Publications

Sharing our research with the scientific community is key to our mission. Read our scientific publications, white papers, and conference presentations below.

We provide access to full summary statistics from published 23andMe research.

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  • Richmond RC, Howe LJ, Heilbron K et al. Show more authors. Richmond RC, Howe LJ, Heilbron K, Jones S, Liu J, 23andMe Research Team, Wang X, Weedon MN, Rutter MK, Lawlor DA, Davey-Smith G, Vetter C Show fewer authors. Correlations in sleeping patterns and circadian preference between spouses Communication Biology. 13 November 2023. Behavior
  • Malawsky DS, Walree EV, Jacobs BM et al. Show more authors. Malawsky DS, Walree EV, Jacobs BM, Heng TH, Huang QQ, Sabir AH, Rahman S, Sharif SM, Khan A, Mirkov MU, 23andMe Research Team, Genes & Health Research Team, Kuwahara H, Gao X, Alkuraya FS, Posthuma D, Newman WG, Griffiths CJ, Mathur R, Heel DAV, Martin HC Show fewer authors. Influence of autozygosity on common disease risk across the phenotypic spectrum Cell. 12 October 2023. Methods
  • Budu-Aggrey A, Kilanowski A, Sobczyk MK et al. Show more authors. Budu-Aggrey A, Kilanowski A, Sobczyk MK, 23andMe Research Team, Shringarpure SS, Mitchell R, Reis K, Reigo A, Estonian Biobank Research Team, Magi R, Nelis M, Tanaka N, Brumpton BM, Thomas LF, Sole-Navais P, Flatley C, Espuela-Ortiz A, Herrera-Luis E, Lominchar JVT, Bork-Jensen J, Marenholz I, Arnau-Soler A, Jeong A, Fawcett KA, Paternoster L Show fewer authors. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation Nature Communications. 04 October 2023. Dermatology
  • Zhang H, Zhan J, Jin J et al. Show more authors. Zhang H, Zhan J, Jin J, Zhang J, Lu W, Zhao R, Ahearn TU, Yu Z, O’Connell J, Jiang Y, Chen T, Okuhara D, 23andMe Research Team, Garcia-Closas M, Lin X, Koelsch BL, Chatterjee N Show fewer authors. A new method for multiancestry polygenic prediction improves performance across diverse populations Nature. 25 September 2023. Ancestry
  • Harney E, Sirak K, Sedig K et al. Show more authors. Harney E, Sirak K, Sedig K, Micheletti S, Curry R, Esselmann SA, Reich D Show fewer authors. Ethical considerations when co-analyzing ancient DNA and data from private genetic databases Science. 07 September 2023. ELSI
  • Rizig M, Bandres-Ciga S, Makarious MB et al. Show more authors. Rizig M, Bandres-Ciga S, Makarious MB, Omolara O, Crea PW, Abiodun OV, Levine KS, Abubakar SA, Achoru CO, Vitale D, Adeniji OA, Agabi OP, Koretsky MJ, Agulanna U, Hall DA, Akinyemi RO,Xie T, Ali MW, Shamim EA, Ani-Osheku I, Padmanaban M, Arigbodi OM, Standaert DG, Bello AH, Dean MN, Erameh CO, Elsayed I, Farombi TH, Okunoye O, Fawale MB, Billingsley KJ, Imarhiagbe FA, Jerez PA, Iwuozo EU, Baker B, Komolafe MA, Malik L, Nwani PO, Daida K, Nwazor EO, Miano-Burkhardt A, Nyandaiti YW, Fang Z, Obiabo YO, Kluss JH, Odeniyi OA, Hernandez DG, Odiase FE, Tayebi N, Ojini FI, Sidranksy E, Onwuegbuzie GA, D’Souza A, Osaigbovo GO, Berhe B, Osemwegie N, Reed X, Oshinaike OO, Leonard HL, Otubogun FM, Alvarado CX, Oyakhire SI, Ozomma SI, Samuel SC, Taiwo FT, Wahab KW, Zubair YA, Iwaki H, Kim JJ, Morris HR, Hardy J, Nalls MA, Heilbron K, Norcliffe-Kaufmann L, Nigeria Parkinson Disease Research Network, International Parkinson’s Disease Genomic Consortium Africa, Black and African American Connections to Parkinson's Disease Study Group, 23andMe Research Team, Blauwendraat C, Houlden H, Singleton A, Okubadejo NU, Global Parkinson’s Genetics Program Show fewer authors. Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study The Lancet. 23 August 2023. Neurology
  • Harney E, Micheletti S, Bruwelheide KS et al. Show more authors. Harney E, Micheletti S, Bruwelheide KS, Freyman WA, Bryc K, Akbari A, Jewett E, Comer E, Gates Jr. HL, Heywood L, THornton J, Curry R, Esselmann SA, Barca KG, Sedig J, Sirak K, Olalde I, Adamski N, Bernardos R, Broomandkhoshbacht N, Ferry M, Qiu L, Stewardson K, Workman JN, Zalzala F, Mallick S, Micco A, Mah M, Zhang Z, 23andMe Research Team, Rohland N, Mountain J, Owsley DW, Reich D Show fewer authors. The genetic legacy of African Americans from Catoctin Furnace Science. 04 August 2023. Ancestry
  • Schootemeijer S, Coker D, Shelton JF et al. Show more authors. Schootemeijer S, Coker D, Shelton JF, Chanoff E, Rowbotham HM, Darweesh SKL, 23andMe Research Team, Bloem BR, Cannon P, de Vries NM Show fewer authors. Exercise knowledge, barriers and motivators among LRRK2 G2019S mutation carriers Parkinsonism & Related Disorders. 11 July 2023. Neurology
  • Han X, Gharahkhani P, Hamel AR et al. Show more authors. Han X, Gharahkhani P, Hamel AR, Ong JS,Rentería ME, Mehta P, Dong X, Pasutto F, Hammond C, Young TL, Hysi P, Lotery AJ, Jorgenson E, Choquet H, Hauser M, Bailey JNC, Nakazawa T, Masato Akiyama, Yukihiro Shiga, Fuller ZL, Wang X, Hewitt AW, Craig JE, Pasquale LR, Mackey DA, Wiggs JL, Khawaja AP, Segrè AV, 23andMe Research Team, International Glaucoma Genetics Consortium, MacGregor S Show fewer authors. Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci Nature Genetics. 29 June 2023. Musculoskeletal
  • Pairo-Castineira E, Rawlik K, Bretherick AD et al. Show more authors. Pairo-Castineira E, Rawlik K, Bretherick AD, Qi T, Wu Y, Nassiri I, McConkey GA, Zechner M, Klaric L, Griffiths F, Oosthuyzen W, Kousathanas A, Richmond A, Millar J, Russell CD, Malinauskas T, Thwaites R, Morrice K, Keating S, Maslove D, Nichol A, Semple MG, Knight J, Shankar-Hari M, Summers C, Hinds C, Horby P, Ling L, McAuley D, Montgomery H, Openshaw PJM, Begg C, Walsh T, Tenesa A, Flores C, Riancho JA, Rojas-Martinez A, Lapunzina P, GenOMICC Investigators, SCOURGE Consortium, ISARICC Investigators, The 23andMe COVID-19 Team, Yang J, Ponting CP, Wilson JF, Vitart V, Abedalthagafi M, Luchessi AD, Parra EJ, Cruz R, Carracedo A, Fawkes A, Murphy L, Rowan K, Pereira AC, Law A, Fairfax B, Hendry SC, Baillie JK Show fewer authors. GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19 Nature. 17 May 2023. Rare Diseases
  • Sanchez-Roige S, Jennings MV, Thorpe HHA et al. Show more authors. Sanchez-Roige S, Jennings MV, Thorpe HHA, Mallari JE, van der Werf LC, Bianchi SB, Huang Y, Lee C, Mallard TT, Barnes SA, Wu JY, Barkley-Levenson AM, Boussaty EC, Snethlage CE, Schafer D, Babic Z, Winters BD, Watters KE, Biederer T, 23andMe Research Team, Mackillop J, Stephens DN, Elson SE, Fontanillas P, Jibran Y. Khokhar, Jared W. Young JW, Palmer AA Show fewer authors. CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice Translational Psychiatry. 12 May 2023. Behavior
  • Garca-Marn LM, Reyes-Prez P, Diaz-Torres S et al. Show more authors. Garca-Marn LM, Reyes-Prez P, Diaz-Torres S, Medina-Rivera A, Martin NG, Mitchell BL, Rentera ME Show fewer authors. Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease risk NPJ Parkinson’s disease. 10 May 2023. Neurology
  • Rahmioglu N, Mortlock S, Ghiasi M et al. Show more authors. Rahmioglu N, Mortlock S, Ghiasi M, Møller PL, Stefansdottir L, Galarneau G, Turman C, Danning R, Law MH, Sapkota Y, Christofidou P, Skarp S, Giri A, Banasik K, Krassowski M, Lepamets M, Marciniak B, Nõukas M, Perro D, Sliz E, Sobalska-Kwapis M, Thorleifsson G, Topbas-Selcuki NF, Vitonis A, Westergaard D, Arnadottir R, Burgdorf KS, Campbell A, Cheuk CSK, Clementi C, Cook J, De Vivo I, DiVasta A, Dorien O, Donoghue JF, Edwards T, Fontanillas P, Fung JN, Geirsson RT, Girling JE, Harkki P, Harris HR, Healey M, Heikinheimo O, Holdsworth-Carson S, Hostettler IC, Houlden H, Houshdaran S, Irwin JC, Jarvelin M, Kamatani Y, Kennedy SH, Kepka E, Kettunen J, Kubo M, Kulig B, Kurra V, Laivuori H, Laufer MR, Lindgren CM, MacGregor S, Mangino M, Martin NG, Matalliotaki C, Matalliotakis M, Murray AD, Ndungu A, Nezhat C, Olsen CM, Opoku-Anane J, Padmanabhan S, Paranjpe M, Peters M, Polak G, Porteous DJ, Rabban J, Rexrode KM, Romanowicz H, Saare M, Saavalainen L, Schork AJ, Sen S, Shafrir AL, Siewierska-Grska A, Słomka M, Smith BH, Smolarz B, Szaflik T, Szyłło K, Takahashi A, Terry KL, Tomassetti C, Treloar SA, Vanhie A, Vincent K, Vo KC, Werring DJ, Zeggini E, Zervou MI, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, The Celmatix Research Team, The 23andMe Research Team, Adachi S, Buring JE, Ridker PM, D’Hooghe T, Goulielmos GN, Hapangama DK, Hayward C, Horne AW, Low S, Martikainen H, Chasman DI, Rogers PAW, Saunders PT, Sirota M, Spector T, Strapagiel D, Tung JY, Whiteman DC, Giudice LC, Velez-Edwards DR, Uimari O, Kraft P, Salumets A, Nyholt DR, Mägi R, Stefansson K, Becker CM, Yurttas-Beim P, Steinthorsdottir V, Nyegaard M, Missmer SA, Montgomery GW, Morris AP, Zondervan KT Show fewer authors. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions Nature Genetics. 13 March 2023. Reproduction
  • Islam MR, The International Headache Genetics Consortium (IHGC), Nyholt DR Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin Human Genetics. 20 February 2023. Neurology
  • Speelberg DHB, Hulshoff MJ, Book E et al. Show more authors. Speelberg DHB, Hulshoff MJ, Book E, Dahodwala N, Korell M, Tanner CM, Marras C Show fewer authors. The Impact of the COVID-19 Pandemic on Care Partners of People with Parkinson's Disease Published Movement Disorders. 03 February 2023. Neurology
  • Aaron Pfennig, Joseph Lachance Challenges of accurately estimating sex-biased admixture from X chromosomal and autosomal ancestry proportions American Journal of Human Genetics. 02 February 2023. Ancestry
  • Gustavson DE, Coleman PL, Wang Y et al. Show more authors. Gustavson DE, Coleman PL, Wang Y, Nitin R, Petty LE, Bush CT, Mosing MA, Wesseldijk LW, Ullén F, 23andMe Research Team, Below JE, Cox NJ, Gordon RL Show fewer authors. Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study ANNALS of the New York Academy of Sciences. 30 January 2023. Traits
  • Campos AI, Ingold N, Huang Y et al. Show more authors. Campos AI, Ingold N, Huang Y, Mitchell BL, Kho PK, Han X, García-Marín LM, Ong JS, 23andMe Research Team, Law MH, Yokoyama JS, Martin NG, Dong X, Cuellar-Partida G, MacGregor S, Aslibekyan S, Rentería ME Show fewer authors. Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring SLEEP. 16 December 2022. Traits
  • Seviiri M, Law MH, Ong JS et al. Show more authors. Seviiri M, Law MH, Ong JS, Gharahkhani P, Fontanills P, 23andMe Research Team, Olsen CM, Whiteman DC, MacGregor S Show fewer authors. A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma Nature. 10 December 2022. Cancer
  • Saunders GRB, Wang X, Chen F et al. Show more authors. Saunders GRB, Wang X, Chen F, Jang S, Liu M, Wang C, Gao S, Jiang Y, Khunsriraksakul C, Otto JM, Addison C, Akiyama M, Albert CM, Aliev F, Alonso A, Arnett DK, Ashley-Koch AE, Ashrani AA, Barnes KC, Barr RG, Bartz TM, Becker DM, Bielak LF, Benjamin EJ, Bis JC, Bjornsdottir G, Blangero J, Bleecker ER, Boardman JD, Boerwinkle E, Boomsma DI, Boorgula MP, Bowden DW, Brody JA, Cade BE, Chasman DI, Chavan S, Chen YI, Chen Z, Cheng I, Cho MH, Choquet H, Cole JW, Cornelis MC, Cucca F, Curran JE, de Andrade M, Dick DM, Docherty AR, Duggirala R, Eaton CB, Ehringer MA, Esko T, Faul JD, Silva LF, Fiorillo E, Fornage M, Freedman BI, Gabrielsen ME, Garrett ME, Gharib SA, Gieger C, Gillespie N, Glahn DC, Gordon SD, Gu CC, Gu D, Gudbjartsson DF, Guo X, Haessler J, Hall ME, Haller T, Harris KM, He J, Herd P, Hewitt JK, Hickie I, Hidalgo B, Hokanson JE, Hopfer C, Hottenga J, Hou L, Huang H, Hung Y, Hunter DJ, Hveem K, Hwang S, Hwu C, Iacono W, Irvin MR, Jee YH, Johnson EO, Joo YY, Jorgenson E, Justice AE, Kamatani Y, Kaplan RC, Kaprio J, Sharon L. R. Kardia, Keller MC, Kelly TN, Kooperberg C, Korhonen T, Kraft P, Krauter K, Kuusisto J, Laakso M, Lasky-Su J, Lee W, Lee JJ, Levy D, Li L, Li K, Li Y, Lin K, Lind PA, Liu C, Lloyd-Jones DM, Lutz SM, Ma J, Mägi R, Manichaikul A, Martin NG, Mathur R, Matoba N, McArdle PF, McGue M, McQueen MB, Medl SE, Metspalu e, Meyers DA, Millwood IY, Mitchell BD, Mohlke KL, Moll M, Montasser ME, Morrison AC, Mulas A, Nielsen JB, North KE, Oelsner EC, Okada Y, Orr V, Palmer ND, Palviainen T, Pit A, Park SL, Peters U, Peters A, Peyser PA, Tinca J. C. Polderman, Rafaels N, Redline S, Reed RM, Reiner AP, Rice JP, Rich SS, Richmond NE, Roan C, Rotter JI, Rueschman MN, Runarsdottir V, Saccone NL, Schwartz DA, Shadyab AH, Shi J, Shringarpure SS, Sicinski K, Skogholt AH, Smith JA, Smith NL, Sotoodehnia N, Stallings MC, Stefansson H, Stefansson K, Stitzel JA, Sun X, Syed M, Tal-Singer R, Taylor AE, Taylor KD, Telen MJ, Thai KK, Tiwari H, Turman C, Tyrfingsson T, Wall TL, Walters RG, Weir DR, Weiss ST, White WB, Whitfield JB, Wiggins KL, Willemsen G, Willer CJ, Winsvold BS, Xu H, Yanek LR, Yin J, Young KL, Young KA, Yu B, Zhao W, Zhou W, Zölner S, Zuccolo L, 23andMe Research Team, The Biobank Japan Project, Batini C, Bergen eW, Bierut LJ, David SP, Sarah A. Gagliano Taliun, Hancock DB, Jiang B, Munaf MR, Thorgeirsson TE, Liu DJ, Vrieze S Show fewer authors. Data related to Genetic diversity fuels gene discovery for tobacco and alcohol use Nature. 07 December 2022. Behavior
  • Krohn L, Heilbron K, Blauwendraat C et al. Show more authors. Krohn L, Heilbron K, Blauwendraat C, Reynolds RH, Yu E, Senkevich K, Rudakou U, Estiar MA, Gustavsson EK, Brolin K, Ruskey JA, Freeman K, Asayesh F, Chia R, Arnulf I, Michele T. M. Hu, Montplaisir JY, Gagnon J, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Högl B, Stefani A, Ibrahim A, Sonka K, Kemlink D, Oertel W, Janzen A, Plazzi G, Biscarini F, Antelmi E, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döing F, Valrie Cochen De Cock, Monaca CC, Heidbreder A, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, 23andMe Research Team, Scholz SW, Ryten M, Bres-Ciga S, Noyce A, Cannon P, Pihlstrom L, Nalls MA, Singleton AB, Rouleau GA, Postuma RB, Gan-Or Z Show fewer authors. Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects Nature Communications. 05 December 2022. Neurology
  • Meng W, Reel PS, Nangia C et al. Show more authors. Meng W, Reel PS, Nangia C, Rajendrakumar AL, Hebert HL, Guo Q, Adams MJ, Zheng H, Lu ZH, 23andMe Research Team, Ray D, Colvin LA, Palmer CNA,McIntosh AM, Smith BH Show fewer authors. A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches Phenomics. 18 November 2022. Neurology
  • Doust C, Fontanillas P, Eising E et al. Show more authors. Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, 23andMe Research Team, Quantitative Trait Working Group of the GenLang Consortium, St Pourcain B, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, Gruen JR, Olson RK, Willcutt EG, DeFries JC, Pennington BF, Smith SD, Wright MJ, Martin NG, Auton A, Bates TC, Fisher SE, Luciano M Show fewer authors. “Discovery of 42 genome-wide significant loci associated with dyslexia ” Nature Genetics. 20 October 2022. Traits
  • Yengo L, Vedantam S, Marouli E et al. Show more authors. Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, Eliasen rU, Jiang Y, Raghavan S, Miao J, Arias JD, Graham SE, Mukamel RE, Spracklen CN, Yin X, Chen S, Ferreira T, Highl HH, Ji Y, Karaderi T, Lin K, Lül K, Malden DE, Medina-Gomez C, Machado M, Moore A, Rüger S, Sim X, Vrieze S, Ahluwalia TS, Akiyama M, Allison MA, Alvarez M, Andersen MK, Ani A, Appadurai V, Arbeeva L, Bhaskar S, Bielak LF, Bollepalli S, Bonnycastle LL, Bork-Jensen J, Bradfield JP, Bradford Y, Braund PS, Brody JA, Burgdorf KS, Cade BE, Cai H, Cai Q, Campbell A, Caadas-Garre M, Catamo E, Chai J, Chai X, Chang L, Chang Y, Chen C, Chesi A, Choi SH, Chung R, Cocca M, Concas MP, Couture C, Cuellar-Partida G, Danning R, Daw EW, Degenhard F, Delgado GE, Delitala A, Demirkan A, Deng X, Devineni P, Dietl A, Dimitriou M, Dimitrov L, Dorajoo R, Ekici AB, Engmann JE, Fairhurst-Hunter Z, Farmaki A, Faul JD, Fernez-Lopez J, Forer L, Francescatto M, Freitag-Wolf S, Fuchsberger C, Galesloot TE, Gao Y, Gao Z, Geller F, Giannakopoulou O, Giulianini F, Gjesing AP, Goel A, Gordon SD, Gorski M, Grove J, Guo X, Gustafsson S, Haessler J, Hansen TF, Havulinna AS, Haworth SJ, He J, Heard-Costa N, Hebbar P, Hindy G, Ho YA, Hofer E, Holliday E, Horn K, Hornsby WE, Hottenga J, Huang H, Huang J, Huerta-Chagoya A, Huffman JE, Hung Y, Huo S, Hwang MY, Iha H, Ikeda DD, Isono M, Jackson AU, Jäer S, Jansen IE, Johansson I, Jonas JB, Jonsson A, Jrgensen T, Kalafati I, Kanai M, Kanoni S, Krhus LL, Kasturiratne A, Katsuya T, Kawaguchi T, Kember RL, Kentistou KA, Kim H, Kim YJ, Kleber ME, Knol MJ, Kurbasic A, Lauzon M, Le P, Lea R, Lee J, Leonard HL, Li SA, Li X, Li X, Liang J, Lin H, Lin S, Liu J, Liu X, Lo KS, Long J, Lores-Motta L, Luan J, Lyssenko V, Lyytikänen L, Mahajan A, Mamakou V, Mangino M, Manichaikul A, Marten J, Mattheisen M, Mavarani L, McDaid AF, Meidtner K, Melendez TL, Mercader JM, Milaneschi Y, Miller JE, Millwood IY, Mishra PP, Mitchell RE, Mllehave LT, Morgan A, Mucha S, Munz M, Nakatochi M, Nelson CP, Nether M, Nho CW, Nielsen AA, Nolte IM, Nongmaithem SS, Noordam R, Ntalla I, Nutile T, Pit A, Christofidou P, Päna K, Pauper M, Eva R. B. Petersen, Petersen LV, Pitkäen N, Polaek O, Poveda A, Preuss MH, Pyarajan S, Raffield LM, Rakugi H, Ramirez J, Rasheed A, Raven D, Rayner NW, Riveros C, Rohde R, Ruggiero D, Ruotsalainen SE, Ryan KA, Sabater-Lleal M, Saxena R, Scholz M, Sendamarai A, Shen B, Shi J, Shin JH, Sidore C, Sitlani CM, Slieker RC, Roelof A. J. Smit, Smith AV, Smith JA, Smyth LJ, Southam L, Steinthorsdottir V, Sun L, Takeuchi F, Divya Sri Priyanka Tallapragada, Taylor KD, Tayo BO, Tchejieu C, Terzikhan N, Tesolin P, Teumer A, Theusch E, Thompson DJ, Thorleifsson G, Timmers PRHJ, Trompet S, Turman C, Vaccargiu S, van der Laan SW, van der Most PJ, van Klinken JB, van Setten J, Verma SS, Verweij N, Veturi Y, Wang CA, Wang C, Wang L, Wang Z, Warren HR, Wei WB, Wickremasinghe AR, Wielscher M, Wiggins KL, Winsvold BS, Wong e, Wu Y, Wuttke M, Xia R, Xie T, Yamamoto K, Yang J, Yao J, Young H, Yousri NA, Yu L, Zeng L, Zhang W, Zhang X, Zhao J, Zhao W, Zhou W, Zimmermann ME, Zoledziewska M, Adair LS, Hieab H. H. Adams, Aguilar-Salinas CA, Al-Mulla F, Arnett DK, Asselbergs FW, vold BO, Attia J, Banas B, Binelli S, Bennett DA, Bergler T, Bharadwaj D, Biino G, Bisgaard H, Boerwinkle E, Böer CA, Bnnelykke K, Boomsma DI, Brglum rD, Borja JB, Bouchard C, Bowden DW, Brslund I, Brumpton B, Buring JE, Caulfield MJ, Chambers JC, Chak GR, Chanock SJ, Chaturvedi N, Chen YI, Chen Z, Cheng C, Christophersen IE, Ciullo M, Cole JW, Collins FS, Cooper RS, Cruz M, Cucca F, Cupples LA, Cutler MJ, Damrauer SM, Dantoft TM, de Borst GJ, de Groot LPGM, De Jager PL, de Kleijn DPV, H. de Silva J, Dedoussis GV, den Hollander AI, Du S, Easton DF, Petra J. M. Elders, Eliassen AH, Ellinor PT, Elmsthl S, Erdmann J, Evans MK, Fatkin D, Feenstra B, Feitosa MF, Ferrucci L, Ford I, Fornage M, Franke e, Franks PW, Freedman BI, Gasparini P, Gieger C, Girotto G, Goddard ME, Golightly YM, Gonzalez-Villalpo C, Gordon-Larsen P, Grallert H, Struan F. A. Grant, Grarup N, Griffiths L, Gudnason V, Haiman C, Hakonarson H, Hansen T, Hartman CA, Hattersley AT, Hayward C, Heckbert SR, Heng C, Hengstenberg C, Hewitt AW, Hishigaki H, Hoyng CB, Huang PL, Huang W, Hunt SC, Hveem K, Hyppöen E, Iacono WG, Ichihara S, Ikram MA, Isasi CR, Jackson RD, Jarvelin M, Jin Z, Jökel K, Joshi PK, Jousilahti P, Jukema JW, Kähonöen M, Kamatani Y, Kang KD, Kaprio J, Sharon L. R. Kardia, Karpe F, Kato N, Kee F, Kessler T, Khera AV, Khor CC, Lambertus A. L. M. Kiemeney, Kim B, Kim EK, Kim H, Kirchhof P, Kivimaki M, Koh W, Koistinen HA, Kolovou GD, Kooner JS, Kooperberg C, Kötgen A, Kovacs P, Kraaijeveld A, Kraft P, Krauss RM, Kumari M, Kutalik Z, Laakso M, Lange LA, Langenberg C, Launer LJ, March LL, Lee H, Lee NR, Lehtimäi T, Li H, Li L, Lieb W, Lin X, Lind L, Linneberg A, Liu C, Liu J, Loeffler M, London B, Lubitz SA, Lye SJ, Mackey DA, Mäi R, Patrik K. E. Magnusson, Marcus GM, Vidal PM, Martin NG, Mäz W, Matsuda F, McGarrah RW, McGue M, McKnight AJ, Medl SE, Mellströ D, Metspalu e, Mitchell BD, Mitchell P, Mook-Kanamori DO, Morris eD, Mucci LA, Munroe PB, Nalls MA, Nazarian S, Nelson AE, Neville MJ, Newton-Cheh C, Nielsen CS, Nöhen MM, Ohlsson C, Oldehinkel AJ, Orozco L, Pahkala K, Pajukanta P, Colin N. A. Palmer, Parra EJ, Pattaro C, Pedersen O, Pennell CE, Brenda W. J. H. Penninx, Perusse L, Peters A, Peyser PA, Porteous DJ, Posthuma D, Power C, Pramstaller PP, Province MA, Qi Q, Qu J, Rader DJ, Raitakari OT, Ralhan S, Rallidis LS, Rao DC, Redline S, Reilly DF, Reiner AP, Rhee SY, Ridker PM, Rienstra M, Ripatti S, Ritchie MD, Roden DM, Rosendaal FR, Rotter JI, Rudan I, Rutters F, Sabanayagam C, Saleheen D, Salomaa V, Samani NJ, Sanghera DK, Sattar N, Schmidt B, Schmidt H, Schmidt R, Schulze MB, Schunkert H, Scott LJ, Scott RJ, Sever P, Shiroma EJ, Shoemaker MB, Shu X, Simonsick EM, Sims M, Singh JR, Singleton eB, Sinner MF, Smith JG, Snieder H, Spector TD, Stampfer MJ, Stark KJ, Strachan DP, Leen M. Hart, Tabara Y, Tang H, Tardif J, Thanaraj TA, Timpson NJ, Töjes A, Tremblay A, Tuomi T, Tuomilehto J, Tusi-Luna M, Uitterlinden eG, Rob M. an Dam, Pim an er Harst, Nathalie Van er Velde, Cornelia M. an Duijn, Natasja M. an Schoor, Vitart V, Vöker U, Vollenweider P, Vözke H, Wacher-Rodarte NH, Walker M, Wang YX, Wareham NJ, Watanabe RM, Watkins H, Weir DR, Werge TM, Widen E, Wilkens LR, Willemsen G, Willett WC, Wilson JF, Wong T, Woo J, Wright AF, Wu J, Xu H, Yajnik CS, Yokota M, Yuan J, Zeggini E, Zemel BS, Zheng W, Zhu X, Zmuda JM, Zonderman AB, Zwart J, 23andMe Research Team, VA Million Veteran Program, DiscovEHR (DiscovEHR MyCode Community Health Initiative), eMERGE (Electronic Medical Records Genomics Network, Lifelines Cohort Study, The PRACTICAL Consortium, Understanding Society Scientific Group, Chasman DI, Cho YS, Heid IM, McCarthy MI, Maggie C. Y. Ng, ODonnell CJ, Rivadeneira F, Thorsteinsdottir U, Sun YV, Tai ES, Boehnke M, Deloukas P, Justice AE, Lindgren CM, Ruth J. F. 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