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Cushman M에 대해
19건.
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외 50명 — 모두 보기
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Nature genetics · 2009 · PMID 19862010 · open access
페이지 12개+
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외 213명 — 모두 보기
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페이지 12개+
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
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외 67명 — 모두 보기
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NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
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페이지 12개+
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FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
페이지 12개+
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외 351명 — 모두 보기
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VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
페이지 12개+
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
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외 101명 — 모두 보기
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페이지 11개
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외 64명 — 모두 보기
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외 23명 — 모두 보기
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American journal of human genetics · 2012 · PMID 22703881
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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
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외 66명 — 모두 보기
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페이지 3개
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
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외 33명 — 모두 보기
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European heart journal · 2012 · PMID 22003152
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A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
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외 196명 — 모두 보기
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NABEC Consortium · UKBEC Consortium 외 컨소시엄 2곳
Nature genetics · 2013 · PMID 23583978 · open access
페이지 2개
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
Liu CT,
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외 81명 — 모두 보기
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PLoS genetics · 2013 · PMID 23966867 · open access
페이지 2개
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
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외 94명 — 모두 보기
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Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
페이지 2개
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
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외 81명 — 모두 보기
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Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium 외 컨소시엄 1곳
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페이지 2개
Genetic predictors of fibrin D-dimer levels in healthy adults
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외 54명 — 모두 보기
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Circulation · 2011 · PMID 21502573
페이지 1개
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
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외 51명 — 모두 보기
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Annals of neurology · 2011 · PMID 21681796
페이지 1개
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
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외 28명 — 모두 보기
Basu S,
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Genetic epidemiology · 2013 · PMID 23650146
페이지 1개
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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.