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성함이나 학술지명, PMID로 찾아보십시오.
Campbell H에 대해
101건, 그중 20건 표시.
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Huang J,
Huffman JE,
Yamakuchi M,
Trompet S,
Asselbergs FW,
Sabater-Lleal M,
Trégouët DA,
Chen WM,
Smith NL,
Kleber ME,
Shin SY,
Becker DM
외 81명 — 모두 보기
Tang W,
Dehghan A,
Johnson AD,
Truong V,
Folkersen L,
Yang Q,
Oudot-Mellkah T,
Buckley BM,
Moore JH,
Williams FM,
Campbell H,
Silbernagel G,
Vitart V,
Rudan I,
Tofler GH,
Navis GJ,
Destefano A,
Wright AF,
Chen MH,
de Craen AJ,
Worrall BB,
Rudnicka AR,
Rumley A,
Bookman EB,
Psaty BM,
Chen F,
Keene KL,
Franco OH,
Böhm BO,
Uitterlinden AG,
Carter AM,
Jukema JW,
Sattar N,
Bis JC,
Bis JC,
Ikram MA,
Sale MM,
McKnight B,
Fornage M,
Ford I,
Taylor K,
Slagboom PE,
McArdle WL,
Hsu FC,
Franco-Cereceda A,
Goodall AH,
Yanek LR,
Furie KL,
Cushman M,
Hofman A,
Witteman JC,
Folsom AR,
Basu S,
Matijevic N,
van Gilst WH,
Wilson JF,
Westendorp RG,
Kathiresan S,
Reilly MP,
Tracy RP,
Polasek O,
Winkelmann BR,
Grant PJ,
Hillege HL,
Cambien F,
Stott DJ,
Lowe GD,
Spector TD,
Meigs JB,
Marz W,
Eriksson P,
Becker LC,
Morange PE,
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Hayward C,
van der Harst P,
Hamsten A,
Lowenstein CJ,
Strachan DP,
O'Donnell CJ
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium 외 컨소시엄 1곳
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
페이지 2개
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
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Esko T
외 470명 — 모두 보기
Fall T,
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Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
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Wang Z,
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Isaacs A,
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LifeLines Cohort Study · ADIPOGen Consortium 외 컨소시엄 12곳
Nature · 2015 · PMID 25673413
페이지 2개
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer
Al-Tassan NA,
Whiffin N,
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Palles C,
Farrington SM,
Dobbins SE,
Harris R,
Gorman M,
Tenesa A,
Meyer BF,
Wakil SM,
Kinnersley B
외 23명 — 모두 보기
Campbell H,
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Scientific reports · 2015 · PMID 25990418 · open access
페이지 2개
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
van Leeuwen EM,
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Manichaikul A,
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Duan Q,
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외 86명 — 모두 보기
Surakka I,
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LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
페이지 2개
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Jiang X,
O'Reilly PF,
Aschard H,
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Hsu YH,
Richards JB,
Dupuis J,
Ingelsson E,
Karasik D,
Pilz S,
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Kestenbaum B
외 93명 — 모두 보기
Zheng J,
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Albanes D,
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Tang W,
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Nature communications · 2018 · PMID 29343764 · open access
페이지 2개
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Tenesa A,
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Porteous ME,
Walker M,
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Barnetson RA,
Theodoratou E,
Cetnarskyj R,
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외 45명 — 모두 보기
Reid FJ,
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Nature genetics · 2008 · PMID 18372901
페이지 1개
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
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외 63명 — 모두 보기
Rowan A,
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CORGI Consortium · EPICOLON Consortium
Nature genetics · 2008 · PMID 18372905
페이지 1개
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
Heard-Costa NL,
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Johansson A,
Harris TB,
Fu M,
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Feitosa MF,
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외 49명 — 모두 보기
Smith AV,
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McArdle PF,
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Boerwinkle E,
Brancati F,
Demerath EW,
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PLoS genetics · 2009 · PMID 19557197 · open access
페이지 1개
Common genetic variants associate with serum phosphorus concentration
Kestenbaum B,
Glazer NL,
Köttgen A,
Felix JF,
Hwang SJ,
Liu Y,
Lohman K,
Kritchevsky SB,
Hausman DB,
Petersen AK,
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외 27명 — 모두 보기
Meitinger T,
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Wichmann HE,
Campbell H,
Hayward C,
Rudan I,
de Boer IH,
Psaty BM,
Rice KM,
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Rivadeneira F,
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Hofman A,
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Kao WH,
Witteman JC,
Siscovick DS,
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Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
페이지 1개
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Human molecular genetics · 2010 · PMID 20639392
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CUBN is a gene locus for albuminuria
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Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
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MAGIC · DIAGRAM Consortium 외 컨소시엄 1곳
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