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66건, 그중 20건 표시.
Defining the role of common variation in the genomic and biological architecture of adult human height
Wood AR,
Esko T,
Yang J,
Vedantam S,
Pers TH,
Gustafsson S,
Chu AY,
Estrada K,
Luan J,
Kutalik Z,
Amin N,
Buchkovich ML
외 433명 — 모두 보기
Croteau-Chonka DC,
Day FR,
Duan Y,
Fall T,
Fehrmann R,
Ferreira T,
Jackson AU,
Karjalainen J,
Lo KS,
Locke AE,
Mägi R,
Mihailov E,
Porcu E,
Randall JC,
Scherag A,
Vinkhuyzen AA,
Westra HJ,
Winkler TW,
Workalemahu T,
Zhao JH,
Absher D,
Albrecht E,
Anderson D,
Baron J,
Beekman M,
Demirkan A,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Fraser RM,
Goel A,
Gong J,
Justice AE,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Lui JC,
Mangino M,
Mateo Leach I,
Medina-Gomez C,
Nalls MA,
Nyholt DR,
Palmer CD,
Pasko D,
Pechlivanis S,
Prokopenko I,
Ried JS,
Ripke S,
Shungin D,
Stancáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Afzal U,
Arnlöv J,
Arscott GM,
Bandinelli S,
Barrett A,
Bellis C,
Bennett AJ,
Berne C,
Blüher M,
Bolton JL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Buckley BM,
Buyske S,
Caspersen IH,
Chines PS,
Clarke R,
Claudi-Boehm S,
Cooper M,
Daw EW,
De Jong PA,
Deelen J,
Delgado G,
Denny JC,
Dhonukshe-Rutten R,
Dimitriou M,
Doney AS,
Dörr M,
Eklund N,
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Folkersen L,
Garcia ME,
Geller F,
Giedraitis V,
Go AS,
Grallert H,
Grammer TB,
Gräßler J,
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de Groot LC,
Groves CJ,
Haessler J,
Hall P,
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Hallmans G,
Hannemann A,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
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Hlatky MA,
Hoffmann W,
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Isaacs A,
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Lichtner P,
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Hengstenberg C,
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Quertermous T,
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Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium 외 컨소시엄 2곳
Nature genetics · 2014 · PMID 25282103 · open access
페이지 12개+
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay M,
Goel A,
Won HH,
Hall LM,
Willenborg C,
Kanoni S,
Saleheen D,
Kyriakou T,
Nelson CP,
Hopewell JC,
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Zeng L
외 139명 — 모두 보기
Dehghan A,
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Chasman DI,
Chen S,
Ford I,
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Huang J,
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Farrall M
Nature genetics · 2015 · PMID 26343387 · open access
페이지 12개+
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
Winkler TW,
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Graff M,
Barata L,
Feitosa MF,
Chu S,
Czajkowski J,
Esko T,
Fall T,
Kilpeläinen TO,
Lu Y,
Mägi R
외 427명 — 모두 보기
Mihailov E,
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CHARGE Consortium · DIAGRAM Consortium 외 컨소시엄 4곳
PLoS genetics · 2015 · PMID 26426971 · open access
페이지 12개+
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
de Vries PS,
Chasman DI,
Sabater-Lleal M,
Chen MH,
Huffman JE,
Steri M,
Tang W,
Teumer A,
Marioni RE,
Grossmann V,
Hottenga JJ,
Trompet S
외 119명 — 모두 보기
Müller-Nurasyid M,
Zhao JH,
Brody JA,
Kleber ME,
Guo X,
Wang JJ,
Auer PL,
Attia JR,
Yanek LR,
Ahluwalia TS,
Lahti J,
Venturini C,
Tanaka T,
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Joshi PK,
Rocanin-Arjo A,
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Zemunik T,
Morrison AC,
Sennblad B,
Tofler G,
de Maat MP,
de Geus EJ,
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Human molecular genetics · 2016 · PMID 26561523
페이지 12개+
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
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ICBP Consortium · AGEN Consortium 외 컨소시엄 3곳
Nature communications · 2016 · PMID 26831199 · open access
페이지 12개+
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
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METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium 외 컨소시엄 1곳
Nature genetics · 2017 · PMID 28416818
페이지 12개+
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
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BIOS Consortium · Understanding Society Scientific Group
Hypertension (Dallas, Tex. : 1979) · 2017 · PMID 28739976
페이지 12개+
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CHD Exome+ Consortium · EPIC-CVD Consortium 외 컨소시엄 9곳
Nature genetics · 2018 · PMID 29273807 · open access
페이지 12개+
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LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
페이지 12개+
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
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외 49명 — 모두 보기
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European journal of human genetics : EJHG · 2019 · PMID 30679814 · open access
페이지 12개+
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외 269명 — 모두 보기
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LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
Cerebral small vessel disease genomics and its implications across the lifespan
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외 105명 — 모두 보기
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International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
페이지 12개+
Genetically Determined Serum Calcium Levels and Markers of Ventricular Repolarization: A Mendelian Randomization Study in the UK Biobank
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Circulation. Genomic and precision medicine · 2021 · PMID 33887147
페이지 12개+
The trans-ancestral genomic architecture of glycemic traits
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외 393명 — 모두 보기
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Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
페이지 12개+
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어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
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
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.