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성함이나 학술지명, PMID로 찾아보십시오.
Gallinger S에 대해
21건, 그중 20건 표시.
Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe JR,
Bien SA,
Harrison TA,
Kang HM,
Chen S,
Schmit SL,
Conti DV,
Qu C,
Jeon J,
Edlund CK,
Greenside P,
Wainberg M
외 188명 — 모두 보기
Schumacher FR,
Smith JD,
Levine DM,
Nelson SC,
Sinnott-Armstrong NA,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Bamia C,
Banbury BL,
Baron JA,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chirlaque MD,
Cho SH,
Connolly CM,
Cross AJ,
Cuk K,
Curtis KR,
de la Chapelle A,
Doheny KF,
Duggan D,
Easton DF,
Elias SG,
Elliott F,
English DR,
Feskens EJM,
Figueiredo JC,
Fischer R,
FitzGerald LM,
Forman D,
Gala M,
Gallinger S,
Gauderman WJ,
Giles GG,
Gillanders E,
Gong J,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hampel H,
Harlid S,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Hunter DJ,
Ibañez-Sanz G,
Idos GE,
Ingersoll R,
Jackson RD,
Jacobs EJ,
Jenkins MA,
Joshi AD,
Joshu CE,
Keku TO,
Key TJ,
Kim HR,
Kobayashi E,
Kolonel LN,
Kooperberg C,
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Kweon SS,
Larsson SC,
Laurie CA,
Le Marchand L,
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Lejbkowicz F,
Lemire M,
Li CI,
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Lieb W,
Lin Y,
Lindblom A,
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Ling H,
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Männistö S,
Markowitz SD,
Martín V,
Masala G,
McNeil CE,
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Murphy N,
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Naccarati A,
Newcomb PA,
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Pardini B,
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Perduca V,
Pharoah PDP,
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Southey MC,
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Su YR,
Tangen CM,
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Thomas DC,
Thomas SS,
Toland AE,
Trichopoulou A,
Ulrich CM,
Van Den Berg DJ,
van Duijnhoven FJB,
Van Guelpen B,
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White E,
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Wu AH,
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Nature genetics · 2019 · PMID 30510241 · open access
페이지 12개+
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
Law PJ,
Timofeeva M,
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Holroyd A
외 86명 — 모두 보기
Penegar S,
Theodoratou E,
Vaughan-Shaw P,
Campbell H,
Zgaga L,
Hayward C,
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Maughan T,
Kaplan R,
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Palin K,
Hänninen UA,
Cajuso T,
Tanskanen T,
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Kaasinen E,
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Eriksson JG,
Rissanen H,
Knekt P,
Pukkala E,
Jousilahti P,
Salomaa V,
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Palotie A,
Renkonen-Sinisalo L,
Lepistö A,
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Buchanan DD,
Win AK,
Hopper J,
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Lindor NM,
Newcomb PA,
Gallinger S,
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Casey G,
Hoffmann P,
Nöthen MM,
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Easton DF,
Pharoah PDP,
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Swerdlow A,
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PRACTICAL consortium
Nature communications · 2019 · PMID 31089142 · open access
페이지 12개+
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Fernandez-Rozadilla C,
Timofeeva M,
Chen Z,
Law P,
Thomas M,
Schmit S,
Díez-Obrero V,
Hsu L,
Fernandez-Tajes J,
Palles C,
Sherwood K,
Briggs S
외 198명 — 모두 보기
Svinti V,
Donnelly K,
Farrington S,
Blackmur J,
Vaughan-Shaw P,
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Long J,
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Guo X,
Lu Y,
Broderick P,
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Harrison T,
Conti D,
Dampier C,
Devall M,
Schumacher F,
Melas M,
Rennert G,
Obón-Santacana M,
Martín-Sánchez V,
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Oh JH,
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Jee SH,
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Kweon SS,
Shin MH,
Shin A,
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Oze I,
Wen W,
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Tanikawa C,
Ren Z,
Gao YT,
Jia WH,
Hopper J,
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Woods M,
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Kaplan R,
Maughan T,
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Kirac I,
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Knekt P,
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Pukkala E,
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Cajuso T,
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Kondelin J,
Palin K,
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Renkonen-Sinisalo L,
Zanke B,
Männistö S,
Albanes D,
Weinstein S,
Ruiz-Narvaez E,
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Nature genetics · 2023 · PMID 36539618
페이지 12개+
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
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외 121명 — 모두 보기
Caporaso N,
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Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium 외 컨소시엄 3곳
Cancer research · 2016 · PMID 27197191
페이지 6개
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Wolpin BM,
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Wang Z,
Arslan AA,
Beane-Freeman L,
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외 106명 — 모두 보기
Gallinger S,
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Nature genetics · 2014 · PMID 25086665 · open access
페이지 5개
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Huyghe JR,
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Hampel H,
Figueiredo JC,
Schmit SL,
Conti DV,
Chen S,
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외 129명 — 모두 보기
Cross AJ,
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Harlid S,
Imaz L,
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Perduca V,
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Albanes D,
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Arnau-Collell C,
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Bassik MC,
Berndt SI,
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Curtis KR,
de la Chapelle A,
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Gala M,
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Grady WM,
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Gut · 2021 · PMID 33632709 · open access
페이지 5개
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Schumacher FR,
Schmit SL,
Jiao S,
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Wang H,
Zhang B,
Hsu L,
Huang SC,
Fischer CP,
Harju JF,
Idos GE,
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외 93명 — 모두 보기
Manion FJ,
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Rennert HS,
Shi W,
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Nature communications · 2015 · PMID 26151821
페이지 4개
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Klein AP,
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Mocci E,
Zhang M,
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외 112명 — 모두 보기
Albanes D,
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외 38명 — 모두 보기
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외 60명 — 모두 보기
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페이지 3개
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외 19명 — 모두 보기
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페이지 3개
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외 50명 — 모두 보기
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페이지 3개
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외 112명 — 모두 보기
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외 171명 — 모두 보기
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외 23명 — 모두 보기
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외 45명 — 모두 보기
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외 65명 — 모두 보기
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외 48명 — 모두 보기
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외 198명 — 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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