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Zhang R,
showing the first 20.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Spracklen CN,
Chen P,
Kim YJ,
Wang X,
Cai H,
Li S,
Long J,
Wu Y,
Wang YX,
Takeuchi F,
Wu JY,
Jung KJ
and 103 more — show all
Hu C,
Akiyama K,
Zhang Y,
Moon S,
Johnson TA,
Li H,
Dorajoo R,
He M,
Cannon ME,
Roman TS,
Salfati E,
Lin KH,
Guo X,
Sheu WHH,
Absher D,
Adair LS,
Assimes TL,
Aung T,
Cai Q,
Chang LC,
Chen CH,
Chien LH,
Chuang LM,
Chuang SC,
Du S,
Fan Q,
Fann CSJ,
Feranil AB,
Friedlander Y,
Gordon-Larsen P,
Gu D,
Gui L,
Guo Z,
Heng CK,
Hixson J,
Hou X,
Hsiung CA,
Hu Y,
Hwang MY,
Hwu CM,
Isono M,
Juang JJ,
Khor CC,
Kim YK,
Koh WP,
Kubo M,
Lee IT,
Lee SJ,
Lee WJ,
Liang KW,
Lim B,
Lim SH,
Liu J,
Nabika T,
Pan WH,
Peng H,
Quertermous T,
Sabanayagam C,
Sandow K,
Shi J,
Sun L,
Tan PC,
Tan SP,
Taylor KD,
Teo YY,
Toh SA,
Tsunoda T,
van Dam RM,
Wang A,
Wang F,
Wang J,
Wei WB,
Xiang YB,
Yao J,
Yuan JM,
Zhang R,
Zhao W,
Chen YI,
Rich SS,
Rotter JI,
Wang TD,
Wu T,
Lin X,
Han BG,
Tanaka T,
Cho YS,
Katsuya T,
Jia W,
Jee SH,
Chen YT,
Kato N,
Jonas JB,
Cheng CY,
Shu XO,
He J,
Zheng W,
Zheng W,
Wong TY,
Huang W,
Kim BJ,
Tai ES,
Mohlke KL,
Sim X
Human molecular genetics · 2017 · PMID 28334899
12 pages+
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
McKay JD,
Hung RJ,
Han Y,
Zong X,
Carreras-Torres R,
Christiani DC,
Caporaso NE,
Johansson M,
Xiao X,
Li Y,
Byun J,
Dunning A
and 128 more — show all
Pooley KA,
Qian DC,
Ji X,
Liu G,
Timofeeva MN,
Bojesen SE,
Wu X,
Le Marchand L,
Albanes D,
Bickeböller H,
Aldrich MC,
Bush WS,
Tardon A,
Rennert G,
Teare MD,
Field JK,
Kiemeney LA,
Lazarus P,
Haugen A,
Lam S,
Schabath MB,
Andrew AS,
Shen H,
Hong YC,
Yuan JM,
Bertazzi PA,
Pesatori AC,
Ye Y,
Diao N,
Su L,
Zhang R,
Brhane Y,
Leighl N,
Johansen JS,
Mellemgaard A,
Saliba W,
Haiman CA,
Wilkens LR,
Fernandez-Somoano A,
Fernandez-Tardon G,
van der Heijden HFM,
Kim JH,
Dai J,
Hu Z,
Davies MPA,
Marcus MW,
Brunnström H,
Manjer J,
Melander O,
Muller DC,
Overvad K,
Trichopoulou A,
Tumino R,
Doherty JA,
Barnett MP,
Chen C,
Goodman GE,
Cox A,
Taylor F,
Woll P,
Brüske I,
Wichmann HE,
Manz J,
Muley TR,
Risch A,
Rosenberger A,
Grankvist K,
Johansson M,
Shepherd FA,
Tsao MS,
Arnold SM,
Haura EB,
Bolca C,
Holcatova I,
Janout V,
Kontic M,
Lissowska J,
Mukeria A,
Ognjanovic S,
Orlowski TM,
Scelo G,
Swiatkowska B,
Zaridze D,
Bakke P,
Skaug V,
Zienolddiny S,
Duell EJ,
Butler LM,
Koh WP,
Gao YT,
Houlston RS,
McLaughlin J,
Stevens VL,
Joubert P,
Lamontagne M,
Nickle DC,
Obeidat M,
Timens W,
Zhu B,
Song L,
Kachuri L,
Artigas MS,
Tobin MD,
Wain LV,
Rafnar T,
Thorgeirsson TE,
Reginsson GW,
Stefansson K,
Hancock DB,
Bierut LJ,
Spitz MR,
Gaddis NC,
Lutz SM,
Gu F,
Johnson EO,
Kamal A,
Pikielny C,
Zhu D,
Lindströem S,
Jiang X,
Tyndale RF,
Chenevix-Trench G,
Beesley J,
Bossé Y,
Chanock S,
Brennan P,
Landi MT,
Amos CI
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 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
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Imamura M,
Takahashi A,
Yamauchi T,
Hara K,
Yasuda K,
Grarup N,
Zhao W,
Wang X,
Huerta-Chagoya A,
Hu C,
Moon S,
Long J
and 52 more — show all
Kwak SH,
Rasheed A,
Saxena R,
Ma RC,
Okada Y,
Iwata M,
Hosoe J,
Shojima N,
Iwasaki M,
Fujita H,
Suzuki K,
Danesh J,
Jørgensen T,
Jørgensen ME,
Witte DR,
Brandslund I,
Christensen C,
Hansen T,
Mercader JM,
Flannick J,
Moreno-Macías H,
Burtt NP,
Zhang R,
Kim YJ,
Zheng W,
Zheng W,
Singh JR,
Tam CH,
Hirose H,
Maegawa H,
Ito C,
Kaku K,
Watada H,
Tanaka Y,
Tobe K,
Kawamori R,
Kubo M,
Cho YS,
Chan JC,
Sanghera D,
Frossard P,
Park KS,
Shu XO,
Kim BJ,
Florez JC,
Tusié-Luna T,
Jia W,
Tai ES,
Pedersen O,
Saleheen D,
Maeda S,
Kadowaki T
Nature communications · 2016 · PMID 26818947 · open access
6 pages
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits
Kim YJ,
Go MJ,
Hu C,
Hong CB,
Kim YK,
Lee JY,
Hwang JY,
Oh JH,
Kim DJ,
Kim NH,
Kim S,
Hong EJ
and 21 more — show all
Kim JH,
Min H,
Kim Y,
Zhang R,
Jia W,
Okada Y,
Takahashi A,
Kubo M,
Tanaka T,
Kamatani N,
Matsuda K,
Park T,
Oh B,
Kimm K,
Kang D,
Shin C,
Cho NH,
Kim HL,
Han BG,
Lee JY,
Cho YS
MAGIC consortium
Nature genetics · 2011 · PMID 21909109
3 pages
A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans
Li H,
Gan W,
Lu L,
Dong X,
Han X,
Hu C,
Yang Z,
Sun L,
Bao W,
Li P,
He M,
Sun L
and 26 more — show all
Wang Y,
Zhu J,
Ning Q,
Tang Y,
Zhang R,
Wen J,
Wang D,
Zhu X,
Guo K,
Zuo X,
Guo X,
Yang H,
Zhou X,
Zhang X,
Qi L,
Loos RJ,
Hu FB,
Wu T,
Liu Y,
Liu L,
Yang Z,
Hu R,
Jia W,
Ji L,
Li Y,
Lin X
DIAGRAM Consortium · AGEN-T2D Consortium
Diabetes · 2013 · PMID 22961080 · open access
3 pages
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease
Tang CS,
Gui H,
Kapoor A,
Kim JH,
Luzón-Toro B,
Pelet A,
Burzynski G,
Lantieri F,
So MT,
Berrios C,
Shin HD,
Fernández RM
and 20 more — show all
Le TL,
Verheij JB,
Matera I,
Cherny SS,
Nandakumar P,
Cheong HS,
Antiñolo G,
Amiel J,
Seo JM,
Kim DY,
Oh JT,
Lyonnet S,
Borrego S,
Ceccherini I,
Hofstra RM,
Chakravarti A,
Kim HY,
Sham PC,
Tam PK,
Garcia-Barceló MM
Human molecular genetics · 2016 · PMID 27702942
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
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
Jin G,
Ma H,
Wu C,
Dai J,
Zhang R,
Shi Y,
Lu J,
Miao X,
Wang M,
Zhou Y,
Chen J,
Li H
and 21 more — show all
Pan S,
Chu M,
Lu F,
Yu D,
Jiang Y,
Dong J,
Hu L,
Chen Y,
Xu L,
Shu Y,
Pan S,
Tan W,
Zhou B,
Lu D,
Wu T,
Zhang Z,
Chen F,
Wang X,
Hu Z,
Lin D,
Shen H
American journal of human genetics · 2012 · PMID 23103227
2 pages
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
Dong J,
Jin G,
Wu C,
Guo H,
Zhou B,
Lv J,
Lu D,
Shi Y,
Shu Y,
Xu L,
Chu M,
Wang C
and 37 more — show all
Zhang R,
Dai J,
Jiang Y,
Yu D,
Ma H,
Zhao X,
Yin Z,
Yang L,
Li Z,
Deng Q,
Cao S,
Qin Z,
Gong J,
Sun C,
Wang J,
Wu W,
Zhou G,
Chen H,
Guan P,
Chen Y,
Liu X,
Liu L,
Xu P,
Han B,
Bai C,
Zhao Y,
Zhang H,
Yan Y,
Liu J,
Amos CI,
Chen F,
Tan W,
Jin L,
Wu T,
Hu Z,
Lin D,
Shen H
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
Exome-Wide Association Analysis Suggests LRP2BP as a Susceptibility Gene for Endothelial Injury in Systemic Sclerosis in the Han Chinese Population
Pu W,
Wu W,
Liu Q,
Ma Y,
Tu W,
Zuo X,
Guo G,
Jiang S,
Zhao Y,
Zuo X,
Wang Q,
Yang L
and 32 more — show all
Xiao R,
Chu H,
Wang L,
Sun L,
Cui J,
Yu L,
Li H,
Li Y,
Shi Y,
Zhang J,
Zhang H,
Liang M,
Chen D,
Ding Y,
Chen X,
Chen Y,
Zhang R,
Zhao H,
Li Y,
Qi Q,
Bai P,
Zhao L,
Reveille JD,
Mayes MD,
Jin L,
Lee EB,
Zhang X,
Xu J,
Zhang Z,
Zhou X,
Zou H,
Wang J
The Journal of investigative dermatology · 2021 · PMID 33069728
2 pages
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Yu HP,
Xiang BD,
Qian J,
Liu H,
Li YF,
Lin Q,
Liu S,
Wei J,
Zhan S,
Jiang B,
Dai J,
Ma L
and 20 more — show all
Zhang L,
Liu Y,
Wen Q,
Gong W,
Li S,
Jiang Y,
Zheng J,
Zhu T,
Zhou Z,
Zeng X,
Wang Z,
Wang JA,
Guo R,
Yang Y,
Wei Q,
Zhou G,
Qiu XQ,
Tang W,
Wang M,
Zhang R
Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147
2 pages
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Lee S,
Miller CL,
Bentley AR,
Brown MR,
Nagarajan P,
Noordam R,
Morrison JL,
Schwander K,
Westerman K,
Kho M,
Kraja AT,
de Vries PS
and 137 more — show all
Ammous F,
Aschard H,
Bartz TM,
Do A,
Dupont CT,
Feitosa MF,
Gudmundsdottir V,
Guo X,
Harris SE,
Hikino K,
Huang Z,
Lefevre C,
Lyytikäinen LP,
Milaneschi Y,
Nardone GG,
Santin A,
Schmidt H,
Shen B,
Sofer T,
Sun Q,
Tan YA,
Tang J,
Thériault S,
van der Most PJ,
Ware EB,
Weiss S,
Xing WY,
Yu C,
Zhao W,
Ansari MAY,
Anugu P,
Attia JR,
Bazzano LA,
Bis JC,
Breyer M,
Cade B,
Chen G,
Collins S,
Corley J,
Davies G,
Dörr M,
Du J,
Edwards TL,
Faquih T,
Faul JD,
Fohner AE,
Fretts AM,
Gangireddy S,
Gepner A,
Graff M,
Hofer E,
Homuth G,
Hood MM,
Jie X,
Kähönen M,
Kardia SLR,
Karvonen-Gutierrez CA,
Launer LJ,
Levy D,
Maheshwari M,
Martin LW,
Matsuda K,
McNeil JJ,
Nolte IM,
Okochi T,
Raffield LM,
Raitakari OT,
Risch L,
Risch M,
Roux AD,
Ruiz-Narvaez EA,
Russ TC,
Saito T,
Schreiner PJ,
Scott RJ,
Shikany J,
Smith JA,
Snieder H,
Spedicati B,
Tai ES,
Taylor AM,
Taylor KD,
Tesolin P,
van Dam RM,
Wang R,
Wenbin W,
Xie T,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Concas MP,
Conen D,
Cox SR,
Evans MK,
Fox ER,
de Las Fuentes L,
Giri A,
Girotto G,
Grabe HJ,
Gu C,
Gudnason V,
Harlow SD,
Holliday E,
Jost JB,
Lacaze P,
Lee S,
Lehtimäki T,
Li C,
Liu CT,
Morrison AC,
North KE,
Penninx BWJH,
Peyser PA,
Province MM,
Psaty BM,
Redline S,
Rosendaal FR,
Rotimi CN,
Rotter JI,
Schmidt R,
Sim X,
Terao C,
Weir DR,
Zhu X,
Franceschini N,
O'Connell JR,
Jaquish CE,
Wang H,
Manning A,
Munroe PB,
Rao DC,
Chen H,
Gauderman WJ,
Bierut LJ,
Winkler TW,
Fornage M
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
2 pages
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Cho YS,
Chen CH,
Hu C,
Long J,
Ong RT,
Sim X,
Takeuchi F,
Wu Y,
Go MJ,
Yamauchi T,
Chang YC,
Kwak SH
and 56 more — show all
Ma RC,
Yamamoto K,
Adair LS,
Aung T,
Cai Q,
Chang LC,
Chen YT,
Gao Y,
Hu FB,
Kim HL,
Kim S,
Kim YJ,
Lee JJ,
Lee NR,
Li Y,
Liu JJ,
Lu W,
Nakamura J,
Nakashima E,
Ng DP,
Tay WT,
Tsai FJ,
Wong TY,
Yokota M,
Zheng W,
Zheng W,
Zhang R,
Wang C,
So WY,
Ohnaka K,
Ikegami H,
Hara K,
Cho YM,
Cho NH,
Chang TJ,
Bao Y,
Hedman ÅK,
Morris AP,
McCarthy MI,
Takayanagi R,
Park KS,
Jia W,
Chuang LM,
Chuang LM,
Chan JC,
Maeda S,
Kadowaki T,
Lee JY,
Wu JY,
Teo YY,
Tai ES,
Shu XO,
Mohlke KL,
Kato N,
Han BG,
Seielstad M
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese
Chu M,
Ji X,
Chen W,
Zhang R,
Sun C,
Wang T,
Luo C,
Gong J,
Zhu M,
Fan J,
Hou Z,
Dai J
and 6 more — show all
Human molecular genetics · 2014 · PMID 24986923
1 page
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
Zhao SX,
Liu W,
Liang J,
Gao GQ,
Zhang XM,
Yao Y,
Wang HN,
Yuan FF,
Xue LQ,
Ma YR,
Zhang LL,
Ye XP
and 25 more — show all
Zhang QY,
Sun F,
Zhang RJ,
Yang SY,
Zhan M,
Du WH,
Liu BL,
Chen X,
Song ZY,
Li XS,
Li P,
Ru Y,
Zuo CL,
Li SX,
Han B,
Zhu H,
Qiao J,
Xuan M,
Su B,
Sun F,
Ma JH,
Chen JL,
Tian HM,
Chen SJ,
Song HD
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
1 page
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Yan C,
Zhu M,
Ding Y,
Yang M,
Wang M,
Li G,
Ren C,
Huang T,
Yang W,
He B,
Wang M,
Yu F
and 22 more — show all
Wang J,
Zhang R,
Wang T,
Ni J,
Chen J,
Jiang Y,
Dai J,
Zhang E,
Ma H,
Wang Y,
Xu D,
Wang S,
Chen Y,
Xu Z,
Zhou J,
Ji G,
Wang Z,
Zhang Z,
Hu Z,
Wei Q,
Shen H,
Jin G
Gut · 2020 · PMID 31383772
1 page
Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study
Jin G,
Lv J,
Yang M,
Wang M,
Zhu M,
Wang T,
Yan C,
Yu C,
Ding Y,
Li G,
Ren C,
Ni J
and 22 more — show all
Zhang R,
Guo Y,
Bian Z,
Zheng Y,
Zhang N,
Jiang Y,
Chen J,
Wang Y,
Xu D,
Zheng H,
Yang L,
Chen Y,
Walters R,
Millwood IY,
Dai J,
Ma H,
Chen K,
Chen Z,
Hu Z,
Wei Q,
Shen H,
Li L
The Lancet. Oncology · 2020 · PMID 33002439
1 page
African ancestry GWAS of dementia in a large military cohort identifies significant risk loci
Sherva R,
Zhang R,
Sahelijo N,
Jun G,
Anglin T,
Chanfreau C,
Cho K,
Fonda JR,
Gaziano JM,
Harrington KM,
Ho YL,
Kremen WS
and 16 more — show all
Litkowski E,
Lynch J,
Neale Z,
Roussos P,
Marra D,
Mez J,
Miller MW,
Salat DH,
Tsuang D,
Wolf E,
Zeng Q,
Panizzon MS,
Merritt VC,
Farrer LA,
Hauger RL,
Logue MW
Molecular psychiatry · 2023 · PMID 36543923
1 page
A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children
Lin YP,
Shi Y,
Zhang R,
Xue X,
Rao S,
Yin L,
Lui KFH,
Pan DJ,
Maurer U,
Choy KW,
Paracchini S,
McBride C
and 1 more — show all
NPJ science of learning · 2024 · PMID 38538593 · open access
1 page
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