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184건, 그중 20건 표시.
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Giri A,
Hellwege JN,
Keaton JM,
Park J,
Qiu C,
Warren HR,
Torstenson ES,
Kovesdy CP,
Sun YV,
Wilson OD,
Robinson-Cohen C,
Roumie CL
외 86명 — 모두 보기
Chung CP,
Birdwell KA,
Damrauer SM,
DuVall SL,
Klarin D,
Cho K,
Wang Y,
Evangelou E,
Cabrera CP,
Wain LV,
Shrestha R,
Mautz BS,
Akwo EA,
Sargurupremraj M,
Debette S,
Boehnke M,
Scott LJ,
Luan J,
Zhao JH,
Willems SM,
Thériault S,
Shah N,
Oldmeadow C,
Almgren P,
Li-Gao R,
Verweij N,
Boutin TS,
Mangino M,
Ntalla I,
Feofanova E,
Surendran P,
Cook JP,
Karthikeyan S,
Lahrouchi N,
Liu C,
Sepúlveda N,
Richardson TG,
Kraja A,
Amouyel P,
Farrall M,
Poulter NR,
Laakso M,
Zeggini E,
Sever P,
Scott RA,
Langenberg C,
Wareham NJ,
Conen D,
Palmer CNA,
Attia J,
Chasman DI,
Ridker PM,
Melander O,
Mook-Kanamori DO,
Harst PV,
Cucca F,
Schlessinger D,
Hayward C,
Spector TD,
Jarvelin MR,
Hennig BJ,
Timpson NJ,
Wei WQ,
Smith JC,
Xu Y,
Matheny ME,
Siew EE,
Lindgren C,
Herzig KH,
Dedoussis G,
Denny JC,
Psaty BM,
Howson JMM,
Munroe PB,
Newton-Cheh C,
Caulfield MJ,
Elliott P,
Gaziano JM,
Concato J,
Wilson PWF,
Tsao PS,
Velez Edwards DR,
Susztak K,
O'Donnell CJ,
Hung AM,
Edwards TL
Understanding Society Scientific Group · International Consortium for Blood Pressure 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30578418 · open access
페이지 12개+
An atlas of genetic influences on osteoporosis in humans and mice
Morris JA,
Kemp JP,
Youlten SE,
Laurent L,
Logan JG,
Chai RC,
Vulpescu NA,
Forgetta V,
Kleinman A,
Mohanty ST,
Sergio CM,
Quinn J
외 47명 — 모두 보기
Nguyen-Yamamoto L,
Luco AL,
Vijay J,
Simon MM,
Pramatarova A,
Medina-Gomez C,
Trajanoska K,
Ghirardello EJ,
Butterfield NC,
Curry KF,
Leitch VD,
Sparkes PC,
Adoum AT,
Mannan NS,
Komla-Ebri DSK,
Pollard AS,
Dewhurst HF,
Hassall TAD,
Beltejar MG,
Adams DJ,
Vaillancourt SM,
Kaptoge S,
Baldock P,
Cooper C,
Reeve J,
Ntzani EE,
Evangelou E,
Ohlsson C,
Karasik D,
Rivadeneira F,
Kiel DP,
Tobias JH,
Gregson CL,
Harvey NC,
Grundberg E,
Goltzman D,
Adams DJ,
Lelliott CJ,
Hinds DA,
Ackert-Bicknell CL,
Hsu YH,
Maurano MT,
Croucher PI,
Williams GR,
Bassett JHD,
Evans DM,
Richards JB
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
페이지 12개+
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Justice AE,
Karaderi T,
Highland HM,
Young KL,
Graff M,
Lu Y,
Turcot V,
Auer PL,
Fine RS,
Guo X,
Schurmann C,
Lempradl A
외 268명 — 모두 보기
Marouli E,
Mahajan A,
Winkler TW,
Winkler TW,
Locke AE,
Medina-Gomez C,
Esko T,
Vedantam S,
Giri A,
Lo KS,
Alfred T,
Mudgal P,
Ng MCY,
Heard-Costa NL,
Feitosa MF,
Manning AK,
Willems SM,
Sivapalaratnam S,
Abecasis G,
Alam DS,
Allison M,
Amouyel P,
Arzumanyan Z,
Balkau B,
Bastarache L,
Bergmann S,
Bielak LF,
Blüher M,
Boehnke M,
Boeing H,
Boerwinkle E,
Böger CA,
Bork-Jensen J,
Bottinger EP,
Bowden DW,
Brandslund I,
Broer L,
Burt AA,
Butterworth AS,
Caulfield MJ,
Cesana G,
Chambers JC,
Chasman DI,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Collins FS,
Cook JP,
Cox AJ,
Crosslin DS,
Danesh J,
de Bakker PIW,
Denus S,
Mutsert R,
Dedoussis G,
Demerath EW,
Dennis JG,
Denny JC,
Di Angelantonio E,
Dörr M,
Drenos F,
Dubé MP,
Dunning AM,
Easton DF,
Elliott P,
Evangelou E,
Farmaki AE,
Feng S,
Ferrannini E,
Ferrieres J,
Florez JC,
Fornage M,
Fox CS,
Franks PW,
Friedrich N,
Gan W,
Gandin I,
Gasparini P,
Giedraitis V,
Girotto G,
Gorski M,
Grallert H,
Grarup N,
Grove ML,
Gustafsson S,
Haessler J,
Hansen T,
Hattersley AT,
Hayward C,
Heid IM,
Holmen OL,
Hovingh GK,
Howson JMM,
Hu Y,
Hung YJ,
Hveem K,
Ikram MA,
Ingelsson E,
Jackson AU,
Jarvik GP,
Jia Y,
Jørgensen T,
Jousilahti P,
Justesen JM,
Kahali B,
Karaleftheri M,
Kardia SLR,
Karpe F,
Kee F,
Kitajima H,
Komulainen P,
Kooner JS,
Kovacs P,
Krämer BK,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka TA,
Lamparter D,
Lange LA,
Langenberg C,
Larson EB,
Lee NR,
Lee WJ,
Lehtimäki T,
Lewis CE,
Li H,
Li J,
Li-Gao R,
Lin LA,
Lin X,
Lind L,
Lindström J,
Linneberg A,
Liu CT,
Liu DJ,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mägi R,
Männistö S,
Marenne G,
Marten J,
Masca NGD,
McCarthy MI,
Meidtner K,
Mihailov E,
Moilanen L,
Moitry M,
Mook-Kanamori DO,
Morgan A,
Morris AP,
Müller-Nurasyid M,
Munroe PB,
Narisu N,
Nelson CP,
Neville M,
Ntalla I,
O'Connell JR,
Owen KR,
Pedersen O,
Peloso GM,
Pennell CE,
Perola M,
Perry JA,
Perry JRB,
Pers TH,
Ewing A,
Polasek O,
Raitakari OT,
Rasheed A,
Raulerson CK,
Rauramaa R,
Reilly DF,
Reiner AP,
Ridker PM,
Rivas MA,
Robertson NR,
Robino A,
Rudan I,
Ruth KS,
Saleheen D,
Salomaa V,
Samani NJ,
Schreiner PJ,
Schulze MB,
Scott RA,
Segura-Lepe M,
Sim X,
Slater AJ,
Small KS,
Smith BH,
Smith JA,
Southam L,
Spector TD,
Speliotes EK,
Stefansson K,
Steinthorsdottir V,
Stirrups KE,
Strauch K,
Stringham HM,
Stumvoll M,
Sun L,
Surendran P,
Swart KMA,
Tardif JC,
Taylor KD,
Teumer A,
Thompson DJ,
Thorleifsson G,
Thorsteinsdottir U,
Thuesen BH,
Tönjes A,
Torres M,
Tsafantakis E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van Duijn CM,
Vanhala M,
Varma R,
Vermeulen SH,
Vestergaard H,
Vitart V,
Vogt TF,
Vuckovic D,
Wagenknecht LE,
Walker M,
Wallentin L,
Wang F,
Wang CA,
Wang S,
Wareham NJ,
Warren HR,
Waterworth DM,
Wessel J,
White HD,
Willer CJ,
Wilson JG,
Wood AR,
Wu Y,
Yaghootkar H,
Yao J,
Yerges-Armstrong LM,
Young R,
Zeggini E,
Zhan X,
Zhang W,
Zhao JH,
Zhao W,
Zheng H,
Zhou W,
Zillikens MC,
Rivadeneira F,
Borecki IB,
Pospisilik JA,
Deloukas P,
Frayling TM,
Lettre G,
Mohlke KL,
Rotter JI,
Kutalik Z,
Hirschhorn JN,
Cupples LA,
Loos RJF,
North KE,
Lindgren CM
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium 외 컨소시엄 8곳
Nature genetics · 2019 · PMID 30778226 · open access
페이지 12개+
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Warrington NM,
Beaumont RN,
Horikoshi M,
Day FR,
Helgeland Ø,
Laurin C,
Bacelis J,
Peng S,
Hao K,
Feenstra B,
Wood AR,
Mahajan A
외 196명 — 모두 보기
Tyrrell J,
Robertson NR,
Rayner NW,
Qiao Z,
Moen GH,
Vaudel M,
Marsit CJ,
Chen J,
Nodzenski M,
Schnurr TM,
Zafarmand MH,
Bradfield JP,
Grarup N,
Kooijman MN,
Li-Gao R,
Geller F,
Ahluwalia TS,
Paternoster L,
Rueedi R,
Huikari V,
Hottenga JJ,
Lyytikäinen LP,
Cavadino A,
Metrustry S,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Vilor-Tejedor N,
Joshi PK,
Painter JN,
Ntalla I,
Myhre R,
Pitkänen N,
van Leeuwen EM,
Joro R,
Lagou V,
Richmond RC,
Espinosa A,
Barton SJ,
Inskip HM,
Holloway JW,
Santa-Marina L,
Estivill X,
Ang W,
Marsh JA,
Reichetzeder C,
Marullo L,
Hocher B,
Lunetta KL,
Murabito JM,
Relton CL,
Kogevinas M,
Chatzi L,
Allard C,
Bouchard L,
Hivert MF,
Zhang G,
Muglia LJ,
Heikkinen J,
Morgen CS,
van Kampen AHC,
van Schaik BDC,
Mentch FD,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Hemani G,
Ring SM,
Bennett AJ,
Gaulton KJ,
Fernandez-Tajes J,
van Zuydam NR,
Medina-Gomez C,
de Haan HG,
Rosendaal FR,
Kutalik Z,
Marques-Vidal P,
Das S,
Willemsen G,
Mbarek H,
Müller-Nurasyid M,
Standl M,
Appel EVR,
Fonvig CE,
Trier C,
van Beijsterveldt CEM,
Murcia M,
Bustamante M,
Bonas-Guarch S,
Hougaard DM,
Mercader JM,
Linneberg A,
Schraut KE,
Lind PA,
Medland SE,
Shields BM,
Knight BA,
Chai JF,
Panoutsopoulou K,
Bartels M,
Sánchez F,
Stokholm J,
Torrents D,
Vinding RK,
Willems SM,
Atalay M,
Chawes BL,
Kovacs P,
Prokopenko I,
Tuke MA,
Yaghootkar H,
Ruth KS,
Jones SE,
Loh PR,
Murray A,
Weedon MN,
Tönjes A,
Stumvoll M,
Michaelsen KF,
Eloranta AM,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Niinikoski H,
Pahkala K,
Raitakari OT,
Jacobsson B,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Montgomery GW,
Campbell H,
Wilson JF,
Vrijkotte TGM,
Vrijheid M,
de Geus EJCN,
Hayes MG,
Kadarmideen HN,
Holm JC,
Beilin LJ,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Hattersley AT,
Spector TD,
Kähönen M,
Viikari JS,
Lehtimäki T,
Boomsma DI,
Sebert S,
Vollenweider P,
Sørensen TIA,
Bisgaard H,
Bønnelykke K,
Murray JC,
Melbye M,
Nohr EA,
Mook-Kanamori DO,
Rivadeneira F,
Hofman A,
Felix JF,
Jaddoe VWV,
Hansen T,
Pisinger C,
Vaag AA,
Pedersen O,
Uitterlinden AG,
Järvelin MR,
Power C,
Hyppönen E,
Scholtens DM,
Lowe WL Jr,
Davey Smith G,
Timpson NJ,
Morris AP,
Wareham NJ,
Hakonarson H,
Grant SFA,
Frayling TM,
Lawlor DA,
Njølstad PR,
Johansson S,
Ong KK,
McCarthy MI,
Perry JRB,
Evans DM,
Freathy RM
EGG Consortium
Nature genetics · 2019 · PMID 31043758
페이지 12개+
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program
Hellwege JN,
Velez Edwards DR,
Giri A,
Qiu C,
Park J,
Torstenson ES,
Keaton JM,
Wilson OD,
Robinson-Cohen C,
Chung CP,
Roumie CL,
Klarin D
외 18명 — 모두 보기
Damrauer SM,
DuVall SL,
Siew E,
Akwo EA,
Wuttke M,
Gorski M,
Li M,
Li Y,
Gaziano JM,
Wilson PWF,
Tsao PS,
O'Donnell CJ,
Kovesdy CP,
Pattaro C,
Köttgen A,
Susztak K,
Edwards TL,
Hung AM
Nature communications · 2019 · PMID 31451708 · open access
페이지 12개+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
외 213명 — 모두 보기
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
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Stefansson K,
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Scholz M,
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Köttgen A
German Chronic Kidney Disease Study · Lifelines Cohort Study 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31578528 · open access
페이지 12개+
The genetic architecture of the human cerebral cortex
Grasby KL,
Jahanshad N,
Painter JN,
Colodro-Conde L,
Bralten J,
Hibar DP,
Lind PA,
Pizzagalli F,
Ching CRK,
McMahon MAB,
Shatokhina N,
Zsembik LCP
외 348명 — 모두 보기
Thomopoulos SI,
Zhu AH,
Strike LT,
Agartz I,
Alhusaini S,
Almeida MAA,
Alnæs D,
Amlien IK,
Andersson M,
Ard T,
Armstrong NJ,
Ashley-Koch A,
Atkins JR,
Bernard M,
Brouwer RM,
Buimer EEL,
Bülow R,
Bürger C,
Cannon DM,
Chakravarty M,
Chen Q,
Cheung JW,
Couvy-Duchesne B,
Dale AM,
Dalvie S,
de Araujo TK,
de Zubicaray GI,
de Zwarte SMC,
den Braber A,
Doan NT,
Dohm K,
Ehrlich S,
Engelbrecht HR,
Erk S,
Fan CC,
Fedko IO,
Foley SF,
Ford JM,
Fukunaga M,
Garrett ME,
Ge T,
Giddaluru S,
Goldman AL,
Green MJ,
Groenewold NA,
Grotegerd D,
Gurholt TP,
Gutman BA,
Hansell NK,
Harris MA,
Harrison MB,
Haswell CC,
Hauser M,
Herms S,
Heslenfeld DJ,
Ho NF,
Hoehn D,
Hoffmann P,
Holleran L,
Hoogman M,
Hottenga JJ,
Ikeda M,
Janowitz D,
Jansen IE,
Jia T,
Jockwitz C,
Kanai R,
Karama S,
Kasperaviciute D,
Kaufmann T,
Kelly S,
Kikuchi M,
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Knodt AR,
Krämer B,
Lam M,
Lancaster TM,
Lee PH,
Lett TA,
Lewis LB,
Lopes-Cendes I,
Luciano M,
Macciardi F,
Marquand AF,
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Melzer TR,
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Mirza-Schreiber N,
Moreira JCV,
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Müller-Myhsok B,
Najt P,
Nakahara S,
Nho K,
Olde Loohuis LM,
Orfanos DP,
Pearson JF,
Pitcher TL,
Pütz B,
Quidé Y,
Ragothaman A,
Rashid FM,
Reay WR,
Redlich R,
Reinbold CS,
Repple J,
Richard G,
Riedel BC,
Risacher SL,
Rocha CS,
Mota NR,
Salminen L,
Saremi A,
Saykin AJ,
Schlag F,
Schmaal L,
Schofield PR,
Secolin R,
Shapland CY,
Shen L,
Shin J,
Shumskaya E,
Sønderby IE,
Sprooten E,
Tansey KE,
Teumer A,
Thalamuthu A,
Tordesillas-Gutiérrez D,
Turner JA,
Uhlmann A,
Vallerga CL,
van der Meer D,
van Donkelaar MMJ,
van Eijk L,
van Erp TGM,
van Haren NEM,
van Rooij D,
van Tol MJ,
Veldink JH,
Verhoef E,
Walton E,
Wang M,
Wang Y,
Wardlaw JM,
Wen W,
Westlye LT,
Whelan CD,
Witt SH,
Wittfeld K,
Wolf C,
Wolfers T,
Wu JQ,
Yasuda CL,
Zaremba D,
Zhang Z,
Zwiers MP,
Artiges E,
Assareh AA,
Ayesa-Arriola R,
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Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium 외 컨소시엄 5곳
Science (New York, N.Y.) · 2020 · PMID 32193296
페이지 12개+
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
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외 46명 — 모두 보기
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Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · open access
페이지 12개+
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
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외 35명 — 모두 보기
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HPAP Consortium · Regeneron Genetics Center 외 컨소시엄 1곳
Nature genetics · 2020 · PMID 32541925 · open access
페이지 12개+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
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외 269명 — 모두 보기
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LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction
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Nature genetics · 2021 · PMID 33414549 · open access
페이지 12개+
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
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외 23명 — 모두 보기
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Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
페이지 12개+
The trans-ancestral genomic architecture of glycemic traits
Chen J,
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외 393명 — 모두 보기
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Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
페이지 12개+
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
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Blood Cell Consortium
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페이지 12개+
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals
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Heid IM,
Winkler TW
VA Million Veteran Program
Nature communications · 2021 · PMID 34272381 · open access
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The power of genetic diversity in genome-wide association studies of lipids
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외 523명 — 모두 보기
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VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
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Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
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Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
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A saturated map of common genetic variants associated with human height
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외 610명 — 모두 보기
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23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
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