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23 matches for
Hu C,
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+
Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe JR,
Bien SA,
Harrison TA,
Kang HM,
Chen S,
Schmit SL,
Conti DV,
Qu C,
Jeon J,
Edlund CK,
Greenside P,
Wainberg M
and 188 more — show all
Schumacher FR,
Smith JD,
Levine DM,
Nelson SC,
Sinnott-Armstrong NA,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Bamia C,
Banbury BL,
Baron JA,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chirlaque MD,
Cho SH,
Connolly CM,
Cross AJ,
Cuk K,
Curtis KR,
de la Chapelle A,
Doheny KF,
Duggan D,
Easton DF,
Elias SG,
Elliott F,
English DR,
Feskens EJM,
Figueiredo JC,
Fischer R,
FitzGerald LM,
Forman D,
Gala M,
Gallinger S,
Gauderman WJ,
Giles GG,
Gillanders E,
Gong J,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hampel H,
Harlid S,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Hunter DJ,
Ibañez-Sanz G,
Idos GE,
Ingersoll R,
Jackson RD,
Jacobs EJ,
Jenkins MA,
Joshi AD,
Joshu CE,
Keku TO,
Key TJ,
Kim HR,
Kobayashi E,
Kolonel LN,
Kooperberg C,
Kühn T,
Küry S,
Kweon SS,
Larsson SC,
Laurie CA,
Le Marchand L,
Leal SM,
Lee SC,
Lejbkowicz F,
Lemire M,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindblom A,
Lindor NM,
Ling H,
Louie TL,
Männistö S,
Markowitz SD,
Martín V,
Masala G,
McNeil CE,
Melas M,
Milne RL,
Moreno L,
Murphy N,
Myte R,
Naccarati A,
Newcomb PA,
Offit K,
Ogino S,
Onland-Moret NC,
Pardini B,
Parfrey PS,
Pearlman R,
Perduca V,
Pharoah PDP,
Pinchev M,
Platz EA,
Prentice RL,
Pugh E,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Rodríguez-Barranco M,
Romm J,
Sakoda LC,
Schafmayer C,
Schoen RE,
Seminara D,
Shah M,
Shelford T,
Shin MH,
Shulman K,
Sieri S,
Slattery ML,
Southey MC,
Stadler ZK,
Stegmaier C,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Thomas SS,
Toland AE,
Trichopoulou A,
Ulrich CM,
Van Den Berg DJ,
van Duijnhoven FJB,
Van Guelpen B,
van Kranen H,
Vijai J,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Win AK,
Wolf CR,
Wolk A,
Woods MO,
Wu AH,
Zaidi SH,
Zanke BW,
Zhang Q,
Zheng W,
Zheng W,
Scacheri PC,
Potter JD,
Bassik MC,
Kundaje A,
Casey G,
Moreno V,
Abecasis GR,
Nickerson DA,
Gruber SB,
Hsu L,
Peters U
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders
Yao X,
Glessner JT,
Li J,
Qi X,
Hou X,
Zhu C,
Li X,
March ME,
Yang L,
Mentch FD,
Hain HS,
Meng X
and 3 more — show all
Translational psychiatry · 2021 · PMID 33479212 · open access
12 pages+
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
Budu-Aggrey A,
Kilanowski A,
Sobczyk MK,
Shringarpure SS,
Mitchell R,
Reis K,
Reigo A,
Mägi R,
Nelis M,
Tanaka N,
Brumpton BM,
Thomas LF
and 120 more — show all
Sole-Navais P,
Flatley C,
Espuela-Ortiz A,
Herrera-Luis E,
Lominchar JVT,
Bork-Jensen J,
Marenholz I,
Arnau-Soler A,
Jeong A,
Fawcett KA,
Baurecht H,
Rodriguez E,
Alves AC,
Kumar A,
Sleiman PM,
Chang X,
Medina-Gomez C,
Hu C,
Xu CJ,
Qi C,
El-Heis S,
Titcombe P,
Antoun E,
Fadista J,
Wang CA,
Thiering E,
Wu B,
Kress S,
Kothalawala DM,
Kadalayil L,
Duan J,
Zhang H,
Hadebe S,
Hoffmann T,
Jorgenson E,
Choquet H,
Risch N,
Njølstad P,
Andreassen OA,
Johansson S,
Almqvist C,
Gong T,
Ullemar V,
Karlsson R,
Magnusson PKE,
Szwajda A,
Burchard EG,
Thyssen JP,
Hansen T,
Kårhus LL,
Dantoft TM,
Jeanrenaud ACSN,
Ghauri A,
Arnold A,
Homuth G,
Lau S,
Nöthen MM,
Hübner N,
Imboden M,
Visconti A,
Falchi M,
Bataille V,
Hysi P,
Ballardini N,
Boomsma DI,
Hottenga JJ,
Müller-Nurasyid M,
Ahluwalia TS,
Stokholm J,
Chawes B,
Schoos AM,
Esplugues A,
Bustamante M,
Raby B,
Arshad S,
German C,
Esko T,
Milani LA,
Metspalu A,
Terao C,
Abuabara K,
Løset M,
Hveem K,
Jacobsson B,
Pino-Yanes M,
Strachan DP,
Grarup N,
Linneberg A,
Lee YA,
Probst-Hensch N,
Weidinger S,
Jarvelin MR,
Melén E,
Hakonarson H,
Irvine AD,
Jarvis D,
Nijsten T,
Duijts L,
Vonk JM,
Koppelmann GH,
Godfrey KM,
Barton SJ,
Feenstra B,
Pennell CE,
Sly PD,
Holt PG,
Williams LK,
Bisgaard H,
Bønnelykke K,
Curtin J,
Simpson A,
Murray C,
Schikowski T,
Bunyavanich S,
Weiss ST,
Holloway JW,
Min JL,
Brown SJ,
Standl M,
Paternoster L
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · 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+
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
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Evangelou E,
Gao H,
Chu C,
Ntritsos G,
Ntritsos G,
Blakeley P,
Butts AR,
Pazoki R,
Suzuki H,
Koskeridis F,
Yiorkas AM,
Karaman I
and 88 more — show all
Elliott J,
Luo Q,
Aeschbacher S,
Bartz TM,
Baumeister SE,
Braund PS,
Brown MR,
Brody JA,
Clarke TK,
Dimou N,
Faul JD,
Homuth G,
Jackson AU,
Kentistou KA,
Joshi PK,
Lemaitre RN,
Lind PA,
Lyytikäinen LP,
Mangino M,
Milaneschi Y,
Nelson CP,
Nolte IM,
Perälä MM,
Polasek O,
Porteous D,
Ratliff SM,
Smith JA,
Stančáková A,
Teumer A,
Tuominen S,
Thériault S,
Vangipurapu J,
Whitfield JB,
Wood A,
Yao J,
Yu B,
Zhao W,
Zhao W,
Arking DE,
Auvinen J,
Liu C,
Männikkö M,
Risch L,
Rotter JI,
Snieder H,
Veijola J,
Blakemore AI,
Boehnke M,
Campbell H,
Conen D,
Eriksson JG,
Grabe HJ,
Guo X,
van der Harst P,
Hartman CA,
Hayward C,
Heath AC,
Jarvelin MR,
Kähönen M,
Kardia SLR,
Kühne M,
Kuusisto J,
Laakso M,
Lahti J,
Lehtimäki T,
McIntosh AM,
Mohlke KL,
Morrison AC,
Martin NG,
Oldehinkel AJ,
Penninx BWJH,
Psaty BM,
Raitakari OT,
Rudan I,
Samani NJ,
Scott LJ,
Spector TD,
Verweij N,
Weir DR,
Wilson JF,
Levy D,
Tzoulaki I,
Bell JD,
Matthews PM,
Rothenfluh A,
Desrivières S,
Schumann G,
Elliott P
Nature human behaviour · 2019 · PMID 31358974
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,
Carracedo Á,
Cecchetti R,
Cervera-Carles L,
Charbonnier C,
Chen HH,
Chillotti C,
Ciccone S,
Claassen JAHR,
Clark C,
Conti E,
Corma-Gómez A,
Costantini E,
Custodero C,
Daian D,
Dalmasso MC,
Daniele A,
Dardiotis E,
Dartigues JF,
de Deyn PP,
de Paiva Lopes K,
de Witte LD,
Debette S,
Deckert J,
Del Ser T,
Denning N,
DeStefano A,
Dichgans M,
Diehl-Schmid J,
Diez-Fairen M,
Rossi PD,
Djurovic S,
Duron E,
Düzel E,
Dufouil C,
Eiriksdottir G,
Engelborghs S,
Escott-Price V,
Espinosa A,
Ewers M,
Faber KM,
Fabrizio T,
Nielsen SF,
Fardo DW,
Farotti L,
Fenoglio C,
Fernández-Fuertes M,
Ferrari R,
Ferreira CB,
Ferri E,
Fin B,
Fischer P,
Fladby T,
Fließbach K,
Fongang B,
Fornage M,
Fortea J,
Foroud TM,
Fostinelli S,
Fox NC,
Franco-Macías E,
Bullido MJ,
Frank-García A,
Froelich L,
Fulton-Howard B,
Galimberti D,
García-Alberca JM,
García-González P,
Garcia-Madrona S,
Garcia-Ribas G,
Ghidoni R,
Giegling I,
Giorgio G,
Goate AM,
Goldhardt O,
Gomez-Fonseca D,
González-Pérez A,
Graff C,
Grande G,
Green E,
Grimmer T,
Grünblatt E,
Grunin M,
Gudnason V,
Guetta-Baranes T,
Haapasalo A,
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Nature genetics · 2010 · PMID 20526339
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Nature communications · 2015 · PMID 26151496 · open access
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Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
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Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
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