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58 matches for
Chen H,
showing the first 20.
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls MA,
Pankratz N,
Lill CM,
Do CB,
Hernandez DG,
Saad M,
DeStefano AL,
Kara E,
Bras J,
Sharma M,
Schulte C,
Keller MF
and 35 more — show all
Arepalli S,
Letson C,
Edsall C,
Stefansson H,
Liu X,
Pliner H,
Lee JH,
Cheng R,
Ikram MA,
Ioannidis JP,
Hadjigeorgiou GM,
Bis JC,
Martinez M,
Perlmutter JS,
Goate A,
Marder K,
Fiske B,
Sutherland M,
Xiromerisiou G,
Myers RH,
Clark LN,
Stefansson K,
Hardy JA,
Heutink P,
Chen H,
Wood NW,
Houlden H,
Payami H,
Brice A,
Scott WK,
Gasser T,
Bertram L,
Eriksson N,
Foroud T,
Singleton AB
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and 10 more consortia
Nature genetics · 2014 · PMID 25064009 · open access
12 pages+
A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos
Feofanova EV,
Chen H,
Dai Y,
Jia P,
Grove ML,
Morrison AC,
Qi Q,
Daviglus M,
Cai J,
North KE,
Laurie CC,
Kaplan RC
and 2 more — show all
American journal of human genetics · 2020 · PMID 33031748
12 pages+
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
Chen H,
Fan S,
Stone J,
Thompson DJ,
Douglas J,
Li S,
Scott C,
Bolla MK,
Wang Q,
Dennis J,
Michailidou K,
Li C
and 44 more — show all
Peters U,
Hopper JL,
Southey MC,
Nguyen-Dumont T,
Nguyen TL,
Fasching PA,
Behrens A,
Cadby G,
Murphy RA,
Aronson K,
Howell A,
Astley S,
Couch F,
Olson J,
Milne RL,
Giles GG,
Haiman CA,
Maskarinec G,
Winham S,
John EM,
Kurian A,
Eliassen H,
Andrulis I,
Evans DG,
Newman WG,
Hall P,
Czene K,
Swerdlow A,
Jones M,
Pollan M,
Fernandez-Navarro P,
McConnell DS,
Kristensen VN,
Rothstein JH,
Wang P,
Habel LA,
Sieh W,
Dunning AM,
Pharoah PDP,
Easton DF,
Gierach GL,
Tamimi RM,
Vachon CM,
Lindström S
NBCS Investigators
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
12 pages+
Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank
Xue Z,
Yuan J,
Chen F,
Yao Y,
Xing S,
Yu X,
Li K,
Wang C,
Bao J,
Qu J,
Su J,
Chen H
EBioMedicine · 2022 · PMID 35841873 · open access
12 pages+
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations
Feofanova EV,
Brown MR,
Alkis T,
Manuel AM,
Li X,
Tahir UA,
Li Z,
Mendez KM,
Kelly RS,
Qi Q,
Chen H,
Larson MG
and 8 more — show all
NHLBI Trans-Omics for Precision Medicine (TOPMed)
Nature communications · 2023 · PMID 37253714 · open access
12 pages+
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Meng X,
Navoly G,
Giannakopoulou O,
Levey DF,
Koller D,
Pathak GA,
Koen N,
Lin K,
Adams MJ,
Rentería ME,
Feng Y,
Gaziano JM
and 66 more — show all
Stein DJ,
Zar HJ,
Campbell ML,
van Heel DA,
Trivedi B,
Finer S,
McQuillin A,
Bass N,
Chundru VK,
Martin HC,
Huang QQ,
Valkovskaya M,
Chu CY,
Kanjira S,
Kuo PH,
Chen HC,
Tsai SJ,
Liu YL,
Kendler KS,
Peterson RE,
Cai N,
Fang Y,
Sen S,
Scott LJ,
Burmeister M,
Loos RJF,
Preuss MH,
Actkins KV,
Davis LK,
Uddin M,
Wani AH,
Wildman DE,
Aiello AE,
Ursano RJ,
Kessler RC,
Kanai M,
Okada Y,
Sakaue S,
Rabinowitz JA,
Maher BS,
Uhl G,
Eaton W,
Cruz-Fuentes CS,
Martinez-Levy GA,
Campos AI,
Millwood IY,
Chen Z,
Li L,
Wassertheil-Smoller S,
Jiang Y,
Tian C,
Martin NG,
Mitchell BL,
Byrne EM,
Awasthi S,
Coleman JRI,
Ripke S,
Sofer T,
Walters RG,
McIntosh AM,
Polimanti R,
Dunn EC,
Stein MB,
Gelernter J,
Lewis CM,
Kuchenbaecker K
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
iGWAS: Image-based genome-wide association of self-supervised deep phenotyping of retina fundus images
Xie Z,
Zhang T,
Kim S,
Lu J,
Zhang W,
Lin CH,
Wu MR,
Davis A,
Channa R,
Giancardo L,
Chen H,
Wang S
and 2 more — show all
PLoS genetics · 2024 · PMID 38728357 · 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+
Large-scale genome-wide analyses of stuttering
Polikowsky HG,
Scartozzi AC,
Shaw DM,
Pruett DG,
Chen HH,
Petty LE,
Petty AS,
Lowther EJ,
Cho SH,
Yu Y,
Mozaffari S,
Avery CL
and 9 more — show all
23andMe Research Team
Nature genetics · 2025 · PMID 40721530 · open access
12 pages+
Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci
Wang Z,
Zhu Q,
Liu Y,
Chen S,
Zhang Y,
Ma Q,
Chen X,
Liu C,
Lei H,
Chen H,
Wang J,
Zheng S
and 4 more — show all
Clinical and translational medicine · 2021 · PMID 33634981 · open access
11 pages
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Morris AP,
Voight BF,
Teslovich TM,
Ferreira T,
Segrè AV,
Steinthorsdottir V,
Strawbridge RJ,
Khan H,
Grallert H,
Mahajan A,
Prokopenko I,
Kang HM
and 192 more — show all
Dina C,
Esko T,
Fraser RM,
Kanoni S,
Kumar A,
Lagou V,
Langenberg C,
Luan J,
Lindgren CM,
Müller-Nurasyid M,
Pechlivanis S,
Rayner NW,
Scott LJ,
Wiltshire S,
Yengo L,
Kinnunen L,
Rossin EJ,
Raychaudhuri S,
Johnson AD,
Dimas AS,
Loos RJ,
Vedantam S,
Chen H,
Florez JC,
Fox C,
Liu CT,
Rybin D,
Couper DJ,
Kao WH,
Li M,
Cornelis MC,
Kraft P,
Sun Q,
van Dam RM,
Stringham HM,
Chines PS,
Fischer K,
Fontanillas P,
Holmen OL,
Hunt SE,
Jackson AU,
Kong A,
Lawrence R,
Meyer J,
Perry JR,
Platou CG,
Potter S,
Rehnberg E,
Robertson N,
Sivapalaratnam S,
Stančáková A,
Stirrups K,
Thorleifsson G,
Tikkanen E,
Wood AR,
Almgren P,
Atalay M,
Benediktsson R,
Bonnycastle LL,
Burtt N,
Carey J,
Charpentier G,
Crenshaw AT,
Doney AS,
Dorkhan M,
Edkins S,
Emilsson V,
Eury E,
Forsen T,
Gertow K,
Gigante B,
Grant GB,
Groves CJ,
Guiducci C,
Herder C,
Hreidarsson AB,
Hui J,
James A,
Jonsson A,
Rathmann W,
Klopp N,
Kravic J,
Krjutškov K,
Langford C,
Leander K,
Lindholm E,
Lobbens S,
Männistö S,
Mirza G,
Mühleisen TW,
Musk B,
Parkin M,
Rallidis L,
Saramies J,
Sennblad B,
Shah S,
Sigurðsson G,
Silveira A,
Steinbach G,
Thorand B,
Trakalo J,
Veglia F,
Wennauer R,
Winckler W,
Zabaneh D,
Campbell H,
van Duijn C,
Uitterlinden AG,
Hofman A,
Sijbrands E,
Abecasis GR,
Owen KR,
Zeggini E,
Trip MD,
Forouhi NG,
Syvänen AC,
Eriksson JG,
Peltonen L,
Nöthen MM,
Balkau B,
Palmer CN,
Lyssenko V,
Tuomi T,
Isomaa B,
Hunter DJ,
Qi L,
Shuldiner AR,
Roden M,
Barroso I,
Wilsgaard T,
Beilby J,
Hovingh K,
Price JF,
Wilson JF,
Rauramaa R,
Lakka TA,
Lind L,
Dedoussis G,
Njølstad I,
Pedersen NL,
Khaw KT,
Wareham NJ,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Korpi-Hyövälti E,
Saltevo J,
Laakso M,
Kuusisto J,
Metspalu A,
Collins FS,
Mohlke KL,
Bergman RN,
Tuomilehto J,
Boehm BO,
Gieger C,
Hveem K,
Cauchi S,
Froguel P,
Baldassarre D,
Tremoli E,
Humphries SE,
Saleheen D,
Danesh J,
Ingelsson E,
Ripatti S,
Salomaa V,
Erbel R,
Jöckel KH,
Moebus S,
Peters A,
Illig T,
de Faire U,
Hamsten A,
Morris AD,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Boerwinkle E,
Melander O,
Kathiresan S,
Nilsson PM,
Deloukas P,
Thorsteinsdottir U,
Groop LC,
Stefansson K,
Hu F,
Pankow JS,
Dupuis J,
Meigs JB,
Altshuler D,
Boehnke M,
McCarthy MI
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators and 4 more consortia
Nature genetics · 2012 · PMID 22885922 · open access
10 pages
Genome-wide association studies reveal new insights into the genetic basis of IgG4-related disease in the Chinese Han population
Yan S,
Peng Y,
Xu J,
Liu Y,
Li Z,
Yang Y,
Peng L,
Zhou J,
Li L,
Liu C,
Chen H,
Wang M
and 14 more — show all
Wu Z,
Zhang S,
Xu H,
Li H,
Feng F,
Fei Y,
Chen Y,
Dong L,
Li M,
Li Z,
Zhang F,
Zuo X,
Zhang W,
Li Y
Annals of the rheumatic diseases · 2026 · PMID 41298177
10 pages
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan A,
Go MJ,
Zhang W,
Below JE,
Gaulton KJ,
Ferreira T,
Horikoshi M,
Johnson AD,
Ng MC,
Prokopenko I,
Saleheen D,
Wang X
and 322 more — show all
Zeggini E,
Abecasis GR,
Adair LS,
Almgren P,
Atalay M,
Aung T,
Baldassarre D,
Balkau B,
Bao Y,
Barnett AH,
Barroso I,
Basit A,
Been LF,
Beilby J,
Bell GI,
Benediktsson R,
Bergman RN,
Boehm BO,
Boerwinkle E,
Bonnycastle LL,
Burtt N,
Cai Q,
Campbell H,
Carey J,
Cauchi S,
Caulfield M,
Chan JC,
Chang LC,
Chang TJ,
Chang YC,
Charpentier G,
Chen CH,
Chen H,
Chen YT,
Chia KS,
Chidambaram M,
Chines PS,
Cho NH,
Cho YM,
Chuang LM,
Chuang LM,
Collins FS,
Cornelis MC,
Couper DJ,
Crenshaw AT,
van Dam RM,
Danesh J,
Das D,
de Faire U,
Dedoussis G,
Deloukas P,
Dimas AS,
Dina C,
Doney AS,
Donnelly PJ,
Dorkhan M,
van Duijn C,
Dupuis J,
Edkins S,
Elliott P,
Emilsson V,
Erbel R,
Eriksson JG,
Escobedo J,
Esko T,
Eury E,
Florez JC,
Fontanillas P,
Forouhi NG,
Forsen T,
Fox C,
Fraser RM,
Frayling TM,
Froguel P,
Frossard P,
Gao Y,
Gertow K,
Gieger C,
Gigante B,
Grallert H,
Grant GB,
Grrop LC,
Groves CJ,
Grundberg E,
Guiducci C,
Hamsten A,
Han BG,
Hara K,
Hassanali N,
Hattersley AT,
Hayward C,
Hedman AK,
Herder C,
Hofman A,
Holmen OL,
Hovingh K,
Hreidarsson AB,
Hu C,
Hu FB,
Hui J,
Humphries SE,
Hunt SE,
Hunter DJ,
Hveem K,
Hydrie ZI,
Ikegami H,
Illig T,
Ingelsson E,
Islam M,
Isomaa B,
Jackson AU,
Jafar T,
James A,
Jia W,
Jöckel KH,
Jonsson A,
Jowett JB,
Kadowaki T,
Kang HM,
Kanoni S,
Kao WH,
Kathiresan S,
Kato N,
Katulanda P,
Keinanen-Kiukaanniemi KM,
Kelly AM,
Khan H,
Khaw KT,
Khor CC,
Kim HL,
Kim S,
Kim YJ,
Kinnunen L,
Klopp N,
Kong A,
Korpi-Hyövälti E,
Kowlessur S,
Kraft P,
Kravic J,
Kristensen MM,
Krithika S,
Kumar A,
Kumate J,
Kuusisto J,
Kwak SH,
Laakso M,
Lagou V,
Lakka TA,
Langenberg C,
Langford C,
Lawrence R,
Leander K,
Lee JM,
Lee NR,
Li M,
Li X,
Li Y,
Liang J,
Liju S,
Lim WY,
Lind L,
Lindgren CM,
Lindholm E,
Liu CT,
Liu JJ,
Lobbens S,
Long J,
Loos RJ,
Lu W,
Luan J,
Lyssenko V,
Ma RC,
Maeda S,
Mägi R,
Männisto S,
Matthews DR,
Meigs JB,
Melander O,
Metspalu A,
Meyer J,
Mirza G,
Mihailov E,
Moebus S,
Mohan V,
Mohlke KL,
Morris AD,
Mühleisen TW,
Müller-Nurasyid M,
Musk B,
Nakamura J,
Nakashima E,
Navarro P,
Ng PK,
Nica AC,
Nilsson PM,
Njølstad I,
Nöthen MM,
Ohnaka K,
Ong TH,
Owen KR,
Palmer CN,
Pankow JS,
Park KS,
Parkin M,
Pechlivanis S,
Pedersen NL,
Peltonen L,
Perry JR,
Peters A,
Pinidiyapathirage JM,
Platou CG,
Potter S,
Price JF,
Qi L,
Radha V,
Rallidis L,
Rasheed A,
Rathman W,
Rauramaa R,
Raychaudhuri S,
Rayner NW,
Rees SD,
Rehnberg E,
Ripatti S,
Robertson N,
Roden M,
Rossin EJ,
Rudan I,
Rybin D,
Saaristo TE,
Salomaa V,
Saltevo J,
Samuel M,
Sanghera DK,
Saramies J,
Scott J,
Scott LJ,
Scott RA,
Segrè AV,
Sehmi J,
Sennblad B,
Shah N,
Shah S,
Shera AS,
Shu XO,
Shuldiner AR,
Sigurđsson G,
Sijbrands E,
Silveira A,
Sim X,
Sivapalaratnam S,
Small KS,
So WY,
Stančáková A,
Stefansson K,
Steinbach G,
Steinthorsdottir V,
Stirrups K,
Strawbridge RJ,
Stringham HM,
Sun Q,
Suo C,
Syvänen AC,
Takayanagi R,
Takeuchi F,
Tay WT,
Teslovich TM,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tikkanen E,
Trakalo J,
Tremoli E,
Trip MD,
Tsai FJ,
Tuomi T,
Tuomilehto J,
Uitterlinden AG,
Valladares-Salgado A,
Vedantam S,
Veglia F,
Voight BF,
Wang C,
Wareham NJ,
Wennauer R,
Wickremasinghe AR,
Wilsgaard T,
Wilson JF,
Wiltshire S,
Winckler W,
Wong TY,
Wood AR,
Wu JY,
Wu Y,
Yamamoto K,
Yamauchi T,
Yang M,
Yengo L,
Yokota M,
Young R,
Zabaneh D,
Zhang F,
Zhang R,
Zheng W,
Zheng W,
Zimmet PZ,
Altshuler D,
Bowden DW,
Cho YS,
Cox NJ,
Cruz M,
Hanis CL,
Kooner J,
Lee JY,
Seielstad M,
Teo YY,
Boehnke M,
Parra EJ,
Chambers JC,
Tai ES,
McCarthy MI,
Morris AP
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 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
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
and 391 more — show all
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
Prokic I,
Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
Alvarez I,
Álvarez V,
Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
Archetti S,
Pastor AA,
Arosio B,
Athanasiu L,
Bailly H,
Banaj N,
Baquero M,
Barral S,
Beiser A,
Pastor AB,
Below JE,
Benchek P,
Benussi L,
Berr C,
Besse C,
Bessi V,
Binetti G,
Bizarro A,
Blesa R,
Boada M,
Boerwinkle E,
Borroni B,
Boschi S,
Bossù P,
Bråthen G,
Bressler J,
Bresner C,
Brodaty H,
Brookes KJ,
Brusco LI,
Buiza-Rueda D,
Bûrger K,
Burholt V,
Bush WS,
Calero M,
Cantwell LB,
Chene G,
Chung J,
Cuccaro ML,
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