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Singleton AB에 대해
25건, 그중 20건 표시.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Ganesh SK,
Zakai NA,
van Rooij FJ,
Soranzo N,
Smith AV,
Nalls MA,
Chen MH,
Kottgen A,
Glazer NL,
Dehghan A,
Kuhnel B,
Aspelund T
외 50명 — 모두 보기
Yang Q,
Tanaka T,
Jaffe A,
Bis JC,
Verwoert GC,
Teumer A,
Fox CS,
Guralnik JM,
Ehret GB,
Rice K,
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Rendon A,
Eiriksdottir G,
Levy D,
Patel KV,
Boerwinkle E,
Rotter JI,
Hofman A,
Sambrook JG,
Hernandez DG,
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Bandinelli S,
Singleton AB,
Coresh J,
Lumley T,
Uitterlinden AG,
Vangils JM,
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Zwaginga JJ,
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Meisinger C,
Deloukas P,
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Spector TD,
Gieger C,
Gudnason V,
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Ferrucci L,
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Harris TB,
Lin JP
Nature genetics · 2009 · PMID 19862010 · open access
페이지 12개+
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls MA,
Pankratz N,
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Do CB,
Hernandez DG,
Saad M,
DeStefano AL,
Kara E,
Bras J,
Sharma M,
Schulte C,
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외 35명 — 모두 보기
Arepalli S,
Letson C,
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Stefansson H,
Liu X,
Pliner H,
Lee JH,
Cheng R,
Ikram MA,
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Houlden H,
Payami H,
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Foroud T,
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International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) 외 컨소시엄 10곳
Nature genetics · 2014 · PMID 25064009 · open access
페이지 12개+
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
Kia DA,
Noyce AJ,
Xue A,
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Young E
외 39명 — 모두 보기
von Coelln R,
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Schulte C,
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Hardy JA,
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Graham RR,
Singleton AB
23andMe Research Team · System Genomics of Parkinson's Disease Consortium 외 컨소시엄 1곳
The Lancet. Neurology · 2019 · PMID 31701892
페이지 12개+
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
Graff M,
Justice AE,
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Marouli E,
Zhang X,
Fine RS,
Lim E,
Buchanan V,
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외 213명 — 모두 보기
Shao Y,
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Cooper RS,
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Dimitrov L,
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Grant SFA,
Guo X,
Hakonarson H,
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Henderson BE,
Hennis A,
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Hirschhorn JN,
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American journal of human genetics · 2021 · PMID 33713608
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
Graham SE,
Mukamel RE,
Spracklen CN,
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Ji Y,
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Cai H,
Cai Q,
Campbell A,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
Cocca M,
Concas MP,
Couture C,
Cuellar-Partida G,
Danning R,
Daw EW,
Degenhard F,
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Delitala A,
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Li SA,
Li X,
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Yu L,
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23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
페이지 12개+
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
Kim JJ,
Vitale D,
Otani DV,
Lian MM,
Heilbron K,
Iwaki H,
Lake J,
Solsberg CW,
Leonard H,
Makarious MB,
Tan EK,
Singleton AB
외 6명 — 모두 보기
23andMe Research Team · Global Parkinson’s Genetics Program (GP2)
Nature genetics · 2024 · PMID 38155330 · open access
페이지 12개+
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Evans DS,
Avery CL,
Nalls MA,
Li G,
Barnard J,
Smith EN,
Tanaka T,
Butler AM,
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Alonso A,
Arking DE,
Berenson GS
외 49명 — 모두 보기
Bis JC,
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Chen W,
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Young T,
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Zonderman AB,
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Whitsel EA,
Reiner AP,
Sotoodehnia N
CHARGE QRS Consortium
Human molecular genetics · 2016 · PMID 27577874
페이지 9개
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
den Hoed M,
Eijgelsheim M,
Esko T,
Brundel BJ,
Peal DS,
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외 256명 — 모두 보기
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페이지 8개
Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry
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외 69명 — 모두 보기
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PLoS genetics · 2011 · PMID 21998595 · open access
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외 6명 — 모두 보기
International Parkinson Disease Genomics Consortium
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페이지 5개
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외 81명 — 모두 보기
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PLoS genetics · 2011 · PMID 21738480 · open access
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페이지 3개
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외 24명 — 모두 보기
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페이지 3개
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외 3명 — 모두 보기
International Parkinson's Disease Genomics Consortium · 23andMe Research Team
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페이지 3개
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
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외 180명 — 모두 보기
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SLALOM Consortium · PARALS Consortium 외 컨소시엄 2곳
Nature genetics · 2021 · PMID 34873335 · open access
페이지 3개
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease
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외 8명 — 모두 보기
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페이지 3개
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외 52명 — 모두 보기
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CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
페이지 2개
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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