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143건, 그중 20건 표시.
A genome-wide association study of serum proteins reveals shared loci with common diseases
Gudjonsson A,
Gudmundsdottir V,
Axelsson GT,
Gudmundsson EF,
Jonsson BG,
Launer LJ,
Lamb JR,
Jennings LL,
Aspelund T,
Emilsson V,
Gudnason V
Nature communications · 2022 · PMID 35078996 · open access
페이지 12개+
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Trpchevska N,
Freidin MB,
Broer L,
Oosterloo BC,
Yao S,
Zhou Y,
Vona B,
Bishop C,
Bizaki-Vallaskangas A,
Canlon B,
Castellana F,
Chasman DI
외 54명 — 모두 보기
Cherny S,
Christensen K,
Concas MP,
Correa A,
Elkon R,
Mengel-From J,
Gao Y,
Giersch ABS,
Girotto G,
Gudjonsson A,
Gudnason V,
Heard-Costa NL,
Hertzano R,
Hjelmborg JVB,
Hjerling-Leffler J,
Hoffman HJ,
Kaprio J,
Kettunen J,
Krebs K,
Kähler AK,
Lallemend F,
Launer LJ,
Lee IM,
Leonard H,
Li CM,
Lowenheim H,
Magnusson PKE,
van Meurs J,
Milani L,
Morton CC,
Mäkitie A,
Nalls MA,
Nardone GG,
Nygaard M,
Palviainen T,
Pratt S,
Quaranta N,
Rämö J,
Saarentaus E,
Sardone R,
Satizabal CL,
Schweinfurth JM,
Seshadri S,
Shiroma E,
Shulman E,
Simonsick E,
Spankovich C,
Tropitzsch A,
Lauschke VM,
Sullivan PF,
Goedegebure A,
Cederroth CR,
Williams FMK,
Nagtegaal AP
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
페이지 12개+
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Wang Z,
Emmerich A,
Pillon NJ,
Moore T,
Hemerich D,
Cornelis MC,
Mazzaferro E,
Broos S,
Ahluwalia TS,
Bartz TM,
Bentley AR,
Bielak LF
외 206명 — 모두 보기
Chong M,
Chu AY,
Berry D,
Dorajoo R,
Dueker ND,
Kasbohm E,
Feenstra B,
Feitosa MF,
Gieger C,
Graff M,
Hall LM,
Haller T,
Hartwig FP,
Hillis DA,
Huikari V,
Heard-Costa N,
Holzapfel C,
Jackson AU,
Johansson Å,
Jørgensen AM,
Kaakinen MA,
Karlsson R,
Kerr KF,
Kim B,
Koolhaas CM,
Kutalik Z,
Lagou V,
Lind PA,
Lorentzon M,
Lyytikäinen LP,
Mangino M,
Metzendorf C,
Monroe KR,
Pacolet A,
Pérusse L,
Pool R,
Richmond RC,
Rivera NV,
Robiou-du-Pont S,
Schraut KE,
Schulz CA,
Stringham HM,
Tanaka T,
Teumer A,
Turman C,
van der Most PJ,
Vanmunster M,
van Rooij FJA,
van Vliet-Ostaptchouk JV,
Zhang X,
Zhao JH,
Zhao W,
Balkhiyarova Z,
Balslev-Harder MN,
Baumeister SE,
Beilby J,
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Boomsma DI,
Brage S,
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Brody JA,
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Ekelund U,
Liu CT,
Cole JW,
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Faul JD,
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Franco OH,
Galesloot TE,
Gordon SD,
Grarup N,
Hartman CA,
Heiss G,
Hui J,
Illig T,
Jago R,
James A,
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Moscati A,
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Reedik M,
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Scott LJ,
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Tremblay A,
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Willemsen G,
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Wong Q,
Xu H,
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Yuan JM,
Zillikens MC,
Zonderman AB,
Ameur A,
Bandinelli S,
Bis JC,
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Smith GD,
de Geus EJC,
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Ferrucci L,
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Fox C,
Garland T Jr,
Gudnason V,
Gyllensten U,
Hansen T,
Hayward C,
Horta BL,
Hyppönen E,
Jarvelin MR,
Johnson WC,
Kardia SLR,
Kiemeney LA,
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Langenberg C,
Lehtimäki T,
Marchand LL,
Magnusson PKE,
Martin NG,
Melbye M,
Metspalu A,
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North KE,
Ohlsson C,
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Pare G,
Park T,
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Pers TH,
Polasek O,
Prokopenko I,
Rotimi CN,
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Snieder H,
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Spector TD,
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Krook A,
Zierath JR,
Thomis MAI,
Loos RJF,
Hoed MD
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
페이지 12개+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
외 610명 — 모두 보기
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
Rüeger S,
Sim X,
Vrieze S,
Ahluwalia TS,
Akiyama M,
Allison MA,
Alvarez M,
Andersen MK,
Ani A,
Appadurai V,
Arbeeva L,
Bhaskar S,
Bielak LF,
Bollepalli S,
Bonnycastle LL,
Bork-Jensen J,
Bradfield JP,
Bradford Y,
Braund PS,
Brody JA,
Burgdorf KS,
Cade BE,
Cai H,
Cai Q,
Campbell A,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
Cocca M,
Concas MP,
Couture C,
Cuellar-Partida G,
Danning R,
Daw EW,
Degenhard F,
Delgado GE,
Delitala A,
Demirkan A,
Deng X,
Devineni P,
Dietl A,
Dimitriou M,
Dimitrov L,
Dorajoo R,
Ekici AB,
Engmann JE,
Fairhurst-Hunter Z,
Farmaki AE,
Faul JD,
Fernandez-Lopez JC,
Forer L,
Francescatto M,
Freitag-Wolf S,
Fuchsberger C,
Galesloot TE,
Gao Y,
Gao Z,
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Gjesing AP,
Goel A,
Gordon SD,
Gorski M,
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Haworth SJ,
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Leonard HL,
Li SA,
Li X,
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Liang J,
Lin H,
Lin SY,
Liu J,
Liu X,
Lo KS,
Long J,
Lores-Motta L,
Luan J,
Lyssenko V,
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Millwood IY,
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Mitchell RE,
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Morgan A,
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Pärna K,
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Ramirez J,
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Raven D,
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Riveros C,
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Smit RAJ,
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Smith JA,
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Southam L,
Steinthorsdottir V,
Sun L,
Takeuchi F,
Tallapragada DSP,
Taylor KD,
Tayo BO,
Tcheandjieu C,
Terzikhan N,
Tesolin P,
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Theusch E,
Thompson DJ,
Thorleifsson G,
Timmers PRHJ,
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Turman C,
Vaccargiu S,
van der Laan SW,
van der Most PJ,
van Klinken JB,
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Verma SS,
Verweij N,
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Wang CA,
Wang C,
Wang L,
Wang Z,
Warren HR,
Bin Wei W,
Wickremasinghe AR,
Wielscher M,
Wiggins KL,
Winsvold BS,
Wong A,
Wu Y,
Wuttke M,
Xia R,
Xie T,
Yamamoto K,
Yang J,
Yao J,
Young H,
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Yu L,
Zeng L,
Zhang W,
Zhang X,
Zhao JH,
Zhao W,
Zhou W,
Zimmermann ME,
Zoledziewska M,
Adair LS,
Adams HHH,
Aguilar-Salinas CA,
Al-Mulla F,
Arnett DK,
Asselbergs FW,
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Banas B,
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Bennett DA,
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Bharadwaj D,
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Brandslund I,
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Chen YI,
Chen Z,
Cheng CY,
Christophersen IE,
Ciullo M,
Cole JW,
Collins FS,
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Kardia SLR,
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Zheng W,
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23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
페이지 12개+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
외 135명 — 모두 보기
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
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Loos RJF,
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Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
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Lu Y,
Rotter JI,
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Luan J,
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Million Veteran Program · Lifelines Cohort Study 외 컨소시엄 2곳
Nature genetics · 2024 · PMID 38689001 · open access
페이지 12개+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
외 145명 — 모두 보기
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
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Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
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Nature genetics · 2025 · PMID 40050429
페이지 12개+
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