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114건, 그중 20건 표시.
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Kilpeläinen TO,
Bentley AR,
Noordam R,
Sung YJ,
Schwander K,
Winkler TW,
Jakupović H,
Chasman DI,
Manning A,
Ntalla I,
Aschard H,
Brown MR
외 217명 — 모두 보기
de las Fuentes L,
Franceschini N,
Guo X,
Vojinovic D,
Aslibekyan S,
Feitosa MF,
Kho M,
Musani SK,
Richard M,
Wang H,
Wang Z,
Bartz TM,
Bielak LF,
Campbell A,
Dorajoo R,
Fisher V,
Hartwig FP,
Horimoto ARVR,
Li C,
Lohman KK,
Marten J,
Sim X,
Smith AV,
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Chai JF,
Chen X,
Divers J,
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Gao C,
Graff M,
Harris SE,
He M,
Hsu FC,
Jackson AU,
Zhao JH,
Kraja AT,
Kühnel B,
Laguzzi F,
Lyytikäinen LP,
Nolte IM,
Rauramaa R,
Riaz M,
Robino A,
Rueedi R,
Stringham HM,
Takeuchi F,
van der Most PJ,
Varga TV,
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Ware EB,
Wen W,
Li X,
Yanek LR,
Amin N,
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Boerwinkle E,
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Cade B,
Canouil M,
Chen YI,
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Connell J,
de Mutsert R,
de Silva HJ,
de Vries PS,
Demirkan A,
Ding J,
Eaton CB,
Faul JD,
Friedlander Y,
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Harris TB,
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Langefeld CD,
Langenberg C,
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Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
페이지 12개+
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Justice AE,
Karaderi T,
Highland HM,
Young KL,
Graff M,
Lu Y,
Turcot V,
Auer PL,
Fine RS,
Guo X,
Schurmann C,
Lempradl A
외 268명 — 모두 보기
Marouli E,
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Abecasis G,
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Balkau B,
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Brandslund I,
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de Bakker PIW,
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Zhao W,
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CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium 외 컨소시엄 8곳
Nature genetics · 2019 · PMID 30778226 · open access
페이지 12개+
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Wuttke M,
Li Y,
Li M,
Sieber KB,
Feitosa MF,
Gorski M,
Tin A,
Wang L,
Chu AY,
Hoppmann A,
Kirsten H,
Giri A
외 315명 — 모두 보기
Chai JF,
Sveinbjornsson G,
Tayo BO,
Nutile T,
Fuchsberger C,
Marten J,
Cocca M,
Ghasemi S,
Xu Y,
Horn K,
Noce D,
van der Most PJ,
Sedaghat S,
Yu Z,
Akiyama M,
Afaq S,
Ahluwalia TS,
Almgren P,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boehnke M,
Boerwinkle E,
Boissel M,
Bottinger EP,
Boutin TS,
Brenner H,
Brumat M,
Burkhardt R,
Butterworth AS,
Campana E,
Campbell A,
Campbell H,
Canouil M,
Carroll RJ,
Catamo E,
Chambers JC,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cheng Y,
Christensen K,
Cifkova R,
Ciullo M,
Concas MP,
Cook JP,
Coresh J,
Corre T,
Sala CF,
Cusi D,
Danesh J,
Daw EW,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Delgado G,
Demirkan A,
Di Angelantonio E,
Dittrich K,
Divers J,
Dorajoo R,
Eckardt KU,
Ehret G,
Elliott P,
Endlich K,
Evans MK,
Felix JF,
Foo VHX,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Friedlander Y,
Froguel P,
Gansevoort RT,
Gao H,
Gasparini P,
Gaziano JM,
Giedraitis V,
Gieger C,
Girotto G,
Giulianini F,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hartman CA,
Hayward C,
Hellwege JN,
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Hofer E,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Indridason OS,
Ingelsson E,
Ising M,
Jaddoe VWV,
Jakobsdottir J,
Jonas JB,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kammerer CM,
Kanai M,
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Kerr SM,
Khor CC,
Kiess W,
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Metspalu A,
Mikaelsdottir EK,
Milaneschi Y,
Miliku K,
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Mook-Kanamori DO,
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Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
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Noordam R,
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Olafsson I,
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Padmanabhan S,
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Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
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Province MA,
Rabelink TJ,
Raffield LM,
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Robino A,
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Saba Y,
Sabanayagam C,
Salomaa V,
Salvi E,
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Strauch K,
Stringham HM,
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Szymczak S,
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Tajuddin SM,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
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Thio CHL,
Thomsen H,
Thorleifsson G,
Toniolo D,
Tönjes A,
Tremblay J,
Tzoulaki I,
Uitterlinden AG,
Vaccargiu S,
van Dam RM,
van der Harst P,
van Duijn CM,
Velez Edward DR,
Verweij N,
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Völker U,
Vollenweider P,
Waeber G,
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Wallentin L,
Wang YX,
Wang C,
Waterworth DM,
Bin Wei W,
White H,
Whitfield JB,
Wild SH,
Wilson JF,
Wojczynski MK,
Wong C,
Wong TY,
Xu L,
Yang Q,
Yasuda M,
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Zhang W,
Zonderman AB,
Rotter JI,
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Vitart V,
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Dehghan A,
Parsa A,
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Ho K,
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Sim X,
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Okada Y,
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Snieder H,
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Hung AM,
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Scholz M,
Teumer A,
Köttgen A,
Pattaro C
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
페이지 12개+
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer A,
Li Y,
Ghasemi S,
Prins BP,
Wuttke M,
Hermle T,
Giri A,
Sieber KB,
Qiu C,
Kirsten H,
Tin A,
Chu AY
외 174명 — 모두 보기
Bansal N,
Feitosa MF,
Wang L,
Chai JF,
Cocca M,
Fuchsberger C,
Gorski M,
Hoppmann A,
Horn K,
Li M,
Marten J,
Noce D,
Nutile T,
Sedaghat S,
Sveinbjornsson G,
Tayo BO,
van der Most PJ,
Xu Y,
Yu Z,
Gerstner L,
Ärnlöv J,
Bakker SJL,
Baptista D,
Biggs ML,
Boerwinkle E,
Brenner H,
Burkhardt R,
Carroll RJ,
Chee ML,
Chee ML,
Chen M,
Cheng CY,
Cook JP,
Coresh J,
Corre T,
Danesh J,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Dittrich K,
Divers J,
Eckardt KU,
Ehret G,
Endlich K,
Felix JF,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Gansevoort RT,
Giedraitis V,
Gögele M,
Grundner-Culemann F,
Gudbjartsson DF,
Gudnason V,
Hamet P,
Harris TB,
Hicks AA,
Holm H,
Foo VHX,
Hwang SJ,
Ikram MA,
Ingelsson E,
Jaddoe VWV,
Jakobsdottir J,
Josyula NS,
Jung B,
Kähönen M,
Khor CC,
Kiess W,
Koenig W,
Körner A,
Kovacs P,
Kramer H,
Krämer BK,
Kronenberg F,
Lange LA,
Langefeld CD,
Lee JJ,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Mahajan A,
Maranville JC,
Mascalzoni D,
McMullen B,
Meisinger C,
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Miliku K,
Mook-Kanamori DO,
Müller-Nurasyid M,
Mychaleckyj JC,
Nauck M,
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Ning B,
Noordam R,
Connell JO,
Olafsson I,
Palmer ND,
Peters A,
Podgornaia AI,
Ponte B,
Poulain T,
Pramstaller PP,
Rabelink TJ,
Raffield LM,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Rivadeneira F,
Runz H,
Ryan KA,
Sabanayagam C,
Saum KU,
Schöttker B,
Shaffer CM,
Shi Y,
Smith AV,
Strauch K,
Stumvoll M,
Sun BB,
Szymczak S,
Tai ES,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorsteinsdottir U,
Tönjes A,
Tremblay J,
Uitterlinden AG,
van der Harst P,
Verweij N,
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Waldenberger M,
Wang C,
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Wong C,
Wong TY,
Yang Q,
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Bochud M,
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Devuyst O,
Edwards TL,
Ho K,
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Parsa A,
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Butterworth AS,
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Pattaro C,
Köttgen A
Nature communications · 2019 · PMID 31511532 · open access
페이지 12개+
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ntalla I,
Weng LC,
Cartwright JH,
Hall AW,
Sveinbjornsson G,
Tucker NR,
Choi SH,
Chaffin MD,
Roselli C,
Barnes MR,
Mifsud B,
Warren HR
외 175명 — 모두 보기
Hayward C,
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Gasparini P,
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Kolcic I,
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Rudan I,
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Lima-Costa MF,
Ribeiro ALP,
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Tarazona-Santos E,
Giedraitis V,
Ingelsson E,
Mahajan A,
Morris AP,
Del Greco M F,
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Lind L,
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Sundström J,
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Sinagra G,
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Kähönen M,
Mishra PP,
Mononen N,
Nikus K,
Caulfield MJ,
Dominiczak A,
Padmanabhan S,
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Shuldiner AR,
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Lehtimäki T,
Lyytikäinen LP,
Raitakari OT,
Barnes CLK,
Campbell H,
Joshi PK,
Wilson JF,
Isaacs A,
Kors JA,
van Duijn CM,
Huang PL,
Gudnason V,
Harris TB,
Launer LJ,
Smith AV,
Bottinger EP,
Loos RJF,
Nadkarni GN,
Preuss MH,
Correa A,
Mei H,
Wilson J,
Meitinger T,
Müller-Nurasyid M,
Peters A,
Waldenberger M,
Mangino M,
Spector TD,
Rienstra M,
van de Vegte YJ,
van der Harst P,
Verweij N,
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Communications biology · 2021 · PMID 33649486 · open access
페이지 12개+
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페이지 12개+
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Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
페이지 12개+
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
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페이지 12개+
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
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외 27명 — 모두 보기
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페이지 12개+
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
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외 154명 — 모두 보기
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페이지 12개+
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
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외 76명 — 모두 보기
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Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
페이지 12개+
A saturated map of common genetic variants associated with human height
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외 610명 — 모두 보기
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페이지 12개+
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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.