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Ma M,
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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+
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
Tahir UA,
Katz DH,
Avila-Pachecho J,
Bick AG,
Pampana A,
Robbins JM,
Yu Z,
Chen ZZ,
Benson MD,
Cruz DE,
Ngo D,
Deng S
and 27 more — show all
Shi X,
Zheng S,
Eisman AS,
Farrell L,
Hall ME,
Correa A,
Tracy RP,
Durda P,
Taylor KD,
Liu Y,
Johnson WC,
Guo X,
Yao J,
Chen YI,
Manichaikul AW,
Ruberg FL,
Blaner WS,
Jain D,
Bouchard C,
Sarzynski MA,
Rich SS,
Rotter JI,
Wang TJ,
Wilson JG,
Clish CB,
Natarajan P,
Gerszten RE
NHLBI Trans-Omics for Precision Medicine 1 Consortium
Nature communications · 2022 · PMID 35995766 · open access
12 pages+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
and 610 more — show all
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
Rüeger 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,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
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 AE,
Faul JD,
Fernandez-Lopez JC,
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 JJ,
Huang H,
Huang J,
Huerta-Chagoya A,
Huffman JE,
Hung YJ,
Huo S,
Hwang MY,
Iha H,
Ikeda DD,
Isono M,
Jackson AU,
Jäger S,
Jansen IE,
Johansson I,
Jonas JB,
Jonsson A,
Jørgensen T,
Kalafati IP,
Kanai M,
Kanoni S,
Kårhus LL,
Kasturiratne A,
Katsuya T,
Kawaguchi T,
Kember RL,
Kentistou KA,
Kim HN,
Kim YJ,
Kleber ME,
Knol MJ,
Kurbasic A,
Lauzon M,
Le P,
Lea R,
Lee JY,
Leonard HL,
Li SA,
Li X,
Li X,
Liang J,
Lin H,
Lin SY,
Liu J,
Liu X,
Lo KS,
Long J,
Lores-Motta L,
Luan J,
Lyssenko V,
Lyytikäinen LP,
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,
Møllehave LT,
Morgan A,
Mucha S,
Munz M,
Nakatochi M,
Nelson CP,
Nethander M,
Nho CW,
Nielsen AA,
Nolte IM,
Nongmaithem SS,
Noordam R,
Ntalla I,
Nutile T,
Pandit A,
Christofidou P,
Pärna K,
Pauper M,
Petersen ERB,
Petersen LV,
Pitkänen N,
Polašek 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,
Smit RAJ,
Smith AV,
Smith JA,
Smyth LJ,
Southam L,
Steinthorsdottir V,
Sun L,
Takeuchi F,
Tallapragada DSP,
Taylor KD,
Tayo BO,
Tcheandjieu 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,
Bin Wei W,
Wickremasinghe AR,
Wielscher M,
Wiggins KL,
Winsvold BS,
Wong A,
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 JH,
Zhao W,
Zhou W,
Zimmermann ME,
Zoledziewska M,
Adair LS,
Adams HHH,
Aguilar-Salinas CA,
Al-Mulla F,
Arnett DK,
Asselbergs FW,
Åsvold BO,
Attia J,
Banas B,
Bandinelli S,
Bennett DA,
Bergler T,
Bharadwaj D,
Biino G,
Bisgaard H,
Boerwinkle E,
Böger CA,
Bønnelykke K,
Boomsma DI,
Børglum AD,
Borja JB,
Bouchard C,
Bowden DW,
Brandslund I,
Brumpton B,
Buring JE,
Caulfield MJ,
Chambers JC,
Chandak GR,
Chanock SJ,
Chaturvedi N,
Chen YI,
Chen Z,
Cheng CY,
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 LCPGM,
De Jager PL,
de Kleijn DPV,
Janaka de Silva H,
Dedoussis GV,
den Hollander AI,
Du S,
Easton DF,
Elders PJM,
Eliassen AH,
Ellinor PT,
Elmståhl S,
Erdmann J,
Evans MK,
Fatkin D,
Feenstra B,
Feitosa MF,
Ferrucci L,
Ford I,
Fornage M,
Franke A,
Franks PW,
Freedman BI,
Gasparini P,
Gieger C,
Girotto G,
Goddard ME,
Golightly YM,
Gonzalez-Villalpando C,
Gordon-Larsen P,
Grallert H,
Grant SFA,
Grarup N,
Griffiths L,
Gudnason V,
Haiman C,
Hakonarson H,
Hansen T,
Hartman CA,
Hattersley AT,
Hayward C,
Heckbert SR,
Heng CK,
Hengstenberg C,
Hewitt AW,
Hishigaki H,
Hoyng CB,
Huang PL,
Huang W,
Hunt SC,
Hveem K,
Hyppönen E,
Iacono WG,
Ichihara S,
Ikram MA,
Isasi CR,
Jackson RD,
Jarvelin MR,
Jin ZB,
Jöckel KH,
Joshi PK,
Jousilahti P,
Jukema JW,
Kähönen M,
Kamatani Y,
Kang KD,
Kaprio J,
Kardia SLR,
Karpe F,
Kato N,
Kee F,
Kessler T,
Khera AV,
Khor CC,
Kiemeney LALM,
Kim BJ,
Kim EK,
Kim HL,
Kirchhof P,
Kivimaki M,
Koh WP,
Koistinen HA,
Kolovou GD,
Kooner JS,
Kooperberg C,
Köttgen A,
Kovacs P,
Kraaijeveld A,
Kraft P,
Krauss RM,
Kumari M,
Kutalik Z,
Laakso M,
Lange LA,
Langenberg C,
Launer LJ,
Le Marchand L,
Lee H,
Lee NR,
Lehtimäki T,
Li H,
Li L,
Lieb W,
Lin X,
Lind L,
Linneberg A,
Liu CT,
Liu J,
Loeffler M,
London B,
Lubitz SA,
Lye SJ,
Mackey DA,
Mägi R,
Magnusson PKE,
Marcus GM,
Vidal PM,
Martin NG,
März W,
Matsuda F,
McGarrah RW,
McGue M,
McKnight AJ,
Medland SE,
Mellström D,
Metspalu A,
Mitchell BD,
Mitchell P,
Mook-Kanamori DO,
Morris AD,
Mucci LA,
Munroe PB,
Nalls MA,
Nazarian S,
Nelson AE,
Neville MJ,
Newton-Cheh C,
Nielsen CS,
Nöthen MM,
Ohlsson C,
Oldehinkel AJ,
Orozco L,
Pahkala K,
Pajukanta P,
Palmer CNA,
Parra EJ,
Pattaro C,
Pedersen O,
Pennell CE,
Penninx BWJH,
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 XO,
Simonsick EM,
Sims M,
Singh JR,
Singleton AB,
Sinner MF,
Smith JG,
Snieder H,
Spector TD,
Stampfer MJ,
Stark KJ,
Strachan DP,
't Hart LM,
Tabara Y,
Tang H,
Tardif JC,
Thanaraj TA,
Timpson NJ,
Tönjes A,
Tremblay A,
Tuomi T,
Tuomilehto J,
Tusié-Luna MT,
Uitterlinden AG,
van Dam RM,
van der Harst P,
Van der Velde N,
van Duijn CM,
van Schoor NM,
Vitart V,
Völker U,
Vollenweider P,
Völzke 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 TY,
Woo JT,
Wright AF,
Wu JY,
Xu H,
Yajnik CS,
Yokota M,
Yuan JM,
Zeggini E,
Zemel BS,
Zheng W,
Zhu X,
Zmuda JM,
Zonderman AB,
Zwart JA,
Chasman DI,
Cho YS,
Heid IM,
McCarthy MI,
Ng MCY,
O'Donnell CJ,
Rivadeneira F,
Thorsteinsdottir U,
Sun YV,
Tai ES,
Boehnke M,
Deloukas P,
Justice AE,
Lindgren CM,
Loos RJF,
Mohlke KL,
North KE,
Stefansson K,
Walters RG,
Winkler TW,
Young KL,
Loh PR,
Yang J,
Esko T,
Assimes TL,
Auton A,
Abecasis GR,
Willer CJ,
Locke AE,
Berndt SI,
Lettre G,
Frayling TM,
Okada Y,
Wood AR,
Visscher PM,
Hirschhorn JN
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
Discerning asthma endotypes through comorbidity mapping
Jia G,
Jia G,
Zhong X,
Im HK,
Schoettler N,
Pividori M,
Hogarth DK,
Sperling AI,
White SR,
Naureckas ET,
Lyttle CS,
Terao C
and 8 more — show all
Nature communications · 2022 · PMID 36344522 · open access
12 pages+
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
Akiyama M
and 205 more — show all
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,
Fernandes Silva L,
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 YJ,
Hunter DJ,
Hveem K,
Hwang SJ,
Hwu CM,
Iacono W,
Irvin MR,
Jee YH,
Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
Kaprio J,
Kardia SLR,
Keller MC,
Kelly TN,
Kooperberg C,
Korhonen T,
Kraft P,
Krauter K,
Kuusisto J,
Laakso M,
Lasky-Su J,
Lee WJ,
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,
Medland SE,
Metspalu A,
Meyers DA,
Millwood IY,
Mitchell BD,
Mohlke KL,
Moll M,
Montasser ME,
Morrison AC,
Mulas A,
Nielsen JB,
North KE,
Oelsner EC,
Okada Y,
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Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Kim BJ,
Thorsteinsdottir U,
Stefansson K,
Zhang J,
Chen Y,
Ho YL,
Lynch JA,
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Genome biology · 2022 · PMID 36575460 · open access
7 pages
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
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Hostettler IC,
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van Eijk KR,
Koido M,
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and 62 more — show all
Walters RG,
Lin K,
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Chen Z,
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Rannikmäe K,
Sudlow CLM,
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Hveem K,
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Dauvillier J,
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Jones GT,
Bown MJ,
Ko NU,
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Klijn CJM,
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Tatlisumak T,
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Lindgren A,
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Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Plagnol V,
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Saad M,
Simón-Sánchez J,
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Sveinbjörnsdóttir S,
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Martinez M
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International Parkinson Disease Genomics Consortium
Lancet (London, England) · 2011 · PMID 21292315
5 pages
Questions about this list
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Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
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My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
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My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
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