연구자에게
내 논문이 여기 있나요?
논문 2,665편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Chen W에 대해
60건, 그중 20건 표시.
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
Onengut-Gumuscu S,
Chen WM,
Burren O,
Cooper NJ,
Quinlan AR,
Mychaleckyj JC,
Farber E,
Bonnie JK,
Szpak M,
Schofield E,
Achuthan P,
Guo H
외 14명 — 모두 보기
Fortune MD,
Stevens H,
Walker NM,
Ward LD,
Kundaje A,
Kellis M,
Daly MJ,
Barrett JC,
Cooper JD,
Deloukas P,
Todd JA,
Wallace C,
Concannon P,
Rich SS
Type 1 Diabetes Genetics Consortium
Nature genetics · 2015 · PMID 25751624 · open access
페이지 12개+
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Pattaro C,
Teumer A,
Gorski M,
Chu AY,
Li M,
Mijatovic V,
Garnaas M,
Tin A,
Sorice R,
Li Y,
Taliun D,
Olden M
외 240명 — 모두 보기
Foster M,
Yang Q,
Chen MH,
Pers TH,
Johnson AD,
Ko YA,
Fuchsberger C,
Tayo B,
Nalls M,
Feitosa MF,
Isaacs A,
Dehghan A,
d'Adamo P,
Adeyemo A,
Dieffenbach AK,
Zonderman AB,
Nolte IM,
van der Most PJ,
Wright AF,
Shuldiner AR,
Morrison AC,
Hofman A,
Smith AV,
Dreisbach AW,
Franke A,
Uitterlinden AG,
Metspalu A,
Tonjes A,
Lupo A,
Robino A,
Johansson Å,
Demirkan A,
Kollerits B,
Freedman BI,
Ponte B,
Oostra BA,
Paulweber B,
Krämer BK,
Mitchell BD,
Buckley BM,
Peralta CA,
Hayward C,
Helmer C,
Rotimi CN,
Shaffer CM,
Müller C,
Sala C,
van Duijn CM,
Saint-Pierre A,
Ackermann D,
Shriner D,
Ruggiero D,
Toniolo D,
Lu Y,
Cusi D,
Czamara D,
Ellinghaus D,
Siscovick DS,
Ruderfer D,
Gieger C,
Grallert H,
Rochtchina E,
Atkinson EJ,
Holliday EG,
Boerwinkle E,
Salvi E,
Bottinger EP,
Murgia F,
Rivadeneira F,
Ernst F,
Kronenberg F,
Hu FB,
Navis GJ,
Curhan GC,
Ehret GB,
Homuth G,
Coassin S,
Thun GA,
Pistis G,
Gambaro G,
Malerba G,
Montgomery GW,
Eiriksdottir G,
Jacobs G,
Li G,
Wichmann HE,
Campbell H,
Schmidt H,
Wallaschofski H,
Völzke H,
Brenner H,
Kroemer HK,
Kramer H,
Lin H,
Leach IM,
Ford I,
Guessous I,
Rudan I,
Prokopenko I,
Borecki I,
Heid IM,
Kolcic I,
Persico I,
Jukema JW,
Wilson JF,
Felix JF,
Divers J,
Lambert JC,
Stafford JM,
Gaspoz JM,
Smith JA,
Faul JD,
Wang JJ,
Ding J,
Hirschhorn JN,
Attia J,
Whitfield JB,
Chalmers J,
Viikari J,
Coresh J,
Denny JC,
Karjalainen J,
Fernandes JK,
Endlich K,
Butterbach K,
Keene KL,
Lohman K,
Portas L,
Launer LJ,
Lyytikäinen LP,
Yengo L,
Franke L,
Ferrucci L,
Rose LM,
Kedenko L,
Rao M,
Struchalin M,
Kleber ME,
Cavalieri M,
Haun M,
Cornelis MC,
Ciullo M,
Pirastu M,
de Andrade M,
McEvoy MA,
Woodward M,
Adam M,
Cocca M,
Nauck M,
Imboden M,
Waldenberger M,
Pruijm M,
Metzger M,
Stumvoll M,
Evans MK,
Sale MM,
Kähönen M,
Boban M,
Bochud M,
Rheinberger M,
Verweij N,
Bouatia-Naji N,
Martin NG,
Hastie N,
Probst-Hensch N,
Soranzo N,
Devuyst O,
Raitakari O,
Gottesman O,
Franco OH,
Polasek O,
Gasparini P,
Munroe PB,
Ridker PM,
Mitchell P,
Muntner P,
Meisinger C,
Smit JH,
Kovacs P,
Wild PS,
Froguel P,
Rettig R,
Mägi R,
Biffar R,
Schmidt R,
Middelberg RP,
Carroll RJ,
Penninx BW,
Scott RJ,
Katz R,
Sedaghat S,
Wild SH,
Kardia SL,
Ulivi S,
Hwang SJ,
Enroth S,
Kloiber S,
Trompet S,
Stengel B,
Hancock SJ,
Turner ST,
Rosas SE,
Stracke S,
Harris TB,
Zeller T,
Zemunik T,
Lehtimäki T,
Illig T,
Aspelund T,
Nikopensius T,
Esko T,
Tanaka T,
Gyllensten U,
Völker U,
Emilsson V,
Vitart V,
Aalto V,
Gudnason V,
Chouraki V,
Chen WM,
Igl W,
März W,
Koenig W,
Lieb W,
Loos RJ,
Liu Y,
Snieder H,
Pramstaller PP,
Parsa A,
O'Connell JR,
Susztak K,
Hamet P,
Tremblay J,
de Boer IH,
Böger CA,
Goessling W,
Chasman DI,
Köttgen A,
Kao WH,
Fox CS
ICBP Consortium · AGEN Consortium 외 컨소시엄 3곳
Nature communications · 2016 · PMID 26831199 · open access
페이지 12개+
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
Ligthart S,
Vaez A,
Võsa U,
Stathopoulou MG,
de Vries PS,
Prins BP,
Van der Most PJ,
Tanaka T,
Naderi E,
Rose LM,
Wu Y,
Karlsson R
외 274명 — 모두 보기
Barbalic M,
Lin H,
Pool R,
Zhu G,
Macé A,
Sidore C,
Trompet S,
Mangino M,
Sabater-Lleal M,
Kemp JP,
Abbasi A,
Kacprowski T,
Verweij N,
Smith AV,
Huang T,
Marzi C,
Feitosa MF,
Lohman KK,
Kleber ME,
Milaneschi Y,
Mueller C,
Huq M,
Vlachopoulou E,
Lyytikäinen LP,
Oldmeadow C,
Deelen J,
Perola M,
Zhao JH,
Feenstra B,
Amini M,
Lahti J,
Schraut KE,
Fornage M,
Suktitipat B,
Chen WM,
Li X,
Nutile T,
Malerba G,
Luan J,
Bak T,
Schork N,
Del Greco M F,
Thiering E,
Mahajan A,
Marioni RE,
Mihailov E,
Eriksson J,
Ozel AB,
Zhang W,
Nethander M,
Cheng YC,
Aslibekyan S,
Ang W,
Gandin I,
Yengo L,
Portas L,
Kooperberg C,
Hofer E,
Rajan KB,
Schurmann C,
den Hollander W,
Ahluwalia TS,
Zhao J,
Draisma HHM,
Ford I,
Timpson N,
Teumer A,
Huang H,
Wahl S,
Liu Y,
Huang J,
Uh HW,
Geller F,
Joshi PK,
Yanek LR,
Trabetti E,
Lehne B,
Vozzi D,
Verbanck M,
Biino G,
Saba Y,
Meulenbelt I,
O'Connell JR,
Laakso M,
Giulianini F,
Magnusson PKE,
Ballantyne CM,
Hottenga JJ,
Montgomery GW,
Rivadineira F,
Rueedi R,
Steri M,
Herzig KH,
Stott DJ,
Menni C,
Frånberg M,
St Pourcain B,
Felix SB,
Pers TH,
Bakker SJL,
Kraft P,
Peters A,
Vaidya D,
Delgado G,
Smit JH,
Großmann V,
Sinisalo J,
Seppälä I,
Williams SR,
Holliday EG,
Moed M,
Langenberg C,
Räikkönen K,
Ding J,
Campbell H,
Sale MM,
Chen YI,
James AL,
Ruggiero D,
Soranzo N,
Hartman CA,
Smith EN,
Berenson GS,
Fuchsberger C,
Hernandez D,
Tiesler CMT,
Giedraitis V,
Liewald D,
Fischer K,
Mellström D,
Larsson A,
Wang Y,
Scott WR,
Lorentzon M,
Beilby J,
Ryan KA,
Pennell CE,
Vuckovic D,
Balkau B,
Concas MP,
Schmidt R,
Mendes de Leon CF,
Bottinger EP,
Kloppenburg M,
Paternoster L,
Boehnke M,
Musk AW,
Willemsen G,
Evans DM,
Madden PAF,
Kähönen M,
Kutalik Z,
Zoledziewska M,
Karhunen V,
Kritchevsky SB,
Sattar N,
Lachance G,
Clarke R,
Harris TB,
Raitakari OT,
Attia JR,
van Heemst D,
Kajantie E,
Sorice R,
Gambaro G,
Scott RA,
Hicks AA,
Ferrucci L,
Standl M,
Lindgren CM,
Starr JM,
Karlsson M,
Lind L,
Li JZ,
Chambers JC,
Mori TA,
de Geus EJCN,
Heath AC,
Martin NG,
Auvinen J,
Buckley BM,
de Craen AJM,
Waldenberger M,
Strauch K,
Meitinger T,
Scott RJ,
McEvoy M,
Beekman M,
Bombieri C,
Ridker PM,
Mohlke KL,
Pedersen NL,
Morrison AC,
Boomsma DI,
Whitfield JB,
Strachan DP,
Hofman A,
Vollenweider P,
Cucca F,
Jarvelin MR,
Jukema JW,
Spector TD,
Hamsten A,
Zeller T,
Uitterlinden AG,
Nauck M,
Gudnason V,
Qi L,
Grallert H,
Borecki IB,
Rotter JI,
März W,
Wild PS,
Lokki ML,
Boyle M,
Salomaa V,
Melbye M,
Eriksson JG,
Wilson JF,
Penninx BWJH,
Becker DM,
Worrall BB,
Gibson G,
Krauss RM,
Ciullo M,
Zaza G,
Wareham NJ,
Oldehinkel AJ,
Palmer LJ,
Murray SS,
Pramstaller PP,
Bandinelli S,
Heinrich J,
Ingelsson E,
Deary IJ,
Mägi R,
Vandenput L,
van der Harst P,
Desch KC,
Kooner JS,
Ohlsson C,
Hayward C,
Lehtimäki T,
Shuldiner AR,
Arnett DK,
Beilin LJ,
Robino A,
Froguel P,
Pirastu M,
Jess T,
Koenig W,
Loos RJF,
Evans DA,
Schmidt H,
Smith GD,
Slagboom PE,
Eiriksdottir G,
Morris AP,
Psaty BM,
Tracy RP,
Nolte IM,
Boerwinkle E,
Visvikis-Siest S,
Reiner AP,
Gross M,
Bis JC,
Franke L,
Franco OH,
Benjamin EJ,
Chasman DI,
Dupuis J,
Snieder H,
Dehghan A,
Alizadeh BZ
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
페이지 12개+
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Landi MT,
Bishop DT,
MacGregor S,
Machiela MJ,
Stratigos AJ,
Ghiorzo P,
Brossard M,
Calista D,
Choi J,
Fargnoli MC,
Zhang T,
Rodolfo M
외 140명 — 모두 보기
Trower AJ,
Menin C,
Martinez J,
Hadjisavvas A,
Song L,
Stefanaki I,
Scolyer R,
Yang R,
Goldstein AM,
Potrony M,
Kypreou KP,
Pastorino L,
Queirolo P,
Pellegrini C,
Cattaneo L,
Zawistowski M,
Gimenez-Xavier P,
Rodriguez A,
Elefanti L,
Manoukian S,
Rivoltini L,
Smith BH,
Loizidou MA,
Del Regno L,
Massi D,
Mandala M,
Khosrotehrani K,
Akslen LA,
Amos CI,
Andresen PA,
Avril MF,
Azizi E,
Soyer HP,
Bataille V,
Dalmasso B,
Bowdler LM,
Burdon KP,
Chen WV,
Codd V,
Craig JE,
Dębniak T,
Falchi M,
Fang S,
Friedman E,
Simi S,
Galan P,
Garcia-Casado Z,
Gillanders EM,
Gordon S,
Green A,
Gruis NA,
Hansson J,
Harland M,
Harris J,
Helsing P,
Henders A,
Hočevar M,
Höiom V,
Hunter D,
Ingvar C,
Kumar R,
Lang J,
Lathrop GM,
Lee JE,
Li X,
Lubiński J,
Mackie RM,
Malt M,
Malvehy J,
McAloney K,
Mohamdi H,
Molven A,
Moses EK,
Neale RE,
Novaković S,
Nyholt DR,
Olsson H,
Orr N,
Fritsche LG,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
Randerson-Moor J,
Requena C,
Rowe C,
Samani NJ,
Sanna M,
Schadendorf D,
Schulze HJ,
Simms LA,
Smithers M,
Song F,
Swerdlow AJ,
van der Stoep N,
Kukutsch NA,
Visconti A,
Wallace L,
Ward SV,
Wheeler L,
Sturm RA,
Hutchinson A,
Jones K,
Malasky M,
Vogt A,
Zhou W,
Pooley KA,
Elder DE,
Han J,
Hicks B,
Hayward NK,
Kanetsky PA,
Brummett C,
Montgomery GW,
Olsen CM,
Hayward C,
Dunning AM,
Martin NG,
Evangelou E,
Mann GJ,
Long G,
Pharoah PDP,
Easton DF,
Barrett JH,
Cust AE,
Abecasis G,
Duffy DL,
Whiteman DC,
Gogas H,
De Nicolo A,
Tucker MA,
Newton-Bishop JA,
Peris K,
Chanock SJ,
Demenais F,
Brown KM,
Puig S,
Nagore E,
Shi J,
Iles MM,
Law MH
GenoMEL Consortium · Q-MEGA and QTWIN Investigators 외 컨소시엄 7곳
Nature genetics · 2020 · PMID 32341527 · open access
페이지 12개+
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
Graff M,
Justice AE,
Young KL,
Marouli E,
Zhang X,
Fine RS,
Lim E,
Buchanan V,
Rand K,
Feitosa MF,
Wojczynski MK,
Yanek LR
외 213명 — 모두 보기
Shao Y,
Rohde R,
Adeyemo AA,
Aldrich MC,
Allison MA,
Ambrosone CB,
Ambs S,
Amos C,
Arnett DK,
Atwood L,
Bandera EV,
Bartz T,
Becker DM,
Berndt SI,
Bernstein L,
Bielak LF,
Blot WJ,
Bottinger EP,
Bowden DW,
Bradfield JP,
Brody JA,
Broeckel U,
Burke G,
Cade BE,
Cai Q,
Caporaso N,
Carlson C,
Carpten J,
Casey G,
Chanock SJ,
Chen G,
Chen M,
Chen YI,
Chen WM,
Chesi A,
Chiang CWK,
Chu L,
Coetzee GA,
Conti DV,
Cooper RS,
Cushman M,
Demerath E,
Deming SL,
Dimitrov L,
Ding J,
Diver WR,
Duan Q,
Evans MK,
Falusi AG,
Faul JD,
Fornage M,
Fox C,
Freedman BI,
Garcia M,
Gillanders EM,
Goodman P,
Gottesman O,
Grant SFA,
Guo X,
Hakonarson H,
Haritunians T,
Harris TB,
Harris CC,
Henderson BE,
Hennis A,
Hernandez DG,
Hirschhorn JN,
McNeill LH,
Howard TD,
Howard B,
Hsing AW,
Hsu YH,
Hu JJ,
Huff CD,
Huo D,
Ingles SA,
Irvin MR,
John EM,
Johnson KC,
Jordan JM,
Kabagambe EK,
Kang SJ,
Kardia SL,
Keating BJ,
Kittles RA,
Klein EA,
Kolb S,
Kolonel LN,
Kooperberg C,
Kuller L,
Kutlar A,
Lange L,
Langefeld CD,
Le Marchand L,
Leonard H,
Lettre G,
Levin AM,
Li Y,
Li J,
Liu Y,
Liu Y,
Liu S,
Lohman K,
Lotay V,
Lu Y,
Maixner W,
Manson JE,
McKnight B,
Meng Y,
Monda KL,
Monroe K,
Moore JH,
Mosley TH,
Mudgal P,
Murphy AB,
Nadukuru R,
Nalls MA,
Nathanson KL,
Nayak U,
N'Diaye A,
Nemesure B,
Neslund-Dudas C,
Neuhouser ML,
Nyante S,
Ochs-Balcom H,
Ogundiran TO,
Ogunniyi A,
Ojengbede O,
Okut H,
Olopade OI,
Olshan A,
Padhukasahasram B,
Palmer J,
Palmer CD,
Palmer ND,
Papanicolaou G,
Patel SR,
Pettaway CA,
Peyser PA,
Press MF,
Rao DC,
Rasmussen-Torvik LJ,
Redline S,
Reiner AP,
Rhie SK,
Rodriguez-Gil JL,
Rotimi CN,
Rotter JI,
Ruiz-Narvaez EA,
Rybicki BA,
Salako B,
Sale MM,
Sanderson M,
Schadt E,
Schreiner PJ,
Schurmann C,
Schwartz AG,
Shriner DA,
Signorello LB,
Singleton AB,
Siscovick DS,
Smith JA,
Smith S,
Speliotes E,
Spitz M,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Sucheston L,
Sun YV,
Tajuddin SM,
Taylor H,
Taylor K,
Tayo BO,
Thun MJ,
Tucker MA,
Vaidya D,
Van Den Berg DJ,
Vedantam S,
Vitolins M,
Wang Z,
Ware EB,
Wassertheil-Smoller S,
Weir DR,
Wiencke JK,
Williams SM,
Williams LK,
Wilson JG,
Witte JS,
Wrensch M,
Wu X,
Yao J,
Zakai N,
Zanetti K,
Zemel BS,
Zhao W,
Zhao JH,
Zheng W,
Zhi D,
Zhou J,
Zhu X,
Ziegler RG,
Zmuda J,
Zonderman AB,
Psaty BM,
Borecki IB,
Cupples LA,
Liu CT,
Haiman CA,
Loos R,
Ng MCY,
North KE
American journal of human genetics · 2021 · PMID 33713608
페이지 12개+
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes
Robertson CC,
Inshaw JRJ,
Onengut-Gumuscu S,
Chen WM,
Santa Cruz DF,
Yang H,
Cutler AJ,
Crouch DJM,
Farber E,
Bridges SL Jr,
Edberg JC,
Kimberly RP
외 19명 — 모두 보기
Buckner JH,
Deloukas P,
Divers J,
Dabelea D,
Lawrence JM,
Marcovina S,
Shah AS,
Greenbaum CJ,
Atkinson MA,
Gregersen PK,
Oksenberg JR,
Pociot F,
Rewers MJ,
Steck AK,
Dunger DB,
Wicker LS,
Concannon P,
Todd JA,
Rich SS
Type 1 Diabetes Genetics Consortium
Nature genetics · 2021 · PMID 34127860 · open access
페이지 12개+
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
McCartney DL,
Min JL,
Richmond RC,
Lu AT,
Sobczyk MK,
Davies G,
Broer L,
Guo X,
Jeong A,
Jung J,
Kasela S,
Katrinli S
외 97명 — 모두 보기
Kuo PL,
Matias-Garcia PR,
Mishra PP,
Nygaard M,
Palviainen T,
Patki A,
Raffield LM,
Ratliff SM,
Richardson TG,
Robinson O,
Soerensen M,
Sun D,
Tsai PC,
van der Zee MD,
Walker RM,
Wang X,
Wang Y,
Xia R,
Xu Z,
Yao J,
Zhao W,
Correa A,
Boerwinkle E,
Dugué PA,
Durda P,
Elliott HR,
Gieger C,
de Geus EJC,
Harris SE,
Hemani G,
Imboden M,
Kähönen M,
Kardia SLR,
Kresovich JK,
Li S,
Lunetta KL,
Mangino M,
Mason D,
McIntosh AM,
Mengel-From J,
Moore AZ,
Murabito JM,
Ollikainen M,
Pankow JS,
Pedersen NL,
Peters A,
Polidoro S,
Porteous DJ,
Raitakari O,
Rich SS,
Sandler DP,
Sillanpää E,
Smith AK,
Southey MC,
Strauch K,
Tiwari H,
Tanaka T,
Tillin T,
Uitterlinden AG,
Van Den Berg DJ,
van Dongen J,
Wilson JG,
Wright J,
Yet I,
Arnett D,
Bandinelli S,
Bell JT,
Binder AM,
Boomsma DI,
Chen W,
Christensen K,
Conneely KN,
Elliott P,
Ferrucci L,
Fornage M,
Hägg S,
Hayward C,
Irvin M,
Kaprio J,
Lawlor DA,
Lehtimäki T,
Lohoff FW,
Milani L,
Milne RL,
Probst-Hensch N,
Reiner AP,
Ritz B,
Rotter JI,
Smith JA,
Taylor JA,
van Meurs JBJ,
Vineis P,
Waldenberger M,
Deary IJ,
Relton CL,
Horvath S,
Marioni RE
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
페이지 12개+
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Trubetskoy V,
Pardiñas AF,
Qi T,
Panagiotaropoulou G,
Awasthi S,
Bigdeli TB,
Bryois J,
Chen CY,
Dennison CA,
Hall LS,
Lam M,
Watanabe K
외 422명 — 모두 보기
Frei O,
Ge T,
Harwood JC,
Koopmans F,
Magnusson S,
Richards AL,
Sidorenko J,
Wu Y,
Zeng J,
Grove J,
Kim M,
Li Z,
Voloudakis G,
Zhang W,
Adams M,
Agartz I,
Atkinson EG,
Agerbo E,
Al Eissa M,
Albus M,
Alexander M,
Alizadeh BZ,
Alptekin K,
Als TD,
Amin F,
Arolt V,
Arrojo M,
Athanasiu L,
Azevedo MH,
Bacanu SA,
Bass NJ,
Begemann M,
Belliveau RA,
Bene J,
Benyamin B,
Bergen SE,
Blasi G,
Bobes J,
Bonassi S,
Braun A,
Bressan RA,
Bromet EJ,
Bruggeman R,
Buckley PF,
Buckner RL,
Bybjerg-Grauholm J,
Cahn W,
Cairns MJ,
Calkins ME,
Carr VJ,
Castle D,
Catts SV,
Chambert KD,
Chan RCK,
Chaumette B,
Cheng W,
Cheung EFC,
Chong SA,
Cohen D,
Consoli A,
Cordeiro Q,
Costas J,
Curtis C,
Davidson M,
Davis KL,
de Haan L,
Degenhardt F,
DeLisi LE,
Demontis D,
Dickerson F,
Dikeos D,
Dinan T,
Djurovic S,
Duan J,
Ducci G,
Dudbridge F,
Eriksson JG,
Fañanás L,
Faraone SV,
Fiorentino A,
Forstner A,
Frank J,
Freimer NB,
Fromer M,
Frustaci A,
Gadelha A,
Genovese G,
Gershon ES,
Giannitelli M,
Giegling I,
Giusti-Rodríguez P,
Godard S,
Goldstein JI,
González Peñas J,
González-Pinto A,
Gopal S,
Gratten J,
Green MF,
Greenwood TA,
Guillin O,
Gülöksüz S,
Gur RE,
Gur RC,
Gutiérrez B,
Hahn E,
Hakonarson H,
Haroutunian V,
Hartmann AM,
Harvey C,
Hayward C,
Henskens FA,
Herms S,
Hoffmann P,
Howrigan DP,
Ikeda M,
Iyegbe C,
Joa I,
Julià A,
Kähler AK,
Kam-Thong T,
Kamatani Y,
Karachanak-Yankova S,
Kebir O,
Keller MC,
Kelly BJ,
Khrunin A,
Kim SW,
Klovins J,
Kondratiev N,
Konte B,
Kraft J,
Kubo M,
Kučinskas V,
Kučinskiene ZA,
Kusumawardhani A,
Kuzelova-Ptackova H,
Landi S,
Lazzeroni LC,
Lee PH,
Legge SE,
Lehrer DS,
Lencer R,
Lerer B,
Li M,
Lieberman J,
Light GA,
Limborska S,
Liu CM,
Lönnqvist J,
Loughland CM,
Lubinski J,
Luykx JJ,
Lynham A,
Macek M Jr,
Mackinnon A,
Magnusson PKE,
Maher BS,
Maier W,
Malaspina D,
Mallet J,
Marder SR,
Marsal S,
Martin AR,
Martorell L,
Mattheisen M,
McCarley RW,
McDonald C,
McGrath JJ,
Medeiros H,
Meier S,
Melegh B,
Melle I,
Mesholam-Gately RI,
Metspalu A,
Michie PT,
Milani L,
Milanova V,
Mitjans M,
Molden E,
Molina E,
Molto MD,
Mondelli V,
Moreno C,
Morley CP,
Muntané G,
Murphy KC,
Myin-Germeys I,
Nenadić I,
Nestadt G,
Nikitina-Zake L,
Noto C,
Nuechterlein KH,
O'Brien NL,
O'Neill FA,
Oh SY,
Olincy A,
Ota VK,
Pantelis C,
Papadimitriou GN,
Parellada M,
Paunio T,
Pellegrino R,
Periyasamy S,
Perkins DO,
Pfuhlmann B,
Pietiläinen O,
Pimm J,
Porteous D,
Powell J,
Quattrone D,
Quested D,
Radant AD,
Rampino A,
Rapaport MH,
Rautanen A,
Reichenberg A,
Roe C,
Roffman JL,
Roth J,
Rothermundt M,
Rutten BPF,
Saker-Delye S,
Salomaa V,
Sanjuan J,
Santoro ML,
Savitz A,
Schall U,
Scott RJ,
Seidman LJ,
Sharp SI,
Shi J,
Siever LJ,
Sigurdsson E,
Sim K,
Skarabis N,
Slominsky P,
So HC,
Sobell JL,
Söderman E,
Stain HJ,
Steen NE,
Steixner-Kumar AA,
Stögmann E,
Stone WS,
Straub RE,
Streit F,
Strengman E,
Stroup TS,
Subramaniam M,
Sugar CA,
Suvisaari J,
Svrakic DM,
Swerdlow NR,
Szatkiewicz JP,
Ta TMT,
Takahashi A,
Terao C,
Thibaut F,
Toncheva D,
Tooney PA,
Torretta S,
Tosato S,
Tura GB,
Turetsky BI,
Üçok A,
Vaaler A,
van Amelsvoort T,
van Winkel R,
Veijola J,
Waddington J,
Walter H,
Waterreus A,
Webb BT,
Weiser M,
Williams NM,
Witt SH,
Wormley BK,
Wu JQ,
Xu Z,
Yolken R,
Zai CC,
Zhou W,
Zhu F,
Zimprich F,
Atbaşoğlu EC,
Ayub M,
Benner C,
Bertolino A,
Black DW,
Bray NJ,
Breen G,
Buccola NG,
Byerley WF,
Chen WJ,
Cloninger CR,
Crespo-Facorro B,
Donohoe G,
Freedman R,
Galletly C,
Gandal MJ,
Gennarelli M,
Hougaard DM,
Hwu HG,
Jablensky AV,
McCarroll SA,
Moran JL,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Neil AL,
Nordentoft M,
Pato MT,
Petryshen TL,
Pirinen M,
Pulver AE,
Schulze TG,
Silverman JM,
Smoller JW,
Stahl EA,
Tsuang DW,
Vilella E,
Wang SH,
Xu S,
Adolfsson R,
Arango C,
Baune BT,
Belangero SI,
Børglum AD,
Braff D,
Bramon E,
Buxbaum JD,
Campion D,
Cervilla JA,
Cichon S,
Collier DA,
Corvin A,
Curtis D,
Forti MD,
Domenici E,
Ehrenreich H,
Escott-Price V,
Esko T,
Fanous AH,
Gareeva A,
Gawlik M,
Gejman PV,
Gill M,
Glatt SJ,
Golimbet V,
Hong KS,
Hultman CM,
Hyman SE,
Iwata N,
Jönsson EG,
Kahn RS,
Kennedy JL,
Khusnutdinova E,
Kirov G,
Knowles JA,
Krebs MO,
Laurent-Levinson C,
Lee J,
Lencz T,
Levinson DF,
Li QS,
Liu J,
Malhotra AK,
Malhotra D,
McIntosh A,
McQuillin A,
Menezes PR,
Morgan VA,
Morris DW,
Mowry BJ,
Murray RM,
Nimgaonkar V,
Nöthen MM,
Ophoff RA,
Paciga SA,
Palotie A,
Pato CN,
Qin S,
Rietschel M,
Riley BP,
Rivera M,
Rujescu D,
Saka MC,
Sanders AR,
Schwab SG,
Serretti A,
Sham PC,
Shi Y,
St Clair D,
Stefánsson H,
Stefansson K,
Tsuang MT,
van Os J,
Vawter MP,
Weinberger DR,
Werge T,
Wildenauer DB,
Yu X,
Yue W,
Holmans PA,
Pocklington AJ,
Roussos P,
Vassos E,
Verhage M,
Visscher PM,
Yang J,
Posthuma D,
Andreassen OA,
Kendler KS,
Owen MJ,
Wray NR,
Daly MJ,
Huang H,
Neale BM,
Sullivan PF,
Ripke S,
Walters JTR,
O'Donovan MC
Indonesia Schizophrenia Consortium · PsychENCODE 외 컨소시엄 3곳
Nature · 2022 · PMID 35396580
페이지 12개+
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Mahajan A,
Spracklen CN,
Zhang W,
Ng MCY,
Petty LE,
Kitajima H,
Yu GZ,
Rüeger S,
Speidel L,
Kim YJ,
Horikoshi M,
Mercader JM
외 337명 — 모두 보기
Taliun D,
Moon S,
Kwak SH,
Robertson NR,
Rayner NW,
Loh M,
Kim BJ,
Chiou J,
Miguel-Escalada I,
Della Briotta Parolo P,
Lin K,
Bragg F,
Preuss MH,
Takeuchi F,
Nano J,
Guo X,
Lamri A,
Nakatochi M,
Scott RA,
Lee JJ,
Huerta-Chagoya A,
Graff M,
Chai JF,
Parra EJ,
Yao J,
Bielak LF,
Tabara Y,
Hai Y,
Steinthorsdottir V,
Cook JP,
Kals M,
Grarup N,
Schmidt EM,
Pan I,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Long J,
Sun M,
Tong L,
Chen WM,
Ahmad M,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Lecoeur C,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Jensen RA,
Tajuddin S,
Kabagambe EK,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Flanagan J,
Abaitua F,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Akiyama M,
Anand SS,
Bertoni A,
Bian Z,
Bork-Jensen J,
Brandslund I,
Brody JA,
Brummett CM,
Buchanan TA,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
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,
Fornage M,
Franco OH,
Frayling TM,
Freedman BI,
Fuchsberger C,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Goodarzi MO,
Gordon-Larsen P,
Gorkin D,
Gross M,
Guo Y,
Hackinger S,
Han S,
Hattersley AT,
Herder C,
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 ME,
Jørgensen T,
Kamatani Y,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kohara K,
Kriebel J,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
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,
Lyssenko V,
Mamakou V,
Mani KR,
Meitinger T,
Metspalu A,
Morris AD,
Nadkarni GN,
Nadler JL,
Nalls MA,
Nayak U,
Nongmaithem SS,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Pereira MA,
Peters A,
Pirie FJ,
Porneala B,
Prasad G,
Preissl S,
Rasmussen-Torvik LJ,
Reiner AP,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sander M,
Sandow K,
Sattar N,
Schönherr S,
Schurmann C,
Shahriar M,
Shi J,
Shin DM,
Shriner D,
Smith JA,
So WY,
Stančáková A,
Stilp AM,
Strauch K,
Suzuki K,
Takahashi A,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tomlinson B,
Torres JM,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Vujkovic M,
Wacher-Rodarte N,
Wheeler E,
Whitsel EA,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamauchi T,
Yengo L,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Hanis CL,
Peyser PA,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Zeggini E,
Yokota M,
Rich SS,
Kooperberg C,
Pankow JS,
Engert JC,
Chen YI,
Froguel P,
Wilson JG,
Sheu WHH,
Kardia SLR,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Groop L,
Mook-Kanamori DO,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Bottinger EP,
Dehghan A,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Palmer CNA,
Liu S,
Abecasis G,
Kooner JS,
Loos RJF,
North KE,
Haiman CA,
Florez JC,
Saleheen D,
Hansen T,
Pedersen O,
Mägi R,
Langenberg C,
Wareham NJ,
Maeda S,
Kadowaki T,
Lee J,
Millwood IY,
Walters RG,
Stefansson K,
Myers SR,
Ferrer J,
Gaulton KJ,
Meigs JB,
Mohlke KL,
Gloyn AL,
Bowden DW,
Below JE,
Chambers JC,
Sim X,
Boehnke M,
Rotter JI,
McCarthy MI,
Morris AP
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
페이지 12개+
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
외 351명 — 모두 보기
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
페이지 12개+
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups
Hoffmann TJ,
Graff RE,
Madduri RK,
Rodriguez AA,
Cario CL,
Feng K,
Jiang Y,
Wang A,
Klein RJ,
Pierce BL,
Eggener S,
Tong L
외 37명 — 모두 보기
Blot W,
Long J,
Goss LB,
Darst BF,
Rebbeck T,
Lachance J,
Andrews C,
Adebiyi AO,
Adusei B,
Aisuodionoe-Shadrach OI,
Fernandez PW,
Jalloh M,
Janivara R,
Chen WC,
Mensah JE,
Agalliu I,
Berndt SI,
Shelley JP,
Schaffer K,
Machiela MJ,
Freedman ND,
Huang WY,
Li SA,
Goodman PJ,
Till C,
Thompson I,
Lilja H,
Ranatunga DK,
Presti J,
Van Den Eeden SK,
Chanock SJ,
Mosley JD,
Conti DV,
Haiman CA,
Justice AC,
Kachuri L,
Witte JS
Nature genetics · 2025 · PMID 39930085 · open access
페이지 12개+
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks CE,
Perry JR,
Sulem P,
Chasman DI,
Franceschini N,
He C,
Lunetta KL,
Visser JA,
Byrne EM,
Cousminer DL,
Gudbjartsson DF,
Esko T
외 162명 — 모두 보기
Feenstra B,
Hottenga JJ,
Koller DL,
Kutalik Z,
Lin P,
Mangino M,
Marongiu M,
McArdle PF,
Smith AV,
Stolk L,
van Wingerden SH,
Zhao JH,
Albrecht E,
Corre T,
Ingelsson E,
Hayward C,
Magnusson PK,
Smith EN,
Ulivi S,
Warrington NM,
Zgaga L,
Alavere H,
Amin N,
Aspelund T,
Bandinelli S,
Barroso I,
Berenson GS,
Bergmann S,
Blackburn H,
Boerwinkle E,
Buring JE,
Busonero F,
Campbell H,
Chanock SJ,
Chen W,
Cornelis MC,
Couper D,
Coviello AD,
d'Adamo P,
de Faire U,
de Geus EJ,
Deloukas P,
Döring A,
Smith GD,
Easton DF,
Eiriksdottir G,
Emilsson V,
Eriksson J,
Ferrucci L,
Folsom AR,
Foroud T,
Garcia M,
Gasparini P,
Geller F,
Gieger C,
Gudnason V,
Hall P,
Hankinson SE,
Ferreli L,
Heath AC,
Hernandez DG,
Hofman A,
Hu FB,
Illig T,
Järvelin MR,
Johnson AD,
Karasik D,
Khaw KT,
Kiel DP,
Kilpeläinen TO,
Kolcic I,
Kraft P,
Launer LJ,
Laven JS,
Li S,
Liu J,
Levy D,
Martin NG,
McArdle WL,
Melbye M,
Mooser V,
Murray JC,
Murray SS,
Nalls MA,
Navarro P,
Nelis M,
Ness AR,
Northstone K,
Oostra BA,
Peacock M,
Palmer LJ,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peltonen L,
Pennell CE,
Pharoah P,
Polasek O,
Plump AS,
Pouta A,
Porcu E,
Rafnar T,
Rice JP,
Ring SM,
Rivadeneira F,
Rudan I,
Sala C,
Salomaa V,
Sanna S,
Schlessinger D,
Schork NJ,
Scuteri A,
Segrè AV,
Shuldiner AR,
Soranzo N,
Sovio U,
Srinivasan SR,
Strachan DP,
Tammesoo ML,
Tikkanen E,
Toniolo D,
Tsui K,
Tryggvadottir L,
Tyrer J,
Uda M,
van Dam RM,
van Meurs JB,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Weedon MN,
Wichmann HE,
Willemsen G,
Wilson JF,
Wright AF,
Young L,
Zhai G,
Zhuang WV,
Bierut LJ,
Boomsma DI,
Boyd HA,
Crisponi L,
Demerath EW,
van Duijn CM,
Econs MJ,
Harris TB,
Hunter DJ,
Loos RJ,
Metspalu A,
Montgomery GW,
Ridker PM,
Spector TD,
Streeten EA,
Stefansson K,
Thorsteinsdottir U,
Uitterlinden AG,
Widen E,
Murabito JM,
Ong KK,
Murray A
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
페이지 11개
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
외 101명 — 모두 보기
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
페이지 11개
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations
Márquez A,
Kerick M,
Zhernakova A,
Gutierrez-Achury J,
Chen WM,
Onengut-Gumuscu S,
González-Álvaro I,
Rodriguez-Rodriguez L,
Rios-Fernández R,
González-Gay MA,
Mayes MD,
Raychaudhuri S
외 3명 — 모두 보기
Coeliac Disease Immunochip Consortium · Rheumatoid Arthritis Consortium International for Immunochip (RACI) 외 컨소시엄 2곳
Genome medicine · 2018 · PMID 30572963 · open access
페이지 11개
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
외 142명 — 모두 보기
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
페이지 10개
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
외 203명 — 모두 보기
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 외 컨소시엄 1곳
PLoS medicine · 2017 · PMID 28898252 · open access
페이지 10개
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
Ho JE,
Chen WY,
Chen MH,
Larson MG,
McCabe EL,
Cheng S,
Ghorbani A,
Coglianese E,
Emilsson V,
Johnson AD,
Walter S,
Franceschini N
외 12명 — 모두 보기
O'Donnell CJ,
Dehghan A,
Lu C,
Levy D,
Newton-Cheh C,
Lin H,
Felix JF,
Schreiter ER,
Vasan RS,
Januzzi JL,
Lee RT,
Wang TJ
CARDIoGRAM Consortium · CHARGE Inflammation Working Group 외 컨소시엄 1곳
The Journal of clinical investigation · 2013 · PMID 23999434
페이지 9개
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
Miller FW,
Chen W,
O'Hanlon TP,
Cooper RG,
Vencovsky J,
Rider LG,
Danko K,
Wedderburn LR,
Lundberg IE,
Pachman LM,
Reed AM,
Ytterberg SR
외 13명 — 모두 보기
Padyukov L,
Selva-O'Callaghan A,
Radstake TR,
Isenberg DA,
Chinoy H,
Ollier WE,
Scheet P,
Peng B,
Lee A,
Byun J,
Lamb JA,
Gregersen PK,
Amos CI
Myositis Genetics Consortium
Genes and immunity · 2015 · PMID 26291516
페이지 9개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.