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Sun YV,
showing the first 19.
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Zimmermann ME,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Peyser PA,
Kato N,
Schulze MB,
Girotto G,
Böger CA,
Jung B,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Tusié-Luna T,
Aguilar-Salinas CA,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Mercader JM,
Costanzo MC,
Jang D,
Burtt NP,
Villalpando CG,
Orozco L,
Fornage M,
Tai E,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Jin ZB,
Qu J,
Hishigaki H,
Lin X,
März W,
Gudnason V,
Tardif JC,
Lettre G,
Hart LM',
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Parra EJ,
Cruz M,
Psaty BM,
Brandslund I,
Pramstaller PP,
Rotimi CN,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Francesco C,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Chuang LM,
Rotter JI,
Dantoft TM,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Li H,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
Willemsen AHM,
Cupples L,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
Hazelhurst S,
Ramsay M,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Baras A,
Justice AE,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Tamiya G,
Yamamoto M,
van Heel DA,
Trembath RC,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Kim BJ,
Thorsteinsdottir U,
Stefansson K,
Zhang J,
Chen Y,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson PWF,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Mohlke KL,
Sun YV,
Morris AP,
Boehnke M,
Brown CD,
Natarajan P,
Deloukas P,
Willer CJ,
Assimes TL,
Peloso GM
Genome biology · 2022 · PMID 36575460 · open access
7 pages
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Klarin D,
Verma SS,
Judy R,
Dikilitas O,
Wolford BN,
Paranjpe I,
Levin MG,
Pan C,
Tcheandjieu C,
Spin JM,
Lynch J,
Assimes TL
and 41 more — show all
Åldstedt Nyrønning L,
Mattsson E,
Edwards TL,
Denny J,
Larson E,
Lee MTM,
Carrell D,
Zhang Y,
Jarvik GP,
Gharavi AG,
Harley J,
Mentch F,
Pacheco JA,
Hakonarson H,
Skogholt AH,
Thomas L,
Gabrielsen ME,
Hveem K,
Nielsen JB,
Zhou W,
Fritsche L,
Huang J,
Natarajan P,
Sun YV,
DuVall SL,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Scali ST,
Berceli SA,
Willer C,
Jones GT,
Bown MJ,
Nadkarni G,
Kullo IJ,
Ritchie M,
Damrauer SM,
Tsao PS
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Tcheandjieu C,
Zhu X,
Hilliard AT,
Clarke SL,
Napolioni V,
Ma S,
Lee KM,
Fang H,
Chen F,
Lu Y,
Tsao NL,
Raghavan S
and 70 more — show all
Koyama S,
Gorman BR,
Vujkovic M,
Klarin D,
Levin MG,
Sinnott-Armstrong N,
Wojcik GL,
Plomondon ME,
Maddox TM,
Waldo SW,
Bick AG,
Pyarajan S,
Huang J,
Song R,
Ho YL,
Buyske S,
Kooperberg C,
Haessler J,
Loos RJF,
Do R,
Verbanck M,
Chaudhary K,
North KE,
Avery CL,
Graff M,
Haiman CA,
Le Marchand L,
Wilkens LR,
Bis JC,
Leonard H,
Shen B,
Lange LA,
Giri A,
Dikilitas O,
Kullo IJ,
Stanaway IB,
Jarvik GP,
Gordon AS,
Hebbring S,
Namjou B,
Kaufman KM,
Ito K,
Ishigaki K,
Kamatani Y,
Verma SS,
Ritchie MD,
Kember RL,
Baras A,
Lotta LA,
Kathiresan S,
Hauser ER,
Miller DR,
Lee JS,
Saleheen D,
Reaven PD,
Cho K,
Gaziano JM,
Natarajan P,
Huffman JE,
Voight BF,
Rader DJ,
Chang KM,
Lynch JA,
Damrauer SM,
Wilson PWF,
Tang H,
Sun YV,
Tsao PS,
O'Donnell CJ,
Assimes TL
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
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,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
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
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program
Raghavan S,
Huang J,
Tcheandjieu C,
Huffman JE,
Litkowski E,
Liu C,
Ho YA,
Hunter-Zinck H,
Zhao H,
Marouli E,
North KE,
Lange E
and 12 more — show all
Lange LA,
Voight BF,
Gaziano JM,
Pyarajan S,
Hauser ER,
Tsao PS,
Wilson PWF,
Chang KM,
Cho K,
O'Donnell CJ,
Sun YV,
Assimes TL
VA Million Veteran Program
PLoS genetics · 2022 · PMID 35653334 · open access
5 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genome-wide association study of peripheral artery disease in the Million Veteran Program
Klarin D,
Lynch J,
Aragam K,
Chaffin M,
Assimes TL,
Huang J,
Lee KM,
Shao Q,
Huffman JE,
Natarajan P,
Arya S,
Small A
and 24 more — show all
Sun YV,
Vujkovic M,
Freiberg MS,
Wang L,
Chen J,
Saleheen D,
Lee JS,
Miller DR,
Reaven P,
Alba PR,
Patterson OV,
DuVall SL,
Boden WE,
Beckman JA,
Gaziano JM,
Concato J,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Tsao PS,
Damrauer SM
VA Million Veteran Program
Nature medicine · 2019 · PMID 31285632 · open access
3 pages
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Levin MG,
Tsao NL,
Singhal P,
Liu C,
Vy HMT,
Paranjpe I,
Backman JD,
Bellomo TR,
Bone WP,
Biddinger KJ,
Hui Q,
Dikilitas O
and 31 more — show all
Satterfield BA,
Yang Y,
Morley MP,
Bradford Y,
Burke M,
Reza N,
Charest B,
Judy RL,
Puckelwartz MJ,
Hakonarson H,
Khan A,
Kottyan LC,
Kullo I,
Luo Y,
McNally EM,
Rasmussen-Torvik LJ,
Day SM,
Do R,
Phillips LS,
Ellinor PT,
Nadkarni GN,
Ritchie MD,
Arany Z,
Cappola TP,
Margulies KB,
Aragam KG,
Haggerty CM,
Joseph J,
Sun YV,
Voight BF,
Damrauer SM
Regeneron Genetics Center
Nature communications · 2022 · PMID 36376295 · open access
3 pages
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Noordam R,
Wang W,
Nagarajan P,
Wang H,
Brown MR,
Bentley AR,
Hui Q,
Kraja AT,
Morrison JL,
O'Connel JR,
Lee S,
Schwander K
and 137 more — show all
Bartz TM,
de Las Fuentes L,
Feitosa MF,
Guo X,
Hanfei X,
Harris SE,
Huang Z,
Kals M,
Lefevre C,
Mangino M,
Milaneschi Y,
van der Most PJ,
Pacheco NL,
Palmer ND,
Rao V,
Rauramaa R,
Sun Q,
Tabara Y,
Vojinovic D,
Wang Y,
Weiss S,
Yang Q,
Zhao W,
Zhu W,
Ansari MAY,
Aschard H,
Anugu P,
Assimes TL,
Attia J,
Baker LD,
Ballantyne C,
Bazzano L,
Boerwinkle E,
Cade B,
Chen HH,
Chen W,
Ida Chen YD,
Chen Z,
Cho K,
De Anda-Duran I,
Dimitrov L,
Do A,
Edwards T,
Faquih T,
Hingorani A,
Fisher-Hoch SP,
Gaziano JM,
Gharib SA,
Giri A,
Ghanbari M,
Grabe HJ,
Graff M,
Charles Gu C,
He J,
Heikkinen S,
Hixson J,
Ho YL,
Hood MM,
Houghton SC,
Karvonen-Gutierrez CA,
Kawaguchi T,
Kilpeläinen TO,
Komulainen P,
Lin HJ,
Linchangco GV Jr,
Luik AI,
Ma J,
Meigs JB,
McCormick JB,
Menni C,
Nolte IM,
Norris JM,
Petty LE,
Polikowsky HG,
Raffield LM,
Rich SS,
Riha RL,
Russ TC,
Ruiz-Narvaez EA,
Sitlani CM,
Smith JA,
Snieder H,
Sofer T,
Shen B,
Tang J,
Taylor KD,
Teder-Laving M,
Triatin R,
Tsai MY,
Völzke H,
Westerman KE,
Xia R,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Zhu X,
Below JE,
Cox SR,
Evans M,
Fornage M,
Fox ER,
Franceschini N,
Harlow SD,
Holliday E,
Ikram MA,
Kelly T,
Lakka TA,
Lawlor DA,
Li C,
Liu CT,
Mägi R,
Manning AK,
Matsuda F,
Morrison AC,
Nauck M,
North KE,
Penninx BW,
Province MA,
Psaty BM,
Rotter JI,
Spector TD,
Wagenknecht LE,
van Dijk KW,
Jaquish CE,
Wilson PW,
Peyser PA,
Munroe PB,
de Vries PS,
Gauderman WJ,
Sun YV,
Chen H,
Miller CL,
Winkler TW,
Rao DC,
Redline S,
van Heemst D
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Monda KL,
Chen GK,
Taylor KC,
Palmer C,
Edwards TL,
Lange LA,
Ng MC,
Adeyemo AA,
Allison MA,
Bielak LF,
Chen G,
Graff M
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Irvin MR,
Rhie SK,
Li G,
Liu Y,
Liu Y,
Lu Y,
Nalls MA,
Sun YV,
Wojczynski MK,
Yanek LR,
Aldrich MC,
Ademola A,
Amos CI,
Bandera EV,
Bock CH,
Britton A,
Broeckel U,
Cai Q,
Caporaso NE,
Carlson CS,
Carpten J,
Casey G,
Chen WM,
Chen F,
Chen YD,
Chiang CW,
Coetzee GA,
Demerath E,
Deming-Halverson SL,
Driver RW,
Dubbert P,
Feitosa MF,
Feng Y,
Freedman BI,
Gillanders EM,
Gottesman O,
Guo X,
Haritunians T,
Harris T,
Harris CC,
Hennis AJ,
Hernandez DG,
McNeill LH,
Howard TD,
Howard BV,
Howard VJ,
Johnson KC,
Kang SJ,
Keating BJ,
Kolb S,
Kuller LH,
Kutlar A,
Langefeld CD,
Lettre G,
Lohman K,
Lotay V,
Lyon H,
Manson JE,
Maixner W,
Meng YA,
Monroe KR,
Morhason-Bello I,
Murphy AB,
Mychaleckyj JC,
Nadukuru R,
Nathanson KL,
Nayak U,
N'diaye A,
Nemesure B,
Wu SY,
Leske MC,
Neslund-Dudas C,
Neuhouser M,
Nyante S,
Ochs-Balcom H,
Ogunniyi A,
Ogundiran TO,
Ojengbede O,
Olopade OI,
Palmer JR,
Ruiz-Narvaez EA,
Palmer ND,
Press MF,
Rampersaud E,
Rasmussen-Torvik LJ,
Rodriguez-Gil JL,
Salako B,
Schadt EE,
Schwartz AG,
Shriner DA,
Siscovick D,
Smith SB,
Wassertheil-Smoller S,
Speliotes EK,
Spitz MR,
Sucheston L,
Taylor H,
Tayo BO,
Tucker MA,
Van Den Berg DJ,
Edwards DR,
Wang Z,
Wiencke JK,
Winkler TW,
Witte JS,
Wrensch M,
Wu X,
Yang JJ,
Levin AM,
Young TR,
Zakai NA,
Cushman M,
Zanetti KA,
Zhao JH,
Zhao W,
Zheng Y,
Zhou J,
Ziegler RG,
Zmuda JM,
Fernandes JK,
Gilkeson GS,
Kamen DL,
Hunt KJ,
Spruill IJ,
Ambrosone CB,
Ambs S,
Arnett DK,
Atwood L,
Becker DM,
Berndt SI,
Bernstein L,
Blot WJ,
Borecki IB,
Bottinger EP,
Bowden DW,
Burke G,
Chanock SJ,
Cooper RS,
Ding J,
Duggan D,
Evans MK,
Fox C,
Garvey WT,
Bradfield JP,
Hakonarson H,
Grant SF,
Hsing A,
Chu L,
Hu JJ,
Huo D,
Ingles SA,
John EM,
Jordan JM,
Kabagambe EK,
Kardia SL,
Kittles RA,
Goodman PJ,
Klein EA,
Kolonel LN,
Le Marchand L,
Liu S,
McKnight B,
Millikan RC,
Mosley TH,
Padhukasahasram B,
Williams LK,
Patel SR,
Peters U,
Pettaway CA,
Peyser PA,
Psaty BM,
Redline S,
Rotimi CN,
Rybicki BA,
Sale MM,
Schreiner PJ,
Signorello LB,
Singleton AB,
Stanford JL,
Strom SS,
Thun MJ,
Vitolins M,
Zheng W,
Moore JH,
Williams SM,
Ketkar S,
Zhu X,
Zonderman AB,
Kooperberg C,
Papanicolaou GJ,
Henderson BE,
Reiner AP,
Hirschhorn JN,
Loos RJ,
North KE,
Haiman CA
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
Liu CT,
Monda KL,
Taylor KC,
Lange L,
Demerath EW,
Palmas W,
Wojczynski MK,
Ellis JC,
Vitolins MZ,
Liu S,
Papanicolaou GJ,
Irvin MR
and 81 more — show all
Xue L,
Griffin PJ,
Nalls MA,
Adeyemo A,
Liu J,
Li G,
Ruiz-Narvaez EA,
Chen WM,
Chen F,
Henderson BE,
Millikan RC,
Ambrosone CB,
Strom SS,
Guo X,
Andrews JS,
Sun YV,
Mosley TH,
Yanek LR,
Shriner D,
Haritunians T,
Rotter JI,
Speliotes EK,
Smith M,
Rosenberg L,
Mychaleckyj J,
Nayak U,
Spruill I,
Garvey WT,
Pettaway C,
Nyante S,
Bandera EV,
Britton AF,
Zonderman AB,
Rasmussen-Torvik LJ,
Chen YD,
Ding J,
Lohman K,
Kritchevsky SB,
Zhao W,
Peyser PA,
Kardia SL,
Kabagambe E,
Broeckel U,
Chen G,
Zhou J,
Wassertheil-Smoller S,
Neuhouser ML,
Rampersaud E,
Psaty B,
Kooperberg C,
Manson JE,
Kuller LH,
Ochs-Balcom HM,
Johnson KC,
Sucheston L,
Ordovas JM,
Palmer JR,
Haiman CA,
McKnight B,
Howard BV,
Becker DM,
Bielak LF,
Liu Y,
Allison MA,
Grant SF,
Burke GL,
Patel SR,
Schreiner PJ,
Borecki IB,
Evans MK,
Taylor H,
Sale MM,
Howard V,
Carlson CS,
Rotimi CN,
Cushman M,
Harris TB,
Reiner AP,
Cupples LA,
North KE,
Fox CS
PLoS genetics · 2013 · PMID 23966867 · open access
2 pages
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Franceschini N,
Fox E,
Zhang Z,
Edwards TL,
Nalls MA,
Sung YJ,
Tayo BO,
Sun YV,
Gottesman O,
Adeyemo A,
Johnson AD,
Young JH
and 94 more — show all
Rice K,
Duan Q,
Chen F,
Li Y,
Tang H,
Fornage M,
Keene KL,
Andrews JS,
Smith JA,
Faul JD,
Guangfa Z,
Guo W,
Liu Y,
Murray SS,
Musani SK,
Srinivasan S,
Velez Edwards DR,
Wang H,
Becker LC,
Bovet P,
Bochud M,
Broeckel U,
Burnier M,
Carty C,
Chasman DI,
Ehret G,
Chen WM,
Chen G,
Chen W,
Ding J,
Dreisbach AW,
Evans MK,
Guo X,
Garcia ME,
Jensen R,
Keller MF,
Lettre G,
Lotay V,
Martin LW,
Moore JH,
Morrison AC,
Mosley TH,
Ogunniyi A,
Palmas W,
Papanicolaou G,
Penman A,
Polak JF,
Ridker PM,
Salako B,
Singleton AB,
Shriner D,
Taylor KD,
Vasan R,
Wiggins K,
Williams SM,
Yanek LR,
Zhao W,
Zonderman AB,
Becker DM,
Berenson G,
Boerwinkle E,
Bottinger E,
Cushman M,
Eaton C,
Nyberg F,
Heiss G,
Hirschhron JN,
Howard VJ,
Karczewsk KJ,
Lanktree MB,
Liu K,
Liu Y,
Loos R,
Margolis K,
Snyder M,
Psaty BM,
Schork NJ,
Weir DR,
Rotimi CN,
Sale MM,
Harris T,
Kardia SL,
Hunt SC,
Arnett D,
Redline S,
Cooper RS,
Risch NJ,
Rao DC,
Rotter JI,
Chakravarti A,
Reiner AP,
Levy D,
Keating BJ,
Zhu X
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
Hartiala JA,
Han Y,
Jia Q,
Hilser JR,
Huang P,
Gukasyan J,
Schwartzman WS,
Cai Z,
Biswas S,
Trégouët DA,
Smith NL,
Seldin M
and 47 more — show all
Pan C,
Mehrabian M,
Lusis AJ,
Bazeley P,
Sun YV,
Liu C,
Quyyumi AA,
Scholz M,
Thiery J,
Delgado GE,
Kleber ME,
März W,
Howe LJ,
Asselbergs FW,
van Vugt M,
Vlachojannis GJ,
Patel RS,
Lyytikäinen LP,
Kähönen M,
Lehtimäki T,
Nieminen TVM,
Kuukasjärvi P,
Laurikka JO,
Chang X,
Heng CK,
Jiang R,
Kraus WE,
Hauser ER,
Ferguson JF,
Reilly MP,
Ito K,
Koyama S,
Kamatani Y,
Komuro I,
Stolze LK,
Romanoski CE,
Khan MD,
Turner AW,
Miller CL,
Aherrahrou R,
Civelek M,
Ma L,
Björkegren JLM,
Kumar SR,
Tang WHW,
Hazen SL,
Allayee H
INVENT Consortium · CHARGE Consortium Hemostasis Working Group and 2 more consortia
European heart journal · 2021 · PMID 33532862
2 pages
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
Rasooly D,
Peloso GM,
Pereira AC,
Dashti H,
Giambartolomei C,
Wheeler E,
Aung N,
Ferolito BR,
Pietzner M,
Farber-Eger EH,
Wells QS,
Kosik NM
and 22 more — show all
Gaziano L,
Posner DC,
Bento AP,
Hui Q,
Liu C,
Aragam K,
Wang Z,
Charest B,
Huffman JE,
Wilson PWF,
Phillips LS,
Whittaker J,
Munroe PB,
Petersen SE,
Cho K,
Leach AR,
Magariños MP,
Gaziano JM,
Langenberg C,
Sun YV,
Joseph J,
Casas JP
VA Million Veteran Program
Nature communications · 2023 · PMID 37429843 · open access
2 pages
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study
Musani SK,
Fox ER,
Kraja A,
Bidulescu A,
Lieb W,
Lin H,
Beecham A,
Chen MH,
Felix JF,
Fox CS,
Kao WH,
Kardia SL
and 11 more — show all
Liu CT,
Nalls MA,
Rundek T,
Sacco RL,
Smith J,
Sun YV,
Wilson G,
Zhang Z,
Mosley TH,
Taylor HA,
Vasan RS
Circulation. Cardiovascular genetics · 2015 · PMID 25561047
1 page
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
Fang H,
Hui Q,
Lynch J,
Honerlaw J,
Assimes TL,
Huang J,
Vujkovic M,
Damrauer SM,
Pyarajan S,
Gaziano JM,
DuVall SL,
O'Donnell CJ
and 6 more — show all
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
1 page
Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program
Peloso GM,
Tcheandjieu C,
McGeary JE,
Posner DC,
Ho YL,
Zhou JJ,
Hilliard AT,
Joseph J,
O'Donnell CJ,
Efird JT,
Crawford DC,
Wu WC
and 4 more — show all
VA Million Veteran Program COVID-19 Science Initiative
Frontiers in genetics · 2021 · PMID 35222515 · open access
1 page
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
and 113 more — show all
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
1 page
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