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51 matches for
Bottinger E,
showing the first 20.
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic D,
Bao EL,
Akbari P,
Lareau CA,
Mousas A,
Jiang T,
Chen MH,
Raffield LM,
Tardaguila M,
Huffman JE,
Ritchie SC,
Megy K
and 100 more — show all
Ponstingl H,
Penkett CJ,
Albers PK,
Wigdor EM,
Sakaue S,
Moscati A,
Manansala R,
Lo KS,
Qian H,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala KN,
Wilson PWF,
Choquet H,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Felix SB,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Guo Q,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nikus K,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Weiss S,
Cai N,
Kundu K,
Watt SB,
Walter K,
Zonderman AB,
Cho K,
Li Y,
Loos RJF,
Knight JC,
Georges M,
Stegle O,
Evangelou E,
Okada Y,
Roberts DJ,
Inouye M,
Johnson AD,
Auer PL,
Astle WJ,
Reiner AP,
Butterworth AS,
Ouwehand WH,
Lettre G,
Sankaran VG,
Soranzo N
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
and 269 more — show all
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
Graff M,
Justice AE,
Young KL,
Marouli E,
Zhang X,
Fine RS,
Lim E,
Buchanan V,
Rand K,
Feitosa MF,
Wojczynski MK,
Yanek LR
and 213 more — show all
Shao Y,
Rohde R,
Adeyemo AA,
Aldrich MC,
Allison MA,
Ambrosone CB,
Ambs S,
Amos C,
Arnett DK,
Atwood L,
Bandera EV,
Bartz T,
Becker DM,
Berndt SI,
Bernstein L,
Bielak LF,
Blot WJ,
Bottinger EP,
Bowden DW,
Bradfield JP,
Brody JA,
Broeckel U,
Burke G,
Cade BE,
Cai Q,
Caporaso N,
Carlson C,
Carpten J,
Casey G,
Chanock SJ,
Chen G,
Chen M,
Chen YI,
Chen WM,
Chesi A,
Chiang CWK,
Chu L,
Coetzee GA,
Conti DV,
Cooper RS,
Cushman M,
Demerath E,
Deming SL,
Dimitrov L,
Ding J,
Diver WR,
Duan Q,
Evans MK,
Falusi AG,
Faul JD,
Fornage M,
Fox C,
Freedman BI,
Garcia M,
Gillanders EM,
Goodman P,
Gottesman O,
Grant SFA,
Guo X,
Hakonarson H,
Haritunians T,
Harris TB,
Harris CC,
Henderson BE,
Hennis A,
Hernandez DG,
Hirschhorn JN,
McNeill LH,
Howard TD,
Howard B,
Hsing AW,
Hsu YH,
Hu JJ,
Huff CD,
Huo D,
Ingles SA,
Irvin MR,
John EM,
Johnson KC,
Jordan JM,
Kabagambe EK,
Kang SJ,
Kardia SL,
Keating BJ,
Kittles RA,
Klein EA,
Kolb S,
Kolonel LN,
Kooperberg C,
Kuller L,
Kutlar A,
Lange L,
Langefeld CD,
Le Marchand L,
Leonard H,
Lettre G,
Levin AM,
Li Y,
Li J,
Liu Y,
Liu Y,
Liu S,
Lohman K,
Lotay V,
Lu Y,
Maixner W,
Manson JE,
McKnight B,
Meng Y,
Monda KL,
Monroe K,
Moore JH,
Mosley TH,
Mudgal P,
Murphy AB,
Nadukuru R,
Nalls MA,
Nathanson KL,
Nayak U,
N'Diaye A,
Nemesure B,
Neslund-Dudas C,
Neuhouser ML,
Nyante S,
Ochs-Balcom H,
Ogundiran TO,
Ogunniyi A,
Ojengbede O,
Okut H,
Olopade OI,
Olshan A,
Padhukasahasram B,
Palmer J,
Palmer CD,
Palmer ND,
Papanicolaou G,
Patel SR,
Pettaway CA,
Peyser PA,
Press MF,
Rao DC,
Rasmussen-Torvik LJ,
Redline S,
Reiner AP,
Rhie SK,
Rodriguez-Gil JL,
Rotimi CN,
Rotter JI,
Ruiz-Narvaez EA,
Rybicki BA,
Salako B,
Sale MM,
Sanderson M,
Schadt E,
Schreiner PJ,
Schurmann C,
Schwartz AG,
Shriner DA,
Signorello LB,
Singleton AB,
Siscovick DS,
Smith JA,
Smith S,
Speliotes E,
Spitz M,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Sucheston L,
Sun YV,
Tajuddin SM,
Taylor H,
Taylor K,
Tayo BO,
Thun MJ,
Tucker MA,
Vaidya D,
Van Den Berg DJ,
Vedantam S,
Vitolins M,
Wang Z,
Ware EB,
Wassertheil-Smoller S,
Weir DR,
Wiencke JK,
Williams SM,
Williams LK,
Wilson JG,
Witte JS,
Wrensch M,
Wu X,
Yao J,
Zakai N,
Zanetti K,
Zemel BS,
Zhao W,
Zhao JH,
Zheng W,
Zhi D,
Zhou J,
Zhu X,
Ziegler RG,
Zmuda J,
Zonderman AB,
Psaty BM,
Borecki IB,
Cupples LA,
Liu CT,
Haiman CA,
Loos R,
Ng MCY,
North KE
American journal of human genetics · 2021 · PMID 33713608
12 pages+
The trans-ancestral genomic architecture of glycemic traits
Chen J,
Spracklen CN,
Marenne G,
Varshney A,
Corbin LJ,
Luan J,
Willems SM,
Wu Y,
Zhang X,
Horikoshi M,
Boutin TS,
Mägi R
and 393 more — show all
Waage J,
Li-Gao R,
Chan KHK,
Yao J,
Anasanti MD,
Chu AY,
Claringbould A,
Heikkinen J,
Hong J,
Hottenga JJ,
Huo S,
Kaakinen MA,
Louie T,
März W,
Moreno-Macias H,
Ndungu A,
Nelson SC,
Nolte IM,
North KE,
Raulerson CK,
Ray D,
Rohde R,
Rybin D,
Schurmann C,
Sim X,
Southam L,
Stewart ID,
Wang CA,
Wang Y,
Wu P,
Zhang W,
Ahluwalia TS,
Appel EVR,
Bielak LF,
Brody JA,
Burtt NP,
Cabrera CP,
Cade BE,
Chai JF,
Chai X,
Chang LC,
Chen CH,
Chen BH,
Chitrala KN,
Chiu YF,
de Haan HG,
Delgado GE,
Demirkan A,
Duan Q,
Engmann J,
Fatumo SA,
Gayán J,
Giulianini F,
Gong JH,
Gustafsson S,
Hai Y,
Hartwig FP,
He J,
Heianza Y,
Huang T,
Huerta-Chagoya A,
Hwang MY,
Jensen RA,
Kawaguchi T,
Kentistou KA,
Kim YJ,
Kleber ME,
Kooner IK,
Lai S,
Lange LA,
Langefeld CD,
Lauzon M,
Li M,
Ligthart S,
Liu J,
Loh M,
Long J,
Lyssenko V,
Mangino M,
Marzi C,
Montasser ME,
Nag A,
Nakatochi M,
Noce D,
Noordam R,
Pistis G,
Preuss M,
Raffield L,
Rasmussen-Torvik LJ,
Rich SS,
Robertson NR,
Rueedi R,
Ryan K,
Sanna S,
Saxena R,
Schraut KE,
Sennblad B,
Setoh K,
Smith AV,
Sparsø T,
Strawbridge RJ,
Takeuchi F,
Tan J,
Trompet S,
van den Akker E,
van der Most PJ,
Verweij N,
Vogel M,
Wang H,
Wang C,
Wang N,
Warren HR,
Wen W,
Wilsgaard T,
Wong A,
Wood AR,
Xie T,
Zafarmand MH,
Zhao JH,
Zhao W,
Amin N,
Arzumanyan Z,
Astrup A,
Bakker SJL,
Baldassarre D,
Beekman M,
Bergman RN,
Bertoni A,
Blüher M,
Bonnycastle LL,
Bornstein SR,
Bowden DW,
Cai Q,
Campbell A,
Campbell H,
Chang YC,
de Geus EJC,
Dehghan A,
Du S,
Eiriksdottir G,
Farmaki AE,
Frånberg M,
Fuchsberger C,
Gao Y,
Gjesing AP,
Goel A,
Han S,
Hartman CA,
Herder C,
Hicks AA,
Hsieh CH,
Hsueh WA,
Ichihara S,
Igase M,
Ikram MA,
Johnson WC,
Jørgensen ME,
Joshi PK,
Kalyani RR,
Kandeel FR,
Katsuya T,
Khor CC,
Kiess W,
Kolcic I,
Kuulasmaa T,
Kuusisto J,
Läll K,
Lam K,
Lawlor DA,
Lee NR,
Lemaitre RN,
Li H,
Lin SY,
Lindström J,
Linneberg A,
Liu J,
Lorenzo C,
Matsubara T,
Matsuda F,
Mingrone G,
Mooijaart S,
Moon S,
Nabika T,
Nadkarni GN,
Nadler JL,
Nelis M,
Neville MJ,
Norris JM,
Ohyagi Y,
Peters A,
Peyser PA,
Polasek O,
Qi Q,
Raven D,
Reilly DF,
Reiner A,
Rivideneira F,
Roll K,
Rudan I,
Sabanayagam C,
Sandow K,
Sattar N,
Schürmann A,
Shi J,
Stringham HM,
Taylor KD,
Teslovich TM,
Thuesen B,
Timmers PRHJ,
Tremoli E,
Tsai MY,
Uitterlinden A,
van Dam RM,
van Heemst D,
van Hylckama Vlieg A,
van Vliet-Ostaptchouk JV,
Vangipurapu J,
Vestergaard H,
Wang T,
Willems van Dijk K,
Zemunik T,
Abecasis GR,
Adair LS,
Aguilar-Salinas CA,
Alarcón-Riquelme ME,
An P,
Aviles-Santa L,
Becker DM,
Beilin LJ,
Bergmann S,
Bisgaard H,
Black C,
Boehnke M,
Boerwinkle E,
Böhm BO,
Bønnelykke K,
Boomsma DI,
Bottinger EP,
Buchanan TA,
Canouil M,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YI,
Cheng CY,
Collins FS,
Correa A,
Cucca F,
de Silva HJ,
Dedoussis G,
Elmståhl S,
Evans MK,
Ferrannini E,
Ferrucci L,
Florez JC,
Franks PW,
Frayling TM,
Froguel P,
Gigante B,
Goodarzi MO,
Gordon-Larsen P,
Grallert H,
Grarup N,
Grimsgaard S,
Groop L,
Gudnason V,
Guo X,
Hamsten A,
Hansen T,
Hayward C,
Heckbert SR,
Horta BL,
Huang W,
Ingelsson E,
James PS,
Jarvelin MR,
Jonas JB,
Jukema JW,
Kaleebu P,
Kaplan R,
Kardia SLR,
Kato N,
Keinanen-Kiukaanniemi SM,
Kim BJ,
Kivimaki M,
Koistinen HA,
Kooner JS,
Körner A,
Kovacs P,
Kuh D,
Kumari M,
Kutalik Z,
Laakso M,
Lakka TA,
Launer LJ,
Leander K,
Li H,
Lin X,
Lind L,
Lindgren C,
Liu S,
Loos RJF,
Magnusson PKE,
Mahajan A,
Metspalu A,
Mook-Kanamori DO,
Mori TA,
Munroe PB,
Njølstad I,
O'Connell JR,
Oldehinkel AJ,
Ong KK,
Padmanabhan S,
Palmer CNA,
Palmer ND,
Pedersen O,
Pennell CE,
Porteous DJ,
Pramstaller PP,
Province MA,
Psaty BM,
Qi L,
Raffel LJ,
Rauramaa R,
Redline S,
Ridker PM,
Rosendaal FR,
Saaristo TE,
Sandhu M,
Saramies J,
Schneiderman N,
Schwarz P,
Scott LJ,
Selvin E,
Sever P,
Shu XO,
Slagboom PE,
Small KS,
Smith BH,
Snieder H,
Sofer T,
Sørensen TIA,
Spector TD,
Stanton A,
Steves CJ,
Stumvoll M,
Sun L,
Tabara Y,
Tai ES,
Timpson NJ,
Tönjes A,
Tuomilehto J,
Tusie T,
Uusitupa M,
van der Harst P,
van Duijn C,
Vitart V,
Vollenweider P,
Vrijkotte TGM,
Wagenknecht LE,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Wei WB,
Wickremasinghe AR,
Willemsen G,
Wilson JF,
Wong TY,
Wu JY,
Xiang AH,
Yanek LR,
Yengo L,
Yokota M,
Zeggini E,
Zheng W,
Zonderman AB,
Rotter JI,
Gloyn AL,
McCarthy MI,
Dupuis J,
Meigs JB,
Scott RA,
Prokopenko I,
Leong A,
Liu CT,
Parker SCJ,
Mohlke KL,
Langenberg C,
Wheeler E,
Morris AP,
Barroso I
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Mahajan A,
Spracklen CN,
Zhang W,
Ng MCY,
Petty LE,
Kitajima H,
Yu GZ,
Rüeger S,
Speidel L,
Kim YJ,
Horikoshi M,
Mercader JM
and 337 more — show all
Taliun D,
Moon S,
Kwak SH,
Robertson NR,
Rayner NW,
Loh M,
Kim BJ,
Chiou J,
Miguel-Escalada I,
Della Briotta Parolo P,
Lin K,
Bragg F,
Preuss MH,
Takeuchi F,
Nano J,
Guo X,
Lamri A,
Nakatochi M,
Scott RA,
Lee JJ,
Huerta-Chagoya A,
Graff M,
Chai JF,
Parra EJ,
Yao J,
Bielak LF,
Tabara Y,
Hai Y,
Steinthorsdottir V,
Cook JP,
Kals M,
Grarup N,
Schmidt EM,
Pan I,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Long J,
Sun M,
Tong L,
Chen WM,
Ahmad M,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Lecoeur C,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Jensen RA,
Tajuddin S,
Kabagambe EK,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Flanagan J,
Abaitua F,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Akiyama M,
Anand SS,
Bertoni A,
Bian Z,
Bork-Jensen J,
Brandslund I,
Brody JA,
Brummett CM,
Buchanan TA,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Das SK,
de Silva HJ,
Dedoussis G,
Dimitrov L,
Doumatey AP,
Du S,
Duan Q,
Eckardt KU,
Emery LS,
Evans DS,
Evans MK,
Fischer K,
Floyd JS,
Ford I,
Fornage M,
Franco OH,
Frayling TM,
Freedman BI,
Fuchsberger C,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Goodarzi MO,
Gordon-Larsen P,
Gorkin D,
Gross M,
Guo Y,
Hackinger S,
Han S,
Hattersley AT,
Herder C,
Howard AG,
Hsueh W,
Huang M,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Ikram MA,
Ingelsson M,
Islam MT,
Isono M,
Jang HM,
Jasmine F,
Jiang G,
Jonas JB,
Jørgensen ME,
Jørgensen T,
Kamatani Y,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kohara K,
Kriebel J,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lyssenko V,
Mamakou V,
Mani KR,
Meitinger T,
Metspalu A,
Morris AD,
Nadkarni GN,
Nadler JL,
Nalls MA,
Nayak U,
Nongmaithem SS,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Pereira MA,
Peters A,
Pirie FJ,
Porneala B,
Prasad G,
Preissl S,
Rasmussen-Torvik LJ,
Reiner AP,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sander M,
Sandow K,
Sattar N,
Schönherr S,
Schurmann C,
Shahriar M,
Shi J,
Shin DM,
Shriner D,
Smith JA,
So WY,
Stančáková A,
Stilp AM,
Strauch K,
Suzuki K,
Takahashi A,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tomlinson B,
Torres JM,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Vujkovic M,
Wacher-Rodarte N,
Wheeler E,
Whitsel EA,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamauchi T,
Yengo L,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Hanis CL,
Peyser PA,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Zeggini E,
Yokota M,
Rich SS,
Kooperberg C,
Pankow JS,
Engert JC,
Chen YI,
Froguel P,
Wilson JG,
Sheu WHH,
Kardia SLR,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Groop L,
Mook-Kanamori DO,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Bottinger EP,
Dehghan A,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Palmer CNA,
Liu S,
Abecasis G,
Kooner JS,
Loos RJF,
North KE,
Haiman CA,
Florez JC,
Saleheen D,
Hansen T,
Pedersen O,
Mägi R,
Langenberg C,
Wareham NJ,
Maeda S,
Kadowaki T,
Lee J,
Millwood IY,
Walters RG,
Stefansson K,
Myers SR,
Ferrer J,
Gaulton KJ,
Meigs JB,
Mohlke KL,
Gloyn AL,
Bowden DW,
Below JE,
Chambers JC,
Sim X,
Boehnke M,
Rotter JI,
McCarthy MI,
Morris AP
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
Petty LE,
Chen HH,
Frankel EG,
Zhu W,
Downie CG,
Graff M,
Lin P,
Sharma P,
Zhang X,
Scartozzi AC,
Roshani R,
Landman JM
and 80 more — show all
Boehnke M,
Bowden DW,
Chambers JC,
Mahajan A,
McCarthy MI,
Ng MCY,
Sim X,
Spracklen CN,
Zhang W,
Preuss M,
Bottinger EP,
Nadkarni GN,
Loos RJF,
Chen YI,
Tan J,
Ipp E,
Genter P,
Emery LS,
Louie T,
Sofer T,
Stilp AM,
Taylor KD,
Xiang AH,
Buchanan TA,
Roll K,
Gao C,
Palmer ND,
Norris JM,
Wagenknecht LE,
Nousome D,
Varma R,
McKean-Cowdin R,
Guo X,
Hai Y,
Hsueh W,
Sandow K,
Parra EJ,
Cruz M,
Valladares-Salgado A,
Wacher-Rodarte N,
Rotter JI,
Goodarzi MO,
Rich SS,
Bertoni A,
Raffel LJ,
Nadler JL,
Kandeel FR,
Duggirala R,
Blangero J,
Lehman DM,
DeFronzo RA,
Thameem F,
Wang Y,
Gahagan S,
Blanco E,
Burrows R,
Huerta-Chagoya A,
Florez JC,
Tusie-Luna T,
González-Villalpando C,
Orozco L,
Haiman CA,
Hanis CL,
Rohde R,
Whitsel EA,
Reiner AP,
Kooperberg C,
Li Y,
Duan Q,
Lee M,
Correa-Burrows P,
Fried SK,
North KE,
McCormick JB,
Fisher-Hoch SP,
Gamazon ER,
Morris AP,
Mercader JM,
Highland HM,
Below JE
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Ng MCY,
Graff M,
Lu Y,
Justice AE,
Mudgal P,
Liu CT,
Young K,
Yanek LR,
Feitosa MF,
Wojczynski MK,
Rand K,
Brody JA
and 101 more — show all
Cade BE,
Dimitrov L,
Duan Q,
Guo X,
Lange LA,
Nalls MA,
Okut H,
Tajuddin SM,
Tayo BO,
Vedantam S,
Bradfield JP,
Chen G,
Chen WM,
Chesi A,
Irvin MR,
Padhukasahasram B,
Smith JA,
Zheng W,
Zheng W,
Allison MA,
Ambrosone CB,
Bandera EV,
Bartz TM,
Berndt SI,
Bernstein L,
Blot WJ,
Bottinger EP,
Carpten J,
Chanock SJ,
Chen YI,
Conti DV,
Cooper RS,
Fornage M,
Freedman BI,
Garcia M,
Goodman PJ,
Hsu YH,
Hu J,
Huff CD,
Ingles SA,
John EM,
Kittles R,
Klein E,
Li J,
McKnight B,
Nayak U,
Nemesure B,
Ogunniyi A,
Olshan A,
Press MF,
Rohde R,
Rybicki BA,
Salako B,
Sanderson M,
Shao Y,
Siscovick DS,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Vaidya D,
Witte JS,
Yao J,
Zhu X,
Ziegler RG,
Zonderman AB,
Adeyemo A,
Ambs S,
Cushman M,
Faul JD,
Hakonarson H,
Levin AM,
Nathanson KL,
Ware EB,
Weir DR,
Zhao W,
Zhi D,
Arnett DK,
Grant SFA,
Kardia SLR,
Oloapde OI,
Rao DC,
Rotimi CN,
Sale MM,
Williams LK,
Zemel BS,
Becker DM,
Borecki IB,
Evans MK,
Harris TB,
Hirschhorn JN,
Li Y,
Patel SR,
Psaty BM,
Rotter JI,
Wilson JG,
Bowden DW,
Cupples LA,
Haiman CA,
Loos RJF,
North KE
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
11 pages
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
Zhao W,
Rasheed A,
Tikkanen E,
Lee JJ,
Butterworth AS,
Howson JMM,
Assimes TL,
Chowdhury R,
Orho-Melander M,
Damrauer S,
Small A,
Asma S
and 78 more — show all
Imamura M,
Yamauch T,
Chambers JC,
Chen P,
Sapkota BR,
Shah N,
Jabeen S,
Surendran P,
Lu Y,
Zhang W,
Imran A,
Abbas S,
Majeed F,
Trindade K,
Qamar N,
Mallick NH,
Yaqoob Z,
Saghir T,
Rizvi SNH,
Memon A,
Rasheed SZ,
Memon FU,
Mehmood K,
Ahmed N,
Qureshi IH,
Tanveer-Us-Salam,
Iqbal W,
Malik U,
Mehra N,
Kuo JZ,
Sheu WH,
Guo X,
Hsiung CA,
Juang JJ,
Taylor KD,
Hung YJ,
Lee WJ,
Quertermous T,
Lee IT,
Hsu CC,
Bottinger EP,
Ralhan S,
Teo YY,
Wang TD,
Alam DS,
Di Angelantonio E,
Epstein S,
Nielsen SF,
Nordestgaard BG,
Tybjaerg-Hansen A,
Young R,
Benn M,
Frikke-Schmidt R,
Kamstrup PR,
Jukema JW,
Sattar N,
Smit R,
Chung RH,
Liang KW,
Anand S,
Sanghera DK,
Ripatti S,
Loos RJF,
Kooner JS,
Tai ES,
Rotter JI,
Chen YI,
Frossard P,
Maeda S,
Kadowaki T,
Reilly M,
Pare G,
Melander O,
Salomaa V,
Rader DJ,
Danesh J,
Voight BF,
Saleheen D
CHD Exome+ Consortium · EPIC-CVD Consortium and 2 more consortia
Nature genetics · 2017 · PMID 28869590 · open access
11 pages
Exome-wide association study of plasma lipids in >300,000 individuals
Liu DJ,
Peloso GM,
Yu H,
Butterworth AS,
Wang X,
Mahajan A,
Saleheen D,
Emdin C,
Alam D,
Alves AC,
Amouyel P,
Di Angelantonio E
and 215 more — show all
Arveiler D,
Assimes TL,
Auer PL,
Baber U,
Ballantyne CM,
Bang LE,
Benn M,
Bis JC,
Boehnke M,
Boerwinkle E,
Bork-Jensen J,
Bottinger EP,
Brandslund I,
Brown M,
Busonero F,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YE,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Connell JM,
Cucca F,
Cupples LA,
Damrauer SM,
Davies G,
Deary IJ,
Dedoussis G,
Denny JC,
Dominiczak A,
Dubé MP,
Ebeling T,
Eiriksdottir G,
Esko T,
Farmaki AE,
Feitosa MF,
Ferrario M,
Ferrieres J,
Ford I,
Fornage M,
Franks PW,
Frayling TM,
Frikke-Schmidt R,
Fritsche LG,
Frossard P,
Fuster V,
Ganesh SK,
Gao W,
Garcia ME,
Gieger C,
Giulianini F,
Goodarzi MO,
Grallert H,
Grarup N,
Groop L,
Grove ML,
Gudnason V,
Hansen T,
Harris TB,
Hayward C,
Hirschhorn JN,
Holmen OL,
Huffman J,
Huo Y,
Hveem K,
Jabeen S,
Jackson AU,
Jakobsdottir J,
Jarvelin MR,
Jensen GB,
Jørgensen ME,
Jukema JW,
Justesen JM,
Kamstrup PR,
Kanoni S,
Karpe F,
Kee F,
Khera AV,
Klarin D,
Koistinen HA,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka T,
Langenberg C,
Langsted A,
Launer LJ,
Lauritzen T,
Liewald DCM,
Lin LA,
Linneberg A,
Loos RJF,
Lu Y,
Lu X,
Mägi R,
Malarstig A,
Manichaikul A,
Manning AK,
Mäntyselkä P,
Marouli E,
Masca NGD,
Maschio A,
Meigs JB,
Melander O,
Metspalu A,
Morris AP,
Morrison AC,
Mulas A,
Müller-Nurasyid M,
Munroe PB,
Neville MJ,
Nielsen JB,
Nielsen SF,
Nordestgaard BG,
Ordovas JM,
Mehran R,
O'Donnell CJ,
Orho-Melander M,
Molony CM,
Muntendam P,
Padmanabhan S,
Palmer CNA,
Pasko D,
Patel AP,
Pedersen O,
Perola M,
Peters A,
Pisinger C,
Pistis G,
Polasek O,
Poulter N,
Psaty BM,
Rader DJ,
Rasheed A,
Rauramaa R,
Reilly DF,
Reiner AP,
Renström F,
Rich SS,
Ridker PM,
Rioux JD,
Robertson NR,
Roden DM,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sanna S,
Sattar N,
Schmidt EM,
Scott RA,
Sever P,
Sevilla RS,
Shaffer CM,
Sim X,
Sivapalaratnam S,
Small KS,
Smith AV,
Smith BH,
Somayajula S,
Southam L,
Spector TD,
Speliotes EK,
Starr JM,
Stirrups KE,
Stitziel N,
Strauch K,
Stringham HM,
Surendran P,
Tada H,
Tall AR,
Tang H,
Tardif JC,
Taylor KD,
Trompet S,
Tsao PS,
Tuomilehto J,
Tybjaerg-Hansen A,
van Zuydam NR,
Varbo A,
Varga TV,
Virtamo J,
Waldenberger M,
Wang N,
Wareham NJ,
Warren HR,
Weeke PE,
Weinstock J,
Wessel J,
Wilson JG,
Wilson PWF,
Xu M,
Yaghootkar H,
Young R,
Zeggini E,
Zhang H,
Zheng NS,
Zhang W,
Zhang Y,
Zhou W,
Zhou Y,
Zoledziewska M,
Howson JMM,
Danesh J,
McCarthy MI,
Cowan CA,
Abecasis G,
Deloukas P,
Musunuru K,
Willer CJ,
Kathiresan S
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
Wheeler E,
Leong A,
Liu CT,
Hivert MF,
Strawbridge RJ,
Podmore C,
Li M,
Yao J,
Sim X,
Hong J,
Chu AY,
Zhang W
and 203 more — show all
Wang X,
Chen P,
Maruthur NM,
Porneala BC,
Sharp SJ,
Jia Y,
Kabagambe EK,
Chang LC,
Chen WM,
Elks CE,
Evans DS,
Fan Q,
Giulianini F,
Go MJ,
Hottenga JJ,
Hu Y,
Jackson AU,
Kanoni S,
Kim YJ,
Kleber ME,
Ladenvall C,
Lecoeur C,
Lim SH,
Lu Y,
Mahajan A,
Marzi C,
Nalls MA,
Navarro P,
Nolte IM,
Rose LM,
Rybin DV,
Sanna S,
Shi Y,
Stram DO,
Takeuchi F,
Tan SP,
van der Most PJ,
Van Vliet-Ostaptchouk JV,
Wong A,
Yengo L,
Zhao W,
Goel A,
Martinez Larrad MT,
Radke D,
Salo P,
Tanaka T,
van Iperen EPA,
Abecasis G,
Afaq S,
Alizadeh BZ,
Bertoni AG,
Bonnefond A,
Böttcher Y,
Bottinger EP,
Campbell H,
Carlson OD,
Chen CH,
Cho YS,
Garvey WT,
Gieger C,
Goodarzi MO,
Grallert H,
Hamsten A,
Hartman CA,
Herder C,
Hsiung CA,
Huang J,
Igase M,
Isono M,
Katsuya T,
Khor CC,
Kiess W,
Kohara K,
Kovacs P,
Lee J,
Lee WJ,
Lehne B,
Li H,
Liu J,
Lobbens S,
Luan J,
Lyssenko V,
Meitinger T,
Miki T,
Miljkovic I,
Moon S,
Mulas A,
Müller G,
Müller-Nurasyid M,
Nagaraja R,
Nauck M,
Pankow JS,
Polasek O,
Prokopenko I,
Ramos PS,
Rasmussen-Torvik L,
Rathmann W,
Rich SS,
Robertson NR,
Roden M,
Roussel R,
Rudan I,
Scott RA,
Scott WR,
Sennblad B,
Siscovick DS,
Strauch K,
Sun L,
Swertz M,
Tajuddin SM,
Taylor KD,
Teo YY,
Tham YC,
Tönjes A,
Wareham NJ,
Willemsen G,
Wilsgaard T,
Hingorani AD,
Egan J,
Ferrucci L,
Hovingh GK,
Jula A,
Kivimaki M,
Kumari M,
Njølstad I,
Palmer CNA,
Serrano Ríos M,
Stumvoll M,
Watkins H,
Aung T,
Blüher M,
Boehnke M,
Boomsma DI,
Bornstein SR,
Chambers JC,
Chasman DI,
Chen YI,
Chen YT,
Cheng CY,
Cucca F,
de Geus EJC,
Deloukas P,
Evans MK,
Fornage M,
Friedlander Y,
Froguel P,
Groop L,
Gross MD,
Harris TB,
Hayward C,
Heng CK,
Ingelsson E,
Kato N,
Kim BJ,
Koh WP,
Kooner JS,
Körner A,
Kuh D,
Kuusisto J,
Laakso M,
Lin X,
Liu Y,
Loos RJF,
Magnusson PKE,
März W,
McCarthy MI,
Oldehinkel AJ,
Ong KK,
Pedersen NL,
Pereira MA,
Peters A,
Ridker PM,
Sabanayagam C,
Sale M,
Saleheen D,
Saltevo J,
Schwarz PE,
Sheu WHH,
Snieder H,
Spector TD,
Tabara Y,
Tuomilehto J,
van Dam RM,
Wilson JG,
Wilson JF,
Wolffenbuttel BHR,
Wong TY,
Wu JY,
Yuan JM,
Zonderman AB,
Soranzo N,
Guo X,
Roberts DJ,
Florez JC,
Sladek R,
Dupuis J,
Morris AP,
Tai ES,
Selvin E,
Rotter JI,
Langenberg C,
Barroso I,
Meigs JB
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
Liu C,
Kraja AT,
Smith JA,
Brody JA,
Franceschini N,
Bis JC,
Rice K,
Morrison AC,
Lu Y,
Weiss S,
Guo X,
Palmas W
and 83 more — show all
Martin LW,
Chen YD,
Surendran P,
Drenos F,
Cook JP,
Auer PL,
Chu AY,
Giri A,
Zhao W,
Jakobsdottir J,
Lin LA,
Stafford JM,
Amin N,
Mei H,
Yao J,
Voorman A,
Larson MG,
Grove ML,
Smith AV,
Hwang SJ,
Chen H,
Huan T,
Kosova G,
Stitziel NO,
Kathiresan S,
Samani N,
Schunkert H,
Deloukas P,
Li M,
Fuchsberger C,
Pattaro C,
Gorski M,
Kooperberg C,
Papanicolaou GJ,
Rossouw JE,
Faul JD,
Kardia SL,
Bouchard C,
Raffel LJ,
Uitterlinden AG,
Franco OH,
Vasan RS,
O'Donnell CJ,
Taylor KD,
Liu K,
Bottinger EP,
Gottesman O,
Daw EW,
Giulianini F,
Ganesh S,
Salfati E,
Harris TB,
Launer LJ,
Dörr M,
Felix SB,
Rettig R,
Völzke H,
Kim E,
Lee WJ,
Lee IT,
Sheu WH,
Tsosie KS,
Edwards DR,
Liu Y,
Correa A,
Weir DR,
Völker U,
Ridker PM,
Boerwinkle E,
Gudnason V,
Reiner AP,
van Duijn CM,
Borecki IB,
Edwards TL,
Chakravarti A,
Rotter JI,
Psaty BM,
Loos RJ,
Fornage M,
Ehret GB,
Newton-Cheh C,
Levy D,
Chasman DI
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 pages
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
Liang J,
Le TH,
Edwards DRV,
Tayo BO,
Gaulton KJ,
Smith JA,
Lu Y,
Jensen RA,
Chen G,
Yanek LR,
Schwander K,
Tajuddin SM
and 69 more — show all
Sofer T,
Kim W,
Kayima J,
McKenzie CA,
Fox E,
Nalls MA,
Young JH,
Sun YV,
Lane JM,
Cechova S,
Zhou J,
Tang H,
Fornage M,
Musani SK,
Wang H,
Lee J,
Adeyemo A,
Dreisbach AW,
Forrester T,
Chu PL,
Cappola A,
Evans MK,
Morrison AC,
Martin LW,
Wiggins KL,
Hui Q,
Zhao W,
Jackson RD,
Ware EB,
Faul JD,
Reiner AP,
Bray M,
Denny JC,
Mosley TH,
Palmas W,
Guo X,
Papanicolaou GJ,
Penman AD,
Polak JF,
Rice K,
Rice K,
Taylor KD,
Boerwinkle E,
Bottinger EP,
Liu K,
Risch N,
Hunt SC,
Kooperberg C,
Zonderman AB,
Laurie CC,
Becker DM,
Cai J,
Loos RJF,
Psaty BM,
Weir DR,
Kardia SLR,
Arnett DK,
Won S,
Edwards TL,
Redline S,
Cooper RS,
Rao DC,
Rotter JI,
Rotimi C,
Levy D,
Chakravarti A,
Zhu X,
Franceschini N,
Franceschini N
PLoS genetics · 2017 · PMID 28498854 · open access
8 pages
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Sung YJ,
Winkler TW,
de las Fuentes L,
Bentley AR,
Brown MR,
Kraja AT,
Schwander K,
Ntalla I,
Guo X,
Franceschini N,
Lu Y,
Cheng CY
and 286 more — show all
Sim X,
Vojinovic D,
Marten J,
Musani SK,
Li C,
Feitosa MF,
Kilpeläinen TO,
Richard MA,
Noordam R,
Aslibekyan S,
Aschard H,
Bartz TM,
Dorajoo R,
Liu Y,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Tayo BO,
Warren HR,
Zhao W,
Zhou Y,
Matoba N,
Sofer T,
Alver M,
Amini M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Giulianini F,
Goel A,
Harris SE,
Hartwig FP,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kähönen M,
Kasturiratne A,
Kühnel B,
Leander K,
Lee WJ,
Lin KH,
'an Luan J,
McKenzie CA,
Meian H,
Nelson CP,
Rauramaa R,
Schupf N,
Scott RA,
Sheu WHH,
Stančáková A,
Takeuchi F,
van der Most PJ,
Varga TV,
Wang H,
Wang Y,
Ware EB,
Weiss S,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Alfred T,
Amin N,
Arking D,
Aung T,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Braund PS,
Brody JA,
Broeckel U,
Cabrera CP,
Cade B,
Caizheng Y,
Campbell A,
Canouil M,
Chakravarti A,
Chauhan G,
Christensen K,
Cocca M,
Collins FS,
Connell JM,
de Mutsert R,
de Silva HJ,
Debette S,
Dörr M,
Duan Q,
Eaton CB,
Ehret G,
Evangelou E,
Faul JD,
Fisher VA,
Forouhi NG,
Franco OH,
Friedlander Y,
Gao H,
Gigante B,
Graff M,
Gu CC,
Gu D,
Gupta P,
Hagenaars SP,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hirata M,
Hofman A,
Howard BV,
Hunt S,
Irvin MR,
Jia Y,
Joehanes R,
Justice AE,
Katsuya T,
Kaufman J,
Kerrison ND,
Khor CC,
Koh WP,
Koistinen HA,
Komulainen P,
Kooperberg C,
Krieger JE,
Kubo M,
Kuusisto J,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Lim SH,
Lin S,
Liu CT,
Liu J,
Liu J,
Liu K,
Liu Y,
Loh M,
Lohman KK,
Long J,
Louie T,
Mägi R,
Mahajan A,
Meitinger T,
Metspalu A,
Milani L,
Momozawa Y,
Morris AP,
Mosley TH Jr,
Munson P,
Murray AD,
Nalls MA,
Nasri U,
Norris JM,
North K,
Ogunniyi A,
Padmanabhan S,
Palmas WR,
Palmer ND,
Pankow JS,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Raitakari OT,
Renström F,
Rice TK,
Ridker PM,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Sabanayagam C,
Salako BL,
Sandow K,
Schmidt CO,
Schreiner PJ,
Scott WR,
Seshadri S,
Sever P,
Sitlani CM,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yuan JM,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Chen YI,
de Faire U,
Deary IJ,
Esko T,
Farrall M,
Forrester T,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Hung YJ,
Jonas JB,
Kato N,
Kooner JS,
Laakso M,
Lehtimäki T,
Liang KW,
Magnusson PKE,
Newman AB,
Oldehinkel AJ,
Pereira AC,
Redline S,
Rettig R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zheng W,
Zheng W,
Kamatani Y,
Laurie CC,
Bouchard C,
Cooper RS,
Evans MK,
Gudnason V,
Kardia SLR,
Kritchevsky SB,
Levy D,
O'Connell JR,
Psaty BM,
van Dam RM,
Sims M,
Arnett DK,
Mook-Kanamori DO,
Kelly TN,
Fox ER,
Hayward C,
Fornage M,
Rotimi CN,
Province MA,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Reiner AP,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Caulfield MJ,
Elliott P,
Rice K,
Munroe PB,
Morrison AC,
Cupples LA,
Rao DC,
Chasman DI
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
Hong J,
Hatchell KE,
Bradfield JP,
Bjonnes A,
Chesi A,
Lai CQ,
Langefeld CD,
Lu L,
Lu Y,
Lutsey PL,
Musani SK,
Nalls MA
and 48 more — show all
Robinson-Cohen C,
Roizen JD,
Saxena R,
Tucker KL,
Ziegler JT,
Arking DE,
Bis JC,
Boerwinkle E,
Bottinger EP,
Bowden DW,
Gilsanz V,
Houston DK,
Kalkwarf HJ,
Kelly A,
Lappe JM,
Liu Y,
Michos ED,
Oberfield SE,
Palmer ND,
Rotter JI,
Sapkota B,
Shepherd JA,
Wilson JG,
Basu S,
de Boer IH,
Divers J,
Freedman BI,
Grant SFA,
Hakanarson H,
Harris TB,
Kestenbaum BR,
Kritchevsky SB,
Loos RJF,
Norris JM,
Norwood AF,
Ordovas JM,
Pankow JS,
Psaty BM,
Sanghera DK,
Wagenknecht LE,
Zemel BS,
Meigs J,
Dupuis J,
Florez JC,
Wang T,
Liu CT,
Engelman CD,
Billings LK
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
6 pages
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Mahajan A,
Wessel J,
Willems SM,
Zhao W,
Robertson NR,
Chu AY,
Gan W,
Kitajima H,
Taliun D,
Rayner NW,
Guo X,
Lu Y
and 228 more — show all
Li M,
Jensen RA,
Hu Y,
Huo S,
Lohman KK,
Zhang W,
Cook JP,
Prins BP,
Flannick J,
Grarup N,
Trubetskoy VV,
Kravic J,
Kim YJ,
Rybin DV,
Yaghootkar H,
Müller-Nurasyid M,
Meidtner K,
Li-Gao R,
Varga TV,
Marten J,
Li J,
Smith AV,
An P,
Ligthart S,
Gustafsson S,
Malerba G,
Demirkan A,
Tajes JF,
Steinthorsdottir V,
Wuttke M,
Lecoeur C,
Preuss M,
Bielak LF,
Graff M,
Highland HM,
Justice AE,
Liu DJ,
Marouli E,
Peloso GM,
Warren HR,
Afaq S,
Afzal S,
Ahlqvist E,
Almgren P,
Amin N,
Bang LB,
Bertoni AG,
Bombieri C,
Bork-Jensen J,
Brandslund I,
Brody JA,
Burtt NP,
Canouil M,
Chen YI,
Cho YS,
Christensen C,
Eastwood SV,
Eckardt KU,
Fischer K,
Gambaro G,
Giedraitis V,
Grove ML,
de Haan HG,
Hackinger S,
Hai Y,
Han S,
Tybjærg-Hansen A,
Hivert MF,
Isomaa B,
Jäger S,
Jørgensen ME,
Jørgensen T,
Käräjämäki A,
Kim BJ,
Kim SS,
Koistinen HA,
Kovacs P,
Kriebel J,
Kronenberg F,
Läll K,
Lange LA,
Lee JJ,
Lehne B,
Li H,
Lin KH,
Linneberg A,
Liu CT,
Liu J,
Loh M,
Mägi R,
Mamakou V,
McKean-Cowdin R,
Nadkarni G,
Neville M,
Nielsen SF,
Ntalla I,
Peyser PA,
Rathmann W,
Rice K,
Rich SS,
Rode L,
Rolandsson O,
Schönherr S,
Selvin E,
Small KS,
Stančáková A,
Surendran P,
Taylor KD,
Teslovich TM,
Thorand B,
Thorleifsson G,
Tin A,
Tönjes A,
Varbo A,
Witte DR,
Wood AR,
Yajnik P,
Yao J,
Yengo L,
Young R,
Amouyel P,
Boeing H,
Boerwinkle E,
Bottinger EP,
Chowdhury R,
Collins FS,
Dedoussis G,
Dehghan A,
Deloukas P,
Ferrario MM,
Ferrières J,
Florez JC,
Frossard P,
Gudnason V,
Harris TB,
Heckbert SR,
Howson JMM,
Ingelsson M,
Kathiresan S,
Kee F,
Kuusisto J,
Langenberg C,
Launer LJ,
Lindgren CM,
Männistö S,
Meitinger T,
Melander O,
Mohlke KL,
Moitry M,
Morris AD,
Murray AD,
de Mutsert R,
Orho-Melander M,
Owen KR,
Perola M,
Peters A,
Province MA,
Rasheed A,
Ridker PM,
Rivadineira F,
Rosendaal FR,
Rosengren AH,
Salomaa V,
Sheu WH,
Sladek R,
Smith BH,
Strauch K,
Uitterlinden AG,
Varma R,
Willer CJ,
Blüher M,
Butterworth AS,
Chambers JC,
Chasman DI,
Danesh J,
van Duijn C,
Dupuis J,
Franco OH,
Franks PW,
Froguel P,
Grallert H,
Groop L,
Han BG,
Hansen T,
Hattersley AT,
Hayward C,
Ingelsson E,
Kardia SLR,
Karpe F,
Kooner JS,
Köttgen A,
Kuulasmaa K,
Laakso M,
Lin X,
Lind L,
Liu Y,
Loos RJF,
Marchini J,
Metspalu A,
Mook-Kanamori D,
Nordestgaard BG,
Palmer CNA,
Pankow JS,
Pedersen O,
Psaty BM,
Rauramaa R,
Sattar N,
Schulze MB,
Soranzo N,
Spector TD,
Stefansson K,
Stumvoll M,
Thorsteinsdottir U,
Tuomi T,
Tuomilehto J,
Wareham NJ,
Wilson JG,
Zeggini E,
Scott RA,
Barroso I,
Frayling TM,
Goodarzi MO,
Meigs JB,
Boehnke M,
Saleheen D,
Morris AP,
Rotter JI,
McCarthy MI
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
Willems SM,
Ng NHJ,
Fernandez J,
Fine RS,
Wheeler E,
Wessel J,
Kitajima H,
Marenne G,
Sim X,
Yaghootkar H,
Wang S,
Chen S
and 228 more — show all
Chen Y,
Chen YI,
Grarup N,
Li-Gao R,
Varga TV,
Asimit JL,
Feng S,
Strawbridge RJ,
Kleinbrink EL,
Ahluwalia TS,
An P,
Appel EV,
Arking DE,
Auvinen J,
Bielak LF,
Bihlmeyer NA,
Bork-Jensen J,
Brody JA,
Campbell A,
Chu AY,
Davies G,
Demirkan A,
Floyd JS,
Giulianini F,
Guo X,
Gustafsson S,
Jackson AU,
Jakobsdottir J,
Järvelin MR,
Jensen RA,
Kanoni S,
Keinanen-Kiukaanniemi S,
Li M,
Lu Y,
Luan J,
Manning AK,
Marten J,
Meidtner K,
Mook-Kanamori DO,
Muka T,
Pistis G,
Prins B,
Rice KM,
Sanna S,
Smith AV,
Smith JA,
Southam L,
Stringham HM,
Tragante V,
van der Laan SW,
Warren HR,
Yao J,
Yiorkas AM,
Zhang W,
Zhao W,
Graff M,
Highland HM,
Justice AE,
Marouli E,
Medina-Gomez C,
Afaq S,
Alhejily WA,
Amin N,
Asselbergs FW,
Bonnycastle LL,
Bots ML,
Brandslund I,
Chen J,
Danesh J,
de Mutsert R,
Dehghan A,
Ebeling T,
Elliott P,
Farmaki AE,
Faul JD,
Franks PW,
Franks S,
Fritsche A,
Gjesing AP,
Goodarzi MO,
Gudnason V,
Hallmans G,
Harris TB,
Herzig KH,
Hivert MF,
Jørgensen T,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Karaleftheri M,
Kardia SLR,
Kinnunen L,
Koistinen HA,
Komulainen P,
Kovacs P,
Kuusisto J,
Laakso M,
Lange LA,
Launer LJ,
Leong A,
Lindström J,
Manning Fox JE,
Männistö S,
Maruthur NM,
Moilanen L,
Mulas A,
Nalls MA,
Neville M,
Pankow JS,
Pattie A,
Petersen ERB,
Puolijoki H,
Rasheed A,
Redmond P,
Renström F,
Roden M,
Saleheen D,
Saltevo J,
Savonen K,
Sebert S,
Skaaby T,
Small KS,
Stančáková A,
Stokholm J,
Strauch K,
Tai ES,
Taylor KD,
Thuesen BH,
Tönjes A,
Tsafantakis E,
Tuomi T,
Tuomilehto J,
Uusitupa M,
Vääräsmäki M,
Vaartjes I,
Zoledziewska M,
Abecasis G,
Balkau B,
Bisgaard H,
Blakemore AI,
Blüher M,
Boeing H,
Boerwinkle E,
Bønnelykke K,
Bottinger EP,
Caulfield MJ,
Chambers JC,
Chasman DI,
Cheng CY,
Collins FS,
Coresh J,
Cucca F,
de Borst GJ,
Deary IJ,
Dedoussis G,
Deloukas P,
den Ruijter HM,
Dupuis J,
Evans MK,
Ferrannini E,
Franco OH,
Grallert H,
Hansen T,
Hattersley AT,
Hayward C,
Hirschhorn JN,
Ikram A,
Ingelsson E,
Karpe F,
Kaw KT,
Kiess W,
Kooner JS,
Körner A,
Lakka T,
Langenberg C,
Lind L,
Lindgren CM,
Linneberg A,
Lipovich L,
Liu CT,
Liu J,
Liu Y,
Loos RJF,
MacDonald PE,
Mohlke KL,
Morris AD,
Munroe PB,
Murray A,
Padmanabhan S,
Palmer CNA,
Pasterkamp G,
Pedersen O,
Peyser PA,
Polasek O,
Porteous D,
Province MA,
Psaty BM,
Rauramaa R,
Ridker PM,
Rolandsson O,
Rorsman P,
Rosendaal FR,
Rudan I,
Salomaa V,
Schulze MB,
Sladek R,
Smith BH,
Spector TD,
Starr JM,
Stumvoll M,
van Duijn CM,
Walker M,
Wareham NJ,
Weir DR,
Wilson JG,
Wong TY,
Zeggini E,
Zonderman AB,
Rotter JI,
Morris AP,
Boehnke M,
Florez JC,
McCarthy MI,
Meigs JB,
Mahajan A,
Scott RA,
Gloyn AL,
Barroso I
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
Gorski M,
van der Most PJ,
Teumer A,
Chu AY,
Li M,
Mijatovic V,
Nolte IM,
Cocca M,
Taliun D,
Gomez F,
Li Y,
Tayo B
and 114 more — show all
Tin A,
Feitosa MF,
Aspelund T,
Attia J,
Biffar R,
Bochud M,
Boerwinkle E,
Borecki I,
Bottinger EP,
Chen MH,
Chouraki V,
Ciullo M,
Coresh J,
Cornelis MC,
Curhan GC,
d'Adamo AP,
Dehghan A,
Dengler L,
Ding J,
Eiriksdottir G,
Endlich K,
Enroth S,
Esko T,
Franco OH,
Gasparini P,
Gieger C,
Girotto G,
Gottesman O,
Gudnason V,
Gyllensten U,
Hancock SJ,
Harris TB,
Helmer C,
Höllerer S,
Hofer E,
Hofman A,
Holliday EG,
Homuth G,
Hu FB,
Huth C,
Hutri-Kähönen N,
Hwang SJ,
Imboden M,
Johansson Å,
Kähönen M,
König W,
Kramer H,
Krämer BK,
Kumar A,
Kutalik Z,
Lambert JC,
Launer LJ,
Lehtimäki T,
de Borst M,
Navis G,
Swertz M,
Liu Y,
Lohman K,
Loos RJF,
Lu Y,
Lyytikäinen LP,
McEvoy MA,
Meisinger C,
Meitinger T,
Metspalu A,
Metzger M,
Mihailov E,
Mitchell P,
Nauck M,
Oldehinkel AJ,
Olden M,
Wjh Penninx B,
Pistis G,
Pramstaller PP,
Probst-Hensch N,
Raitakari OT,
Rettig R,
Ridker PM,
Rivadeneira F,
Robino A,
Rosas SE,
Ruderfer D,
Ruggiero D,
Saba Y,
Sala C,
Schmidt H,
Schmidt R,
Scott RJ,
Sedaghat S,
Smith AV,
Sorice R,
Stengel B,
Stracke S,
Strauch K,
Toniolo D,
Uitterlinden AG,
Ulivi S,
Viikari JS,
Völker U,
Vollenweider P,
Völzke H,
Vuckovic D,
Waldenberger M,
Jin Wang J,
Yang Q,
Chasman DI,
Tromp G,
Snieder H,
Heid IM,
Fox CS,
Köttgen A,
Pattaro C,
Böger CA,
Fuchsberger C
Scientific reports · 2017 · PMID 28452372 · open access
4 pages
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
Nielsen JB,
Fritsche LG,
Zhou W,
Teslovich TM,
Holmen OL,
Gustafsson S,
Gabrielsen ME,
Schmidt EM,
Beaumont R,
Wolford BN,
Lin M,
Brummett CM
and 33 more — show all
Preuss MH,
Refsgaard L,
Bottinger EP,
Graham SE,
Surakka I,
Chu Y,
Skogholt AH,
Dalen H,
Boyle AP,
Oral H,
Herron TJ,
Kitzman J,
Jalife J,
Svendsen JH,
Olesen MS,
Njølstad I,
Løchen ML,
Baras A,
Gottesman O,
Marcketta A,
O'Dushlaine C,
Ritchie MD,
Wilsgaard T,
Loos RJF,
Frayling TM,
Boehnke M,
Ingelsson E,
Carey DJ,
Dewey FE,
Kang HM,
Abecasis GR,
Hveem K,
Willer CJ
American journal of human genetics · 2018 · PMID 29290336
4 pages
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
Chen Z,
Tang H,
Qayyum R,
Schick UM,
Nalls MA,
Handsaker R,
Li J,
Lu Y,
Yanek LR,
Keating B,
Meng Y,
van Rooij FJ
and 24 more — show all
Okada Y,
Kubo M,
Rasmussen-Torvik L,
Keller MF,
Lange L,
Evans M,
Bottinger EP,
Linderman MD,
Ruderfer DM,
Hakonarson H,
Papanicolaou G,
Zonderman AB,
Gottesman O,
Thomson C,
Ziv E,
Singleton AB,
Loos RJ,
Sleiman PM,
Ganesh S,
McCarroll S,
Becker DM,
Wilson JG,
Lettre G,
Reiner AP
BioBank Japan Project · CHARGE Consortium
Human molecular genetics · 2013 · PMID 23446634
3 pages
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
Below JE,
Parra EJ,
Gamazon ER,
Torres J,
Krithika S,
Candille S,
Lu Y,
Manichakul A,
Peralta-Romero J,
Duan Q,
Li Y,
Morris AP
and 13 more — show all
Gottesman O,
Bottinger E,
Wang XQ,
Taylor KD,
Ida Chen YD,
Rotter JI,
Rich SS,
Loos RJ,
Tang H,
Cox NJ,
Cruz M,
Hanis CL,
Valladares-Salgado A
Scientific reports · 2016 · PMID 26780889 · open access
3 pages
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