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Fornage M,
showing the first 20.
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Suzuki K,
Hatzikotoulas K,
Southam L,
Taylor HJ,
Yin X,
Lorenz KM,
Mandla R,
Huerta-Chagoya A,
Melloni GEM,
Kanoni S,
Rayner NW,
Bocher O
and 351 more — show all
Arruda AL,
Sonehara K,
Namba S,
Lee SSK,
Preuss MH,
Petty LE,
Schroeder P,
Vanderwerff B,
Kals M,
Bragg F,
Lin K,
Guo X,
Zhang W,
Yao J,
Kim YJ,
Graff M,
Takeuchi F,
Nano J,
Lamri A,
Nakatochi M,
Moon S,
Scott RA,
Cook JP,
Lee JJ,
Pan I,
Taliun D,
Parra EJ,
Chai JF,
Bielak LF,
Tabara Y,
Hai Y,
Thorleifsson G,
Grarup N,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Kwak SH,
Long J,
Sun M,
Tong L,
Chen WM,
Nongmaithem SS,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Brody JA,
Kabagambe E,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Broadaway KA,
Williamson A,
Kamali Z,
Cui J,
Thangam M,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Ahluwalia TS,
Anand SS,
Bertoni A,
Bork-Jensen J,
Brandslund I,
Buchanan TA,
Burant CF,
Butterworth AS,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Danesh J,
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,
Franco OH,
Frayling TM,
Freedman BI,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Gordon-Larsen P,
Gross M,
Guare LA,
Hackinger S,
Hakaste L,
Han S,
Hattersley AT,
Herder C,
Horikoshi M,
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 T,
Kamanu FK,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee KM,
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,
Lynch JA,
Lyssenko V,
Maeda S,
Mamakou V,
Mansuri SR,
Matsuda K,
Meitinger T,
Melander O,
Metspalu A,
Mo H,
Morris AD,
Moura FA,
Nadler JL,
Nalls MA,
Nayak U,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Patil S,
Pei P,
Pereira MA,
Peters A,
Pirie FJ,
Polikowsky HG,
Porneala B,
Prasad G,
Rasmussen-Torvik LJ,
Reiner AP,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sandow K,
Sankareswaran A,
Sattar N,
Schönherr S,
Shahriar M,
Shen B,
Shi J,
Shin DM,
Shojima N,
Smith JA,
So WY,
Stančáková A,
Steinthorsdottir V,
Stilp AM,
Strauch K,
Taylor KD,
Thorand B,
Thorsteinsdottir U,
Tomlinson B,
Tran TC,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Wacher-Rodarte N,
Wheeler E,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamamoto K,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zawistowski M,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Fornage M,
Hanis CL,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Yokota M,
Kardia SLR,
Peyser PA,
Pankow JS,
Engert JC,
Bonnefond A,
Froguel P,
Wilson JG,
Sheu WHH,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Mook-Kanamori DO,
Tuomi T,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
Chen YI,
Rich SS,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Ghanbari M,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Bowden DW,
Palmer CNA,
Kooner JS,
Kooperberg C,
Liu S,
North KE,
Saleheen D,
Hansen T,
Pedersen O,
Wareham NJ,
Lee J,
Kim BJ,
Millwood IY,
Walters RG,
Stefansson K,
Ahlqvist E,
Goodarzi MO,
Mohlke KL,
Langenberg C,
Haiman CA,
Loos RJF,
Florez JC,
Rader DJ,
Ritchie MD,
Zöllner S,
Mägi R,
Marston NA,
Ruff CT,
van Heel DA,
Finer S,
Denny JC,
Yamauchi T,
Kadowaki T,
Chambers JC,
Ng MCY,
Sim X,
Below JE,
Tsao PS,
Chang KM,
McCarthy MI,
Meigs JB,
Mahajan A,
Spracklen CN,
Mercader JM,
Boehnke M,
Rotter JI,
Vujkovic M,
Voight BF,
Morris AP,
Zeggini E
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
Williams FM,
Carter AM,
Hysi PG,
Surdulescu G,
Hodgkiss D,
Soranzo N,
Traylor M,
Bevan S,
Dichgans M,
Rothwell PM,
Sudlow C,
Farrall M
and 46 more — show all
Silander K,
Kaunisto M,
Wagner P,
Saarela O,
Kuulasmaa K,
Virtamo J,
Salomaa V,
Amouyel P,
Arveiler D,
Ferrieres J,
Wiklund PG,
Ikram MA,
Hofman A,
Boncoraglio GB,
Parati EA,
Helgadottir A,
Gretarsdottir S,
Thorsteinsdottir U,
Thorleifsson G,
Stefansson K,
Seshadri S,
DeStefano A,
Gschwendtner A,
Psaty B,
Longstreth W,
Mitchell BD,
Cheng YC,
Clarke R,
Ferrario M,
Bis JC,
Levi C,
Attia J,
Holliday EG,
Scott RJ,
Fornage M,
Sharma P,
Furie KL,
Rosand J,
Nalls M,
Meschia J,
Mosely TH,
Evans A,
Palotie A,
Markus HS,
Grant PJ,
Spector TD
EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 and 3 more consortia
Annals of neurology · 2013 · PMID 23381943 · open access
11 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
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
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium
Jiang MZ,
Gaynor SM,
Li X,
Van Buren E,
Stilp A,
Stilp A,
Buth E,
Wang FF,
Manansala R,
Gogarten SM,
Li Z,
Polfus LM
and 35 more — show all
Salimi S,
Bis JC,
Pankratz N,
Yanek LR,
Durda P,
Tracy RP,
Rich SS,
Rotter JI,
Mitchell BD,
Lewis JP,
Psaty BM,
Pratte KA,
Silverman EK,
Kaplan RC,
Avery C,
North KE,
Mathias RA,
Faraday N,
Lin H,
Wang B,
Carson AP,
Norwood AF,
Gibbs RA,
Kooperberg C,
Lundin J,
Peters U,
Dupuis J,
Hou L,
Fornage M,
Benjamin EJ,
Reiner AP,
Bowler RP,
Lin X,
Auer PL,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Inflammation Working Group
Human molecular genetics · 2024 · PMID 38747556
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
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
Sabater-Lleal M,
Huang J,
Chasman D,
Naitza S,
Dehghan A,
Johnson AD,
Teumer A,
Reiner AP,
Folkersen L,
Basu S,
Rudnicka AR,
Trompet S
and 133 more — show all
Mälarstig A,
Baumert J,
Bis JC,
Guo X,
Hottenga JJ,
Shin SY,
Lopez LM,
Lahti J,
Tanaka T,
Yanek LR,
Oudot-Mellakh T,
Wilson JF,
Navarro P,
Huffman JE,
Zemunik T,
Redline S,
Mehra R,
Pulanic D,
Rudan I,
Wright AF,
Kolcic I,
Polasek O,
Wild SH,
Campbell H,
Curb JD,
Wallace R,
Liu S,
Eaton CB,
Becker DM,
Becker LC,
Bandinelli S,
Räikkönen K,
Widen E,
Palotie A,
Fornage M,
Green D,
Gross M,
Davies G,
Harris SE,
Liewald DC,
Starr JM,
Williams FM,
Grant PJ,
Spector TD,
Strawbridge RJ,
Silveira A,
Sennblad B,
Rivadeneira F,
Uitterlinden AG,
Franco OH,
Hofman A,
van Dongen J,
Willemsen G,
Boomsma DI,
Yao J,
Swords Jenny N,
Haritunians T,
McKnight B,
Lumley T,
Taylor KD,
Rotter JI,
Psaty BM,
Peters A,
Gieger C,
Illig T,
Grotevendt A,
Homuth G,
Völzke H,
Kocher T,
Goel A,
Franzosi MG,
Seedorf U,
Clarke R,
Steri M,
Tarasov KV,
Sanna S,
Schlessinger D,
Stott DJ,
Sattar N,
Buckley BM,
Rumley A,
Lowe GD,
McArdle WL,
Chen MH,
Tofler GH,
Song J,
Boerwinkle E,
Folsom AR,
Rose LM,
Franco-Cereceda A,
Teichert M,
Ikram MA,
Mosley TH,
Bevan S,
Dichgans M,
Rothwell PM,
Sudlow CL,
Hopewell JC,
Chambers JC,
Saleheen D,
Kooner JS,
Danesh J,
Nelson CP,
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LifeLines Cohort Study · EchoGen consortium and 6 more consortia
Nature genetics · 2011 · PMID 21909110 · open access
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Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
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Questions about this list
Why is my paper here? I never gave you permission.
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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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