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86 matches for
Li X,
showing the first 20.
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies
Tian J,
Zhang M,
Zhang F,
Gao K,
Lu Z,
Cai Y,
Chen C,
Ning C,
Li Y,
Qian S,
Bai H,
Liu Y
and 10 more — show all
Genome medicine · 2024 · PMID 38872215 · open access
12 pages+
Cross-population GWAS and proteomics improve risk prediction and reveal mechanisms in atrial fibrillation
Yuan S,
Chen J,
Ruan X,
Li Y,
Abramowitz SA,
Wang L,
Jiang F,
Xiong Y,
Levin MG,
Voight BF,
Gill D,
Burgess S
and 5 more — show all
Nature communications · 2025 · PMID 40645996 · open access
12 pages+
Genetic landscape and functional exploration of kidney cancer predisposition in cross-ancestral populations
Dai H,
Chu X,
Du H,
Yang S,
Yao Y,
Yu X,
Zhao Y,
Dong P,
Lyu Z,
Wang W,
Li H,
Mi Z
and 19 more — show all
Sheng C,
Li X,
Zheng H,
Song F,
Song F,
Sun M,
Dai J,
Lan Q,
Rothman N,
Hu Z,
Wei Q,
Ye D,
Yao X,
Jia W,
Chanock SJ,
Shen H,
Purdue MP,
Li MJ,
Chen K
Nature communications · 2026 · PMID 42000752 · open access
12 pages+
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Liu S,
Zheng H,
Gu Y,
Yang Z,
Zhen J,
Wei Y,
Liu Y,
Chen Y,
Wan Z,
Guo X,
Hu L,
Chen X
and 11 more — show all
Li X,
Qiu X,
Huang S,
Chen GB,
Hu Z,
Namba S,
Kanai M,
Matsuda K,
Okada Y,
Zhang Q,
Wei F
Nature genetics · 2026 · PMID 42509370
12 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
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Lu Y,
Vitart V,
Burdon KP,
Khor CC,
Bykhovskaya Y,
Mirshahi A,
Hewitt AW,
Koehn D,
Hysi PG,
Ramdas WD,
Zeller T,
Vithana EN
and 78 more — show all
Cornes BK,
Tay WT,
Tai ES,
Cheng CY,
Liu J,
Foo JN,
Saw SM,
Thorleifsson G,
Stefansson K,
Dimasi DP,
Mills RA,
Mountain J,
Ang W,
Hoehn R,
Verhoeven VJ,
Grus F,
Wolfs R,
Castagne R,
Lackner KJ,
Springelkamp H,
Yang J,
Jonasson F,
Leung DY,
Chen LJ,
Tham CC,
Rudan I,
Vatavuk Z,
Hayward C,
Gibson J,
Cree AJ,
MacLeod A,
Ennis S,
Polasek O,
Campbell H,
Wilson JF,
Viswanathan AC,
Fleck B,
Li X,
Siscovick D,
Taylor KD,
Rotter JI,
Yazar S,
Ulmer M,
Li J,
Yaspan BL,
Ozel AB,
Richards JE,
Moroi SE,
Haines JL,
Kang JH,
Pasquale LR,
Allingham RR,
Ashley-Koch A,
Mitchell P,
Wang JJ,
Wright AF,
Pennell C,
Spector TD,
Young TL,
Klaver CC,
Martin NG,
Montgomery GW,
Anderson MG,
Aung T,
Willoughby CE,
Wiggs JL,
Pang CP,
Thorsteinsdottir U,
Lotery AJ,
Hammond CJ,
van Duijn CM,
Hauser MA,
Rabinowitz YS,
Pfeiffer N,
Mackey DA,
Craig JE,
Macgregor S,
Wong TY
NEIGHBOR Consortium
Nature genetics · 2013 · PMID 23291589
10 pages
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
and 142 more — show all
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
Guo X,
Mazur J,
Huffman JE,
Williams KM,
Polasek O,
Campbell H,
Rudan I,
Vatavuk Z,
Wilson JF,
Joshi PK,
McMahon G,
St Pourcain B,
Evans DM,
Simpson CL,
Schwantes-An TH,
Igo RP,
Mirshahi A,
Cougnard-Gregoire A,
Bellenguez C,
Blettner M,
Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
Beuerman RW,
Siantar R,
Tai ES,
Vithana E,
Mihailov E,
Khor CC,
Hayward C,
Luben RN,
Foster PJ,
Klein BE,
Klein R,
Wong HS,
Mitchell P,
Metspalu A,
Aung T,
Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
Teo YY,
Mackey DA,
Oexle K,
Yoshimura N,
Paterson AD,
Pfeiffer N,
Wong TY,
Baird PN,
Stambolian D,
Wilson JE,
Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
Rahi JS,
Korobelnik JF,
Kemp JP,
Timpson NJ,
Smith GD,
Craig JE,
Burdon KP,
Fogarty RD,
Iyengar SK,
Chew E,
Janmahasatian S,
Martin NG,
MacGregor S,
Xu L,
Schache M,
Nangia V,
Panda-Jonas S,
Wright AF,
Fondran JR,
Lass JH,
Feng S,
Zhao JH,
Khaw KT,
Wareham NJ,
Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
Raffel LJ,
Cotch MF,
Li X,
Yip SP,
Yap MK,
Biino G,
Vaccargiu S,
Fossarello M,
Fleck B,
Yazar S,
Tideman JW,
Tedja M,
Deangelis MM,
Morrison M,
Farrer L,
Zhou X,
Chen W,
Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Chambers JC,
Zhang W,
Sehmi J,
Li X,
Wass MN,
Van der Harst P,
Holm H,
Sanna S,
Kavousi M,
Baumeister SE,
Coin LJ,
Deng G
and 124 more — show all
Gieger C,
Heard-Costa NL,
Hottenga JJ,
Kühnel B,
Kumar V,
Lagou V,
Liang L,
Luan J,
Vidal PM,
Mateo Leach I,
O'Reilly PF,
Peden JF,
Rahmioglu N,
Soininen P,
Speliotes EK,
Yuan X,
Thorleifsson G,
Alizadeh BZ,
Atwood LD,
Borecki IB,
Brown MJ,
Charoen P,
Cucca F,
Das D,
de Geus EJ,
Dixon AL,
Döring A,
Ehret G,
Eyjolfsson GI,
Farrall M,
Forouhi NG,
Friedrich N,
Goessling W,
Gudbjartsson DF,
Harris TB,
Hartikainen AL,
Heath S,
Hirschfield GM,
Hofman A,
Homuth G,
Hyppönen E,
Janssen HL,
Johnson T,
Kangas AJ,
Kema IP,
Kühn JP,
Lai S,
Lathrop M,
Lerch MM,
Li Y,
Liang TJ,
Lin JP,
Loos RJ,
Martin NG,
Moffatt MF,
Montgomery GW,
Munroe PB,
Musunuru K,
Nakamura Y,
O'Donnell CJ,
Olafsson I,
Penninx BW,
Pouta A,
Prins BP,
Prokopenko I,
Puls R,
Ruokonen A,
Savolainen MJ,
Schlessinger D,
Schouten JN,
Seedorf U,
Sen-Chowdhry S,
Siminovitch KA,
Smit JH,
Spector TD,
Tan W,
Teslovich TM,
Tukiainen T,
Uitterlinden AG,
Van der Klauw MM,
Vasan RS,
Wallace C,
Wallaschofski H,
Wichmann HE,
Willemsen G,
Würtz P,
Xu C,
Yerges-Armstrong LM,
Abecasis GR,
Ahmadi KR,
Boomsma DI,
Caulfield M,
Cookson WO,
van Duijn CM,
Froguel P,
Matsuda K,
McCarthy MI,
Meisinger C,
Mooser V,
Pietiläinen KH,
Schumann G,
Snieder H,
Sternberg MJ,
Stolk RP,
Thomas HC,
Thorsteinsdottir U,
Uda M,
Waeber G,
Wareham NJ,
Waterworth DM,
Watkins H,
Whitfield JB,
Witteman JC,
Wolffenbuttel BH,
Fox CS,
Ala-Korpela M,
Stefansson K,
Vollenweider P,
Völzke H,
Schadt EE,
Scott J,
Järvelin MR,
Elliott P,
Kooner JS
Alcohol Genome-wide Association (AlcGen) Consortium · Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study and 5 more consortia
Nature genetics · 2011 · PMID 22001757
9 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
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Vujkovic M,
Ramdas S,
Lorenz KM,
Guo X,
Darlay R,
Cordell HJ,
He J,
Gindin Y,
Chung C,
Myers RP,
Schneider CV,
Park J
and 78 more — show all
Lee KM,
Serper M,
Carr RM,
Kaplan DE,
Haas ME,
MacLean MT,
Witschey WR,
Zhu X,
Tcheandjieu C,
Kember RL,
Kranzler HR,
Verma A,
Giri A,
Klarin DM,
Sun YV,
Huang J,
Huffman JE,
Creasy KT,
Hand NJ,
Liu CT,
Long MT,
Yao J,
Budoff M,
Tan J,
Li X,
Lin HJ,
Chen YI,
Taylor KD,
Chang RK,
Krauss RM,
Vilarinho S,
Brancale J,
Nielsen JB,
Locke AE,
Jones MB,
Verweij N,
Baras A,
Reddy KR,
Neuschwander-Tetri BA,
Schwimmer JB,
Sanyal AJ,
Chalasani N,
Ryan KA,
Mitchell BD,
Gill D,
Wells AD,
Manduchi E,
Saiman Y,
Mahmud N,
Miller DR,
Reaven PD,
Phillips LS,
Muralidhar S,
DuVall SL,
Lee JS,
Assimes TL,
Pyarajan S,
Cho K,
Edwards TL,
Damrauer SM,
Wilson PW,
Gaziano JM,
O'Donnell CJ,
Khera AV,
Grant SFA,
Brown CD,
Tsao PS,
Saleheen D,
Lotta LA,
Bastarache L,
Anstee QM,
Daly AK,
Meigs JB,
Rotter JI,
Lynch JA,
Rader DJ,
Voight BF,
Chang KM
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
Genome-wide association analysis of left ventricular imaging-derived phenotypes identifies 72 risk loci and yields genetic insights into hypertrophic cardiomyopathy
Ning C,
Fan L,
Jin M,
Wang W,
Hu Z,
Cai Y,
Chen L,
Lu Z,
Zhang M,
Chen C,
Li Y,
Zhang F
and 23 more — show all
Wang W,
Liu Y,
Chen S,
Jiang Y,
He C,
Wang Z,
Chen X,
Li H,
Li G,
Ma Q,
Geng H,
Tian W,
Zhang H,
Liu B,
Xia Q,
Yang X,
Liu Z,
Li B,
Zhu Y,
Li X,
Zhang S,
Tian J,
Miao X
Nature communications · 2023 · PMID 38036550 · open access
8 pages
Genome-wide association study identifies 48 common genetic variants associated with handedness
Cuellar-Partida G,
Tung JY,
Eriksson N,
Albrecht E,
Aliev F,
Andreassen OA,
Barroso I,
Beckmann JS,
Boks MP,
Boomsma DI,
Boyd HA,
Breteler MMB
and 106 more — show all
Campbell H,
Chasman DI,
Cherkas LF,
Davies G,
de Geus EJC,
Deary IJ,
Deloukas P,
Dick DM,
Duffy DL,
Eriksson JG,
Esko T,
Feenstra B,
Geller F,
Gieger C,
Giegling I,
Gordon SD,
Han J,
Hansen TF,
Hartmann AM,
Hayward C,
Heikkilä K,
Hicks AA,
Hirschhorn JN,
Hottenga JJ,
Huffman JE,
Hwang LD,
Ikram MA,
Kaprio J,
Kemp JP,
Khaw KT,
Klopp N,
Konte B,
Kutalik Z,
Lahti J,
Li X,
Loos RJF,
Luciano M,
Magnusson SH,
Mangino M,
Marques-Vidal P,
Martin NG,
McArdle WL,
McCarthy MI,
Medina-Gomez C,
Melbye M,
Melville SA,
Metspalu A,
Milani L,
Mooser V,
Nelis M,
Nyholt DR,
O'Connell KS,
Ophoff RA,
Palmer C,
Palotie A,
Palviainen T,
Pare G,
Paternoster L,
Peltonen L,
Penninx BWJH,
Polasek O,
Pramstaller PP,
Prokopenko I,
Raikkonen K,
Ripatti S,
Rivadeneira F,
Rudan I,
Rujescu D,
Smit JH,
Smith GD,
Smoller JW,
Soranzo N,
Spector TD,
Pourcain BS,
Starr JM,
Stefánsson H,
Steinberg S,
Teder-Laving M,
Thorleifsson G,
Stefánsson K,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
van Rooij FJA,
Vink JM,
Vollenweider P,
Vuoksimaa E,
Waeber G,
Wareham NJ,
Warrington N,
Waterworth D,
Werge T,
Wichmann HE,
Widen E,
Willemsen G,
Wright AF,
Wright MJ,
Xu M,
Zhao JH,
Kraft P,
Hinds DA,
Lindgren CM,
Mägi R,
Neale BM,
Evans DM,
Medland SE
Nature human behaviour · 2021 · PMID 32989287
7 pages
Genome-wide association meta-analysis identifies 29 new acne susceptibility loci
Mitchell BL,
Saklatvala JR,
Dand N,
Hagenbeek FA,
Li X,
Min JL,
Thomas L,
Bartels M,
Jan Hottenga J,
Lupton MK,
Boomsma DI,
Dong X
and 8 more — show all
Nature communications · 2022 · PMID 35132056 · open access
7 pages
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
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5 pages
Questions about this list
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