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98건, 그중 20건 표시.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
외 269명 — 모두 보기
Giri A,
Tragante V,
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Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
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Lu Y,
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Masca NGD,
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Mook-Kanamori DO,
Mosen-Ansorena D,
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Poveda A,
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Zhao W,
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LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
The power of genetic diversity in genome-wide association studies of lipids
Graham SE,
Clarke SL,
Wu KH,
Kanoni S,
Zajac GJM,
Ramdas S,
Surakka I,
Ntalla I,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
외 523명 — 모두 보기
Hwang MY,
Han S,
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Verma A,
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VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
페이지 12개+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
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외 610명 — 모두 보기
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23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
페이지 12개+
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Biobank Japan · EPIC-CVD 외 컨소시엄 1곳
Nature genetics · 2022 · PMID 36474045 · open access
페이지 12개+
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
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Nature communications · 2023 · PMID 37120605 · open access
페이지 12개+
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease
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외 20명 — 모두 보기
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Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2023 · PMID 37872160 · open access
페이지 12개+
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
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VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
페이지 12개+
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
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23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
페이지 12개+
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
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외 5명 — 모두 보기
Genes & Health Research Team
Nature communications · 2024 · PMID 39414775 · open access
페이지 12개+
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
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페이지 9개
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페이지 9개
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페이지 8개
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
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페이지 8개
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페이지 8개
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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.