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성함이나 학술지명, PMID로 찾아보십시오.
De Vivo I에 대해
17건.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Perry JR,
Day F,
Elks CE,
Sulem P,
Thompson DJ,
Ferreira T,
He C,
Chasman DI,
Esko T,
Thorleifsson G,
Albrecht E,
Ang WQ
외 186명 — 모두 보기
Corre T,
Cousminer DL,
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Franceschini N,
Ganna A,
Johnson AD,
Kjellqvist S,
Lunetta KL,
McMahon G,
Nolte IM,
Paternoster L,
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Smith AV,
Stolk L,
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Ulivi S,
Wagner EK,
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Byrne EM,
Hottenga JJ,
Koller DL,
Mangino M,
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Yerges-Armstrong LM,
Zhao JH,
Andrulis IL,
Anton-Culver H,
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Bandinelli S,
Beckmann MW,
Benitez J,
Blomqvist C,
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Collée JM,
Couch FJ,
Couper D,
Coveillo AD,
Cox A,
Czene K,
D'adamo AP,
Smith GD,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dieffenbach AK,
Dunning AM,
Eiriksdottir G,
Eriksson JG,
Fasching PA,
Ferrucci L,
Flesch-Janys D,
Flyger H,
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Franke L,
Garcia ME,
García-Closas M,
Geller F,
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Gudnason V,
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Hofman A,
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Hopper JL,
Hu FB,
Hunter DJ,
Karasik D,
Kiel DP,
Knight JA,
Kosma VM,
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Lai S,
Lambrechts D,
Lindblom A,
Mägi R,
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Mannermaa A,
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Masson G,
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Melbye M,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Nevanlinna H,
Neven P,
Nohr EA,
Oldehinkel AJ,
Oostra BA,
Palotie A,
Peacock M,
Pedersen NL,
Peterlongo P,
Peto J,
Pharoah PD,
Postma DS,
Pouta A,
Pylkäs K,
Radice P,
Ring S,
Rivadeneira F,
Robino A,
Rose LM,
Rudolph A,
Salomaa V,
Sanna S,
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Tyrer J,
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Vollenweider P,
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Waldenberger M,
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Wang Q,
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Winqvist R,
Wolffenbuttel BH,
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Australian Ovarian Cancer Study · GENICA Network 외 컨소시엄 4곳
Nature · 2014 · PMID 25231870 · open access
페이지 12개+
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
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외 230명 — 모두 보기
Elks CE,
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Cox A,
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De Vivo I,
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PRACTICAL consortium · kConFab Investigators 외 컨소시엄 4곳
Nature genetics · 2015 · PMID 26414677 · open access
페이지 12개+
Genetic insights into biological mechanisms governing human ovarian ageing
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외 256명 — 모두 보기
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Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium 외 컨소시엄 6곳
Nature · 2021 · PMID 34349265
페이지 12개+
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
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외 121명 — 모두 보기
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DBDS Genomic Consortium · FinnGen Study 외 컨소시엄 3곳
Nature genetics · 2023 · PMID 36914876
페이지 8개
Identification of nine new susceptibility loci for endometrial cancer
O'Mara TA,
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외 114명 — 모두 보기
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Nature communications · 2018 · PMID 30093612 · open access
페이지 6개
Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights
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외 88명 — 모두 보기
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UROMOL Consortium
European urology · 2023 · PMID 37210288
페이지 4개
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
Song H,
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외 62명 — 모두 보기
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Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
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LifeLines Cohort Study · InterAct Consortium 외 컨소시엄 4곳
Nature genetics · 2017 · PMID 28436984
페이지 1개
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
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외 30명 — 모두 보기
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외 128명 — 모두 보기
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Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions
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외 49명 — 모두 보기
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Journal of the National Cancer Institute · 2023 · PMID 36929942
페이지 1개
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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.