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성함이나 학술지명, PMID로 찾아보십시오.
Andrade M에 대해
26건, 그중 20건 표시.
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay M,
Goel A,
Won HH,
Hall LM,
Willenborg C,
Kanoni S,
Saleheen D,
Kyriakou T,
Nelson CP,
Hopewell JC,
Webb TR,
Zeng L
외 139명 — 모두 보기
Dehghan A,
Alver M,
Armasu SM,
Auro K,
Bjonnes A,
Chasman DI,
Chen S,
Ford I,
Franceschini N,
Gieger C,
Grace C,
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Huang J,
Hwang SJ,
Kim YK,
Kleber ME,
Lau KW,
Lu X,
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Lyytikäinen LP,
Mihailov E,
Morrison AC,
Pervjakova N,
Qu L,
Rose LM,
Salfati E,
Saxena R,
Scholz M,
Smith AV,
Tikkanen E,
Uitterlinden A,
Yang X,
Zhang W,
Zhao W,
de Andrade M,
de Vries PS,
van Zuydam NR,
Anand SS,
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Lieb W,
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Boerwinkle E,
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Collins R,
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Esko T,
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Franco OH,
Franzosi MG,
Granger CB,
Gu D,
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Hall AS,
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Nature genetics · 2015 · PMID 26343387 · 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,
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Li Y,
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외 240명 — 모두 보기
Foster M,
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ICBP Consortium · AGEN Consortium 외 컨소시엄 3곳
Nature communications · 2016 · PMID 26831199 · open access
페이지 12개+
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Thibord F,
Klarin D,
Brody JA,
Chen MH,
Levin MG,
Chasman DI,
Goode EL,
Hveem K,
Teder-Laving M,
Martinez-Perez A,
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외 76명 — 모두 보기
Ito K,
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Wang X,
Wang X,
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Komuro I,
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Loos RJF,
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Pankow JS,
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Morelli VM,
Ridker PM,
Vlieg AVH,
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Kraft P,
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Min Lee K,
Psaty BM,
Heidi Skogholt A,
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Suchon P,
Rich SS,
Vy HMT,
Tang W,
Jackson RD,
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Morange PE,
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Damrauer SM,
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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+
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
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외 205명 — 모두 보기
Albert CM,
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Chen YI,
Chen Z,
Cheng I,
Cho MH,
Choquet H,
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Ehringer MA,
Esko T,
Faul JD,
Fernandes Silva L,
Fiorillo E,
Fornage M,
Freedman BI,
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Garrett ME,
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Gu CC,
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Hou L,
Huang H,
Hung YJ,
Hunter DJ,
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Hwang SJ,
Hwu CM,
Iacono W,
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Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
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Kardia SLR,
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23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
페이지 12개+
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
Cordell HJ,
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Ueno K,
Darlay R,
Aiba Y,
Hitomi Y,
Kawashima M,
Nishida N,
Khor SS,
Gervais O,
Kawai Y,
Nagasaki M
외 31명 — 모두 보기
Tokunaga K,
Tang R,
Shi Y,
Li Z,
Juran BD,
Atkinson EJ,
Gerussi A,
Carbone M,
Asselta R,
Cheung A,
de Andrade M,
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Sun D,
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Ma X,
Nakamura M,
Mells GF
PBC Consortia · Canadian PBC Consortium 외 컨소시엄 5곳
Journal of hepatology · 2021 · PMID 34033851 · open access
페이지 10개
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
Manning AK,
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Chen H,
Rybin D,
Liu CT,
Bielak LF,
Prokopenko I,
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Barnes D
외 204명 — 모두 보기
Cadby G,
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DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
페이지 8개
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
Ji SG,
Juran BD,
Mucha S,
Folseraas T,
Jostins L,
Melum E,
Kumasaka N,
Atkinson EJ,
Schlicht EM,
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Gutierrez-Achury J
외 58명 — 모두 보기
Boberg KM,
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Chapman RW,
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UK-PSC Consortium · International IBD Genetics Consortium 외 컨소시엄 1곳
Nature genetics · 2017 · PMID 27992413 · open access
페이지 8개
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype
Stanaway IB,
Hall TO,
Rosenthal EA,
Palmer M,
Naranbhai V,
Knevel R,
Namjou-Khales B,
Carroll RJ,
Kiryluk K,
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Howell KM
외 28명 — 모두 보기
Mapes BM,
Lin FTJ,
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de Andrade M,
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Peterson JF,
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외 120명 — 모두 보기
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외 90명 — 모두 보기
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외 60명 — 모두 보기
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페이지 3개
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외 191명 — 모두 보기
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외 105명 — 모두 보기
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외 2명 — 모두 보기
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외 21명 — 모두 보기
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외 73명 — 모두 보기
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외 52명 — 모두 보기
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페이지 2개
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외 45명 — 모두 보기
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페이지 2개
CUBN is a gene locus for albuminuria
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외 103명 — 모두 보기
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페이지 1개
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
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외 29명 — 모두 보기
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페이지 1개
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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
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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
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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
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