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20건.
Defining the role of common variation in the genomic and biological architecture of adult human height
Wood AR,
Esko T,
Yang J,
Vedantam S,
Pers TH,
Gustafsson S,
Chu AY,
Estrada K,
Luan J,
Kutalik Z,
Amin N,
Buchkovich ML
외 433명 — 모두 보기
Croteau-Chonka DC,
Day FR,
Duan Y,
Fall T,
Fehrmann R,
Ferreira T,
Jackson AU,
Karjalainen J,
Lo KS,
Locke AE,
Mägi R,
Mihailov E,
Porcu E,
Randall JC,
Scherag A,
Vinkhuyzen AA,
Westra HJ,
Winkler TW,
Workalemahu T,
Zhao JH,
Absher D,
Albrecht E,
Anderson D,
Baron J,
Beekman M,
Demirkan A,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Fraser RM,
Goel A,
Gong J,
Justice AE,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Lui JC,
Mangino M,
Mateo Leach I,
Medina-Gomez C,
Nalls MA,
Nyholt DR,
Palmer CD,
Pasko D,
Pechlivanis S,
Prokopenko I,
Ried JS,
Ripke S,
Shungin D,
Stancáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Afzal U,
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Bandinelli S,
Barrett A,
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Bennett AJ,
Berne C,
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Buyske S,
Caspersen IH,
Chines PS,
Clarke R,
Claudi-Boehm S,
Cooper M,
Daw EW,
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Deelen J,
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Denny JC,
Dhonukshe-Rutten R,
Dimitriou M,
Doney AS,
Dörr M,
Eklund N,
Eury E,
Folkersen L,
Garcia ME,
Geller F,
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Grallert H,
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de Groot LC,
Groves CJ,
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Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium 외 컨소시엄 2곳
Nature genetics · 2014 · PMID 25282103 · open access
페이지 12개+
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
Heilmann-Heimbach S,
Herold C,
Hochfeld LM,
Hillmer AM,
Nyholt DR,
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외 24명 — 모두 보기
Fier HL,
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Nature communications · 2017 · PMID 28272467 · open access
페이지 12개+
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Morris AP,
Voight BF,
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Ferreira T,
Segrè AV,
Steinthorsdottir V,
Strawbridge RJ,
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외 192명 — 모두 보기
Dina C,
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Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators 외 컨소시엄 4곳
Nature genetics · 2012 · PMID 22885922 · open access
페이지 10개
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan A,
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외 322명 — 모두 보기
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Lu W,
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Ma RC,
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Mühleisen TW,
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Altshuler D,
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Cho YS,
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Chambers JC,
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McCarthy MI,
Morris AP
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium 외 컨소시엄 3곳
Nature genetics · 2014 · PMID 24509480 · open access
페이지 9개
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
외 391명 — 모두 보기
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,
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Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
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Pastor AA,
Arosio B,
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Banaj N,
Baquero M,
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Below JE,
Benchek P,
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Berr C,
Besse C,
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Binetti G,
Bizarro A,
Blesa R,
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Boerwinkle E,
Borroni B,
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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,
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EADB · GR@ACE 외 컨소시엄 7곳
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페이지 9개
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis
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외 57명 — 모두 보기
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Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) · Esophageal Adenocarcinoma GenEtics Consortium (EAGLE) 외 컨소시엄 1곳
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페이지 6개
Genome-wide association study reveals two new risk loci for bipolar disorder
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외 51명 — 모두 보기
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페이지 4개
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
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외 27명 — 모두 보기
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페이지 3개
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외 21명 — 모두 보기
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페이지 3개
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외 22명 — 모두 보기
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페이지 2개
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
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외 26명 — 모두 보기
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페이지 2개
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups
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외 38명 — 모두 보기
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PLoS genetics · 2010 · PMID 20421936 · open access
페이지 2개
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
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외 64명 — 모두 보기
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Bipolar Disorder Genome Study (BiGS) Consortium
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페이지 2개
Genetic studies of body mass index yield new insights for obesity biology
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외 470명 — 모두 보기
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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.