016-9644-x
45. Läll, K; Mägi, R; Morris, AP; Metspalu, A; Fischer, K. “Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores”. Genetics in Medicine, 2016 Aug 11. doi: 10.1038/gim.2016.103.
46. Maillard AM, Hippolyte L, Rodriguez-Herreros B, Chawner SJ, Dremmel D, Agüera Z, Fagundo AB, Pain A, Martin-Brevet S, Hilbert A, Kurz S, Etienne R, Draganski B, Jimenez-Murcia S, Männik K, Metspalu A, Reigo A, Isidor B, Le Caignec C, David A, Mignot C, Keren B; 16p11.2 European Consortium, van den Bree MB, Munsch S, Fernandez-Aranda F, Beckmann JS, Reymond A, Jacquemont S. “16p11.2 Locus modulates response to satiety before the onset of obesity.” International Journal of Obesity 2016; 40(5): 870-876. doi: 10.1038/ijo.2015.247.
47. Marioni RE, Ritchie SJ, Joshi PK, Hagenaars SP, Okbay A, Fischer K, Adams MJ, Hill WD, Davies G; Social Science Genetic Association Consortium (… Mihailov, E; Pervjakova, N; Mägi, R; Milani, L; Metspalu, A…), Nagy R, Amador C, Läll K, Metspalu A, Liewald DC, Campbell A, Wilson JF, Hayward C, Esko T, Porteous DJ, Gale CR, Deary IJ. “Genetic variants linked to education predict longevity”. PNAS 2016, 113(47): 13366-13371. doi: 10.1073/pnas.1605334113
48. Mehta D, Tropf FC, Gratten J, Bakshi A, Zhu Z, Bacanu SA, Hemani G, Magnusson PK, Barban N, Esko T, Metspalu A, Snieder H, Mowry BJ, Kendler KS, Yang J, Visscher PM, McGrath JJ, Mills MC, Wray NR, Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium (…Tõnu Esko, Andres Metspalu, Lili Milani, Mari Nelis…), LifeLines Cohort Study, and Twins UK, … Scott RJ, Seidman LJ, Toncheva D, Tooney PA, Waddington J, Weinberger DR, Weiser M, Wu JQ. “Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women”. JAMA Psychiatry. 2016, 73(5):497-505. doi: 10.1001/jamapsychiatry.2016.0129.
49. Mihailov, E; Nikopensius, T; Reigo, A; Nikkolo; C; Kals, M; Aruaas, K; Milani, L; Seepter, H; Metspalu, A. “Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia”. Hernia, 2016. DOI: 10.1007/s10029-016-1491-9
50. Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators (.... Tõnu Esko, Evalin Mihailov, Maris Alver, Markus Perola, Andres Metspalu ...).“Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease”. N Engl J Med 2016; 374:1134-1144. DOI: 10.1056/NEJMoa1507652.
51. Okbay A, Baselmans BM, De Neve JE, Turley P, Nivard MG, Fontana MA, Meddens SF, Linnér RK, Rietveld CA, ... Mihailov E, ...Metspalu A, ...Esko T, Krueger RF, Beauchamp JP, Koellinger PD, Benjamin DJ, Bartels M, Cesarini D. “Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.” Nat Genet. 2016, 48(6), pp: 624-633. doi: 10.1038/ng.3552. 
52. Okbay A, Beauchamp JP, Fontana MA, Lee JJ, Pers TH, Rietveld CA, Turley P, Chen GB, ... Mihailov E, … Mägi R, ... Metspalu A, Pendleton N, Penninx BW, Perola M, ... Esko T, Koellinger PD, Cesarini D, Benjamin DJ. “Genome-wide association study identifies 74 loci associated with educational attainment”. Nature 2016, 533(7604):539-42. doi: 10.1038/nature17671.
53. Pagani L, Lawson DJ, Jagoda E, Mörseburg A, Eriksson A, Mitt M, Clemente F, Hudjashov G, DeGiorgio M, Saag L, Wall JD, Cardona A, Mägi R, ... Mihailov E, Karunas A, Litvinov S, Khusainova R, Ekomasova N, Akhmetova V, Khidiyatova I, Marjanović D, Yepiskoposyan L, Behar DM, Balanovska E, Metspalu A, Derenko M, Malyarchuk B, Voevoda M, Fedorova SA, Osipova LP, Lahr MM, Gerbault P, Leavesley M, Migliano AB, Petraglia M, Balanovsky O, Khusnutdinova EK, Metspalu E, Thomas MG, Manica A, Nielsen R, Villems R, Willerslev E, Kivisild T, Metspalu M. “Genomic analyses inform on migration events during the peopling of Eurasia”. Nature 2016, 538(7624): 238-242. DOI: 10.1038/nature19792
54. Pajusalu S, Talvik I, Noormets K, Talvik T, Põder H, Joost K, Puusepp S, Piirsoo A, Stenzel W, Goebel HH, Nikopensius T, Annilo T, Nõukas M, Metspalu A, Õunap K, Reimand T. “De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion.” Neuromuscul Disord. 2016, 26(3): 236-239. 
dx.doi.org/10.1016/j.nmd.2015.11.011
55. Pallister T, Haller T, Thorand B, Altmaier E, Cassidy A, Martin T, Jennings A, Mohney RP, Gieger C, MacGregor A, Kastenmüller G, Metspalu A, Spector TD, Menni C. “Metabolites of milk intake: a metabolomic approach in UK twins with findings replicated in two European cohorts.” Eur J Nutr (2016). doi:10.1007/s00394-016-1278-x
56. Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, ... Metspalu A, … Mägi R, ... Nikopensius T, Esko T, Tanaka T, Gyllensten U, Völker U, Emilsson V, Vitart V, Aalto V, Gudnason V, Chouraki V, Chen WM, Igl W, März W, Koenig W, Lieb W, Loos RJ, Liu Y, Snieder H, Pramstaller PP, Parsa A, O'Connell JR, Susztak K, Hamet P, Tremblay J, de Boer IH, Böger CA, Goessling W, Chasman DI, Köttgen A, Kao WH, Fox CS. “Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function”. Nat Commun. 2016 ;7:10023. doi: 10.1038/ncomms10023.
57. Pervjakova N, Kasela S, Morris AP, Kals M, Metspalu A, Lindgren CM, Salumets A, Mägi R. “Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues.”  Epigenomics. 2016, 8(6): 789-799. DOI:10.2217/epi.16.8
58. Pettai K, Milani L, Tammiste A, Võsa U, Kolde R, Eller T, Nutt D, Metspalu A, Maron E. “Whole-genome expression analysis reveals genes associated with treatment response to escitalopram in major depression.” Eur Neuropsychopharmacol. 2016 Jul 22. pii: S0924-977X(16)30091-8. doi: 10.1016/j.euroneuro.2016.06.007.
59. Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen MH, Auer PL, … Kals M, Metspalu A, Esko T, … O'Donnell CJ, Johnsen JM, Reiner AP, Ganesh SK, Sankaran VG. “Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.” Am J Hum Genet. 2016; 99(2):481-488. doi: 10.1016/j.ajhg.2016.06.016.
60. Roberto G, Leal I, Sattar N, Loomis AK, Avillach P, Egger P, van Wijngaarden R, Ansell D, Reisberg S, Tammesoo ML, Alavere H, Pasqua A, Pedersen L, Cunningham J, Tramontan L, Mayer MA, Herings R, Coloma P, Lapi F, Sturkenboom M, van der Lei J, Schuemie MJ, Rijnbeek P, Gini R. “Identifying Cases of Type 2 Diabetes in Heterogeneous Data Sources: Strategy from the EMIF Project.” PLoS One, 2016, 11(8):e0160648. doi: 10.1371/journal.pone.0160648
61. Shadrina, MI; Shulskaya, MV; Klyushnikov, SA; Nikopensius, T; Nelis, M; Kivistik, PA; Komar, AA; Limborska, SA; Illarioshkin, SN; Slominsky, PA. “ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia.” Cerebellum Ataxias, 2016, 3:2. doi: 10.1186/s40673-016-0040-8
62. Sekar A; Bialas AR; de Rivera H; Davis A; Hammond TR; Kamitaki N; Tooley K; Presumey J; Baum M; Van Doren V; Genovese G; Rose SA; Handsaker RE; Schizophrenia Working Group of the Psychiatric Genomics Consortium (...Andres Metspalu, Lili Milani, Mari Nelis, Tõnu Esko...) ; Daly MJ; Carroll MC; Stevens B; McCarroll SA. “Schizophrenia risk from complex variation of complement component 4.” Nature 2016; 530(7589): 177-183. doi: 10.1038/nature16549.
63. Spjuth O, Krestyaninova M, Hastings J, Shen HY, Heikkinen J, Waldenberger M, Langhammer A, Ladenvall C, Esko T, Persson MÅ, Heggland J, Dietrich J, Ose S, Gieger C, Ried JS, Peters A, Fortier I, de Geus EJ, Klovins J, Zaharenko L, Willemsen G, Hottenga JJ, Litton JE, Karvanen J, Boomsma DI, Groop L, Rung J, Palmgren J, Pedersen NL, McCarthy MI, van Duijn CM, Hveem K, Metspalu A, Ripatti S, Prokopenko I, Harris JR. “Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research.” Eur J Hum Genet. 2016; 24(4): 521-528. doi: 10.1038/ejhg.2015.165. 
64. Stringer S, Minică CC, Verweij KJ, Mbarek H, Bernard M, Derringer J, van Eijk KR, Isen JD, Loukola A, Maciejewski DF, Mihailov E, … Mägi R, … Metspalu A, Gelernter J, Boomsma DI, Iacono WG, Martin NG, Gillespie NA, Derks EM, Vink JM. “Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium”. Transl Psychiatry. 2016;6:e769. doi: 10.1038/tp.2016.36.
65. Stuart PE, Nair RP, Tsoi LC, Tejasvi T, Das S, Kang HM, Ellinghaus E, Chandran V, Callis-Duffin K, Ike R, Li Y, Wen X, Enerbäck C, Gudjonsson JE, Kõks S, Kingo K, Esko T, Mrowietz U, Reis A, Wichmann HE, Gieger C, Hoffmann P, Nöthen MM, Winkelmann J, Kunz M, Moreta EG, Mease PJ, Ritchlin CT, Bowcock AM, Krueger GG, Lim HW, Weidinger S, Weichenthal M, Voorhees JJ, Rahman P, Gregersen PK, Franke A, Gladman DD, Abecasis GR, Elder JT. “Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.” Am J Hum Genet. 2015 Dec 3;97(6):816-36. 
doi: 10.1016/j.ajhg.2015.10.019. 
66. Surendran P, Drenos F, Young R, Warren H, Cook JP, Manning AK, Grarup N, Sim X, ... Mihailov E, ... Perola M, ... EchoGen Consortium, Traylor M, Markus HS; METASTROKE Consortium, Highland HM, Justice AE, Marouli E; GIANT Consortium (… Tõnu Esko, Reedik Mägi, Andres, Metspalu, Evelin Mihailov, Lili Milani, Andrew P. Morris, Markus Perola…) , Lindström J, Uusitupa M, Komulainen P, Lakka TA, Rauramaa R, Polasek O, Rudan I, Rolandsson O, Franks PW, ... Esko T, Mägi R, Metspalu A, CHARGE+ Exome Chip Blood Pressure Consortium, Tobin MD, Nordestgaard BG; T2D-GENES Consortium (…Tõnu Esko, Lili Milani, Evelin Mihailov, Andres Metspalu, Reedik Mägi…); GoT2DGenes Consortium; ExomeBP Consortium; CHD Exome+ Consortium, Caulfield MJ, Mahajan A, Morris AP, Tomaszewski M, Samani NJ, Saleheen D, Asselbergs FW, Lindgren CM, Danesh J, Wain LV, Butterworth AS, Howson JM, Munroe PB. “Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.” Nat Genet. 2016; 48(10): 1151-1161. doi: 10.1038/ng.3654
67. Tajuddin SM, Schick UM, Eicher JD, Chami N, Giri A, Brody JA, Hill WD, Kacprowski T, Li J, Lyytikäinen LP, Manichaikul A, Mihailov E, ... Mägi R, ... Esko T, Faraday N, Wilson JG, Cushman M, Johnson AD, Edwards TL, Zakai NA, Lettre G, Reiner AP, Auer PL. “Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.” Am J Hum Genet. 2016 Jul 7;99(1):22-39. doi: 10.1016/j.ajhg.2016.05.003.
68. Tamm R, Mägi R, Tremmel R, Winter S, Mihailov E, Smid A, Möricke A, Klein K, Schrappe M, Stanulla M, Houlston R, Weinshilboum R, Mlinarič Raščan I, Metspalu A, Milani L, Schwab M, Schaeffeler E. “Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: a meta-analysis of three genome-wide association studies”. Clinical Pharmacology and Therapeutics, 2016. doi: 10.1002/cpt.540. [Epub ahead of print]
69. Thiery, Odile; Vasar, Martti; Jairus, Teele; Davison, John; Roux, Christophe; Kivistik, Paula-Ann; Metspalu, Andres; Milani, Lili; Saks, Ülle; Moora, Mari; Zobel, Martin; Öpik, Maarja. “Sequence variation in nuclear ribosomal SSU, ITS and LSU regions of Rhizophagus irregularis and Gigaspora margarita is high and isolate-dependent”. Molecular Ecology, 2016, 25 (12): 2816−2832, 10.1111/mec.13655.
70. Teumer A, Qi Q, Nethander M, Aschard H, Bandinelli S, Beekman M, Berndt SI, ...  Magi R, ... van Duijn CM, van Heemst D, Vandenput L, Vasan RS, Völker U, Willems SM, Ohlsson C, Wallaschofski H, Kaplan RC. “Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits”. Aging Cell, 2016;15(5):811-24. doi: 10.1111/acel.12490.
71. Tiirats, A; Viltrop, T; Nõukas, M; Reimann, E; Salumets, A; Kõks, S. “C14orf132 gene is possibly related to extremely low birth weight”. BMC Genetics, 2016,  17:132. DOI 10.1186/s12863-016-0439-5 
72. van den Berg, SM; de Moor, MH; Verweij, KJ; Krueger, RF; Luciano, M; Arias, Vasquez, A; Matteson, LK; Derringer, J; Esko, T; ... Mihailov, E; ... Metspalu, A; Kaprio, J; Deary, IJ; Räikkönen, K; Wilson, JF; Keltikangas-Järvinen, L; Bierut, LJ; Hettema, JM; Grabe, HJ; Penninx, BW; van, Duijn, CM; Evans, DM; Schlessinger, D; Pedersen, NL; Terracciano, A; McGue, M; Martin, NG; Boomsma, DI. “Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium”. Behav Genet. 2016;46(2):170-82. doi: 10.1007/s10519-015-9735-5.
73. van der Harst P, van Setten J, Verweij N, Vogler G, Franke L, Maurano MT, Wang X, Mateo Leach I, ... Esko T, ... Metspalu A, ... Gasparini P, Jukema JW, Kääb S, Gudnason V, Felix SB, Heckbert SR, de Boer RA, Newton-Cheh C, Hicks AA, Chambers JC, Jamshidi Y, Visel A, Christoffels VM, Isaacs A, Samani NJ, de Bakker PI. “52 Genetic Loci Influencing Myocardial Mass.” J Am Coll Cardiol. 2016 Sep 27;68(13):1435-48. doi: 10.1016/j.jacc.2016.07.729.
74. Veerus P, Fischer K, Hemminki E, Hovi SL, Hakama M. “Effect of characteristics of women on attendance in blind and non-blind randomised trials: analysis of recruitment data from the EPHT Trial”. BMJ open, 2016, 6(10): e011099. doi: 10.1136/bmjopen-2016-011099
75. Vogt S, Wahl S, Kettunen J, Breitner S, Kastenmüller G, Gieger C, Suhre K, Waldenberger M, Kratzsch J, Perola M, Salomaa V, Blankenberg S, Zeller T, Soininen P, Kangas AJ, Peters A, Grallert H, Ala-Korpela M, Thorand B. “Characterization of the metabolic profile associated with serum 25-hydroxyvitamin D: a cross-sectional analysis in population-based data”. International Journal of Epidemiology 2016,  45(5): 1469-1481. doi: 10.1093/ije/dyw222
76. Walford GA, Gustafsson S, Rybin D, Stančáková A, Chen H, Liu CT, Hong J, Jensen RA, Rice K, Morris AP, Mägi R, ... Collins FS, Mohlke KL, Tuomilehto J, März W, Kovacs P, Stumvoll M, Psaty BM, Kuusisto J, Laakso M, Meigs JB, Dupuis J, Ingelsson E, Florez JC. “Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci”. Diabetes, 2016, 65(10):3200-11. doi: 10.2337/db16-0199.
77. Wang J, Thingholm LB, Skiecevičienė J, Rausch P, Kummen M, Hov JR, Degenhardt F, Heinsen FA, Rühlemann MC, Szymczak S, Holm K, Esko T, Sun J, Pricop-Jeckstadt M, Al-Dury S, Bohov P, Bethune J, Sommer F, Ellinghaus D, Berge RK, Hübenthal M, Koch M, Schwarz K, Rimbach G, Hübbe P, Pan WH, Sheibani-Tezerji R, Häsler R, Rosenstiel P, D'Amato M, Cloppenborg-Schmidt K, Künzel S, Laudes M, Marschall HU, Lieb W, Nöthlings U, Karlsen TH, Baines JF, Franke A. “Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota”. Nature Genetics 2016, 48(11): 1396-1406. DOI: 10.1038/ng.3695
78. Ware JJ, Chen X, Vink J, Loukola A, Minica C, Pool R, Milaneschi Y, Mangino M, Menni C, Chen J, Peterson RE, Auro K, Lyytikäinen LP, Wedenoja J, Stiby AI, Hemani G, Willemsen G, Hottenga JJ, Korhonen T, Heliövaara M, Perola M, Rose RJ, Paternoster L, Timpson N, Wassenaar CA, Zhu AZ, Davey Smith G, Raitakari OT, Lehtimäki T, Kähönen M, Koskinen S, Spector T, Penninx BW, Salomaa V, Boomsma DI, Tyndale RF, Kaprio J, Munafò MR. “Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2”. Scientific Reports 2016 Feb 1;6:20092. doi: 10.1038/srep20092.
79. Würtz P, Wang Q, Soininen P, Kangas AJ, Fatemifar G, Tynkkynen T, Tiainen M, Perola M, Tillin T, Hughes AD, Mäntyselkä P, Kähönen M, Lehtimäki T, Sattar N, Hingorani AD, Casas JP, Salomaa V, Kivimäki M, Järvelin MR, Davey Smith G, Vanhala M, Lawlor DA, Raitakari OT, Chaturvedi N, Kettunen J, Ala-Korpela M. “Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase.” J Am Coll Cardiol. 2016;67(10):1200-10. doi:10.1016/j.jacc.2015.12.060.
80. Yang J, Bakshi A, Zhu Z, Hemani G, Vinkhuyzen AA, Nolte IM, van Vliet-Ostaptchouk JV, Snieder H; Lifelines Cohort Study, Esko T, Milani L, Mägi R, Metspalu A, Hamsten A, Magnusson PK, Pedersen NL, Ingelsson E, Visscher PM. “Genome-wide genetic homogeneity between sexes and populations for human height and body mass index”. Hum Mol Genet. 2015 Dec 20;24(25):7445-9. doi: 10.1093/hmg/ddv443. Epub 2015 Oct 22.
81. Zanoni P, Khetarpal SA, Larach DB, Hancock-Cerutti WF, Millar JS, Cuchel M, … Perola M, … CHD Exome+ Consortium; CARDIoGRAM Exome Consortium (… Tõnu Esko, Evelin Mihailov, Maris Alver, Andres Metspalu ...); Global Lipids Genetics Consortium (…Tõnu Esko…). “Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease.” Science. 2016; 351(6278): 1166-1171. doi: 10.1126/science.aad3517.
82. Zhu, Weifei; Jill C. Gregory, Elin Org, Jennifer A. Buffa, Nilaksh Gupta, Zeneng Wang, Lin Li, Xiaoming Fu, Yuping Wu, Margarete Mehrabian, R. Balfour Sartor, Thomas M. McIntyre, Roy L. Silverstein, W.H. Wilson Tang, Joseph A. DiDonato, J. Mark Brown, Aldons J. Lusis and Stanley L. Hazen. “Gut Microbial Metabolite TMAO Enhances Platelet Hyperreactivity and Thrombosis Risk.” Cell. 2016 Mar 24; 165(1):111-24. doi: 10.1016/j.cell.2016.02.011.
83. Org E1,2, Mehrabian M1, Parks BW1,3, Shipkova P4, Liu X5, Drake TA6, Lusis AJ1,7,8. "Sex differences and hormonal effects on gut microbiota composition in mice."  2016 Jul 3;7(4):313-322. Epub 2016 Jun 29.
1. Andiappan, AK; Narayanan, S; Myers, RA; Lee, B; Nieuwenhuis, MA; Nardin, A; Park, CS; Shin, HD; Kim, JH; Westra, HJ; Franke, L; Esko, T; Metspalu, A; Teo, YY; Saw, SM; Chuen, KC; Jianjun, L; Koppelman, GH; Postma, DS; Poidinger, M; Connolly, JE; Wang, DY; Rotzschke, O; Curotto, de Lafaille, MA; Chew, FT. “Genetic variants of inducible costimulator are associated with allergic asthma susceptibility”. Journal of Allergy and Clinical Immunology. 2015, 135(2), pp: 556-558, e13.  DOI: 10.1016/j.jaci.2014.06.028
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2014

1. Ahrens, W; Pohlabeln, H; Foraita, R; Nelis, M; Lagiou, P; Lagiou, A; Bouchardy, C; Slamova, A; Schejbalova, M; Merletti, F; Richiardi, L; Kjaerheim, K; Agudo, A; Castellsague, X; Macfarlane, TV; Macfarlane, GJ; Lee, YCA; Talamini, R; Barzan, L; Canova, C; Simonato, L; Thomson, P; McKinney, PA; McMahon, AD; Znaor, A; Healy, CM; McCartan, BE; Metspalu, A; Marron, M; Hashibe, M; Conway, DI; Brennan, P. “Oral health, dental care and mouthwash associated with upper aerodigestive tract cancer risk in Europe: The ARCAGE study”.  Oral Oncology. 2014, Vol. 50(6), pp: 616-625. DOI: 10.1016/j.oraloncology.2014.03.001 

2. Allebrandt KV, Teder-Laving M, Kantermann T, Peters A, Campbell H, Rudan I, Wilson JF, Metspalu A, Roenneberg T. “Chronotype and sleep duration: the influence of season of assessment.” Chronobiol Int. 2014 Jun;31(5):731-40. doi: 10.3109/07420528.2014.901347
3. Andiappan, AK; Narayanan, S; Myers, RA; Lee, B; Nieuwenhuis, MA; Nardin, A; Park, CS; Shin, HD; Kim, JH; Westra, HJ; Franke, L; Esko, T; Metspalu, A; Teo, YY; Saw, SM; Chuen, KC; Jianjun, L; Koppelman, GH; Postma, DS; Poidinger, M; Connolly, JE; Wang, DY; Rotzschke, O; Curotto, de Lafaille, MA; Chew, FT. “Genetic variants of inducible costimulator are associated with allergic asthma susceptibility”. Journal of Allergy and Clinical Immunology. 2014, DOI: 10.1016/j.jaci.2014.06.028
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2013

  1. Okada Y et al.

Genetics of rheumatoid arthritis contributes to biology and drug discovery.

Nature. 2013 Dec 25. doi: 10.1038/nature12873. [Epub ahead of print] PubMed PMID: 24390342.

Co-authors (EGCUT) – Esko T, Metspalu A

  1. Vaher U et al.

De Novo SCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders.

J Child Neurol. 2013 Dec 18. [Epub ahead of print] PubMed PMID: 24352161.

Co-authors (EGCUT) – Vaher U, Nõukas M, Nikopensius T, Kals M, Annilo T, Nelis M, Metspalu A

  1. Rodriguez-Fontenla C et al.

Assessment of osteoarthritis candidate genes in a meta-analysis of 9 genome-wide association studies.

Arthritis Rheum. 2013 Dec 10. doi: 10.1002/art.38300. [Epub ahead of print] PubMed PMID: 24338622.

Co-authors (EGCUT) – Esko T, Metspalu A

  1. Parsa A et al.

Common variants in mendelian kidney disease genes and their association with renal function.

J Am Soc Nephrol. 2013 Dec;24(12):2105-2117. doi: 10.1681/ASN.2012100983. Epub 2013 Sep 12. PubMed PMID: 24029420; PubMed Central PMCID: PMC3839542.

Co-authors (EGCUT) – Esko T, Mägi R, Metspalu A, Nikopensius T

  1. Yao C et al.

Sex- and age-interacting eQTLs in human complex diseases. Hum Mol Genet. 2013 Nov 28. [Epub ahead of print] PubMed PMID: 24242183.

Co-authors (EGCUT) – Esko T, Metspalu A

  1. Global Lipids Genetics Consortium et al.

Discovery and refinement of loci associated with lipid levels.

Nat Genet. 2013 Nov;45(11):1274-1283. doi: 10.1038/ng.2797. Epub 2013 Oct 6. PubMed PMID: 24097068; PubMed Central PMCID: PMC3838666.

Co-authors (EGCUT) – Esko T, Fischer K, Perola M, Metspalu A, Mihailov E

  1. Do R et al.

Common variants associated with plasma triglycerides and risk for coronary artery disease.

Nat Genet. 2013 Nov;45(11):1345-1352. doi: 10.1038/ng.2795. Epub 2013 Oct 6. PubMed PMID: 24097064.

Co-authors (EGCUT) – Esko T, Fischer K, Mihailov E, Perola M, Metspalu A

  1. Nikopensius T et al.

A missense mutation in DUSP6 is associated with Class III malocclusion.

J Dent Res. 2013 Oct;92(10):893-898. doi: 10.1177/0022034513502790. Epub 2013 Aug 21. PubMed PMID: 23965468.

Co-authors (EGCUT) – Nikopensius T, Annilo T, Kals M, Kivistik PA, Milani L, Metspalu A

  1. Tammiste A et al.

Whole-exome sequencing identifies a polymorphism in the BMP5 gene associated with SSRI treatment response in major depression.

J Psychopharmacol. 2013 Oct;27(10):915-920. doi: 10.1177/0269881113499829. Epub 2013 Aug 7. PubMed PMID: 23926243.

Co-authors (EGCUT) – Tammiste A, Ng PC, Metspalu A, Esko T, Fischer K, Pettai K, Võsa U, Tšernikova N

  1. Westra HJ et al.

Systematic identification of trans eQTLs as putative drivers of known disease associations.

Nat Genet. 2013 Oct;45(10):1238-1243. doi: 10.1038/ng.2756. Epub 2013 Sep 8. PubMed PMID: 24013639.

Co-authors (EGCUT) – Esko T, Reinmaa E, Fischer K, Nelis M, Milani L,Perola M, Metspalu A

  1. Evans DM et al.

Mining the human phenome using allelic scores that index biological intermediates.

PLoS Genet. 2013 Oct;9(10):e1003919. doi:10.1371/journal.pgen.1003919. Epub 2013 Oct 31. PubMed PMID: 24204319; PubMed Central PMCID: PMC3814299.

Co-authors (EGCUT) – GIANT Consortium: Esko T, Mägi R, Nelis M, Fischer K, Mihailov E, Perola M, Metspalu A (Snieder H, Morris AD)

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A common biological basis of obesity and nicotine addiction.

Transl Psychiatry. 2013 Oct 1;3:e308. doi:10.1038/tp.2013.81. PubMed PMID: 24084939; PubMed Central PMCID: PMC3818010.

Co-authors (EGCUT) – ENGAGE consortium: Esko T, Mägi R, Nelis M, Metspalu A

  1. Dymerska D et al.

Lynch syndrome mutations shared by the Baltic States and Poland.

Clin Genet. 2013 Sep 5. doi: 10.1111/cge.12251. [Epub ahead of print] PubMed PMID: 24032978.

Co-authors (EGCUT) – Metspalu A

  1. Evangelou E et al.

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.

Ann Rheum Dis. 2013 Sep 4. doi:10.1136/annrheumdis-2012-203114. [Epub ahead of print] PubMed PMID: 23989986.

Co-authors (EGCUT) – Esko T, Milani L, Metspalu A

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Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.

Hum Mol Genet. 2013 Sep 1;22(17):3597-3607. doi: 10.1093/hmg/ddt205. Epub 2013 May 12. PubMed PMID: 23669352; PubMed Central PMCID: PMC3736869.

Co-authors (EGCUT) – Esko T, Nelis M, Nikopensius T, Metspalu A, Mägi R

  1. Ivanov M et al.

Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function.

Genome Biol. 2013 Aug 19;14(8):R83. [Epub ahead of print] PubMed PMID: 23958281.

Co-authors (EGCUT) – Kals M, Metspalu A, Milani L

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Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.

Am J Hum Genet. 2013 Aug 8;93(2):264-277. doi: 10.1016/j.ajhg.2013.06.016. PubMed PMID: 24144296; PubMed Central PMCID: PMC3772747.

Co-authors (EGCUT) – Haller T, Metspalu A

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Meta-analysis of gene-level associations for rare variants based on single-variant statistics.

Am J Hum Genet. 2013 Aug 8;93(2):236-248. doi: 10.1016/j.ajhg.2013.06.011. Epub 2013 Jul 25. PubMed PMID: 23891470; PubMed Central PMCID: PMC3738834.

Co-authors (EGCUT) – GIANT Consortium: Esko T, Mägi R, Nelis M, Fischer K, Mihailov E, Perola M, Metspalu A (Snieder H, Morris AD)

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Association of adiposity genetic variants with menarche timing in 92,105 women of European descent.

Am J Epidemiol. 2013 Aug 1;178(3):451-460. doi: 10.1093/aje/kws473. Epub  2013 Apr 4. PubMed PMID: 23558354; PubMed Central PMCID: PMC3816344.

Co-authors (EGCUT) – Esko T, Mihailov E, Metspalu A

  1. Amin N et al.

Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions.

Eur J Hum Genet. 2013 Aug;21(8):876-882. doi: 10.1038/ejhg.2012.263. Epub 2012 Dec 5. PubMed PMID: 23211697; PubMed Central PMCID: PMC3722675.

Co-authors (EGCUT) – Metspalu A, Esko T

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A genome-wide association study of sleep habits and insomnia.

Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):439-451. doi: 10.1002/ajmg.b.32168. Epub 2013 May 31. PubMed PMID: 23728906.

Co-authors (EGCUT) – Esko T, Teder-Laving M, Metspalu A

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The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males.

Ann Rheum Dis. 2013 Jul;72(7):1264-1265. doi: 10.1136/annrheumdis-2012-203182. Epub 2013 Mar 16. PubMed PMID: 23505243; PubMed Central PMCID: PMC3686326.

Co-authors (EGCUT) – Esko T, Metspalu A

  1. Fears R et al.

The perspective from EASAC and FEAM on direct-to-consumer genetic testing for health-related purposes.

Eur J Hum Genet. 2013 Jul;21(7):703-707. doi: 10.1038/ejhg.2012.238. Epub 2012 Nov 21. Review. PubMed PMID: 23169492; PubMed Central PMCID: PMC3722941.

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Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.

Genome Res. 2013 Jul;23(7):1130-1141. doi: 10.1101/gr.155127.113. Epub 2013 Apr 9. PubMed PMID: 23570689; PubMed Central PMCID: PMC3698506.

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  1. Cousminer DL et al.

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.

Hum Mol Genet. 2013 Jul 1;22(13):2735-2747. doi: 10.1093/hmg/ddt104. Epub 2013 Feb 27. PubMed PMID: 23449627; PubMed Central PMCID: PMC3674797.

Co-authors (EGCUT) – GIANT Consortium: Esko T, Mägi R, Nelis M, Fischer K, Mihailov E, Perola M, Metspalu A (Snieder H, Morris AD)

  1. Rietveld CA et al.

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.

Science. 2013 Jun 21;340(6139):1467-1471. doi: 10.1126/science.1235488. Epub 2013 May 30. PubMed PMID: 23722424; PubMed Central PMCID: PMC3751588.

Co-authors (EGCUT) – Esko T, Milani L, Fischer K, Reinmaa E, Perola M, Metspalu A

  1. Võsa U et al.

Meta-analysis of microRNA expression in lung cancer.

Int J Cancer. 2013 Jun 15;132(12):2884-2893.doi: 10.1002/ijc.27981. Epub 2012 Dec 27. PubMed PMID: 23225545.

Co-authors (EGCUT) – Võsa U, Metspalu A, Annilo T

  1. Esko T et al.

Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity.

Eur J Hum Genet. 2013 Jun;21(6):659-665. doi: 10.1038/ejhg.2012.229. Epub 2012 Dec 19. PubMed PMID: 23249956; PubMed Central PMCID: PMC3658181.

Co-authors (EGCUT) – Esko T, Nelis M, Metspalu A

  1. Nikopensius T et al.

Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).

J Dent Res. 2013 Jun;92(6):507-511. doi: 10.1177/0022034513487210. Epub 2013 Apr 19. PubMed PMID: 23603338.

Co-authors (EGCUT) – Annilo T, Kals M, Mägi R, Metspalu A

  1. den Hoed M et al.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.

Nat Genet. 2013 Jun;45(6):621-631. doi: 10.1038/ng.2610. Epub 2013 Apr 14. PubMed PMID: 23583979; PubMed Central PMCID: PMC3696959.

Co-authors (EGCUT) – Esko T, Mihailov E, Fischer K, Milani L, Metspalu A, Perola M

  1. Randall JC et al.

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.

PLoS Genet. 2013 Jun;9(6):e1003500. doi: 10.1371/journal.pgen.1003500. Epub 2013 Jun 6. PubMed PMID: 23754948; PubMed Central PMCID: PMC3674993.

Co-authors (EGCUT) – Esko T, Mägi R, Nelis M, Metspalu A, Perola M, Fischer K

  1. Berndt SI et al.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

Nat Genet. 2013 May;45(5):501-512. doi: 10.1038/ng.2606. Epub 2013 Apr 7. PubMed PMID: 23563607.

Co-authors (EGCUT) – Mägi R, Mihailov E, Milani L, Metspalu A, Morris AD, Snieder H, Esko T, Fischer K

  1. Lener MR et al.

Can selenium levels act as a marker of colorectal cancer risk?

BMC Cancer. 2013 Apr 29;13:214. doi:10.1186/1471-2407-13-214. PubMed PMID: 23627542; PubMed Central PMCID:PMC3641950.

Co-authors (EGCUT) – Tammesoo ML, Metspalu A

  1. Perry JR et al.

A genome-wide association study of early menopause and the combined impact of identified variants.

Hum Mol Genet. 2013 Apr 1;22(7):1465-1472. doi: 10.1093/hmg/dds551. Epub 2013 Jan 9. PubMed PMID: 23307926; PubMed Central PMCID: PMC3596848.

Co-authors (EGCUT) – Esko T, Metspalu A

  1. Codd V et al.

Identification of seven loci affecting mean telomere length and their association with disease.

Nat Genet. 2013 Apr;45(4):422-427, 427e1-2. doi: 10.1038/ng.2528. PubMed PMID: 23535734.

Co-authors (EGCUT) – Fischer K, Esko T, Mihailov E, Metspalu A, Perola M

  1. Ivanov M et al.

In-solution hybrid capture of bisulfite-converted DNA for targeted bisulfite sequencing of 174 ADME genes.

Nucleic Acids Res. 2013 Apr 1;41(6):e72. doi:10.1093/nar/gks1467. Epub 2013 Jan 15. PubMed PMID: 23325842; PubMed Central PMCID: PMC3616706.

Co-authors (EGCUT) – Kals M, Milani L

  1. Verhoeven V et al.

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.

Nat Genet. 2013 Mar;45(3):314-318. doi: 10.1038/ng.2554. Epub 2013 Feb 10. Erratum in: Nat Genet. 2013 Jun;45(2):712. Janmahasathian, Sarayut [corrected to Sarayut Janmahasatian]. PubMed PMID: 23396134; PubMed Central PMCID: PMC3740568.

Co-authors (EGCUT) – Haller T, Metspalu A

  1. Köttgen A et al.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.

Nat Genet. 2013 Feb;45(2):145-154. doi: 10.1038/ng.2500. Epub 2012 Dec 23. PubMed PMID: 23263486; PubMed Central PMCID: PMC3663712.

Co-authors (EGCUT) – Esko T, Org E, Metspalu A, Snieder H, Haller T

  1. Allebrandt KV et al.

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.

Mol Psychiatry. 2013 Jan;18(1):122-132. doi: 10.1038/mp.2011.142. Epub 2011 Nov 22. PubMed PMID: 22105623.

Co-authors (EGCUT) – Esko T, Teder-Laving M, Metspalu A

  1. CARDIoGRAMplusC4D Consortium et al.

Large-scale association analysis identifies new risk loci for coronary artery disease.

Nat Genet. 2013 Jan;45(1):25-33. doi: 10.1038/ng.2480. Epub 2012 Dec 2. PubMed PMID: 23202125; PubMed Central PMCID: PMC3679547.

Co-authors (EGCUT) – Esko T, Fischer K, Mihailov E, Maouche S, Morris AD, Metspalu A, Perola M, Milani L

  1. Kumar V et al.

Human disease-associated genetic variation impacts large intergenic non-coding RNA expression.

PLoS Genet. 2013;9(1):e1003201. doi: 10.1371/journal.pgen.1003201. Epub 2013 Jan 17. PubMed PMID: 23341781; PubMed Central PMCID: PMC3547830.

Co-authors (EGCUT) – Esko T, Reinmaa E, Võsa U, Metspalu A

  1. Fall T et al.

European Network for Genetic and Genomic Epidemiology (ENGAGE) consortium. The role of adiposity in cardiometabolic traits: a mendelian randomization analysis. PLoS Med. 2013;10(6):e1001474. doi: 10.1371/journal.pmed.1001474. Epub 2013 Jun 25. PubMed  PMID: 23824655; PubMed Central PMCID: PMC3692470.

Co-authors (EGCUT) – Mägi R, Fischer K, Kals M, Esko T, Metspalu A

  1. Pichler I et al.

Serum iron levels and the risk of Parkinson disease: a mendelian randomization study.

PLoS Med. 2013;10(6):e1001462. doi: 10.1371/journal.pmed.1001462. Epub 2013 Jun 4. Erratum in: PLoS Med. 2013 Jun;10(6). doi:10.1371/annotation/c4d81646-0c0e-4a3e-9425-b220bae2d8b6. PubMed PMID: 23750121; PubMed Central PMCID: PMC3672214.

Co-authors (EGCUT) – Esko T, Metspalu A

  1. Vimaleswaran KS et al.

Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts.

PloS Med. 2013;10(2):e1001383. doi: 10.1371/journal.pmed.1001383. Epub 2013 Feb 5. PubMed PMID: 23393431; PubMed Central PMCID: PMC3564800.

Co-authors (EGCUT) – Mägi R, Esko T, Metspalu A

  1. Walters RG et al.

Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.

PLoS One. 2013;8(3):e58048. doi: 10.1371/journal.pone.0058048. Epub 2013 Mar 12. PubMed PMID: 23554873; PubMed Central PMCID: PMC3595275.

Co-authors (EGCUT) – Esko T, Metspalu A

  1. Khrunin AV et al.

A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe.

PLoS One. 2013;8(3):e58552. doi: 10.1371/journal.pone.0058552. Epub 2013 Mar 7. PubMed PMID: 23505534; PubMed Central PMCID: PMC3591355.

Co-authors (EGCUT) – Esko T, Nelis M, Metspalu A

  1. Mägi R et al.

Contribution of 32 GWAS-identified common variants to severe obesity in European adults referred for bariatric surgery.

PLoS One. 2013 Aug 7;8(8):e70735. doi: 10.1371/journal.pone.0070735. eCollection 2013. PubMed PMID: 23950990.

Co-authors (EGCUT) –

  1. Haller T et al.

RegScan: a GWAS tool for quick estimation of allele effects on continuous traits and their combinations. Brief Bioinform. 2013 Sep 5. [Epub ahead of print] PubMed PMID: 24008273.

Co-authors (EGCUT) – Mägi R, Kals M, Esko T, Fischer K

  1. Migliano A et al.

Evolution of the pygmy phenotype: evidence of positive selection from genome-wide scans in African, Asian and Melanesian pygmies. Hum Biol. 2013 Feb-Jun;85(1-3):251-284. PubMed PMID: 24297229.

Co-authors (EGCUT) – Mägi R, Nelis M

2012 (41)

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.
Chasman DI, Fuchsberger C, Pattaro C, Teumer A, Böger CA, Endlich K, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, Foster MC, O''Seaghdha CM, Glazer N, Isaacs A, Liu CT, Smith AV, O''Connell JR, Struchalin M, Tanaka T, Li G, Johnson AD, Gierman HJ, Feitosa MF, Hwang SJ, Atkinson EJ, Lohman K, Cornelis MC, Johansson A, Tönjes A, Dehghan A, Lambert JC, Holliday EG, Sorice R, Kutalik Z, Lehtimäki T, Esko T, Deshmukh H, Ulivi S, Chu AY, Murgia F, Trompet S, Imboden M, Coassin S, Pistis G; CARDIoGRAM Consortium; ICBP Consortium; CARe Consortium; WTCCC2, Harris TB, Launer LJ, Aspelund T, Eiriksdottir G, Mitchell BD, Boerwinkle E, Schmidt H, Cavalieri M, Rao M, Hu F, Demirkan A, Oostra BA, de Andrade M, Turner ST, Ding J, Andrews JS, Freedman BI, Giulianini F, Koenig W, Illig T, Meisinger C, Gieger C, Zgaga L, Zemunik T, Boban M, Minelli C, Wheeler HE, Igl W, Zaboli G, Wild SH, Wright AF, Campbell H, Ellinghaus D, Nöthlings U, Jacobs G, Biffar R, Ernst F, Homuth G, Kroemer HK, Nauck M, Stracke S, Völker U, Völzke H, Kovacs P, Stumvoll M, Mägi R, Hofman A, Uitterlinden AG, Rivadeneira F, Aulchenko YS, Polasek O, Hastie N, Vitart V, Helmer C, Wang JJ, Stengel B, Ruggiero D, Bergmann S, Kähönen M, Viikari J, Nikopensius T, Province M, Ketkar S, Colhoun H, Doney A, Robino A, Krämer BK, Portas L, Ford I, Buckley BM, Adam M, Thun GA, Paulweber B, Haun M, Sala C, Mitchell P, Ciullo M, Kim SK, Vollenweider P, Raitakari O, Metspalu A, Palmer C, Gasparini P, Pirastu M, Jukema JW, Probst-Hensch NM, Kronenberg F, Toniolo D, Gudnason V, Shuldiner AR, Coresh J, Schmidt R, Ferrucci L, Siscovick DS, van Duijn CM, Borecki IB, Kardia SL, Liu Y, Curhan GC, Rudan I, Gyllensten U, Wilson JF, Franke A, Pramstaller PP, Rettig R, Prokopenko I, Witteman J, Hayward C, Ridker PM, Parsa A, Bochud M, Heid IM, Kao WH, Fox CS, Köttgen A.
Avaldatud: Human Molecular Genetics. 2012 Dec 15;21(24):5329-43.
DOI: 10.1093/hmg/dds369


A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
Manning AK, Hivert MF, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu CT, Bielak LF, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga JJ, Ingelsson E, Jackson AU, Johnson T, Kanoni S, Ladenvall C, Lagou V, Lahti J, Lecoeur C, Liu Y, Martinez-Larrad MT, Montasser ME, Navarro P, Perry JR, Rasmussen-Torvik LJ, Salo P, Sattar N, Shungin D, Strawbridge RJ, Tanaka T, van Duijn CM, An P, de Andrade M, Andrews JS, Aspelund T, Atalay M, Aulchenko Y, Balkau B, Bandinelli S, Beckmann JS, Beilby JP, Bellis C, Bergman RN, Blangero J, Boban M, Boehnke M, Boerwinkle E, Bonnycastle LL, Boomsma DI, Borecki IB, Böttcher Y, Bouchard C, Brunner E, Budimir D, Campbell H, Carlson O, Chines PS, Clarke R, Collins FS, Corbatón-Anchuelo A, Couper D, de Faire U, Dedoussis GV, Deloukas P, Dimitriou M, Egan JM, Eiriksdottir G, Erdos MR, Eriksson JG, Eury E, Ferrucci L, Ford I, Forouhi NG, Fox CS, Franzosi MG, Franks PW, Frayling TM, Froguel P, Galan P, de Geus E, Gigante B, Glazer NL, Goel A, Groop L, Gudnason V, Hallmans G, Hamsten A, Hansson O, Harris TB, Hayward C, Heath S, Hercberg S, Hicks AA, Hingorani A, Hofman A, Hui J, Hung J, Jarvelin MR, Jhun MA, Johnson PC, Jukema JW, Jula A, Kao WH, Kaprio J, Kardia SL, Keinanen-Kiukaanniemi S, Kivimaki M, Kolcic I, Kovacs P, Kumari M, Kuusisto J, Kyvik KO, Laakso M, Lakka T, Lannfelt L, Lathrop GM, Launer LJ, Leander K, Li G, Lind L, Lindstrom J, Lobbens S, Loos RJ, Luan J, Lyssenko V, Mägi R, Magnusson PK, Marmot M, Meneton P, Mohlke KL, Mooser V, Morken MA, Miljkovic I, Narisu N, O''Connell J, Ong KK, Oostra BA, Palmer LJ, Palotie A, Pankow JS, Peden JF, Pedersen NL, Pehlic M, Peltonen L, Penninx B, Pericic M, Perola M, Perusse L, Peyser PA, Polasek O, Pramstaller PP, Province MA, Räikkönen K, Rauramaa R, Rehnberg E, Rice K, Rotter JI, Rudan I, Ruokonen A, Saaristo T, Sabater-Lleal M, Salomaa V, Savage DB, Saxena R, Schwarz P, Seedorf U, Sennblad B, Serrano-Rios M, Shuldiner AR, Sijbrands EJ, Siscovick DS, Smit JH, Small KS, Smith NL, Smith AV, Stančáková A, Stirrups K, Stumvoll M, Sun YV, Swift AJ, Tönjes A, Tuomilehto J, Trompet S, Uitterlinden AG, Uusitupa M, Vikström M, Vitart V, Vohl MC, Voight BF, Vollenweider P, Waeber G, Waterworth DM, Watkins H, Wheeler E, Widen E, Wild SH, Willems SM, Willemsen G, Wilson JF, Witteman JC, Wright AF, Yaghootkar H, Zelenika D, Zemunik T, Zgaga L; DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium; Multiple Tissue Human Expression Resource (MUTHER) Consortium, Wareham NJ, McCarthy MI, Barroso I, Watanabe RM, Florez JC, Dupuis J, Meigs JB, Langenberg C.
Avaldatud: Nat Genet. 2012 May 13;44(6):659-69
DOI: 10.1038/ng.2274


Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases
Mägi R, Asimit JL, Day-Williams AG, Zeggini E, Morris AP.
Avaldatud: Genet Epidemiol. 2012 Sep 5
DOI: 10.1002/gepi.21675


A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site.
Nürnberg ST, Rendon A, Smethurst PA, Paul DS, Voss K, Thon JN, Lloyd-Jones H, Sambrook JG, Tijssen MR; HaemGen Consortium, Italiano JE Jr, Deloukas P, Gottgens B, Soranzo N, Ouwehand WH.
Avaldatud: Blood. 2012 Dec 6;120(24):4859-68.
DOI: doi: 10.1182/blood-2012-01-401893


The perspective from EASAC and FEAM on direct-to-consumer genetic testing for health-related purposes
Robin Fears*, Volker ter Meulen and for the EASAC–FEAM Working Group (Participants in the Working Group were: Stefania Boccia, Martina Cornel, Marc Delpech, Anne De Paepe, Xavier Estivill, Mats Hansson, Katia Karalis, Andres Metspalu, Markus Nöthen, Peter Propping, Jorge Sequeiros, Ron Zimmern, Volker ter Meulen (Chair), Robin Fears (secretariat).
Avaldatud: European Journal of Human Genetics (2012), 1–5
DOI: doi:10.1038/ejhg.2012.238


A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila
Allebrandt KV, Amin N, Müller-Myhsok B, Esko T, Teder-Laving M, Azevedo RV, Hayward C, van Mill J, Vogelzangs N, Green EW, Melville SA, Lichtner P, Wichmann HE, Oostra BA, Janssens AC, Campbell H, Wilson JF, Hicks AA, Pramstaller PP, Dogas Z, Rudan I, Merrow M, Penninx B, Kyriacou CP, Metspalu A, van Duijn CM, Meitinger T, Roenneberg T.
Avaldatud: Mol Psychiatry. Nov 22.
DOI: 10.1038/mp.2011.142


Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.
Chasman DI, Fuchsberger C, Pattaro C, Teumer A, Böger CA, Endlich K, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, Foster MC, O''Seaghdha CM, Glazer N, Isaacs A, Liu CT, Smith AV, O''Connell JR, Struchalin M, Tanaka T, Li G, Johnson AD, Gierman HJ, Feitosa MF, Hwang SJ, Atkinson EJ, Lohman K, Cornelis MC, Johansson A, Tönjes A, Dehghan A, Lambert JC, Holliday EG, Sorice R, Kutalik Z, Lehtimäki T, Esko T, Deshmukh H, Ulivi S, Chu AY, Murgia F, Trompet S, Imboden M, Coassin S, Pistis G; CARDIoGRAM Consortium; ICBP Consortium; CARe Consortium; WTCCC2, Harris TB, Launer LJ, Aspelund T, Eiriksdottir G, Mitchell BD, Boerwinkle E, Schmidt H, Cavalieri M, Rao M, Hu F, Demirkan A, Oostra BA, de Andrade M, Turner ST, Ding J, Andrews JS, Freedman BI, Giulianini F, Koenig W, Illig T, Meisinger C, Gieger C, Zgaga L, Zemunik T, Boban M, Minelli C, Wheeler HE, Igl W, Zaboli G, Wild SH, Wright AF, Campbell H, Ellinghaus D, Nöthlings U, Jacobs G, Biffar R, Ernst F, Homuth G, Kroemer HK, Nauck M, Stracke S, Völker U, Völzke H, Kovacs P, Stumvoll M, Mägi R, Hofman A, Uitterlinden AG, Rivadeneira F, Aulchenko YS, Polasek O, Hastie N, Vitart V, Helmer C, Wang JJ, Stengel B, Ruggiero D, Bergmann S, Kähönen M, Viikari J, Nikopensius T, Province M, Ketkar S, Colhoun H, Doney A, Robino A, Krämer BK, Portas L, Ford I, Buckley BM, Adam M, Thun GA, Paulweber B, Haun M, Sala C, Mitchell P, Ciullo M, Kim SK, Vollenweider P, Raitakari O, Metspalu A, Palmer C, Gasparini P, Pirastu M, Jukema JW, Probst-Hensch NM, Kronenberg F, Toniolo D, Gudnason V, Shuldiner AR, Coresh J, Schmidt R, Ferrucci L, Siscovick DS, van Duijn CM, Borecki IB, Kardia SL, Liu Y, Curhan GC, Rudan I, Gyllensten U, Wilson JF, Franke A, Pramstaller PP, Rettig R, Prokopenko I, Witteman J, Hayward C, Ridker PM, Parsa A, Bochud M, Heid IM, Kao WH, Fox CS, Köttgen A.
Avaldatud: Hum Mol Genet 2012; 21(24): 5329-5343


Meta-analysis of microrna expression in lung cancer
Võsa U, Vooder T, Kolde R, Vilo J, Metspalu A, Annilo T.
Avaldatud: International Journal of Cancer. Published online: 27 DEC 2012
DOI: doi:10.1002/ijc.27981


Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions
Amin N, Hottenga JJ, Hansell NK, Janssens AC, de Moor MH, Madden PA, Zorkoltseva IV, Penninx BW, Terracciano A, Uda M, Tanaka T, Esko T, Realo A, Ferrucci L, Luciano M, Davies G, Metspalu A, Abecasis GR, Deary IJ, Raikkonen K, Bierut LJ, Costa PT, Saviouk V, Zhu G, Kirichenko AV, Isaacs A, Aulchenko YS, Willemsen G, Heath AC, Pergadia ML, Medland SE, Axenovich TI, de Geus E, Montgomery GW, Wright MJ, Oostra BA, Martin NG, Boomsma DI, van Duijn CM.
Avaldatud: European Journal of Human Genetics
DOI: 10.1038/ejhg.2012.263.


Large-scale association analysis identifies new risk loci for coronary artery disease
The CARDIoGRAMplusC4D Consortium, Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, Ingelsson E, Saleheen D, Erdmann J, Goldstein BA, Stirrups K, König IR, Cazier JB, Johansson A, Hall AS, Lee JY, Willer CJ, Chambers JC, Esko T, Folkersen L, Goel A, Grundberg E, Havulinna AS, Ho WK, Hopewell JC, Eriksson N, Kleber ME, Kristiansson K, Lundmark P, Lyytikäinen LP, Rafelt S, Shungin D, Strawbridge RJ, Thorleifsson G, Tikkanen E, Van Zuydam N, Voight BF, Waite LL, Zhang W, Ziegler A, Absher D, Altshuler D, Balmforth AJ, Barroso I, Braund PS, Burgdorf C, Claudi-Boehm S, Cox D, Dimitriou M, Do R; DIAGRAM Consortium; CARDIOGENICS Consortium, Doney AS, Mokhtari NE, Eriksson P, Fischer K, Fontanillas P, Franco-Cereceda A, Gigante B, Groop L, Gustafsson S, Hager J, Hallmans G, Han BG, Hunt SE, Kang HM, Illig T, Kessler T, Knowles JW, Kolovou G, Kuusisto J, Langenberg C, Langford C, Leander K, Lokki ML, Lundmark A, McCarthy MI, Meisinger C, Melander O, Mihailov E, Maouche S, Morris AD, Müller-Nurasyid M; MuTHER Consortium, Nikus K, Peden JF, Rayner NW, Rasheed A, Rosinger S, Rubin D, Rumpf MP, Schäfer A, Sivananthan M, Song C, Stewart AF, Tan ST, Thorgeirsson G, Schoot CE, Wagner PJ; Wellcome Trust Case Control Consortium, Wells GA, Wild PS, Yang TP, Amouyel P, Arveiler D, Basart H, Boehnke M, Boerwinkle E, Brambilla P, Cambien F, Cupples AL, de Faire U, Dehghan A, Diemert P, Epstein SE, Evans A, Ferrario MM, Ferrières J, Gauguier D, Go AS, Goodall AH, Gudnason V, Hazen SL, Holm H, Iribarren C, Jang Y, Kähönen M, Kee F, Kim HS, Klopp N, Koenig W, Kratzer W, Kuulasmaa K, Laakso M, Laaksonen R, Lee JY, Lind L, Ouwehand WH, Parish S, Park JE, Pedersen NL, Peters A, Quertermous T, Rader DJ, Salomaa V, Schadt E, Shah SH, Sinisalo J, Stark K, Stefansson K, Trégouët DA, Virtamo J, Wallentin L, Wareham N, Zimmermann ME, Nieminen MS, Hengstenberg C, Sandhu MS, Pastinen T, Syvänen AC, Hovingh GK, Dedoussis G, Franks PW, Lehtimäki T, Metspalu A, Zalloua PA, Siegbahn A, Schreiber S, Ripatti S, Blankenberg SS, Perola M, Clarke R, Boehm BO, O''''''''Donnell C, Reilly MP, März W, Collins R, Kathiresan S, Hamsten A, Kooner JS, Thorsteinsdottir U, Danesh J, Palmer CN, Roberts R, Watkins H, Schunkert H, Samani NJ.
Avaldatud: Nature Genetics Dec 2.
DOI: 10.1038/ng.2480.


DNA methylation dynamics in the hepatic CYP3A4 gene promoter
Kacevska M, Ivanov M, Wyss A, Kasela S, Milani L, Rane A, Ingelman-Sundberg M.
Avaldatud: Biochimie. 2012 Nov; 94(11):2338-44.
DOI: 10.1016/j.biochi.2012.07.013.


Genetic effects on variability: FTO genotype is associated with phenotypic variance of body mass index
Yang J, Loos RJ, Powell JE, Medland SE, Speliotes EK, Chasman DI, Rose LM, Thorleifsson G, Steinthorsdottir V, Mägi R, Waite L, Smith AV, Yerges-Armstrong LM, Monda KL, Hadley D, Mahajan A, Li G, Kapur K, Vitart V, Huffman JE, Wang SR, Palmer C, Esko T, Fischer K, Zhao JH, Demirkan A, Isaacs A, Feitosa MF, Luan J, Heard-Costa NL, White C, Jackson AU, Preuss M, Ziegler A, Eriksson J, Kutalik Z, Frau F, Nolte IM, Van Vliet-Ostaptchouk JV, Hottenga JJ, Jacobs KB, Verweij N, Goel A, Medina-Gomez C, Estrada K, Bragg-Gresham JL, Sanna S, Sidore C, Tyrer J, Teumer A, Prokopenko I, Mangino M, Lindgren CM, Assimes TL, Shuldiner AR, Hui J, Beilby JP, McArdle WL, Hall P, Haritunians T, Zgaga L, Kolcic I, Polasek O, Zemunik T, Oostra BA, Junttila MJ, Grönberg H, Schreiber S, Peters A, Hicks AA, Stephens J, Foad NS, Laitinen J, Pouta A, Kaakinen M, Willemsen G, Vink JM, Wild SH, Navis G, Asselbergs FW, Homuth G, John U, Iribarren C, Harris T, Launer L, Gudnason V, O''''Connell JR, Boerwinkle E, Cadby G, Palmer LJ, James AL, Musk AW, Ingelsson E, Psaty BM, Beckmann JS, Waeber G, Vollenweider P, Hayward C, Wright AF, Rudan I, Groop LC, Metspalu A, Tee Khaw K, van Duijn CM, Borecki IB, Province MA, Wareham NJ, Tardif JC, Huikuri HV, Cupples LA, Atwood LD, Fox CS, Boehnke M, Collins FS, Mohlke KL, Erdmann J, Schunkert H, Hengstenberg C, Stark K, Lorentzon M, Ohlsson C, Cusi D, Staessen JA, Van der Klauw MM, Pramstaller PP, Kathiresan S, Jolley JD, Ripatti S, Jarvelin MR, de Geus EJ, Boomsma DI, Penninx B, Wilson JF, Campbell H, Chanock SJ, van der Harst P, Hamsten A, Watkins H, Hofman A, Witteman JC, Zillikens MC, Uitterlinden AG, Rivadeneira F, Zillikens MC, Kiemeney LA, Vermeulen SH, Abecasis GR, Schlessinger D, Schipf S, Stumvoll M, Tönjes A, Spector TD, North KE, Lettre G, McCarthy MI, Berndt SI, Heath AC, Madden PA, Nyholt DR, Montgomery GW, Martin NG, McKnight B, Strachan DP, Hill WG, Snieder H, Ridker PM, Thorsteinsdottir U, Stefansson K, Frayling TM, Hirschhorn JN, Goddard ME, Visscher PM.
Avaldatud: Nature, Vol: 490 (7419) pp: 267-72; Published: 2012-Oct-11
DOI: 10.1038/nature11401


History of the Diagnosis of a Sexually Transmitted Disease is Linked to Normal Variation in Personality Traits.
Mõttus R, Realo A, Allik J, Esko T, Metspalu A.
Avaldatud: The Journal of Sexual Medicine; Volume 9, Issue 11, Pages 2733–2981
DOI: 10.1111/j.1743-6109.2012.02891.x.


Influence of Common Genetic Variation on Lung Cancer Risk: Meta-Analysis of 14,900 Cases and 29,485 Controls.
Timofeeva MN, Hung RJ, Rafnar T, Christiani DC, Field JK, Bickeboller H, Risch A, McKay JD, Wang Y, Dai J, Gaborieau V, McLaughlin J, Brenner D, Narod S, Caporaso NE, Albanes D, Thun M, Eisen T, Wichmann HE, Rosenberger A, Han Y, Chen W, Zhu D, Spitz M, Wu X, Pande M, Zhao Y, Zaridze D, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Mates D, Bencko V, Foretova L, Janout V, Krokan HE, Gabrielsen ME, Skorpen F, Vatten L, Njølstad I, Chen C, Goodman G, Lathrop M, Benhamou S, Vooder T, Välk K, Nelis M, Metspalu A, Raji O, Chen Y, Gosney J, Liloglou T, Muley T, Dienemann H, Thorleifsson G, Shen H, Stefansson K, Brennan P, Amos CI, Houlston R, Landi MT; for TRICL Research Team.
Avaldatud: Human Molecular Genetics. Volume: 21 Issue: 22 Pages: 4980-95
DOI: 10.1093/hmg/dds334


A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.
Marjamaa A, Oikarinen L, Porthan K, Ripatti S, Peloso G, Noseworthy PA, Viitasalo M, Nieminen MS, Toivonen L, Kontula K, Peltonen L, Havulinna AS, Jula A, O''Donnell CJ, Newton-Cheh C, Perola M, Salomaa V.
Avaldatud: Heart Rhythm. 2012 Jul;9 (7):1099-103. Epub 2012 Feb 15.
DOI: 10.1016/j.hrthm.2012.02.019


Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
Scott RA, Lagou V, Welch RP, Wheeler E, Montasser ME, Luan J, Mägi R, Strawbridge RJ, Rehnberg E, Gustafsson S, Kanoni S, Rasmussen-Torvik LJ, Yengo L, Lecoeur C, Shungin D, Sanna S, Sidore C, Johnson PC, Jukema JW, Johnson T, Mahajan A, Verweij N, Thorleifsson G, Hottenga JJ, Shah S, Smith AV, Sennblad B, Gieger C, Salo P, Perola M, Timpson NJ, Evans DM, Pourcain BS, Wu Y, Andrews JS, Hui J, Bielak LF, Zhao W, Horikoshi M, Navarro P, Isaacs A, O''''Connell JR, Stirrups K, Vitart V, Hayward C, Esko T, Mihailov E, Fraser RM, Fall T, Voight BF, Raychaudhuri S, Chen H, Lindgren CM, Morris AP, Rayner NW, Robertson N, Rybin D, Liu CT, Beckmann JS, Willems SM, Chines PS, Jackson AU, Kang HM, Stringham HM, Song K, Tanaka T, Peden JF, Goel A, Hicks AA, An P, Müller-Nurasyid M, Franco-Cereceda A, Folkersen L, Marullo L, Jansen H, Oldehinkel AJ, Bruinenberg M, Pankow JS, North KE, Forouhi NG, Loos RJ, Edkins S, Varga TV, Hallmans G, Oksa H, Antonella M, Nagaraja R, Trompet S, Ford I, Bakker SJ, Kong A, Kumari M, Gigante B, Herder C, Munroe PB, Caulfield M, Antti J, Mangino M, Small K, Miljkovic I, Liu Y, Atalay M, Kiess W, James AL, Rivadeneira F, Uitterlinden AG, Palmer CN, Doney AS, Willemsen G, Smit JH, Campbell S, Polasek O, Bonnycastle LL, Hercberg S, Dimitriou M, Bolton JL, Fowkes GR, Kovacs P, Lindström J, Zemunik T, Bandinelli S, Wild SH, Basart HV, Rathmann W, Grallert H; DIAbetes Genetics Replication and Meta-analysis (DIAGRAM) Consortium, Maerz W, Kleber ME, Boehm BO, Peters A, Pramstaller PP, Province MA, Borecki IB, Hastie ND, Rudan I, Campbell H, Watkins H, Farrall M, Stumvoll M, Ferrucci L, Waterworth DM, Bergman RN, Collins FS, Tuomilehto J, Watanabe RM, de Geus EJ, Penninx BW, Hofman A, Oostra BA, Psaty BM, Vollenweider P, Wilson JF, Wright AF, Hovingh GK, Metspalu A, Uusitupa M, Magnusson PK, Kyvik KO, Kaprio J, Price JF, Dedoussis GV, Deloukas P, Meneton P, Lind L, Boehnke M, Shuldiner AR, van Duijn CM, Morris AD, Toenjes A, Peyser PA, Beilby JP, Körner A, Kuusisto J, Laakso M, Bornstein SR, Schwarz PE, Lakka TA, Rauramaa R, Adair LS, Smith GD, Spector TD, Illig T, de Faire U, Hamsten A, Gudnason V, Kivimaki M, Hingorani A, Keinanen-Kiukaanniemi SM, Saaristo TE, Boomsma DI, Stefansson K, van der Harst P, Dupuis J, Pedersen NL, Sattar N, Harris TB, Cucca F, Ripatti S, Salomaa V, Mohlke KL, Balkau B, Froguel P, Pouta A, Jarvelin MR, Wareham NJ, Bouatia-Naji N, McCarthy MI, Franks PW, Meigs JB, Teslovich TM, Florez JC, Langenberg C, Ingelsson E, Prokopenko I, Barroso I.
Avaldatud: Nature Genetics 2012 Sep; 44(9):991-1005. Epub 2012 Aug 12.
DOI: 10.1038/ng.2385


Methylation markers of early-stage non-small cell lung cancer
Lokk K, Vooder T, Kolde R, Välk K, Võsa U, Roosipuu R, Milani L, Fischer K, Koltsina M, Urgard E, Annilo T, Metspalu A, Tõnisson N.
Avaldatud: PLos One 2012;7(6):e39813. Epub 2012 Jun 29.
DOI: 10.1371/journal.pone.0039813


Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
the DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Morris AP, Voight BF, Teslovich TM, Ferreira T, Segrè AV, Steinthorsdottir V, Strawbridge RJ, Khan H, Grallert H, Mahajan A, Prokopenko I, Kang HM, Dina C, Esko T, Fraser RM, Kanoni S, Kumar A, Lagou V, Langenberg C, Luan J, Lindgren CM, Müller-Nurasyid M, Pechlivanis S, Rayner NW, Scott LJ, Wiltshire S, Yengo L, Kinnunen L, Rossin EJ, Raychaudhuri S, Johnson AD, Dimas AS, Loos RJ, Vedantam S, Chen H, Florez JC, Fox C, Liu CT, Rybin D, Couper DJ, Kao WH, Li M, Cornelis MC, Kraft P, Sun Q, van Dam RM, Stringham HM, Chines PS, Fischer K, Fontanillas P, Holmen OL, Hunt SE, Jackson AU, Kong A, Lawrence R, Meyer J, Perry JR, Platou CG, Potter S, Rehnberg E, Robertson N, Sivapalaratnam S, Stančáková A, Stirrups K, Thorleifsson G, Tikkanen E, Wood AR, Almgren P, Atalay M, Benediktsson R, Bonnycastle LL, Burtt N, Carey J, Charpentier G, Crenshaw AT, Doney AS, Dorkhan M, Edkins S, Emilsson V, Eury E, Forsen T, Gertow K, Gigante B, Grant GB, Groves CJ, Guiducci C, Herder C, Hreidarsson AB, Hui J, James A, Jonsson A, Rathmann W, Klopp N, Kravic J, Krjutškov K, Langford C, Leander K, Lindholm E, Lobbens S, Männistö S, Mirza G, Mühleisen TW, Musk B, Parkin M, Rallidis L, Saramies J, Sennblad B, Shah S, Sigurðsson G, Silveira A, Steinbach G, Thorand B, Trakalo J, Veglia F, Wennauer R, Winckler W, Zabaneh D, Campbell H, van Duijn C, Uitterlinden AG, Hofman A, Sijbrands E, Abecasis GR, Owen KR, Zeggini E, Trip MD, Forouhi NG, Syvänen AC, Eriksson JG, Peltonen L, Nöthen MM, Balkau B, Palmer CN, Lyssenko V, Tuomi T, Isomaa B, Hunter DJ, Qi L; Wellcome Trust Case Control Consortium; Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators; Genetic Investigation of ANthropometric Traits (GIANT) Consortium; Asian Genetic Epidemiology Network–Type 2 Diabetes (AGEN-T2D) Consortium; South Asian Type 2 Diabetes (SAT2D) Consortium, Shuldiner AR, Roden M, Barroso I, Wilsgaard T, Beilby J, Hovingh K, Price JF, Wilson JF, Rauramaa R, Lakka TA, Lind L, Dedoussis G, Njølstad I, Pedersen NL, Khaw KT, Wareham NJ, Keinanen-Kiukaanniemi SM, Saaristo TE, Korpi-Hyövälti E, Saltevo J, Laakso M, Kuusisto J, Metspalu A, Collins FS, Mohlke KL, Bergman RN, Tuomilehto J, Boehm BO, Gieger C, Hveem K, Cauchi S, Froguel P, Baldassarre D, Tremoli E, Humphries SE, Saleheen D, Danesh J, Ingelsson E, Ripatti S, Salomaa V, Erbel R, Jöckel KH, Moebus S, Peters A, Illig T, de Faire U, Hamsten A, Morris AD, Donnelly PJ, Frayling TM, Hattersley AT, Boerwinkle E, Melander O, Kathiresan S, Nilsson PM, Deloukas P, Thorsteinsdottir U, Groop LC, Stefansson K, Hu F, Pankow JS, Dupuis J, Meigs JB, Altshuler D, Boehnke M, McCarthy MI.
Avaldatud: Nature Genetics. 2012 Sep;44(9):981-90. Epub 2012 Aug 12.
DOI: 10.1038/ng.2383


Results from a blind and a non-blind randomised trial run in parallel: experience from the Estonian Postmenopausal Hormone Therapy (EPHT) Trial
Veerus P, Fischer K, Hakama M, Hemminki E; EPHT Trial
Avaldatud: BMC Medical Research Methodology. 2012 Apr 4;12:44.


Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium
Kazma R, Babron MC, Gaborieau V, Génin E, Brennan P, Hung RJ, McLaughlin JR, Krokan HE, Elvestad MB, Skorpen F, Anderssen E, Vooder T, Välk K, Metspalu A, Field JK, Lathrop M, Sarasin A, Benhamou S; ILCCO consortium.
Avaldatud: Carcinogenesis. 2012 May;33(5):1059-64. Epub 2012 Mar 1.
DOI: 10.1093/carcin/bgs116.


Genome-wide Meta-analysis of Common Variant Differences between Men and Women
Boraska V, Jeroncic A, Colonna V, Southam L, Nyholt DR, William Rayner N, Perry JR, Toniolo D, Albrecht E, Ang W, Bandinelli S, Barbalic M, Barroso I, Beckmann JS, Biffar R, Boomsma D, Campbell H, Corre T, Erdmann J, Esko T, Fischer K, Franceschini N, Frayling TM, Girotto G, Gonzalez JR, Harris TB, Heath AC, Heid IM, Hoffmann W, Hofman A, Horikoshi M, Hua Zhao J, Jackson AU, Hottenga JJ, Jula A, Kähönen M, Khaw KT, Kiemeney LA, Klopp N, Kutalik Z, Lagou V, Launer LJ, Lehtimäki T, Lemire M, Lokki ML, Loley C, Luan J, Mangino M, Mateo Leach I, Medland SE, Mihailov E, Montgomery GW, Navis G, Newnham J, Nieminen MS, Palotie A, Panoutsopoulou K, Peters A, Pirastu N, Polasek O, Rehnström K, Ripatti S, Ritchie GR, Rivadeneira F, Robino A, Samani NJ, Shin SY, Sinisalo J, Smit JH, Soranzo N, Stolk L, Swinkels DW, Tanaka T, Teumer A, Tönjes A, Traglia M, Tuomilehto J, Valsesia A, van Gilst WH, van Meurs JB, Smith AV, Viikari J, Vink JM, Waeber G, Warrington NM, Widen E, Willemsen G, Wright AF, Zanke BW, Zgaga L; Wellcome Trust Case Control Consortium (WTCCC), Boehnke M, d''''Adamo AP, de Geus E, Demerath EW, den Heijer M, Eriksson JG, Ferrucci L, Gieger C, Gudnason V, Hayward C, Hengstenberg C, Hudson TJ, Järvelin MR, Kogevinas M, Loos RJ, Martin NG, Metspalu A, Pennell CE, Penninx BW, Perola M, Raitakari O, Salomaa V, Schreiber S, Schunkert H, Spector TD, Stumvoll M, Uitterlinden AG, Ulivi S, van der Harst P, Vollenweider P, Völzke H, Wareham NJ, Wichmann HE, Wilson JF, Rudan I, Xue Y, Zeggini E.
Avaldatud: Human Molecular Genetics. Vol: 21, Issue: 21, pp: 4805-15. Published: 2012-Nov-1.
DOI: 10.1093/hmg/dds304


Toward a roadmap in global biobanking for health
Harris JR, Burton P, Knoppers BM, Lindpaintner K, Bledsoe M, Brookes AJ, Budin-Ljøsne I, Chisholm R, Cox D, Deschênes M, Fortier I, Hainaut P, Hewitt R, Kaye J, Litton JE, Metspalu A, Ollier B, Palmer LJ, Palotie A, Pasterk M, Perola M, Riegman PH, van Ommen GJ, Yuille M, Zatloukal K.
Avaldatud: European Journal of Human Genetics, Jun 20.
DOI: 10.1038/ejhg.2012.96.


Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations
Yukinori Okada, Xueling Sim, Min Jin Go, Jer-Yuarn Wu, Dongfeng Gu, Fumihiko Takeuchi, Atsushi Takahashi, Shiro Maeda, Tatsuhiko Tsunoda, Peng Chen, Su-Chi Lim, Tien-Yin Wong, Jianjun Liu, Terri L Young, Tin Aung, Mark Seielstad, Yik-Ying Teo, Young Jin Kim, Jong-Young Lee, Bok-Ghee Han, Daehee Kang, Chien-Hsiun Chen, Fuu-Jen Tsai, Li-Ching Chang, S-J Cathy Fann, Hao Mei, Dabeeru C Rao, James E Hixson, Shufeng Chen, Tomohiro Katsuya, Masato Isono, Toshio Ogihara, John C Chambers, Weihua Zhang, Jaspal S Kooner, The KidneyGen Consortium, The CKDGen Consortium, Eva Albrecht, The GUGC consortium, Kazuhiko Yamamoto, Michiaki Kubo, Yusuke Nakamura, Naoyuki Kamatani, Norihiro Kato, Jiang He, Yuan-Tsong Chen, Yoon Shin Cho, E-Shyong Tai & Toshihiro Tanaka
Avaldatud: Nature Genetics 44, 904–909 (Published online 15 July)
DOI: 10.1038/ng.2352


Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O''Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T, Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM, Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A, Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtimäki T, Woodward OM, Okada Y, Tin A, Müller C, Oldmeadow C, Putku M, Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK, Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M, Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR Jr, Liu K, D''Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G, Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B, Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ, Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E, Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R, Döring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann HE, Davies G, Gow AJ, Bruinenberg M; LifeLines Cohort Study, Stolk RP, Kooner JS, Zhang W, Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G, Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Leach IM, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F, Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R, Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM, Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa V, Shin SY, Spector TD, Sala C, Ridker PM, Kähönen M, Viikari J, Hengstenberg C, Nelson CP; CARDIoGRAM Consortium; DIAGRAM Consortium; ICBP Consortium; MAGIC Consortium, Meschia JF, Nalls MA, Sharma P, Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M, Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S, Probst-Hensch NM, Völzke H, Gudnason V, Parsa A, Schmidt R, Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Polašek O, Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH, Chambers JC, März W, Pramstaller PP, Snieder H, Gyllensten U, Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S, Dunlop MG, Tönjes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI, Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M, Gieger C.
Avaldatud: Nature Genetics
DOI: 10.1038/ng.2500


Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity
Tõnu Esko, Massimo Mezzavilla, Mari Nelis, Christelle Borel, Tadeusz Debniak, Eveliina Jakkula, Antonio Julia, Sena Karachanak, Andrey Khrunin, Peter Kisfali, Veronika Krulisova, Zita Aušrelé Kučinskiené, Karola Rehnström, Michela Traglia, Liene Nikitina-Zake, Fritz Zimprich, Stylianos E Antonarakis, Xavier Estivill, Damjan Glavač, Ivo Gut, Janis Klovins, Michael Krawczak, Vaidutis Kučinskas, Mark Lathrop, Milan Macek, Sara Marsa, Thomas Meitinger, Béla Melegh, Svetlana Limborska, Jan Lubinski, Aarno Paolotie, Stefan Schreiber, Draga Toncheva, Daniela Toniolo, H-Erich Wichmann, Alexander Zimprich, Mait Metspalu, Paolo Gasparini, Andres Metspalu and Pio D''Adamo4
Avaldatud: European Journal of Human Genetics
DOI: 10.1038/ejhg.2012.229


Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Lam C Tsoi, Sarah L Spain, Jo Knight, Eva Ellinghaus, Philip E Stuart, Francesca Capon, Jun Ding, Yanming Li, Trilokraj Tejasvi, Johann E Gudjonsson, Hyun M Kang, Michael H Allen, Ross McManus, Giuseppe Novelli, Lena Samuelsson, Joost Schalkwijk, Mona Ståhle, A David Burden, Catherine H Smith, Michael J Cork, Xavier Estivill, Anne M Bowcock, Gerald G Krueger, Wolfgang Weger, Jane Worthington, Rachid Tazi-Ahnini, Frank O Nestle, Adrian Hayday, Per Hoffmann, Juliane Winkelmann, Cisca Wijmenga, Cordelia Langford, Sarah Edkins, Robert Andrews, Hannah Blackburn, Amy Strange, Gavin Band, Richard D Pearson, Damjan Vukcevic, Chris C A Spencer, Panos Deloukas, Ulrich Mrowietz, Stefan Schreiber, Stephan Weidinger, Sulev Koks, Külli Kingo, Tonu Esko, Andres Metspalu, Henry W Lim, John J Voorhees, Michael Weichenthal, H Erich Wichmann, Vinod Chandran, Cheryl F Rosen, Proton Rahman, Dafna D Gladman, Christopher E M Griffiths, Andre Reis, Juha Kere, Collaborative Association Study of Psoriasis (CASP), Genetic Analysis of Psoriasis Consortium, Psoriasis Association Genetics Extension, Wellcome Trust Case Control Consortium 2, Rajan P Nair, Andre Franke, Jonathan N W N Barker, Goncalo R Abecasis, James T Elder & Richard C Trembath
Avaldatud: Nature Genetics 44, 1341–1348 (Published online 11 November 2012)
DOI: doi:10.1038/ng.2467


Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study (link)
arcOGEN Consortium and arcOGEN Collaborators, /…/, Esko T, Metspalu A et al.
Avaldatud: The Lancet. Published Online July 3, 2012
DOI: 10.1016/S0140-6736(12)60681-3


Evidence of Inbreeding Depression on Human Height
Ruth McQuillan, Niina Eklund, Nicola Pirastu, Maris Kuningas, Brian P. McEvoy, To ̃nu Esko, Tanguy Corre, Gail Davies, Marika Kaakinen, Leo-Pekka Lyytika ̈inen, Kati Kristiansson, Aki S. Havulinna, Martin Go ̈gele, Veronique Vitart, Albert Tenesa, Yurii Aulchenko, Caroline Hayward, A ̊sa Johansson, Mladen Boban, Sheila Ulivi, Antonietta Robino, Vesna Boraska, Wilmar Igl, Sarah H. Wild, Lina Zgaga, Najaf Amin, Evropi Theodoratou, Ozren Polasˇek, Giorgia Girotto, Lorna M. Lopez, Cinzia Sala, Jari Lahti, Tiina Laatikainen, Inga Prokopenko, Mart Kals, Jorma Viikari, Jian Yang, Anneli Pouta, Karol Estrada, Albert Hofman, Nelson Freimer, Nicholas G. Martin, Mika Ka ̈ho ̈nen, Lili Milani, Markku Helio ̈vaara, Erkki Vartiainen, Katri Ra ̈ikko ̈nen, Corrado Masciullo, John M. Starr, Andrew A. Hicks, Laura Esposito, Ivana Kolcˇic ́, Susan M. Farrington, Ben Oostra, Tatijana Zemunik, Harry Campbell, Mirna Kirin, Marina Pehlic, Flavio Faletra, David Porteous, Giorgio Pistis, Elisabeth Wide ́n, Veikko Salomaa, Seppo Koskinen, Krista Fischer, Terho Lehtima ̈ki, Andrew Heath, Mark I. McCarthy, Fernando Rivadeneira, Grant W. Montgomery, Henning Tiemeier, Anna-Liisa Hartikainen, Pamela A. F. Madden, Pio d’Adamo, Nicholas D. Hastie, Ulf Gyllensten, Alan F. Wright, Cornelia M. van Duijn, Malcolm Dunlop, Igor Rudan, Paolo Gasparini, Peter P. Pramstaller, Ian J. Deary, Daniela Toniolo, Johan G. Eriksson, Antti Jula, Olli T. Raitakari, Andres Metspalu, Markus Perola, Marjo-Riitta Ja ̈rvelin, Andre ́ Uitterlinden, Peter M. Visscher, James F. Wilson1* on behalf of the ROHgen Consortium
Avaldatud: PLOS Genetics; e1002655, July 19, 2012, Volume 8, Issue 7


Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. (link)
Verhoeven VJ, Hysi PG, Saw SM, Vitart V, Mirshahi A, Guggenheim JA, Cotch MF, Yamashiro K, Baird PN, Mackey DA, Wojciechowski R, Ikram MK, Hewitt AW, Duggal P, Janmahasatian S, Khor CC, Fan Q, Zhou X, Young TL, Tai ES, Goh LK, Li YJ, Aung T, Vithana E, Teo YY, Tay W, Sim X, Rudan I, Hayward C, Wright AF, Polasek O, Campbell H, Wilson JF, Fleck BW, Nakata I, Yoshimura N, Yamada R, Matsuda F, Ohno-Matsui K, Nag A, McMahon G, Pourcain BS, Lu Y, Rahi JS, Cumberland PM, Bhattacharya S, Simpson CL, Atwood LD, Li X, Raffel LJ, Murgia F, Portas L, Despriet DD, van Koolwijk LM, Wolfram C, Lackner KJ, Tönjes A, Mägi R, Lehtimäki T, Kähönen M, Esko T, Metspalu A, Rantanen T, Pärssinen O, Klein BE, Meitinger T, Spector TD, Oostra BA, Smith AV, de Jong PT, Hofman A, Amin N, Karssen LC, Rivadeneira F, Vingerling JR, Eiríksdóttir G, Gudnason V, Döring A, Bettecken T, Uitterlinden AG, Williams C, Zeller T, Castagné R, Oexle K, van Duijn CM, Iyengar SK, Mitchell P, Wang JJ, Höhn R, Pfeiffer N, Bailey-Wilson JE, Stambolian D, Wong TY, Hammond CJ, Klaver CC.
Avaldatud: Hum Genet. 2012 Jun 5.


Common variants at 6q22 and 17q21 are associated with intracranial volume (link)
M Arfan Ikram, Myriam Fornage, Albert V Smith, Sudha Seshadri, Reinhold Schmidt, Stéphanie Debette, Henri A Vrooman, Sigurdur Sigurdsson, Stefan Ropele, H Rob Taal, Dennis O Mook-Kanamori, Laura H Coker, W T Longstreth Jr, Wiro J Niessen, Anita L DeStefano, Alexa Beiser, Alex P Zijdenbos, Maksim Struchalin, Clifford R Jack Jr, Fernando Rivadeneira, Andre G Uitterlinden, David S Knopman, Anna-Liisa Hartikainen, Craig E Pennell, Elisabeth Thiering, Eric A P Steegers, Hakon Hakonarson, Joachim Heinrich, Lyle J Palmer, Marjo-Riitta Jarvelin, Mark I McCarthy, Struan F A Grant, Beate St Pourcain, Nicholas J Timpson, George Davey Smith, Ulla Sovio, Mike A Nalls, Rhoda Au, Albert Hofman, Haukur Gudnason, Aad van der Lugt, Tamara B Harris, William M Meeks, Meike W Vernooij, Mark A van Buchem, Diane Catellier, Vincent W V Jaddoe, Vilmundur Gudnason, B Gwen Windham, Philip A Wolf, Cornelia M van Duijn, Thomas H Mosley Jr, Helena Schmidt, Lenore J Launer, Monique M B Breteler & Charles DeCarli for the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium & Early Growth Genetics (EGG) Consortium
Avaldatud: Nature Genetics 44, 539–544 (2012)
DOI: 10.1038/ng.2245


Common variants at 12q15 and 12q24 are associated with infant head circumference (link)
H Rob Taal, Beate St Pourcain, Elisabeth Thiering, Shikta Das, Dennis O Mook-Kanamori, Nicole M Warrington, Marika Kaakinen, Eskil Kreiner-Møller, Jonathan P Bradfield, Rachel M Freathy, Frank Geller, Mònica Guxens, Diana L Cousminer, Marjan Kerkhof, Nicholas J Timpson, M Arfan Ikram, Lawrence J Beilin, Klaus Bønnelykke, Jessica L Buxton, Pimphen Charoen, Bo Lund Krogsgaard Chawes, Johan Eriksson, David M Evans, Albert Hofman, John P Kemp, Cecilia E Kim, Norman Klopp, Jari Lahti, Stephen J Lye, George McMahon, Frank D Mentch, Martina Müller-Nurasyid, Paul F O''''''''Reilly, Inga Prokopenko, Fernando Rivadeneira, Eric A P Steegers, Jordi Sunyer, Carla Tiesler, Hanieh Yaghootkar, The Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium, Monique M B Breteler, Stéphanie Debette, Myriam Fornage, Vilmundur Gudnason, Lenore J Launer, Aad van der Lugt, Thomas H Mosley Jr, Sudha Seshadri, Albert V Smith, Meike W Vernooij, Early Genetics & Lifecourse Epidemiology (EAGLE) Consortium, Alexandra I F Blakemore, Rosetta M Chiavacci, Bjarke Feenstra, Julio Fernandez-Banet, Struan F A Grant, Anna-Liisa Hartikainen, Albert J van der Heijden, Carmen Iñiguez, Mark Lathrop, Wendy L McArdle, Anne Mølgaard, John P Newnham, Lyle J Palmer, Aarno Palotie, Annneli Pouta, Susan M Ring, Ulla Sovio, Marie Standl, Andre G Uitterlinden, H-Erich Wichmann, Nadja Hawwa Vissing, Charles DeCarli, Cornelia M van Duijn, Mark I McCarthy, Gerard H Koppelman, Xavier Estivill, Andrew T Hattersley, Mads Melbye, Hans Bisgaard, Craig E Pennell, Elisabeth Widen, Hakon Hakonarson, George Davey Smith, Joachim Heinrich, Marjo-Riitta Jarvelin, Vincent W V Jaddoe & Early Growth Genetics (EGG) Consortium
Avaldatud: Nature Genetics 44, 532–538 (2012)
DOI: 10.1038/ng.2238


Seventy-five genetic loci influencing the human red blood cell
Pim van der Harst, Weihua Zhang, Irene Mateo Leach, Augusto Rendon, Niek Verweij, Joban Sehmi, Dirk S. Paul, Ulrich Elling, Hooman Allayee, Xinzhong Li, Aparna Radhakrishnan, Sian-Tsung Tan, Katrin Voss, Christian X. Weichenberger, Cornelis A. Albers, Abtehale Al-Hussani, Folkert W. Asselbergs, Marina Ciullo, Fabrice Danjou, Christian Dina, Tõnu Esko, David M. Evans, Lude Franke, Martin Gögele, Jaana Hartiala, Micha Hersch, Hilma Holm, Jouke-Jan Hottenga, Stavroula Kanoni, Marcus E. Kleber, Vasiliki Lagou, Claudia Langenberg, Lorna M. Lopez, Leo-Pekka Lyytikäinen, Olle Melander, Federico Murgia, Ilja M. Nolte, Paul F. O’Reilly, Sandosh Padmanabhan, Afshin Parsa, Nicola Pirastu, Eleonora Porcu, Laura Portas, Inga Prokopenko, Janina S. Ried, So-Youn Shin, Clara S. Tang, Alexander Teumer, Michela Traglia, Sheila Ulivi, Harm-Jan Westra, Jian Yang, Jing Hua Zhao, Franco Anni, Abdel Abdellaoui, Antony Attwood, Beverley Balkau, Stefania Bandinelli, François Bastardot, Beben Benyamin, Bernhard O. Boehm, William O. Cookson, Debashish Das, Paul I. W. de Bakker, Rudolf A. de Boer, Eco J. C. de Geus, Marleen H. de Moor, Maria Dimitriou, Francisco S. Domingues, Angela Döring, Gunnar Engström, Gudmundur Ingi Eyjolfsson, Luigi Ferrucci, Krista Fischer, Renzo Galanello, Stephen F. Garner, Bernd Genser, Quince D. Gibson, Giorgia Girotto, Daniel Fannar Gudbjartsson, Sarah E. Harris, Anna-Liisa Hartikainen, Claire E. Hastie, Bo Hedblad, Thomas Illig, Jennifer Jolley, Mika Kähönen, Ido P. Kema, John P. Kemp, Liming Liang, Heather Lloyd-Jones, Ruth J. F. Loos, Stuart Meacham, Sarah E. Medland, Christa Meisinger, Yasin Memari, Evelin Mihailov, Kathy Miller, Miriam F. Moffatt, Matthias Nauck, Maria Novatchkova, Teresa Nutile, Isleifur Olafsson, Pall T. Onundarson, Debora Parracciani, Brenda W. Penninx, Lucia Perseu, Antonio Piga, Giorgio Pistis, Anneli Pouta, Ursula Puc, Olli Raitakari, Susan M. Ring, Antonietta Robino, Daniela Ruggiero, Aimo Ruokonen, Aude Saint-Pierre, Cinzia Sala, Andres Salumets, Jennifer Sambrook, Hein Schepers, Carsten Oliver Schmidt, Herman H. W. Silljé, Rob Sladek, Johannes H. Smit, John M. Starr, Jonathan Stephens, Patrick Sulem, Toshiko Tanaka, Unnur Thorsteinsdottir, Vinicius Tragante, Wiek H. van Gilst, L. Joost van Pelt, Dirk J. van Veldhuisen, Uwe Völker, John B. Whitfield, Gonneke Willemsen, Bernhard R. Winkelmann, Gerald Wirnsberger, Ale Algra, Francesco Cucca, Adamo Pio d’Adamo, John Danesh, Ian J. Deary, Anna F. Dominiczak, Paul Elliott, Paolo Fortina, Philippe Froguel, Paolo Gasparini, Andreas Greinacher, Stanley L. Hazen, Marjo-Riitta Jarvelin, Kay Tee Khaw, Terho Lehtimäki, Winfried Maerz, Nicholas G. Martin, Andres Metspalu, Braxton D. Mitchell, Grant W. Montgomery, Carmel Moore, Gerjan Navis, Mario Pirastu, Peter P. Pramstaller, Ramiro Ramirez-Solis, Eric Schadt, James Scott, Alan R. Shuldiner, George Davey Smith, J. Gustav Smith, Harold Snieder, Rossella Sorice, Tim D. Spector, Kari Stefansson, Michael Stumvoll, W. H. Wilson Tang, Daniela Toniolo, Anke Tönjes, Peter M. Visscher, Peter Vollenweider, Nicholas J. Wareham, Bruce H. R. Wolffenbuttel, Dorret I. Boomsma, Jacques S. Beckmann, George V. Dedoussis, Panos Deloukas, Manuel A. Ferreira, Serena Sanna, Manuela Uda, Andrew A. Hicks, Josef Martin Penninger, Christian Gieger, Jaspal S. Kooner, Willem H. Ouwehand, Nicole Soranzo & John C. Chambers
Avaldatud: Nature - Received 06 February 2012 Accepted 15 October 2012 Published online 05 December 2012
DOI: 10.1038/nature11677


Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci (link)
David Ellinghaus, Eva Ellinghaus, Rajan P. Nair, Philip E. Stuart, Tõnu Esko, Andres Metspalu, Sophie Debrus, John V. Raelson, Trilokraj Tejasvi, Majid Belouchi, Sarah L. West, Jonathan N. Barker, Sulev Kõks, Külli Kingo, Tobias Balschun, Orazio Palmieri, Vito Annese, Christian Gieger, H. Erich Wichmann, Michael Kabesch, Richard C. Trembath, Christopher G. Mathew, Gonçalo R. Abecasis, Stephan Weidinger, Susanna Nikolaus, Stefan Schreiber, James T. Elder, Michael Weichenthal, Michael Nothnagel, Andre Franke Institute of Clinical Molecular Biology, Christian-Albrechts-University, 24105 Kiel, Germany Department of Dermatology, University of Michigan, Ann Arbor, MI 48109, USA Estonian Genome Center, University of Tartu, 50409 Tartu, Estonia Institute of Molecular and Cell Biology, University of Tartu, 50409 Tartu, Estonia Gatineau, QC J9J 2X6, Canada PGX-Services, Montreal, QC H2T 1S1, Canada Genizon BioSciences, Inc., St. Laurent, QC H4T 2C7, Canada Division of Genetics and Molecular Medicine, King''''''''s College London, London SE1 9RT, UK Department of Physiology, Centre of Translational Medicine and Centre of Translational Genomics, University of Tartu, 50409 Tartu, Estonia Department of Dermatology and Venerology, University of Tartu, 50409 Tartu, Estonia Division of Gastroenterology, Istituto di Ricovero e Cura a Carattere Scientifico-Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo 71013, Italy Unit of Gastroenterology SOD2, Azienda Ospedaliero Universitaria Careggi, Florence 50134, Italy Institute of Genetic Epidemiology, Helmholtz Centre Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany Institute of Epidemiology I, Helmholtz Centre Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany Institute of Medical Informatics, Biometry and Epidemiology, Ludwig-Maximilians-University, 81377 Munich, Germany Klinikum Grosshadern, 81377 Munich, Germany Department of Paediatric Pneumology, Allergy and Neonatology, Hannover Medical School, 30625 Hannover, Germany Department of Biostatistics, Center for Statistical Genetics, University of Michigan, Ann Arbor, MI 48109, USA 19 Department of Dermatology, Allergology, and Venerology, University Hospital Schleswig-Holstein, Christian-Albrechts-University, 24105 Kiel, Germany PopGen Biobank, Christian-Albrechts-University Kiel, 24105 Kiel, Germany Department of General Internal Medicine, University Hospital Schleswig-Holstein, 24105 Kiel, Germany 22 Ann Arbor Veterans Affairs Hopital, Ann Arbor, MI 48105, USA 23 Institute of Medical Informatics and Statistics, Christian-Albrechts University, 24105 Kiel, Germany
Avaldatud: AJHG Volume 90, Issue 4, 6 April 2012, Pages 636–647
DOI: 10.1016/j.ajhg.2012.02.020.


The Estonian Genome Center of the University of Tartu at the disposal of scientists. Tartu Ülikooli Eesti geenivaramu on teadlaste käsutuses.
Alavere H, Fischer K, Esko T, Leitsalu-Moynihan L, Metspalu A.
Avaldatud: Est Med J 91 / Eesti Arst 2012;91(4):190-198.


Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function (link)
Pattaro C, Köttgen A, Teumer A, Garnaas M, Böger CA, Fuchsberger C, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, Foster MC, O''''Seaghdha CM, Glazer N, Isaacs A, Liu CT, Smith AV, O''''Connell JR, Struchalin M, Tanaka T, Li G, Johnson AD, Gierman HJ, Feitosa M, Hwang SJ, Atkinson EJ, Lohman K, Cornelis MC, Johansson A, Tönjes A, Dehghan A, Chouraki V, Holliday EG, Sorice R, Kutalik Z, Lehtimäki T, Esko T, Deshmukh H, Ulivi S, Chu AY, Murgia F, Trompet S, Imboden M, Kollerits B, Pistis G; CARDIoGRAM Consortium; ICBP Consortium; CARe Consortium; Wellcome Trust Case Control Consortium 2 (WTCCC2), Harris TB, Launer LJ, Aspelund T, Eiriksdottir G, Mitchell BD, Boerwinkle E, Schmidt H, Cavalieri M, Rao M, Hu FB, Demirkan A, Oostra BA, de Andrade M, Turner ST, Ding J, Andrews JS, Freedman BI, Koenig W, Illig T, Döring A, Wichmann HE, Kolcic I, Zemunik T, Boban M, Minelli C, Wheeler HE, Igl W, Zaboli G, Wild SH, Wright AF, Campbell H, Ellinghaus D, Nöthlings U, Jacobs G, Biffar R, Endlich K, Ernst F, Homuth G, Kroemer HK, Nauck M, Stracke S, Völker U, Völzke H, Kovacs P, Stumvoll M, Mägi R, Hofman A, Uitterlinden AG, Rivadeneira F, Aulchenko YS, Polasek O, Hastie N, Vitart V, Helmer C, Wang JJ, Ruggiero D, Bergmann S, Kähönen M, Viikari J, Nikopensius T, Province M, Ketkar S, Colhoun H, Doney A, Robino A, Giulianini F, Krämer BK, Portas L, Ford I, Buckley BM, Adam M, Thun GA, Paulweber B, Haun M, Sala C, Metzger M, Mitchell P, Ciullo M, Kim SK, Vollenweider P, Raitakari O, Metspalu A, Palmer C, Gasparini P, Pirastu M, Jukema JW, Probst-Hensch NM, Kronenberg F, Toniolo D, Gudnason V, Shuldiner AR, Coresh J, Schmidt R, Ferrucci L, Siscovick DS, van Duijn CM, Borecki I, Kardia SL, Liu Y, Curhan GC, Rudan I, Gyllensten U, Wilson JF, Franke A, Pramstaller PP, Rettig R, Prokopenko I, Witteman JC, Hayward C, Ridker P, Parsa A, Bochud M, Heid IM, Goessling W, Chasman DI, Kao WH, Fox CS
Avaldatud: PLoS Genetics 8(3): e1002584 March 29, 2012
DOI: 10.1371/journal.pgen.1002584


A genome-wide association meta-analysis identifies new childhood obesity loci
Jonathan P Bradfield, H Rob Taal, Nicholas J Timpson, André Scherag, Cecile Lecoeur, Nicole M Warrington, Elina Hypponen, Claus Holst, Beatriz Valcarcel, Elisabeth Thiering, Rany M Salem, Fredrick R Schumacher, Diana L Cousminer, Patrick M A Sleiman, Jianhua Zhao, Robert I Berkowitz, Karani S Vimaleswaran, Ivonne Jarick, Craig E Pennell, David M Evans, Beate St Pourcain, Diane J Berry, Dennis O Mook-Kanamori, Albert Hofman, Fernando Rivadeneira, André G Uitterlinden, Cornelia M van Duijn, Ralf J P van der Valk, Johan C de Jongste, Dirkje S Postma, Dorret I Boomsma, W James Gauderman, Mohamed T Hassanein, Cecilia M Lindgren, Reedik Mägi, Colin A G Boreham, Charlotte E Neville, Luis A Moreno, Paul Elliott, Anneli Pouta, Anna-Liisa Hartikainen, Mingyao Li, Olli Raitakari, Terho Lehtimäki, Johan G Eriksson, Aarno Palotie, Jean Dallongeville, Shikta Das, Panos Deloukas, George McMahon, Susan M Ring, John P Kemp, Jessica L Buxton, Alexandra I F Blakemore, Mariona Bustamante, Mònica Guxens, Joel N Hirschhorn, Matthew W Gillman, Eskil Kreiner-Møller, Hans Bisgaard, Frank D Gilliland, Joachim Heinrich, Eleanor Wheeler, Inês Barroso, Stephen O’Rahilly, Aline Meirhaeghe, Thorkild I A Sørensen, Chris Power, Lyle J Palmer, Anke Hinney, Elisabeth Widen, I Sadaf Farooqi, Mark I McCarthy, Philippe Froguel, David Meyre, Johannes Hebebrand, Marjo-Riitta Jarvelin, Vincent W V Jaddoe, George Davey Smith, Hakon Hakonarson & Struan F A Grant for the Early Growth Genetics (EGG) Consortium
Avaldatud: Nature Genetics, Published Online 15. April 2012


Coexpression Network Analysis in Abdominal and Gluteal Adipose Tissue Reveals Regulatory Genetic Loci for Metabolic Syndrome and Related Phenotypes
Josine L. Min, George Nicholson, Ingileif Halgrimsdottir, Kristian Almstrup, Andreas Petri, Amy Barrett, Mary Travers, Nigel W. Rayner, Reedik Mägi, Fredrik H. Pettersson, John Broxholme, Matt J. Neville, Quin F. Wills, Jane Cheeseman, The GIANT Consortium", The MolPAGE Consortium", Maxine Allen, Chris C. Holmes, Tim D. Spector, Jan Fleckner, Mark I. McCarthy, Fredrik Karpe, Cecilia M. Lindgren, Krina T. Zondervan
Avaldatud: PLoS Genetics, February 2012 | Volume 8 | Issue 2,
DOI: 10.1371/journal.pgen.1002505


Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (link)
Stolk L, Perry JR, Chasman DI, He C, Mangino M, Sulem P, Barbalic M, Broer L, Byrne EM, Ernst F, Esko T, Franceschini N, Gudbjartsson DF, Hottenga JJ, Kraft P, McArdle PF, Porcu E, Shin SY, Smith AV, van Wingerden S, Zhai G, Zhuang WV, Albrecht E, Alizadeh BZ, Aspelund T, Bandinelli S, Lauc LB, Beckmann JS, Boban M, Boerwinkle E, Broekmans FJ, Burri A, Campbell H, Chanock SJ, Chen C, Cornelis MC, Corre T, Coviello AD, d''Adamo P, Davies G, de Faire U, de Geus EJ, Deary IJ, Dedoussis GV, Deloukas P, Ebrahim S, Eiriksdottir G, Emilsson V, Eriksson JG, Fauser BC, Ferreli L, Ferrucci L, Fischer K, Folsom AR, Garcia ME, Gasparini P, Gieger C, Glazer N, Grobbee DE, Hall P, Haller T, Hankinson SE, Hass M, Hayward C, Heath AC, Hofman A, Ingelsson E, Janssens AC, Johnson AD, Karasik D, Kardia SL, Keyzer J, Kiel DP, Kolcic I, Kutalik Z, Lahti J, Lai S, Laisk T, Laven JS, Lawlor DA, Liu J, Lopez LM, Louwers YV, Magnusson PK, Marongiu M, Martin NG, Klaric IM, Masciullo C, McKnight B, Medland SE, Melzer D, Mooser V, Navarro P, Newman AB, Nyholt DR, Onland-Moret NC, Palotie A, Paré G, Parker AN, Pedersen NL, Peeters PH, Pistis G, Plump AS, Polasek O, Pop VJ, Psaty BM, Räikkönen K, Rehnberg E, Rotter JI, Rudan I, Sala C, Salumets A, Scuteri A, Singleton A, Smith JA, Snieder H, Soranzo N, Stacey SN, Starr JM, Stathopoulou MG, Stirrups K, Stolk RP, Styrkarsdottir U, Sun YV, Tenesa A, Thorand B, Toniolo D, Tryggvadottir L, Tsui K, Ulivi S, van Dam RM, van der Schouw YT, van Gils CH, van Nierop P, Vink JM, Visscher PM, Voorhuis M, Waeber G, Wallaschofski H, Wichmann HE, Widen E, Wijnands-van Gent CJ, Willemsen G, Wilson JF, Wolffenbuttel BH, Wright AF, Yerges-Armstrong LM, Zemunik T, Zgaga L, Zillikens MC, Zygmunt M, Study TL, Arnold AM, Boomsma DI, Buring JE, Crisponi L, Demerath EW, Gudnason V, Harris TB, Hu FB, Hunter DJ, Launer LJ, Metspalu A, Montgomery GW, Oostra BA, Ridker PM, Sanna S, Schlessinger D, Spector TD, Stefansson K, Streeten EA, Thorsteinsdottir U, Uda M, Uitterlinden AG, van Duijn CM, Völzke H, Murray A, Murabito JM, Visser JA, Lunetta KL.
Avaldatud: Nat Genet. 2012 Jan 22;44(3):260-8
DOI: 10.1038/ng.1051


Post-translational stabilization of thiopurine S-methyltransferase by S-adenosyl-l-methionine reveals regulation of TPMT*1 and *3C allozymes.
Milek M, Smid A, Tamm R, Kuzelicki NK, Metspalu A, Mlinaric-Rascan I.
Avaldatud: Biochem Pharmacol. Epub 2012 Jan 17.
DOI: 10.1016/j.bcp.2012.01.010


Personality traits and eating habits in a large sample of Estonians
Mõttus R, Realo A, Allik J, Deary IJ, Esko T, Metspalu A.
Avaldatud: Health Psychology. Epub 2012 Jan 23.
DOI: 10.1037/a0027041


Longevity candidate genes and their association with personality traits in the elderly.
Luciano M, Lopez LM, de Moor MH, Harris SE, Davies G, Nutile T, Krueger RF, Esko T, Schlessinger D, Toshiko T, Derringer JL, Realo A, Hansell NK, Pergadia ML, Pesonen AK, Sanna S, Terracciano A, Madden PA, Penninx B, Spinhoven P, Hartman CA, Oostra BA, Janssens AC, Eriksson JG, Starr JM, Cannas A, Ferrucci L, Metspalu A, Wright MJ, Heath AC, van Duijn CM, Bierut LJ, Raikkonen K, Martin NG, Ciullo M, Rujescu D, Boomsma DI, Deary IJ.
Avaldatud: Am J Med Genet B Neuropsychiatr Genet. 2012 Mar;159B(2):192-200. doi: 10.1002/ajmg.b.32013. Epub 2011 Dec 27
DOI: 10.1002/ajmg.b.32013.

2011 (32)

The Lin28/let-7 axis regulates glucose metabolism.
Zhu H, Shyh-Chang N, Segrè AV, Shinoda G, Shah SP, Einhorn WS, Takeuchi A, Engreitz JM, Hagan JP, Kharas MG, Urbach A, Thornton JE, Triboulet R, Gregory RI; DIAGRAM Consortium; MAGIC Investigators, Altshuler D, Daley GQ.
Avaldatud: Cell. 2011 Sep 30;147(1):81-94
DOI: doi: 10.1016/j.cell.2011.08.033


Assessing the impact of missing genotype data in rare variant association analysis
Mägi R, Kumar A, Morris AP.
Avaldatud: BMC Proc. 2011 Nov 29;5 Suppl 9:S107
DOI: 10.1186/1753-6561-5-S9-S107


A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
Manning AK, Hivert MF, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu CT, Bielak LF, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga JJ, Ingelsson E, Jackson AU, Johnson T, Kanoni S, Ladenvall C, Lagou V, Lahti J, Lecoeur C, Liu Y, Martinez-Larrad MT, Montasser ME, Navarro P, Perry JR, Rasmussen-Torvik LJ, Salo P, Sattar N, Shungin D, Strawbridge RJ, Tanaka T, van Duijn CM, An P, de Andrade M, Andrews JS, Aspelund T, Atalay M, Aulchenko Y, Balkau B, Bandinelli S, Beckmann JS, Beilby JP, Bellis C, Bergman RN, Blangero J, Boban M, Boehnke M, Boerwinkle E, Bonnycastle LL, Boomsma DI, Borecki IB, Böttcher Y, Bouchard C, Brunner E, Budimir D, Campbell H, Carlson O, Chines PS, Clarke R, Collins FS, Corbatón-Anchuelo A, Couper D, de Faire U, Dedoussis GV, Deloukas P, Dimitriou M, Egan JM, Eiriksdottir G, Erdos MR, Eriksson JG, Eury E, Ferrucci L, Ford I, Forouhi NG, Fox CS, Franzosi MG, Franks PW, Frayling TM, Froguel P, Galan P, de Geus E, Gigante B, Glazer NL, Goel A, Groop L, Gudnason V, Hallmans G, Hamsten A, Hansson O, Harris TB, Hayward C, Heath S, Hercberg S, Hicks AA, Hingorani A, Hofman A, Hui J, Hung J, Jarvelin MR, Jhun MA, Johnson PC, Jukema JW, Jula A, Kao WH, Kaprio J, Kardia SL, Keinanen-Kiukaanniemi S, Kivimaki M, Kolcic I, Kovacs P, Kumari M, Kuusisto J, Kyvik KO, Laakso M, Lakka T, Lannfelt L, Lathrop GM, Launer LJ, Leander K, Li G, Lind L, Lindstrom J, Lobbens S, Loos RJ, Luan J, Lyssenko V, Mägi R, Magnusson PK, Marmot M, Meneton P, Mohlke KL, Mooser V, Morken MA, Miljkovic I, Narisu N, O''Connell J, Ong KK, Oostra BA, Palmer LJ, Palotie A, Pankow JS, Peden JF, Pedersen NL, Pehlic M, Peltonen L, Penninx B, Pericic M, Perola M, Perusse L, Peyser PA, Polasek O, Pramstaller PP, Province MA, Räikkönen K, Rauramaa R, Rehnberg E, Rice K, Rotter JI, Rudan I, Ruokonen A, Saaristo T, Sabater-Lleal M, Salomaa V, Savage DB, Saxena R, Schwarz P, Seedorf U, Sennblad B, Serrano-Rios M, Shuldiner AR, Sijbrands EJ, Siscovick DS, Smit JH, Small KS, Smith NL, Smith AV, Stančáková A, Stirrups K, Stumvoll M, Sun YV, Swift AJ, Tönjes A, Tuomilehto J, Trompet S, Uitterlinden AG, Uusitupa M, Vikström M, Vitart V, Vohl MC, Voight BF, Vollenweider P, Waeber G, Waterworth DM, Watkins H, Wheeler E, Widen E, Wild SH, Willems SM, Willemsen G, Wilson JF, Witteman JC, Wright AF, Yaghootkar H, Zelenika D, Zemunik T, Zgaga L; DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium; Multiple Tissue Human Expression Resource (MUTHER) Consortium, Wareham NJ, McCarthy MI, Barroso I, Watanabe RM, Florez JC, Dupuis J, Meigs JB, Langenberg C.
Avaldatud: Nat Genet. 2012 May 13;44(6):659-69.
DOI: 10.1038/ng.2274


A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (link)
McKay JD, Truong T, Gaborieau V, Chabrier A, Chuang SC, Byrnes G, Zaridze D, Shangina O, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Bucur A, Bencko V, Holcatova I, Janout V, Foretova L, Lagiou P, Trichopoulos D, Benhamou S, Bouchardy C, Ahrens W, Merletti F, Richiardi L, Talamini R, Barzan L, Kjaerheim K, Macfarlane GJ, Macfarlane TV, Simonato L, Canova C, Agudo A, Castellsagué X, Lowry R, Conway DI, McKinney PA, Healy CM, Toner ME, Znaor A, Curado MP, Koifman S, Menezes A, Wünsch-Filho V, Neto JE, Garrote LF, Boccia S, Cadoni G, Arzani D, Olshan AF, Weissler MC, Funkhouser WK, Luo J, Lubiński J, Trubicka J, Lener M, Oszutowska D, Schwartz SM, Chen C, Fish S, Doody DR, Muscat JE, Lazarus P, Gallagher CJ, Chang SC, Zhang ZF, Wei Q, Sturgis EM, Wang LE, Franceschi S, Herrero R, Kelsey KT, McClean MD, Marsit CJ, Nelson HH, Romkes M, Buch S, Nukui T, Zhong S, Lacko M, Manni JJ, Peters WH, Hung RJ, McLaughlin J, Vatten L, Njølstad I, Goodman GE, Field JK, Liloglou T, Vineis P, Clavel-Chapelon F, Palli D, Tumino R, Krogh V, Panico S, González CA, Quirós JR, Martínez C, Navarro C, Ardanaz E, Larrañaga N, Khaw KT, Key T, Bueno-de-Mesquita HB, Peeters PH, Trichopoulou A, Linseisen J, Boeing H, Hallmans G, Overvad K, Tjønneland A, Kumle M, Riboli E, Välk K, Vooder T, Metspalu A, Zelenika D, Boland A, Delepine M, Foglio M, Lechner D, Blanché H, Gut IG, Galan P, Heath S, Hashibe M, Hayes RB, Boffetta P, Lathrop M, Brennan P.
Avaldatud: PLoS Genet. 2011 Mar;7(3):e1001333. Epub 2011 Mar 17. Erratum in: PLoS Genet. 2011 Apr;7(4).


Manifesto for a European Anxiety Disorders Research Network
David S. Baldwin, Christer Allgulander, Alfredo Carlo Altamura, Jules Angst, Borwin Bandelow, Johan den Boer, Patrice Boyer, Simon Davies, Bernardo dell''Osso, Elias Eriksson, Naomi Fineberg, Mats Fredrikson, Andres Herran, Eduard Maron, Andres Metspalu, David Nutt, Nic van der Wee, Jose Luis Vázquez-Barquero and Joseph Zohar
Avaldatud: European Neuropsychopharmacology, Volume 20, Issue 6, June 2010, Pages 426-432


A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila. (link)
Allebrandt KV, Amin N, Müller-Myhsok B, Esko T, Teder-Laving M, Azevedo RV, Hayward C, van Mill J, Vogelzangs N, Green EW, Melville SA, Lichtner P, Wichmann HE, Oostra BA, Janssens AC, Campbell H, Wilson JF, Hicks AA, Pramstaller PP, Dogas Z, Rudan I, Merrow M, Penninx B, Kyriacou CP, Metspalu A, van Duijn CM, Meitinger T, Roenneberg T.
Avaldatud: Mol Psychiatry. 2011 Nov 22.
DOI: doi: 10.1038/mp.2011.142.


Genome-Wide Meta-Analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL.
Ellinghaus E, Stuart PE, Ellinghaus D, Nair RP, Debrus S, Raelson JV, Belouchi M, Tejasvi T, Li Y, Tsoi LC, Onken AT, Esko T, Metspalu A, Rahman P, Gladman DD, Bowcock AM, Helms C, Krueger GG, Koks S, Kingo K, Gieger C, Wichmann HE, Mrowietz U, Weidinger S, Schreiber S, Abecasis GR, Elder JT, Weichenthal M, Franke A.
Avaldatud: J Invest Dermatol. 2011 Dec 15.
DOI: doi: 10.1038/jid.2011.415.


New gene functions in megakaryopoiesis and platelet formation. (link)
Gieger C, Radhakrishnan A, Cvejic A, Tang W, Porcu E, Pistis G, Serbanovic-Canic J, Elling U, Goodall AH, Labrune Y, Lopez LM, Mägi R, Meacham S, Okada Y, Pirastu N, Sorice R, Teumer A, Voss K, Zhang W, Ramirez-Solis R, Bis JC, Ellinghaus D, Gögele M, Hottenga JJ, Langenberg C, Kovacs P, O''Reilly PF, Shin SY, Esko T, Hartiala J, Kanoni S, Murgia F, Parsa A, Stephens J, van der Harst P, Ellen van der Schoot C, Allayee H, Attwood A, Balkau B, Bastardot F, Basu S, Baumeister SE, Biino G, Bomba L, Bonnefond A, Cambien F, Chambers JC, Cucca F, D''Adamo P, Davies G, de Boer RA, de Geus EJ, Döring A, Elliott P, Erdmann J, Evans DM, Falchi M, Feng W, Folsom AR, Frazer IH, Gibson QD, Glazer NL, Hammond C, Hartikainen AL, Heckbert SR, Hengstenberg C, Hersch M, Illig T, Loos RJ, Jolley J, Tee Khaw K, Kühnel B, Kyrtsonis MC, Lagou V, Lloyd-Jones H, Lumley T, Mangino M, Maschio A, Mateo Leach I, McKnight B, Memari Y, Mitchell BD, Montgomery GW, Nakamura Y, Nauck M, Navis G, Nöthlings U, Nolte IM, Porteous DJ, Pouta A, Pramstaller PP, Pullat J, Ring SM, Rotter JI, Ruggiero D, Ruokonen A, Sala C, Samani NJ, Sambrook J, Schlessinger D, Schreiber S, Schunkert H, Scott J, Smith NL, Snieder H, Starr JM, Stumvoll M, Takahashi A, Tang WH, Taylor K, Tenesa A, Lay Thein S, Tönjes A, Uda M, Ulivi S, van Veldhuisen DJ, Visscher PM, Völker U, Wichmann HE, Wiggins KL, Willemsen G, Yang TP, Hua Zhao J, Zitting P, Bradley JR, Dedoussis GV, Gasparini P, Hazen SL, Metspalu A, Pirastu M, Shuldiner AR, Joost van Pelt L, Zwaginga JJ, Boomsma DI, Deary IJ, Franke A, Froguel P, Ganesh SK, Jarvelin MR, Martin NG, Meisinger C, Psaty BM, Spector TD, Wareham NJ, Akkerman JW, Ciullo M, Deloukas P, Greinacher A, Jupe S, Kamatani N, Khadake J, Kooner JS, Penninger J, Prokopenko I, Stemple D, Toniolo D, Wernisch L, Sanna S, Hicks AA, Rendon A, Ferreira MA, Ouwehand WH, Soranzo N
Avaldatud: Nature. 2011 Nov 30;480(7376):201-8.
DOI: doi: 10.1038/nature10659.


Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
Chambers JC, Zhang W, Sehmi J, Li X, Wass MN, Van der Harst P, Holm H, Sanna S, Kavousi M, Baumeister SE, Coin LJ, Deng G, Gieger C, Heard-Costa NL, Hottenga JJ, Kühnel B, Kumar V, Lagou V, Liang L, Luan J, Vidal PM, Mateo Leach I, O''Reilly PF, Peden JF, Rahmioglu N, Soininen P, Speliotes EK, Yuan X, Thorleifsson G, Alizadeh BZ, Atwood LD, Borecki IB, Brown MJ, Charoen P, Cucca F, Das D, de Geus EJ, Dixon AL, Döring A, Ehret G, Eyjolfsson GI, Farrall M, Forouhi NG, Friedrich N, Goessling W, Gudbjartsson DF, Harris TB, Hartikainen AL, Heath S, Hirschfield GM, Hofman A, Homuth G, Hyppönen E, Janssen HL, Johnson T, Kangas AJ, Kema IP, Kühn JP, Lai S, Lathrop M, Lerch MM, Li Y, Liang TJ, Lin JP, Loos RJ, Martin NG, Moffatt MF, Montgomery GW, Munroe PB, Musunuru K, Nakamura Y, O''Donnell CJ, Olafsson I, Penninx BW, Pouta A, Prins BP, Prokopenko I, Puls R, Ruokonen A, Savolainen MJ, Schlessinger D, Schouten JN, Seedorf U, Sen-Chowdhry S, Siminovitch KA, Smit JH, Spector TD, Tan W, Teslovich TM, Tukiainen T, Uitterlinden AG, Van der Klauw MM, Vasan RS, Wallace C, Wallaschofski H, Wichmann HE, Willemsen G, Würtz P, Xu C, Yerges-Armstrong LM; Alcohol Genome-wide Association (AlcGen) Consortium; Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study; Genetic Investigation of Anthropometric Traits (GIANT) Consortium (incl. Esko T., Mägi R., Teder-Laving, M, Nelis, M, Alevere H., Tammesoo M.-L., Metspalu A.); Global Lipids Genetics Consortium; Genetics of Liver Disease (GOLD) Consortium; International Consortium for Blood Pressure (ICBP-GWAS); Meta-analyses of Glucose and Insulin-Related Traits Consortium (MAGIC), Abecasis GR, Ahmadi KR, Boomsma DI, Caulfield M, Cookson WO, van Duijn CM, Froguel P, Matsuda K, McCarthy MI, Meisinger C, Mooser V, Pietiläinen KH, Schumann G, Snieder H, Sternberg MJ, Stolk RP, Thomas HC, Thorsteinsdottir U, Uda M, Waeber G, Wareham NJ, Waterworth DM, Watkins H, Whitfield JB, Witteman JC, Wolffenbuttel BH, Fox CS, Ala-Korpela M, Stefansson K, Vollenweider P, Völzke H, Schadt EE, Scott J, Järvelin MR, Elliott P, Kooner JS.
Avaldatud: Nat Genet. 2011 Oct 16;43(11):1131-8
DOI: doi: 10.1038/ng.970.


The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data
CM Middeldorp, MHM de Moor, LM McGrath, SD Gordon, DH Blackwood, PT Costa, A Terracciano, RF Krueger, EJC de Geus, DR Nyholt, T Tanaka, T Esko, PAF Madden, J Derringer, N Amin, G Willemsen, J-J Hottenga, MA Distel M Uda, S Sanna, P Spinhoven, CA Hartman, S Ripke, PF Sullivan, A Realo, J Allik, AC Heath, ML Pergadia, A Agrawal, P Lin, RA Grucza, E Widen, DL Cousminer, JG Eriksson, A Palotie, JH Barnett, PH Lee, M Luciano, A Tenesa, G Davies, LM Lopez, NK Hansell, SE Medland, L Ferrucci, D Schlessinger, GW Montgomery, MJ Wright, YS Aulchenko, ACJW Janssens, BA Oostra, A Metspalu, GR Abecasis, IJ Deary, K Räikkönen, LJ Bierut, NG Martin, NR Wray, CM van Duijn, JW Smoller, BWJH Penninx and DI Boomsma
Avaldatud: Translational Psychiatry (2011) 1,e49
DOI: doi:10.1038/tp.2011.45


Longevity candidate genes and their association with personality traits in the elderly.
Luciano M, Lopez LM, de Moor MH, Harris SE, Davies G, Nutile T, Krueger RF, Esko T, Schlessinger D, Toshiko T, Derringer JL, Realo A, Hansell NK, Pergadia ML, Pesonen AK, Sanna S, Terracciano A, Madden PA, Penninx B, Spinhoven P, Hartman CA, Oostra BA, Janssens AC, Eriksson JG, Starr JM, Cannas A, Ferrucci L, Metspalu A, Wright MJ, Heath AC, van Duijn CM, Bierut LJ, Raikkonen K, Martin NG, Ciullo M, Rujescu D, Boomsma DI, Deary IJ.
Avaldatud: Am J Med Genet B Neuropsychiatr Genet. 2011 Dec 27.
DOI: doi: 10.1002/ajmg.b.32013.


Giving and Withholding of Information following Genomic Screening: Challenges Identified in a Study of Primary Care Physicians in Estonia
Liis Leitsalu, Laura Hercher, Andres Metspalu
Avaldatud: J Genet Counsel, Published on-line 08.12.11,
DOI: DOI 10.1007/s10897-011-9424-3


The role of a Bioresource Research Impact Factor as an incentive to share human bioresources.
Cambon-Thomsen, A., Thorisson, G. a, Mabile, L., Andrieu, S., Bertier, G., Boeckhout, M., Carpenter, J., Dagher, G., Dalgleish, R., Deschênes, M., di Donato, J.H., Filocamo, M., Goldberg, M., Hewitt, R., Hofman, P., Kauffmann, F., Leitsalu, L., Lomba, I., Melegh, B., Metspalu, A., Miranda, L., Napolitani, F., Oestergaard, M.Z., Parodi, B., Pasterk, M., Reiche, A., Rial-Sebbag, E., Rivalle, G., Rochaix, P., Susbielle, G., Tarasova, L., Thomsen, M., Zawati, M.H. & Zins, M.
Avaldatud: Nature genetics 43, 503-4


A Variant in MCF2L Is Associated with Osteoarthritis.
Day-Williams, A.G., Southam, L., Panoutsopoulou, K., Rayner, N.W., Esko, T., Estrada, K., Helgadottir, H.T., Hofman, A., Ingvarsson, T., Jonsson, H., Keis, A., Kerkhof, H.J.M., Thorleifsson, G., Arden, N.K., Carr, A., Chapman, K., Deloukas, P., Loughlin, J., McCaskie, A., Ollier, W.E.R., Ralston, S.H., Spector, T.D., Wallis, G.A., Wilkinson, J.M., Aslam, N., Birell, F., Carluke, I., Joseph, J., Rai, A., Reed, M., Walker, K., Doherty, S.A., Jonsdottir, I., Maciewicz, R.A., Muir, K.R., Metspalu, A., Rivadeneira, F., Stefansson, K., Styrkarsdottir, U., Uitterlinden, A.G., van Meurs, J.B.J., Zhang, W., Valdes, A.M., Doherty, M. & Zeggini, E.
Avaldatud: American journal of human genetics 89, 446-50


New gene functions in megakaryopoiesis and platelet formation.
Gieger, C., Radhakrishnan, A., Cvejic, A., Tang, W., Porcu, E., Pistis, G., Serbanovic-Canic, J., Elling, U., Goodall, A.H., Labrune, Y., Lopez, L.M., Mägi, R., Meacham, S., Okada, Y., Pirastu, N., Sorice, R., Teumer, A., Voss, K., Zhang, W., Ramirez-Solis, R., Bis, J.C., Ellinghaus, D., Gögele, M., Hottenga, J.-J., Langenberg, C., Kovacs, P., O’Reilly, P.F., Shin, S.-Y., Esko, T., Hartiala, J., Kanoni, S., Murgia, F., Parsa, A., Stephens, J., van der Harst, P., Ellen van der Schoot, C., Allayee, H., Attwood, A., Balkau, B., Bastardot, F., Basu, S., Baumeister, S.E., Biino, G., Bomba, L., Bonnefond, A., Cambien, F., Chambers, J.C., Cucca, F., D’Adamo, P., Davies, G., de Boer, R.A., de Geus, E.J.C., Döring, A., Elliott, P., Erdmann, J., Evans, D.M., Falchi, M., Feng, W., Folsom, A.R., Frazer, I.H., Gibson, Q.D., Glazer, N.L., Hammond, C., Hartikainen, A.-L., Heckbert, S.R., Hengstenberg, C., Hersch, M., Illig, T., Loos, R.J.F., Jolley, J., Tee Khaw, K., Kühnel, B., Kyrtsonis, M.-C., Lagou, V., Lloyd-Jones, H., Lumley, T., Mangino, M., Maschio, A., Mateo Leach, I., McKnight, B., Memari, Y., Mitchell, B.D., Montgomery, G.W., Nakamura, Y., Nauck, M., Navis, G., Nöthlings, U., Nolte, I.M., Porteous, D.J., Pouta, A., Pramstaller, P.P., Pullat, J., Ring, S.M., Rotter, J.I., Ruggiero, D., Ruokonen, A., Sala, C., Samani, N.J., Sambrook, J., Schlessinger, D., Schreiber, S., Schunkert, H., Scott, J., Smith, N.L., Snieder, H., Starr, J.M., Stumvoll, M., Takahashi, A., Wilson Tang, W.H., Taylor, K., Tenesa, A., Lay Thein, S., Tönjes, A., Uda, M., Ulivi, S., van Veldhuisen, D.J., Visscher, P.M., Völker, U., Wichmann, H.-E., Wiggins, K.L., Willemsen, G., Yang, T.-P., Hua Zhao, J., Zitting, P., Bradley, J.R., Dedoussis, G.V., Gasparini, P., Hazen, S.L., Metspalu, A., Pirastu, M., Shuldiner, A.R., Joost van Pelt, L., Zwaginga, J.-J., Boomsma, D.I., Deary, I.J., Franke, A., Froguel, P., Ganesh, S.K., Jarvelin, M.-R., Martin, N.G., Meisinger, C., Psaty, B.M., Spector, T.D., Wareham, N.J., Akkerman, J.-W.N., Ciullo, M., Deloukas, P., Greinacher, A., Jupe, S., Kamatani, N., Khadake, J., Kooner, J.S., Penninger, J., Prokopenko, I., Stemple, D., Toniolo, D., Wernisch, L., Sanna, S., Hicks, A.A., Rendon, A., Ferreira, M.A., Ouwehand, W.H. & Soranzo, N.
Avaldatud: Nature


A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. (link)
Surakka I, Isaacs A, Karssen LC, Laurila PP, Middelberg RP, Tikkanen E, Ried JS, Lamina C, Mangino M, Igl W, Hottenga JJ, Lagou V, van der Harst P, Mateo Leach I, Esko T, Kutalik Z, Wainwright NW, Struchalin MV, Sarin AP, Kangas AJ, Viikari JS, Perola M, Rantanen T, Petersen AK, Soininen P, Johansson A, Soranzo N, Heath AC, Papamarkou T, Prokopenko I, Tönjes A, Kronenberg F, Döring A, Rivadeneira F, Montgomery GW, Whitfield JB, Kähönen M, Lehtimäki T, Freimer NB, Willemsen G, de Geus EJ, Palotie A, Sandhu MS, Waterworth DM, Metspalu A, Stumvoll M, Uitterlinden AG, Jula A, Navis G, Wijmenga C, Wolffenbuttel BH, Taskinen MR, Ala-Korpela M, Kaprio J, Kyvik KO, Boomsma DI, Pedersen NL, Gyllensten U, Wilson JF, Rudan I, Campbell H, Pramstaller PP, Spector TD, Witteman JC, Eriksson JG, Salomaa V, Oostra BA, Raitakari OT, Wichmann HE, Gieger C, Järvelin MR, Martin NG, Hofman A, McCarthy MI, Peltonen L, van Duijn CM, Aulchenko YS, Ripatti S; for the ENGAGE Consortium
Avaldatud: PLoS Genet. 2011 Oct;7(10):e1002333. Epub 2011 Oct 20.


The role of COX-2 and Nrf2/ARE in anti-inflammation and antioxidative stress: Aging and anti-aging.
Luo, C., Urgard, E., Vooder, T. & Metspalu, A.
Avaldatud: Medical hypotheses 77, 174-8


Human microRNAs miR-22, miR-138-2, miR-148a, and miR-488 are associated with panic disorder and regulate several anxiety candidate genes and related pathways.
Muiños-Gimeno, M., Espinosa-Parrilla, Y., Guidi, M., Kagerbauer, B., Sipilä, T., Maron, E., Pettai, K., Kananen, L., Navinés, R., Martín-Santos, R., Gratacòs, M., Metspalu, A., Hovatta, I. & Estivill, X.
Avaldatud: Biological psychiatry 69, 526-33


Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate.
Nikopensius, T., Kempa, I., Ambrozaitytė, L., Jagomägi, T., Saag, M., Matulevičienė, A., Utkus, A., Krjutškov, K., Tammekivi, V., Piekuse, L., Akota, I., Barkane, B., Krumina, A., Klovins, J., Lace, B., Kučinskas, V. & Metspalu, A.
Avaldatud: Birth defects research. Part A, Clinical and molecular teratology 91, 218-25


Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study.
Panoutsopoulou, K., Southam, L., Elliott, K.S., Wrayner, N., Zhai, G., Beazley, C., Thorleifsson, G., Arden, N.K., Carr, A., Chapman, K., Deloukas, P., Doherty, M., McCaskie, A., Ollier, W.E.R., Ralston, S.H., Spector, T.D., Valdes, A.M., Wallis, G.A., Wilkinson, J.M., Arden, E., Battley, K., Blackburn, H., Blanco, F.J., Bumpstead, S., Cupples, L.A., Day-Williams, A.G., Dixon, K., Doherty, S.A., Esko, T., Evangelou, E., Felson, D., Gomez-Reino, J.J., Gonzalez, A., Gordon, A., Gwilliam, R., Halldorsson, B.V., Hauksson, V.B., Hofman, A., Hunt, S.E., Ioannidis, J.P.A., Ingvarsson, T., Jonsdottir, I., Jonsson, H., Keen, R., Kerkhof, H.J.M., Kloppenburg, M.G., Koller, N., Lakenberg, N., Lane, N.E., Lee, A.T., Metspalu, A., Meulenbelt, I., Nevitt, M.C., O’Neill, F., Parimi, N., Potter, S.C., Rego-Perez, I., Riancho, J.A., Sherburn, K., Slagboom, P.E., Stefansson, K., Styrkarsdottir, U., Sumillera, M., Swift, D., Thorsteinsdottir, U., Tsezou, A., Uitterlinden, A.G., van Meurs, J.B.J., Watkins, B., Wheeler, M., Mitchell, S., Zhu, Y., Zmuda, J.M., Zeggini, E. & Loughlin, J.
Avaldatud: Annals of the rheumatic diseases 70, 864-7


Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.
Schumann, G., Coin, L.J., Lourdusamy, A., Charoen, P., Berger, K.H., Stacey, D., Desrivières, S., Aliev, F.A., Khan, A.A., Amin, N., Aulchenko, Y.S., Bakalkin, G., Bakker, S.J., Balkau, B., Beulens, J.W., Bilbao, A., de Boer, R.A., Beury, D., Bots, M.L., Breetvelt, E.J., Cauchi, S., Cavalcanti-Proença, C., Chambers, J.C., Clarke, T.-K., Dahmen, N., de Geus, E.J., Dick, D., Ducci, F., Easton, A., Edenberg, H.J., Esko, T., Esk, T., Fernández-Medarde, A., Foroud, T., Freimer, N.B., Girault, J.-A., Grobbee, D.E., Guarrera, S., Gudbjartsson, D.F., Hartikainen, A.-L., Heath, A.C., Hesselbrock, V., Hofman, A., Hottenga, J.-J., Isohanni, M.K., Kaprio, J., Khaw, K.-T., Kuehnel, B., Laitinen, J., Lobbens, S., Luan, J., Mangino, M., Maroteaux, M., Matullo, G., McCarthy, M.I., Mueller, C., Navis, G., Numans, M.E., Núñez, A., Nyholt, D.R., Onland-Moret, C.N., Oostra, B.A., O’Reilly, P.F., Palkovits, M., Penninx, B.W., Polidoro, S., Pouta, A., Prokopenko, I., Ricceri, F., Santos, E., Smit, J.H., Soranzo, N., Song, K., Sovio, U., Stumvoll, M., Surakk, I., Thorgeirsson, T.E., Thorsteinsdottir, U., Troakes, C., Tyrfingsson, T., Tönjes, A., Uiterwaal, C.S., Uitterlinden, A.G., van der Harst, P., van der Schouw, Y.T., Staehlin, O., Vogelzangs, N., Vollenweider, P., Waeber, G., Wareham, N.J., Waterworth, D.M., Whitfield, J.B., Wichmann, E.H., Willemsen, G., Witteman, J.C., Yuan, X., Zhai, G., Zhao, J.H., Zhang, W., Martin, N.G., Metspalu, A., Doering, A., Scott, J., Spector, T.D., Loos, R.J., Boomsma, D.I., Mooser, V., Peltonen, L., Stefansson, K., van Duijn, C.M., Vineis, P., Sommer, W.H., Kooner, J.S., Spanagel, R., Heberlein, U.A., Jarvelin, M.-R. & Elliott, P.
Avaldatud: Proceedings of the National Academy of Sciences of the United States of America 108, 7119-24


Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.
Speliotes, E.K., Yerges-Armstrong, L.M., Wu, J., Hernaez, R., Kim, L.J., Palmer, C.D., Gudnason, V., Eiriksdottir, G., Garcia, M.E., Launer, L.J., Nalls, M.A., Clark, J.M., Mitchell, B.D., Shuldiner, A.R., Butler, J.L., Tomas, M., Hoffmann, U., Hwang, S.-J., Massaro, J.M., O’Donnell, C.J., Sahani, D.V., Salomaa, V., Schadt, E.E., Schwartz, S.M., Siscovick, D.S., Voight, B.F., Carr, J.J., Feitosa, M.F., Harris, T.B., Fox, C.S., Smith, A.V., Kao, W.H.L., Hirschhorn, J.N. & Borecki, I.B.
Avaldatud: PLoS genetics 7, e1001324


Identification of miR-374a as a prognostic marker for survival in patients with early-stage nonsmall cell lung cancer.
Võsa, U., Vooder, T., Kolde, R., Fischer, K., Välk, K., Tõnisson, N., Roosipuu, R., Vilo, J., Metspalu, A. & Annilo, T.
Avaldatud: Genes, chromosomes & cancer 50, 812-22


Investigating gene expression profile of non-small cell lung cancer.
Vooder, T. & Metspalu, A.
Avaldatud: Cent. Eur. J. Med.


Metagenes associated with survival in NSCLC.
Urgard, E., Vooder, T., Võsa, U., Välk, K., Liu, M., Luo, C., Hoti, F., Roosipuu, R., Annilo, T., Laine, J., Frenz, C.M., Zhang, L. & Metspalu, A.
Avaldatud: Cancer Informatics, 10, 175-183


The Estonian Biobank – the gateway for the stratified medicine.,
Metspalu, A., Leitsalu L., Milani M., Esko T., Allik A., Lilienthal K., Tammesoo M-L., Haller T., Kaasik A-T., Nelis M., Hass M., Fischer K., Krjutskov K., Leego E., Alavere H., Perola M.
Avaldatud: Research in Estonia Present and Future, 283-301


A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (link)
McKay JD, Truong T, Gaborieau V, Chabrier A, Chuang SC, Byrnes G, Zaridze D, Shangina O, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Bucur A, Bencko V, Holcatova I, Janout V, Foretova L, Lagiou P, Trichopoulos D, Benhamou S, Bouchardy C, Ahrens W, Merletti F, Richiardi L, Talamini R, Barzan L, Kjaerheim K, Macfarlane GJ, Macfarlane TV, Simonato L, Canova C, Agudo A, Castellsagué X, Lowry R, Conway DI, McKinney PA, Healy CM, Toner ME, Znaor A, Curado MP, Koifman S, Menezes A, Wünsch-Filho V, Neto JE, Garrote LF, Boccia S, Cadoni G, Arzani D, Olshan AF, Weissler MC, Funkhouser WK, Luo J, Lubiński J, Trubicka J, Lener M, Oszutowska D, Schwartz SM, Chen C, Fish S, Doody DR, Muscat JE, Lazarus P, Gallagher CJ, Chang SC, Zhang ZF, Wei Q, Sturgis EM, Wang LE, Franceschi S, Herrero R, Kelsey KT, McClean MD, Marsit CJ, Nelson HH, Romkes M, Buch S, Nukui T, Zhong S, Lacko M, Manni JJ, Peters WH, Hung RJ, McLaughlin J, Vatten L, Njølstad I, Goodman GE, Field JK, Liloglou T, Vineis P, Clavel-Chapelon F, Palli D, Tumino R, Krogh V, Panico S, González CA, Quirós JR, Martínez C, Navarro C, Ardanaz E, Larrañaga N, Khaw KT, Key T, Bueno-de-Mesquita HB, Peeters PH, Trichopoulou A, Linseisen J, Boeing H, Hallmans G, Overvad K, Tjønneland A, Kumle M, Riboli E, Välk K, Vooder T, Metspalu A, Zelenika D, Boland A, Delepine M, Foglio M, Lechner D, Blanché H, Gut IG, Galan P, Heath S, Hashibe M, Hayes RB, Boffetta P, Lathrop M, Brennan P.
Avaldatud: PLoS Genet. 2011 Mar;7(3):e1001333. Epub 2011 Mar 17. Erratum in: PLoS Genet. 2011 Apr;7(4).


Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic Traits
Elizabeth K. Speliotes, Laura M. Yerges-Armstrong, Jun Wu, Ruben Hernaez, Lauren J., Kim, Cameron D. Palmer, Vilmundur Gudnason, Gudny Eiriksdottir, Melissa E. Garcia, Lenore J. Launer, Michael A. Nalls, Jeanne M. Clark, Braxton D. Mitchell, Alan R. Shuldiner, Johannah L. Butler, Marta Tomas, Udo Hoffmann, Shih-Jen Hwang, Joseph M., Massaro, Christopher J. O’Donnell, Dushyant V. Sahani, Veikko Salomaa, Eric E. Schadt, Stephen M. Schwartz, David S. Siscovick, NASH CRN, GIANT Consortium (Reedik Mägi, Tõnu Esko, Helene Alavere, Mari Nelis, Makus Perola, Mari-Liis Tammesoo, Maris Teder-Laving, Andres Metspalu), MAGIC, Investigators", Benjamin F. Voight, J. Jeffrey Carr, Mary F. Feitosa, Tamara B. Harris, Caroline S. Fox, Albert V. Smith, W. H. Linda Kao, Joel N. Hirschhorn, Ingrid B. Borecki., GOLD Consortium"
Avaldatud: PLoS Genetics, March 2011, Volume 7, Issue 3, e1001324


Metagenes associated with survival in NSCLC (link)
Urgard, Egon; Vooder, Tõnu; Võsa, Urmo; Välk, Kristjan; Liu, Mingming; Luo, Cheng; Hoti, Fabian; Roosipuu, Retlav; Annilo, Tarmo; Laine, Jukka; . Frenz, Christopher M; Zhang, Liqing; Metspalu, Andres
Avaldatud: Cancer Informatics 2011:10 175–183
DOI: doi: 10.4137/CIN.S7135


Systems medicine and integrated care to combat chronic noncommunicable diseases. (link)
Bousquet J, Anto JM, Sterk PJ, Adcock IM, Chung KF, Roca J, Agusti A, Brightling C, Cambon-Thomsen A, Cesario A, Abdelhak S, Antonarakis SE, Avignon A, Ballabio A, Baraldi E, Baranov A, Bieber T, Bockaert J, Brahmachari S, Brambilla C, Bringer J, Dauzat M, Ernberg I, Fabbri L, Froguel P, Galas D, Gojobori T, Hunter P, Jorgensen C, Kauffmann F, Kourilsky P, Kowalski ML, Lancet D, Pen CL, Mallet J, Mayosi B, Mercier J, Metspalu A, Nadeau JH, Ninot G, Noble D, Oztürk M, Palkonen S, Préfaut C, Rabe K, Renard E, Roberts RG, Samolinski B, Schünemann HJ, Simon HU, Soares MB, Superti-Furga G, Tegner J, Verjovski-Almeida S, Wellstead P, Wolkenhauer O, Wouters E, Balling R, Brookes AJ, Charron D, Pison C, Chen Z, Hood L, Auffray C.
Avaldatud: Genome Med. 2011 Jul 6;3(7):43.


Comprehensive catalog of European biobanks. (link)
Wichmann HE, Kuhn KA, Waldenberger M, Schmelcher D, Schuffenhauer S, Meitinger T, Wurst SH, Lamla G, Fortier I, Burton PR, Peltonen L, Perola M, Metspalu A, Riegman P, Landegren U, Taussig MJ, Litton JE, Fransson MN, Eder J, Cambon-Thomsen A, Bovenberg J, Dagher G, van Ommen GJ, Griffith M, Yuille M, Zatloukal K.
Avaldatud: Nat Biotechnol. 2011 Sep 8;29(9):795-7
DOI: doi: 10.1038/nbt.1958


Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. (link)
Strawbridge RJ, Dupuis J, Prokopenko I, Barker A, Ahlqvist E, Rybin D, Petrie JR, Travers ME, Bouatia-Naji N, Dimas AS, Nica A, Wheeler E, Chen H, Voight BF, Taneera J, Kanoni S, Peden JF, Turrini F, Gustafsson S, Zabena C, Almgren P, Barker DJ, Barnes D, Dennison EM, Eriksson JG, Eriksson P, Eury E, Folkersen L, Fox CS, Frayling TM, Goel A, Gu HF, Horikoshi M, Isomaa B, Jackson AU, Jameson KA, Kajantie E, Kerr-Conte J, Kuulasmaa T, Kuusisto J, Loos RJ, Luan J, Makrilakis K, Manning AK, Martínez-Larrad MT, Narisu N, Nastase Mannila M, Ohrvik J, Osmond C, Pascoe L, Payne F, Sayer AA, Sennblad B, Silveira A, Stancáková A, Stirrups K, Swift AJ, Syvänen AC, Tuomi T, van ''t Hooft FM, Walker M, Weedon MN, Xie W, Zethelius B; DIAGRAM Consortium; GIANT Consortium (incl. Andres Metspalu, Maris Teder-Laving, Mari-Liis Tammesoo, Helene Alavere, Mari Nelis); MuTHER Consortium; CARDIoGRAM Consortium; C4D Consortium, Ongen H, Mälarstig A, Hopewell JC, Saleheen D, Chambers J, Parish S, Danesh J, Kooner J, Ostenson CG, Lind L, Cooper CC, Serrano-Ríos M, Ferrannini E, Forsen TJ, Clarke R, Franzosi MG, Seedorf U, Watkins H, Froguel P, Johnson P, Deloukas P, Collins FS, Laakso M, Dermitzakis ET, Boehnke M, McCarthy MI, Wareham NJ, Groop L, Pattou F, Gloyn AL, Dedoussis GV, Lyssenko V, Meigs JB, Barroso I, Watanabe RM, Ingelsson E, Langenberg C, Hamsten A, Florez JC.
Avaldatud: Diabetes. 2011 Oct;60(10):2624-34. Epub 2011 Aug 26.

2010 (33)

CLOCK gene variants associate with sleep duration in two independent populations.

Allebrandt, K.V., Teder-Laving, M., Akyol, M., Pichler, I., Müller-Myhsok, B., Pramstaller, P., Merrow, M., Meitinger, T., Metspalu, A. & Roenneberg, T.
Avaldatud: Biological psychiatry 67, 1040-7


Manifesto for a European anxiety disorders research network.
Baldwin, D.S., Allgulander, C., Altamura, A.C., Angst, J., Bandelow, B., den Boer, J., Boyer, P., Davies, S., Dell’osso, B., Eriksson, E., Fineberg, N., Fredrikson, M., Herran, A., Maron, E., Metspalu, A., Nutt, D., van der Wee, N., Vázquez-Barquero, J.L. & Zohar, J.
Avaldatud: European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 20, 426-32


Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements.
Braschinsky, M., Tamm, R., Beetz, C., Sachez-Ferrero, E., Raukas, E., Lüüs, S.-M., Gross-Paju, K., Boillot, C., Canzian, F., Metspalu, A. & Haldre, S.
Avaldatud: BMC neurology 10, 17


Meta-analysis of genome-wide association studies for personality.
de Moor, M.H.M., Costa, P.T., Terracciano, A., Krueger, R.F., de Geus, E.J.C., Toshiko, T., Penninx, B.W.J.H., Esko, T., Madden, P.A.F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J.-J., Distel, M.A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C.A., Sullivan, P., Realo, A., Allik, J., Heath, A.C., Pergadia, M.L., Agrawal, A., Lin, P., Grucza, R., Nutile, T., Ciullo, M., Rujescu, D., Giegling, I., Konte, B., Widen, E., Cousminer, D.L., Eriksson, J.G., Palotie, A., Peltonen, L., Luciano, M., Tenesa, A., Davies, G., Lopez, L.M., Hansell, N.K., Medland, S.E., Ferrucci, L., Schlessinger, D., Montgomery, G.W., Wright, M.J., Aulchenko, Y.S., Janssens, A.C.J.W., Oostra, B.A., Metspalu, A., Abecasis, G.R., Deary, I.J., Räikkönen, K., Bierut, L.J., Martin, N.G., van Duijn, C.M. & Boomsma, D.I.
Avaldatud: Molecular psychiatry


Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
Elks, C.E., Perry, J.R.B., Sulem, P., Chasman, D.I., Franceschini, N., He, C., Lunetta, K.L., Visser, J.A., Byrne, E.M., Cousminer, D.L., Gudbjartsson, D.F., Esko, T., Feenstra, B., Hottenga, J.-J., Koller, D.L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P.F., Smith, A.V., Stolk, L., van Wingerden, S.H., Zhao, J.H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P.K.E., Smith, E.N., Ulivi, S., Warrington, N.M., Zgaga, L., Alavere, H., Amin, N., Aspelund, T., Bandinelli, S., Barroso, I., Berenson, G.S., Bergmann, S., Blackburn, H., Boerwinkle, E., Buring, J.E., Busonero, F., Campbell, H., Chanock, S.J., Chen, W., Cornelis, M.C., Couper, D., Coviello, A.D., d’ Adamo, P., de Faire, U., de Geus, E.J.C., Deloukas, P., Döring, A., Smith, G.D., Easton, D.F., Eiriksdottir, G., Emilsson, V., Eriksson, J., Ferrucci, L., Folsom, A.R., Foroud, T., Garcia, M., Gasparini, P., Geller, F., Gieger, C., Gudnason, V., Hall, P., Hankinson, S.E., Ferreli, L., Heath, A.C., Hernandez, D.G., Hofman, A., Hu, F.B., Illig, T., Järvelin, M.-R., Johnson, A.D., Karasik, D., Khaw, K.-T., Kiel, D.P., Kilpeläinen, T.O., Kolcic, I., Kraft, P., Launer, L.J., Laven, J.S.E., Li, S., Liu, J., Levy, D., Martin, N.G., McArdle, W.L., Melbye, M., Mooser, V., Murray, J.C., Murray, S.S., Nalls, M.A., Navarro, P., Nelis, M., Ness, A.R., Northstone, K., Oostra, B.A., Peacock, M., Palmer, L.J., Palotie, A., Paré, G., Parker, A.N., Pedersen, N.L., Peltonen, L., Pennell, C.E., Pharoah, P., Polasek, O., Plump, A.S., Pouta, A., Porcu, E., Rafnar, T., Rice, J.P., Ring, S.M., Rivadeneira, F., Rudan, I., Sala, C., Salomaa, V., Sanna, S., Schlessinger, D., Schork, N.J., Scuteri, A., Segrè, A.V., Shuldiner, A.R., Soranzo, N., Sovio, U., Srinivasan, S.R., Strachan, D.P., Tammesoo, M.-L., Tikkanen, E., Toniolo, D., Tsui, K., Tryggvadottir, L., Tyrer, J., Uda, M., van Dam, R.M., van Meurs, J.B.J., Vollenweider, P., Waeber, G., Wareham, N.J., Waterworth, D.M., Weedon, M.N., Wichmann, H.E., Willemsen, G., Wilson, J.F., Wright, A.F., Young, L., Zhai, G., Zhuang, W.V., Bierut, L.J., Boomsma, D.I., Boyd, H.A., Crisponi, L., Demerath, E.W., van Duijn, C.M., Econs, M.J., Harris, T.B., Hunter, D.J., Loos, R.J.F., Metspalu, A., Montgomery, G.W., Ridker, P.M., Spector, T.D., Streeten, E.A., Stefansson, K., Thorsteinsdottir, U., Uitterlinden, A.G., Widen, E., Murabito, J.M., Ong, K.K. & Murray, A.
Avaldatud: Nature genetics 42, 1077-85


Common variants in KCNN3 are associated with lone atrial fibrillation.
Ellinor, P.T., Lunetta, K.L., Glazer, N.L., Pfeufer, A., Alonso, A., Chung, M.K., Sinner, M.F., de Bakker, P.I.W., Mueller, M., Lubitz, S.A., Fox, E., Darbar, D., Smith, N.L., Smith, J.D., Schnabel, R.B., Soliman, E.Z., Rice, K.M., Van Wagoner, D.R., Beckmann, B.-M., van Noord, C., Wang, K., Ehret, G.B., Rotter, J.I., Hazen, S.L., Steinbeck, G., Smith, A.V., Launer, L.J., Harris, T.B., Makino, S., Nelis, M., Milan, D.J., Perz, S., Esko, T., Köttgen, A., Moebus, S., Newton-Cheh, C., Li, M., Möhlenkamp, S., Wang, T.J., Kao, W.H.L., Vasan, R.S., Nöthen, M.M., MacRae, C.A., Stricker, B.H.C., Hofman, A., Uitterlinden, A.G., Levy, D., Boerwinkle, E., Metspalu, A., Topol, E.J., Chakravarti, A., Gudnason, V., Psaty, B.M., Roden, D.M., Meitinger, T., Wichmann, H.-E., Witteman, J.C.M., Barnard, J., Arking, D.E., Benjamin, E.J., Heckbert, S.R. & Kääb, S.
Avaldatud: Nature genetics 42, 240-4


Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies.
Fortier, I., Burton, P.R., Robson, P.J., Ferretti, V., Little, J., L’Heureux, F., Deschênes, M., Knoppers, B.M., Doiron, D., Keers, J.C., Linksted, P., Harris, J.R., Lachance, G., Boileau, C., Pedersen, N.L., Hamilton, C.M., Hveem, K., Borugian, M.J., Gallagher, R.P., McLaughlin, J., Parker, L., Potter, J.D., Gallacher, J., Kaaks, R., Liu, B., Sprosen, T., Vilain, A., Atkinson, S.A., Rengifo, A., Morton, R., Metspalu, A., Wichmann, H.E., Tremblay, M., Chisholm, R.L., Garcia-Montero, A., Hillege, H., Litton, J.-E., Palmer, L.J., Perola, M., Wolffenbuttel, B.H.R., Peltonen, L. & Hudson, T.J.
Avaldatud: International journal of epidemiology 39, 1383-93


Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
Heid, I.M., Jackson, A.U., Randall, J.C., Winkler, T.W., Qi, L., Steinthorsdottir, V., Thorleifsson, G., Zillikens, M.C., Speliotes, E.K., Mägi, R., Workalemahu, T., White, C.C., Bouatia-Naji, N., Harris, T.B., Berndt, S.I., Ingelsson, E., Willer, C.J., Weedon, M.N., Luan, J., Vedantam, S., Esko, T., Kilpeläinen, T.O., Kutalik, Z., Li, S., Monda, K.L., Dixon, A.L., Holmes, C.C., Kaplan, L.M., Liang, L., Min, J.L., Moffatt, M.F., Molony, C., Nicholson, G., Schadt, E.E., Zondervan, K.T., Feitosa, M.F., Ferreira, T., Allen, H.L., Weyant, R.J., Wheeler, E., Wood, A.R., Estrada, K., Goddard, M.E., Lettre, G., Mangino, M., Nyholt, D.R., Purcell, S., Smith, A.V., Visscher, P.M., Yang, J., McCarroll, S.A., Nemesh, J., Voight, B.F., Absher, D., Amin, N., Aspelund, T., Coin, L., Glazer, N.L., Hayward, C., Heard-Costa, N.L., Hottenga, J.-J., Johansson, A., Johnson, T., Kaakinen, M., Kapur, K., Ketkar, S., Knowles, J.W., Kraft, P., Kraja, A.T., Lamina, C., Leitzmann, M.F., McKnight, B., Morris, A.P., Ong, K.K., Perry, J.R.B., Peters, M.J., Polasek, O., Prokopenko, I., Rayner, N.W., Ripatti, S., Rivadeneira, F., Robertson, N.R., Sanna, S., Sovio, U., Surakka, I., Teumer, A., van Wingerden, S., Vitart, V., Zhao, J.H., Cavalcanti-Proença, C., Chines, P.S., Fisher, E., Kulzer, J.R., Lecoeur, C., Narisu, N., Sandholt, C., Scott, L.J., Silander, K., Stark, K., Tammesoo, M.-L., Teslovich, T.M., Timpson, N.J., Watanabe, R.M., Welch, R., Chasman, D.I., Cooper, M.N., Jansson, J.-O., Kettunen, J., Lawrence, R.W., Pellikka, N., Perola, M., Vandenput, L., Alavere, H., Almgren, P., Atwood, L.D., Bennett, A.J., Biffar, R., Bonnycastle, L.L., Bornstein, S.R., Buchanan, T.A., Campbell, H., Day, I.N.M., Dei, M., Dörr, M., Elliott, P., Erdos, M.R., Eriksson, J.G., Freimer, N.B., Fu, M., Gaget, S., Geus, E.J.C., Gjesing, A.P., Grallert, H., Grässler, J., Groves, C.J., Guiducci, C., Hartikainen, A.-L., Hassanali, N., Havulinna, A.S., Herzig, K.-H., Hicks, A.A., Hui, J., Igl, W., Jousilahti, P., Jula, A., Kajantie, E., Kinnunen, L., Kolcic, I., Koskinen, S., Kovacs, P., Kroemer, H.K., Krzelj, V., Kuusisto, J., Kvaloy, K., Laitinen, J., Lantieri, O., Lathrop, G.M., Lokki, M.-L., Luben, R.N., Ludwig, B., McArdle, W.L., McCarthy, A., Morken, M.A., Nelis, M., Neville, M.J., Paré, G., Parker, A.N., Peden, J.F., Pichler, I., Pietiläinen, K.H., Platou, C.G.P., Pouta, A., Ridderstråle, M., Samani, N.J., Saramies, J., Sinisalo, J., Smit, J.H., Strawbridge, R.J., Stringham, H.M., Swift, A.J., Teder-Laving, M., Thomson, B., Usala, G., van Meurs, J.B.J., van Ommen, G.-J., Vatin, V., Volpato, C.B., Wallaschofski, H., Walters, G.B., Widen, E., Wild, S.H., Willemsen, G., Witte, D.R., Zgaga, L., Zitting, P., Beilby, J.P., James, A.L., Kähönen, M., Lehtimäki, T., Nieminen, M.S., Ohlsson, C., Palmer, L.J., Raitakari, O., Ridker, P.M., Stumvoll, M., Tönjes, A., Viikari, J., Balkau, B., Ben-Shlomo, Y., Bergman, R.N., Boeing, H., Smith, G.D., Ebrahim, S., Froguel, P., Hansen, T., Hengstenberg, C., Hveem, K., Isomaa, B., Jørgensen, T., Karpe, F., Khaw, K.-T., Laakso, M., Lawlor, D.A., Marre, M., Meitinger, T., Metspalu, A., Midthjell, K., Pedersen, O., Salomaa, V., Schwarz, P.E.H., Tuomi, T., Tuomilehto, J., Valle, T.T., Wareham, N.J., Arnold, A.M., Beckmann, J.S., Bergmann, S., Boerwinkle, E., Boomsma, D.I., Caulfield, M.J., Collins, F.S., Eiriksdottir, G., Gudnason, V., Gyllensten, U., Hamsten, A., Hattersley, A.T., Hofman, A., Hu, F.B., Illig, T., Iribarren, C., Jarvelin, M.-R., Kao, W.H.L., Kaprio, J., Launer, L.J., Munroe, P.B., Oostra, B., Penninx, B.W., Pramstaller, P.P., Psaty, B.M., Quertermous, T., Rissanen, A., Rudan, I., Shuldiner, A.R., Soranzo, N., Spector, T.D., Syvanen, A.-C., Uda, M., Uitterlinden, A., Völzke, H., Vollenweider, P., Wilson, J.F., Witteman, J.C., Wright, A.F., Abecasis, G.R., Boehnke, M., Borecki, I.B., Deloukas, P., Frayling, T.M., Groop, L.C., Haritunians, T., Hunter, D.J., Kaplan, R.C., North, K.E., O’Connell, J.R., Peltonen, L., Schlessinger, D., Strachan, D.P., Hirschhorn, J.N., Assimes, T.L., Wichmann, H.-E., Thorsteinsdottir, U., van Duijn, C.M., Stefansson, K., Cupples, L.A., Loos, R.J.F., Barroso, I., McCarthy, M.I., Fox, C.S., Mohlke, K.L. & Lindgren, C.M.
Avaldatud: Nature genetics 42, 949-60


MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.
Jagomägi, T., Nikopensius, T., Krjutskov, K., Tammekivi, V., Viltrop, T., Saag, M. & Metspalu, A.
Avaldatud: European journal of oral sciences 118, 213-20


Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits.
Kepp, K., Org, E., Sõber, S., Kelgo, P., Viigimaa, M., Veldre, G., Tõnisson, N., Juhanson, P., Putku, M., Kindmark, A., Kozich, V. & Laan, M.
Avaldatud: BMC medical genetics 11, 15


Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Lango Allen, H., Estrada, K., Lettre, G., Berndt, S.I., Weedon, M.N., Rivadeneira, F., Willer, C.J., Jackson, A.U., Vedantam, S., Raychaudhuri, S., Ferreira, T., Wood, A.R., Weyant, R.J., Segrè, A.V., Speliotes, E.K., Wheeler, E., Soranzo, N., Park, J.-H., Yang, J., Gudbjartsson, D., Heard-Costa, N.L., Randall, J.C., Qi, L., Vernon Smith, A., Mägi, R., Pastinen, T., Liang, L., Heid, I.M., Luan, J., Thorleifsson, G., Winkler, T.W., Goddard, M.E., Sin Lo, K., Palmer, C., Workalemahu, T., Aulchenko, Y.S., Johansson, A., Zillikens, M.C., Feitosa, M.F., Esko, T., Johnson, T., Ketkar, S., Kraft, P., Mangino, M., Prokopenko, I., Absher, D., Albrecht, E., Ernst, F., Glazer, N.L., Hayward, C., Hottenga, J.-J., Jacobs, K.B., Knowles, J.W., Kutalik, Z., Monda, K.L., Polasek, O., Preuss, M., Rayner, N.W., Robertson, N.R., Steinthorsdottir, V., Tyrer, J.P., Voight, B.F., Wiklund, F., Xu, J., Zhao, J.H., Nyholt, D.R., Pellikka, N., Perola, M., Perry, J.R.B., Surakka, I., Tammesoo, M.-L., Altmaier, E.L., Amin, N., Aspelund, T., Bhangale, T., Boucher, G., Chasman, D.I., Chen, C., Coin, L., Cooper, M.N., Dixon, A.L., Gibson, Q., Grundberg, E., Hao, K., Juhani Junttila, M., Kaplan, L.M., Kettunen, J., König, I.R., Kwan, T., Lawrence, R.W., Levinson, D.F., Lorentzon, M., McKnight, B., Morris, A.P., Müller, M., Suh Ngwa, J., Purcell, S., Rafelt, S., Salem, R.M., Salvi, E., Sanna, S., Shi, J., Sovio, U., Thompson, J.R., Turchin, M.C., Vandenput, L., Verlaan, D.J., Vitart, V., White, C.C., Ziegler, A., Almgren, P., Balmforth, A.J., Campbell, H., Citterio, L., De Grandi, A., Dominiczak, A., Duan, J., Elliott, P., Elosua, R., Eriksson, J.G., Freimer, N.B., Geus, E.J.C., Glorioso, N., Haiqing, S., Hartikainen, A.-L., Havulinna, A.S., Hicks, A.A., Hui, J., Igl, W., Illig, T., Jula, A., Kajantie, E., Kilpeläinen, T.O., Koiranen, M., Kolcic, I., Koskinen, S., Kovacs, P., Laitinen, J., Liu, J., Lokki, M.-L., Marusic, A., Maschio, A., Meitinger, T., Mulas, A., Paré, G., Parker, A.N., Peden, J.F., Petersmann, A., Pichler, I., Pietiläinen, K.H., Pouta, A., Ridderstråle, M., Rotter, J.I., Sambrook, J.G., Sanders, A.R., Schmidt, C.O., Sinisalo, J., Smit, J.H., Stringham, H.M., Bragi Walters, G., Widen, E., Wild, S.H., Willemsen, G., Zagato, L., Zgaga, L., Zitting, P., Alavere, H., Farrall, M., McArdle, W.L., Nelis, M., Peters, M.J., Ripatti, S., van Meurs, J.B.J., Aben, K.K., Ardlie, K.G., Beckmann, J.S., Beilby, J.P., Bergman, R.N., Bergmann, S., Collins, F.S., Cusi, D., den Heijer, M., Eiriksdottir, G., Gejman, P.V., Hall, A.S., Hamsten, A., Huikuri, H.V., Iribarren, C., Kähönen, M., Kaprio, J., Kathiresan, S., Kiemeney, L., Kocher, T., Launer, L.J., Lehtimäki, T., Melander, O., Mosley, T.H., Musk, A.W., Nieminen, M.S., O’Donnell, C.J., Ohlsson, C., Oostra, B., Palmer, L.J., Raitakari, O., Ridker, P.M., Rioux, J.D., Rissanen, A., Rivolta, C., Schunkert, H., Shuldiner, A.R., Siscovick, D.S., Stumvoll, M., Tönjes, A., Tuomilehto, J., van Ommen, G.-J., Viikari, J., Heath, A.C., Martin, N.G., Montgomery, G.W., Province, M.A., Kayser, M., Arnold, A.M., Atwood, L.D., Boerwinkle, E., Chanock, S.J., Deloukas, P., Gieger, C., Grönberg, H., Hall, P., Hattersley, A.T., Hengstenberg, C., Hoffman, W., Lathrop, G.M., Salomaa, V., Schreiber, S., Uda, M., Waterworth, D., Wright, A.F., Assimes, T.L., Barroso, I., Hofman, A., Mohlke, K.L., Boomsma, D.I., Caulfield, M.J., Cupples, L.A., Erdmann, J., Fox, C.S., Gudnason, V., Gyllensten, U., Harris, T.B., Hayes, R.B., Jarvelin, M.-R., Mooser, V., Munroe, P.B., Ouwehand, W.H., Penninx, B.W., Pramstaller, P.P., Quertermous, T., Rudan, I., Samani, N.J., Spector, T.D., Völzke, H., Watkins, H., Wilson, J.F., Groop, L.C., Haritunians, T., Hu, F.B., Kaplan, R.C., Metspalu, A., North, K.E., Schlessinger, D., Wareham, N.J., Hunter, D.J., O’Connell, J.R., Strachan, D.P., Wichmann, H.-E., Borecki, I.B., van Duijn, C.M., Schadt, E.E., Thorsteinsdottir, U., Peltonen, L., Uitterlinden, A.G., Visscher, P.M., Chatterjee, N., Loos, R.J.F., Boehnke, M., McCarthy, M.I., Ingelsson, E., Lindgren, C.M., Abecasis, G.R., Stefansson, K., Frayling, T.M. & Hirschhorn, J.N.
Avaldatud: Nature 467, 832-8


Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals.
Lips, E.H., Gaborieau, V., McKay, J.D., Chabrier, A., Hung, R.J., Boffetta, P., Hashibe, M., Zaridze, D., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., Field, J.K., Liloglou, T., Xinarianos, G., McLaughlin, J., Liu, G., Skorpen, F., Elvestad, M.B., Hveem, K., Vatten, L., Study, E., Benhamou, S., Lagiou, P., Holcátová, I., Merletti, F., Kjaerheim, K., Agudo, A., Castellsagué, X., Macfarlane, T.V., Barzan, L., Canova, C., Lowry, R., Conway, D.I., Znaor, A., Healy, C., Curado, M.P., Koifman, S., Eluf-Neto, J., Matos, E., Menezes, A., Fernandez, L., Metspalu, A., Heath, S., Lathrop, M. & Brennan, P.
Avaldatud: International journal of epidemiology 39, 563-77


A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.
Männik, K., Parkel, S., Palta, P., Zilina, O., Puusepp, H., Esko, T., Mägi, R., Nõukas, M., Veidenberg, A., Nelis, M., Metspalu, A., Remm, M., Ounap, K. & Kurg, A.
Avaldatud: European journal of medical genetics 54, 136-43


Advances in molecular genetics of panic disorder.
Maron, E., Hettema, J.M. & Shlik, J.
Avaldatud: Molecular psychiatry 15, 681-701


Peripheral gene expression profiling of CCK-4-induced panic in healthy subjects.
Maron, E., Kallassalu, K., Tammiste, A., Kolde, R., Vilo, J., Tõru, I., Vasar, V., Shlik, J. & Metspalu, A.
Avaldatud: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 153B, 269-74


Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients.
Nikopensius, T., Birnbaum, S., Ludwig, K.U., Jagomägi, T., Saag, M., Herms, S., Knapp, M., Hoffmann, P., Nöthen, M.M., Metspalu, A. & Mangold, E.
Avaldatud: European journal of oral sciences 118, 317-9


Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
Nikopensius, T., Jagomägi, T., Krjutskov, K., Tammekivi, V., Saag, M., Prane, I., Piekuse, L., Akota, I., Barkane, B., Krumina, A., Ambrozaityte, L., Matuleviciene, A., Kucinskiene, Z.A., Lace, B., Kucinskas, V. & Metspalu, A.
Avaldatud: Birth defects research. Part A, Clinical and molecular teratology 88, 748-56


HGV2009 meeting: bigger and better studies provide more answers and more questions.
Reekie, K., Metspalu, A., Chanock, S.J., Liu, E.T., Mardis, E.R., Scherer, S.W., Kwok, P.-Y. & Brookes, A.J.
Avaldatud: Human mutation 31, 886-8


Polymorphisms in MMP-2 and MMP-9 promoter regions are associated with endometriosis.
Saare, M., Lamp, M., Kaart, T., Karro, H., Kadastik, U., Metspalu, A., Peters, M. & Salumets, A.
Avaldatud: Fertility and sterility 94, 1560-3


Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
Speliotes, E.K., Willer, C.J., Berndt, S.I., Monda, K.L., Thorleifsson, G., Jackson, A.U., Allen, H.L., Lindgren, C.M., Luan, J., Mägi, R., Randall, J.C., Vedantam, S., Winkler, T.W., Qi, L., Workalemahu, T., Heid, I.M., Steinthorsdottir, V., Stringham, H.M., Weedon, M.N., Wheeler, E., Wood, A.R., Ferreira, T., Weyant, R.J., Segrè, A.V., Estrada, K., Liang, L., Nemesh, J., Park, J.-H., Gustafsson, S., Kilpeläinen, T.O., Yang, J., Bouatia-Naji, N., Esko, T., Feitosa, M.F., Kutalik, Z., Mangino, M., Raychaudhuri, S., Scherag, A., Smith, A.V., Welch, R., Zhao, J.H., Aben, K.K., Absher, D.M., Amin, N., Dixon, A.L., Fisher, E., Glazer, N.L., Goddard, M.E., Heard-Costa, N.L., Hoesel, V., Hottenga, J.-J., Johansson, A., Johnson, T., Ketkar, S., Lamina, C., Li, S., Moffatt, M.F., Myers, R.H., Narisu, N., Perry, J.R.B., Peters, M.J., Preuss, M., Ripatti, S., Rivadeneira, F., Sandholt, C., Scott, L.J., Timpson, N.J., Tyrer, J.P., van Wingerden, S., Watanabe, R.M., White, C.C., Wiklund, F., Barlassina, C., Chasman, D.I., Cooper, M.N., Jansson, J.-O., Lawrence, R.W., Pellikka, N., Prokopenko, I., Shi, J., Thiering, E., Alavere, H., Alibrandi, M.T.S., Almgren, P., Arnold, A.M., Aspelund, T., Atwood, L.D., Balkau, B., Balmforth, A.J., Bennett, A.J., Ben-Shlomo, Y., Bergman, R.N., Bergmann, S., Biebermann, H., Blakemore, A.I.F., Boes, T., Bonnycastle, L.L., Bornstein, S.R., Brown, M.J., Buchanan, T.A., Busonero, F., Campbell, H., Cappuccio, F.P., Cavalcanti-Proença, C., Chen, Y.-D.I., Chen, C.-M., Chines, P.S., Clarke, R., Coin, L., Connell, J., Day, I.N.M., Heijer, M. den, Duan, J., Ebrahim, S., Elliott, P., Elosua, R., Eiriksdottir, G., Erdos, M.R., Eriksson, J.G., Facheris, M.F., Felix, S.B., Fischer-Posovszky, P., Folsom, A.R., Friedrich, N., Freimer, N.B., Fu, M., Gaget, S., Gejman, P.V., Geus, E.J.C., Gieger, C., Gjesing, A.P., Goel, A., Goyette, P., Grallert, H., Grässler, J., Greenawalt, D.M., Groves, C.J., Gudnason, V., Guiducci, C., Hartikainen, A.-L., Hassanali, N., Hall, A.S., Havulinna, A.S., Hayward, C., Heath, A.C., Hengstenberg, C., Hicks, A.A., Hinney, A., Hofman, A., Homuth, G., Hui, J., Igl, W., Iribarren, C., Isomaa, B., Jacobs, K.B., Jarick, I., Jewell, E., John, U., Jørgensen, T., Jousilahti, P., Jula, A., Kaakinen, M., Kajantie, E., Kaplan, L.M., Kathiresan, S., Kettunen, J., Kinnunen, L., Knowles, J.W., Kolcic, I., König, I.R., Koskinen, S., Kovacs, P., Kuusisto, J., Kraft, P., Kvaløy, K., Laitinen, J., Lantieri, O., Lanzani, C., Launer, L.J., Lecoeur, C., Lehtimäki, T., Lettre, G., Liu, J., Lokki, M.-L., Lorentzon, M., Luben, R.N., Ludwig, B., Manunta, P., Marek, D., Marre, M., Martin, N.G., McArdle, W.L., McCarthy, A., McKnight, B., Meitinger, T., Melander, O., Meyre, D., Midthjell, K., Montgomery, G.W., Morken, M.A., Morris, A.P., Mulic, R., Ngwa, J.S., Nelis, M., Neville, M.J., Nyholt, D.R., O’Donnell, C.J., O’Rahilly, S., Ong, K.K., Oostra, B., Paré, G., Parker, A.N., Perola, M., Pichler, I., Pietiläinen, K.H., Platou, C.G.P., Polasek, O., Pouta, A., Rafelt, S., Raitakari, O., Rayner, N.W., Ridderstråle, M., Rief, W., Ruokonen, A., Robertson, N.R., Rzehak, P., Salomaa, V., Sanders, A.R., Sandhu, M.S., Sanna, S., Saramies, J., Savolainen, M.J., Scherag, S., Schipf, S., Schreiber, S., Schunkert, H., Silander, K., Sinisalo, J., Siscovick, D.S., Smit, J.H., Soranzo, N., Sovio, U., Stephens, J., Surakka, I., Swift, A.J., Tammesoo, M.-L., Tardif, J.-C., Teder-Laving, M., Teslovich, T.M., Thompson, J.R., Thomson, B., Tönjes, A., Tuomi, T., van Meurs, J.B.J., van Ommen, G.-J., Vatin, V., Viikari, J., Visvikis-Siest, S., Vitart, V., Vogel, C.I.G., Voight, B.F., Waite, L.L., Wallaschofski, H., Walters, G.B., Widen, E., Wiegand, S., Wild, S.H., Willemsen, G., Witte, D.R., Witteman, J.C., Xu, J., Zhang, Q., Zgaga, L., Ziegler, A., Zitting, P., Beilby, J.P., Farooqi, I.S., Hebebrand, J., Huikuri, H.V., James, A.L., Kähönen, M., Levinson, D.F., Macciardi, F., Nieminen, M.S., Ohlsson, C., Palmer, L.J., Ridker, P.M., Stumvoll, M., Beckmann, J.S., Boeing, H., Boerwinkle, E., Boomsma, D.I., Caulfield, M.J., Chanock, S.J., Collins, F.S., Cupples, L.A., Smith, G.D., Erdmann, J., Froguel, P., Grönberg, H., Gyllensten, U., Hall, P., Hansen, T., Harris, T.B., Hattersley, A.T., Hayes, R.B., Heinrich, J., Hu, F.B., Hveem, K., Illig, T., Jarvelin, M.-R., Kaprio, J., Karpe, F., Khaw, K.-T., Kiemeney, L.A., Krude, H., Laakso, M., Lawlor, D.A., Metspalu, A., Munroe, P.B., Ouwehand, W.H., Pedersen, O., Penninx, B.W., Peters, A., Pramstaller, P.P., Quertermous, T., Reinehr, T., Rissanen, A., Rudan, I., Samani, N.J., Schwarz, P.E.H., Shuldiner, A.R., Spector, T.D., Tuomilehto, J., Uda, M., Uitterlinden, A., Valle, T.T., Wabitsch, M., Waeber, G., Wareham, N.J., Watkins, H., Wilson, J.F., Wright, A.F., Zillikens, M.C., Chatterjee, N., McCarroll, S.A., Purcell, S., Schadt, E.E., Visscher, P.M., Assimes, T.L., Borecki, I.B., Deloukas, P., Fox, C.S., Groop, L.C., Haritunians, T., Hunter, D.J., Kaplan, R.C., Mohlke, K.L., O’Connell, J.R., Peltonen, L., Schlessinger, D., Strachan, D.P., van Duijn, C.M., Wichmann, H.-E., Frayling, T.M., Thorsteinsdottir, U., Abecasis, G.R., Barroso, I., Boehnke, M., Stefansson, K., North, K.E., McCarthy, M.I., Hirschhorn, J.N., Ingelsson, E. & Loos, R.J.F.
Avaldatud: Nature genetics 42, 937-48


Novel human pathological mutations. Gene symbol: SPAST. Disease: Hereditary spastic paraplegia.
Tamm, R.
Avaldatud: Human genetics 127, 112


Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study.
Theodoraki, E.V., Nikopensius, T., Suhorutsenko, J., Peppes, V., Fili, P., Kolovou, G., Papamikos, V., Richter, D., Zakopoulos, N., Krjutskov, K., Metspalu, A. & Dedoussis, G.V.
Avaldatud: BMC medical genetics 11, 28


Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.
Thorgeirsson, T.E., Gudbjartsson, D.F., Surakka, I., Vink, J.M., Amin, N., Geller, F., Sulem, P., Rafnar, T., Esko, T., Walter, S., Gieger, C., Rawal, R., Mangino, M., Prokopenko, I., Mägi, R., Keskitalo, K., Gudjonsdottir, I.H., Gretarsdottir, S., Stefansson, H., Thompson, J.R., Aulchenko, Y.S., Nelis, M., Aben, K.K., den Heijer, M., Dirksen, A., Ashraf, H., Soranzo, N., Valdes, A.M., Steves, C., Uitterlinden, A.G., Hofman, A., Tönjes, A., Kovacs, P., Hottenga, J.J., Willemsen, G., Vogelzangs, N., Döring, A., Dahmen, N., Nitz, B., Pergadia, M.L., Saez, B., De Diego, V., Lezcano, V., Garcia-Prats, M.D., Ripatti, S., Perola, M., Kettunen, J., Hartikainen, A.-L., Pouta, A., Laitinen, J., Isohanni, M., Huei-Yi, S., Allen, M., Krestyaninova, M., Hall, A.S., Jones, G.T., van Rij, A.M., Mueller, T., Dieplinger, B., Haltmayer, M., Jonsson, S., Matthiasson, S.E., Oskarsson, H., Tyrfingsson, T., Kiemeney, L.A., Mayordomo, J.I., Lindholt, J.S., Pedersen, J.H., Franklin, W.A., Wolf, H., Montgomery, G.W., Heath, A.C., Martin, N.G., Madden, P.A.F., Giegling, I., Rujescu, D., Järvelin, M.-R., Salomaa, V., Stumvoll, M., Spector, T.D., Wichmann, H.-E., Metspalu, A., Samani, N.J., Penninx, B.W., Oostra, B.A., Boomsma, D.I., Tiemeier, H., van Duijn, C.M., Kaprio, J., Gulcher, J.R., McCarthy, M.I., Peltonen, L., Thorsteinsdottir, U. & Stefansson, K.
Avaldatud: Nature genetics 42, 448-53


Gene expression profiles of non-small cell lung cancer: survival prediction and new biomarkers.
Välk, K., Vooder, T., Kolde, R., Reintam, M.-A., Petzold, C., Vilo, J. & Metspalu, A.
Avaldatud: Oncology 79, 283-92


Comparison of DNA extraction methods for multiplex polymerase chain reaction.
Viltrop, T., Krjutskov, K., Palta, P. & Metspalu, A.
Avaldatud: Analytical biochemistry 398, 260-2


Gene Expression-Based Approaches in Differentiation of Metastases and Second Primary Tumour.
Vooder, T., Välk, K., Kolde, R., Roosipuu, R., Vilo, J. & Metspalu, A.
Avaldatud: Case reports in oncology 3, 255-261


A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
Walters, R.G., Jacquemont, S., Valsesia, A., de Smith, A.J., Martinet, D., Andersson, J., Falchi, M., Chen, F., Andrieux, J., Lobbens, S., Delobel, B., Stutzmann, F., El-Sayed Moustafa, J.S., Chèvre, J.-C., Lecoeur, C., Vatin, V., Bouquillon, S., Buxton, J.L., Boute, O., Holder-Espinasse, M., Cuisset, J.-M., Lemaitre, M.-P., Ambresin, A.-E., Brioschi, A., Gaillard, M., Giusti, V., Fellmann, F., Ferrarini, A., Hadjikhani, N., Campion, D., Guilmatre, A., Goldenberg, A., Calmels, N., Mandel, J.-L., Le Caignec, C., David, A., Isidor, B., Cordier, M.-P., Dupuis-Girod, S., Labalme, A., Sanlaville, D., Béri-Dexheimer, M., Jonveaux, P., Leheup, B., Ounap, K., Bochukova, E.G., Henning, E., Keogh, J., Ellis, R.J., Macdermot, K.D., van Haelst, M.M., Vincent-Delorme, C., Plessis, G., Touraine, R., Philippe, A., Malan, V., Mathieu-Dramard, M., Chiesa, J., Blaumeiser, B., Kooy, R.F., Caiazzo, R., Pigeyre, M., Balkau, B., Sladek, R., Bergmann, S., Mooser, V., Waterworth, D., Reymond, A., Vollenweider, P., Waeber, G., Kurg, A., Palta, P., Esko, T., Metspalu, A., Nelis, M., Elliott, P., Hartikainen, A.-L., McCarthy, M.I., Peltonen, L., Carlsson, L., Jacobson, P., Sjöström, L., Huang, N., Hurles, M.E., O’Rahilly, S., Farooqi, I.S., Männik, K., Jarvelin, M.-R., Pattou, F., Meyre, D., Walley, A.J., Coin, L.J.M., Blakemore, A.I.F., Froguel, P. & Beckmann, J.S.
Avaldatud: Nature 463, 671-5


Variance determines self-observer agreement on the Big Five personality traits.
Allik, J., Realo, A., Mõttus, R., Esko, T., Pullat, J. & Metspalu, A.
Avaldatud: Journal of Research in Personality 44, 4, 421-426


Hereditaarset spastilist parapleegiat süsteemselt käsitlenud uuring Eestis tõi esile uusi andmeid.
Braschinsky, M., Rannikmäe, K., Tamm, R., Metspalu, A., Gross-Paju, K. & Haldre, S.
Avaldatud: Eesti Arst, 89(3), 165-170


Gene Expression Profiles of Non-Small Cell Lung Cancer: Survival Prediction and New Biomarkers
Kristjan Välk, Tõnu Vooder, Raivo Kolde, Mari-Ann Reintam, Cathleen Petzold, Jaak Vilo, Andres Metspalu
Avaldatud: Oncology 2010;79:283–292


A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Walters RG, Jacquemont S, Valsesia A, de Smith AJ, Martinet D, Andersson J, Falchi M, Chen F, Andrieux J, Lobbens S, Delobel B, Stutzmann F, El-Sayed Moustafa JS, Chèvre JC, Lecoeur C, Vatin V, Bouquillon S, Buxton JL, Boute O, Holder-Espinasse M, Cuisset JM, Lemaitre MP, Ambresin AE, Brioschi A, Gaillard M, Giusti V, Fellmann F, Ferrarini A, Hadjikhani N, Campion D, Guilmatre A, Goldenberg A, Calmels N, Mandel JL, Le Caignec C, David A, Isidor B, Cordier MP, Dupuis-Girod S, Labalme A, Sanlaville D, Béri-Dexheimer M, Jonveaux P, Leheup B, Ounap K, Bochukova EG, Henning E, Keogh J, Ellis RJ, Macdermot KD, van Haelst MM, Vincent-Delorme C, Plessis G, Touraine R, Philippe A, Malan V, Mathieu-Dramard M, Chiesa J, Blaumeiser B, Kooy RF, Caiazzo R, Pigeyre M, Balkau B, Sladek R, Bergmann S, Mooser V, Waterworth D, Reymond A, Vollenweider P, Waeber G, Kurg A, Palta P, Esko T, Metspalu A, Nelis M, Elliott P, Hartikainen AL, McCarthy MI, Peltonen L, Carlsson L, Jacobson P, Sjöström L, Huang N, Hurles ME, O''Rahilly S, Farooqi IS, Männik K, Jarvelin MR, Pattou F, Meyre D, Walley AJ, Coin LJ, Blakemore AI, Froguel P, Beckmann JS.
Avaldatud: Nature. 2010 Feb 4;463(7281):671-5.
DOI: 10.1038/nature08727


Meta-analysis of sex-specific genome-wide association studies
Magi R, Lindgren CM, Morris AP.
Avaldatud: Genet Epidemiol. 2010 Dec;34(8):846-53
DOI: 10.1002/gepi.20540


Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies, Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O''Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND; CARDIoGRAM consortium; CKDGen Consortium; KidneyGen Consortium; EchoGen consortium; CHARGE-HF consortium, Aspelund T, Garcia M, Chang YP, O''Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stančáková A, Raffel LJ, Yao J, Kathiresan S, O''Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT Jr, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T.
Avaldatud: Nature. 2011 Sep 11;478(7367):103-9
DOI: doi: 10.1038/nature10405

2009 (10)

Genetic associations of 115 polymorphisms with cancers of the upper aerodigestive tract across 10 European countries: the ARCAGE project.

Canova, C., Hashibe, M., Simonato, L., Nelis, M., Metspalu, A., Lagiou, P., Trichopoulos, D., Ahrens, W., Pigeot, I., Merletti, F., Richiardi, L., Talamini, R., Barzan, L., Macfarlane, G.J., Macfarlane, T.V., Holcátová, I., Bencko, V., Benhamou, S., Bouchardy, C., Kjaerheim, K., Lowry, R., Agudo, A., Castellsagué, X., Conway, D.I., McKinney, P.A., Znaor, A., McCartan, B.E., Healy, C.M., Marron, M. & Brennan, P.
Avaldatud: Cancer research 69, 2956-65


Analysis of allele and haplotype diversity across 25 genomic regions in three Eastern European populations.
Khrunin, A., Mihailov, E., Nikopensius, T., Krjutskov, K., Limborska, S. & Metspalu, A.
Avaldatud: Human heredity 68, 35-44


Evaluation of the 124-plex SNP typing microarray for forensic testing.
Krjutskov, K., Viltrop, T., Palta, P., Metspalu, E., Tamm, E., Suvi, S., Sak, K., Merilo, A., Sork, H., Teek, R., Nikopensius, T., Kivisild, T. & Metspalu, A.
Avaldatud: Forensic science international. Genetics 4, 43-8


Selection for genetic variation inducing pro-inflammatory responses under adverse environmental conditions in a Ghanaian population.
Kuningas, M., May, L., Tamm, R., van Bodegom, D., van den Biggelaar, A.H.J., Meij, J.J., Frölich, M., Ziem, J.B., Suchiman, H.E.D., Metspalu, A., Slagboom, P.E. & Westendorp, R.G.J.
Avaldatud: PloS one 4, e7795


Alcohol-related cancers and genetic susceptibility in Europe: the ARCAGE project: study samples and data collection.
Lagiou, P., Georgila, C., Minaki, P., Ahrens, W., Pohlabeln, H., Benhamou, S., Bouchardy, C., Slamova, A., Schejbalova, M., Merletti, F., Richiardi, L., Kjaerheim, K., Agudo, A., Castellsague, X., Macfarlane, T.V., Macfarlane, G.J., Talamini, R., Barzan, L., Canova, C., Simonato, L., Lowry, R., Conway, D.I., McKinney, P.A., Znaor, A., McCartan, B.E., Healy, C., Nelis, M., Metspalu, A., Marron, M., Hashibe, M. & Brennan, P.J.
Avaldatud: European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 18, 76-84


A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Landi, M.T., Chatterjee, N., Yu, K., Goldin, L.R., Goldstein, A.M., Rotunno, M., Mirabello, L., Jacobs, K., Wheeler, W., Yeager, M., Bergen, A.W., Li, Q., Consonni, D., Pesatori, A.C., Wacholder, S., Thun, M., Diver, R., Oken, M., Virtamo, J., Albanes, D., Wang, Z., Burdette, L., Doheny, K.F., Pugh, E.W., Laurie, C., Brennan, P., Hung, R., Gaborieau, V., McKay, J.D., Lathrop, M., McLaughlin, J., Wang, Y., Tsao, M.-S., Spitz, M.R., Wang, Y., Krokan, H., Vatten, L., Skorpen, F., Arnesen, E., Benhamou, S., Bouchard, C., Metspalu, A., Metsapalu, A., Vooder, T., Nelis, M., Välk, K., Field, J.K., Chen, C., Goodman, G., Sulem, P., Thorleifsson, G., Rafnar, T., Eisen, T., Sauter, W., Rosenberger, A., Bickeböller, H., Risch, A., Chang-Claude, J., Wichmann, H.E., Stefansson, K., Houlston, R., Amos, C.I., Fraumeni, J.F., Savage, S.A., Bertazzi, P.A., Tucker, M.A., Chanock, S. & Caporaso, N.E.
Avaldatud: American journal of human genetics 85, 679-91


Serotonin transporter promoter region polymorphisms do not influence treatment response to escitalopram in patients with major depression.
Maron, E., Tammiste, A., Kallassalu, K., Eller, T., Vasar, V., Nutt, D.J. & Metspalu, A.
Avaldatud: European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 19, 451-6


Genetic structure of Europeans: a view from the North-East.
Nelis, M., Esko, T., Mägi, R., Zimprich, F., Zimprich, A., Toncheva, D., Karachanak, S., Piskácková, T., Balascák, I., Peltonen, L., Jakkula, E., Rehnström, K., Lathrop, M., Heath, S., Galan, P., Schreiber, S., Meitinger, T., Pfeufer, A., Wichmann, H.-E., Melegh, B., Polgár, N., Toniolo, D., Gasparini, P., D’Adamo, P., Klovins, J., Nikitina-Zake, L., Kucinskas, V., Kasnauskiene, J., Lubinski, J., Debniak, T., Limborska, S., Khrunin, A., Estivill, X., Rabionet, R., Marsal, S., Julià, A., Antonarakis, S.E., Deutsch, S., Borel, C., Attar, H., Gagnebin, M., Macek, M., Krawczak, M., Remm, M. & Metspalu, A.
Avaldatud: PloS one 4, e5472


Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients.
Nikopensius, T., Ambrozaityte, L., Ludwig, K.U., Birnbaum, S., Jagomägi, T., Saag, M., Matuleviciene, A., Linkeviciene, L., Herms, S., Knapp, M., Hoffmann, P., Nöthen, M.M., Kucinskas, V., Metspalu, A. & Mangold, E.
Avaldatud: American journal of medical genetics. Part A 149A, 2551-3


ROS1 Asp2213Asn polymorphism is not associated with coronary artery disease in a Greek case-control study.
Theodoraki, E.V., Nikopensius, T., Suhorutsenko, J., Papamikos, V., Kolovou, G.D., Peppes, V., Panagiotakos, D., Limberi, S., Zakopoulos, N., Metspalu, A. & Dedoussis, G.V.
Avaldatud: Clinical chemistry and laboratory medicine : CCLM / FESCC 47, 1471-3

2008 (6)

Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays.

Krjutskov, K., Andreson, R., Mägi, R., Nikopensius, T., Khrunin, A., Mihailov, E., Tammekivi, V., Sork, H., Remm, M. & Metspalu, A.
Avaldatud: Nucleic acids research 36, e75


Arrayed primer extension on in situ synthesized 5’-->3’ oligonucleotides in microchannels.
Pullat, J., Kusnezow, W., Jaakson, K., Beier, M., Hoheisel, J.D. & Metspalu, A.
Avaldatud: New biotechnology 25, 133-41


Arrayed primer extension reaction for genotyping on oligonucleotide microarray.
Pullat, J. & Metspalu, A.
Avaldatud: Methods in molecular biology (Clifton, N.J.) 444, 161-7


Androgen receptor gene haplotype is associated with male infertility.
Saare, M., Belousova, A., Punab, M., Peters, M., Haller, K., Ausmees, K., Poolamets, O., Karro, H., Metspalu, A. & Salumets, A.
Avaldatud: International journal of andrology 31, 395-402


Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population.
Tamm, R., Oselin, K., Kallassalu, K., Magi, R., Anier, K., Remm, M. & Metspalu, A.
Avaldatud: Clinical chemistry and laboratory medicine : CCLM / FESCC 46, 974-9


Aromatase gene (CYP19A1) allele variants are essential to controlled ovarian hyperstimulation outcome
Altmäe, S., Haller, K., Peters, M., Saare, M., Hovatta, O., Stavreus-Evers, A., Velthut, A., Karro, H., Metspalu, A. & Salumets, A.
Avaldatud: RBMOnline, Volume 17, No 3

2007 (2)

Allelic estrogen receptor 1 (ESR1) gene variants predict the outcome of ovarian stimulation in in vitro fertilization.
Altmäe, S., Haller, K., Peters, M., Hovatta, O., Stavreus-Evers, A., Karro, H., Metspalu, A. & Salumets, A.
Avaldatud: Molecular human reproduction 13, 521-6


Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples.
Pullat, J., Fleischer, R., Becker, N., Beier, M., Metspalu, A. & Hoheisel, J.D.
Avaldatud: BMC genomics 8, 282

2005 (1)

L''Estonie parie sur les biotechnologies.
Eensaar, R. & Metspalu, A.
Avaldatud: Biofutur 257: 51-54

2004 (2)

[The Estonian Genome Project in the context of European genome research]
Metspalu, A., Köhler, F., Laschinski, G., Ganten, D. & Roots, I.
Avaldatud: Deutsche medizinische Wochenschrift (1946) 129 Suppl , S25-8


The Estonian Genome Project.
Metspalu, A.
Avaldatud: Drug Development Research 62, 97-101

2002 (2)

Estonian Genome Project--before the take-off and take-off.
Metspalu, A.
Avaldatud: Bioinformatics (Oxford, England) 18 Suppl 2, S152


Comment to: Pálsson, G. and Hardardóttir "For Whom the Cell Tolls"
Metspalu, A.
Avaldatud: Current Anthropology 43, 2