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Ntalla I에 대해
31건, 그중 11건 표시.
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
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외 527명 — 모두 보기
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Genome biology · 2022 · PMID 36575460 · open access
페이지 8개
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Sung YJ,
Winkler TW,
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Ntalla I,
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외 286명 — 모두 보기
Sim X,
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CHARGE Neurology Working Group · COGENT-Kidney Consortium 외 컨소시엄 2곳
American journal of human genetics · 2018 · PMID 29455858
페이지 7개
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
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외 27명 — 모두 보기
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UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
페이지 6개
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
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외 228명 — 모두 보기
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ExomeBP Consortium · MAGIC Consortium 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29632382 · open access
페이지 6개
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Prins BP,
Mead TJ,
Brody JA,
Sveinbjornsson G,
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페이지 4개
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COGENT-Kidney Consortium · EPIC-InterAct Consortium 외 컨소시엄 2곳
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페이지 1개
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외 198명 — 모두 보기
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Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
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페이지 1개
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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.