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Willemsen G에 대해
73건, 그중 13건 표시.
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,
Sabo A,
Bis JC,
Huffman JE,
Manichaikul A,
Smith AV,
Feitosa MF,
Demissie S,
Joshi PK,
Duan Q,
Marten J,
van Klinken JB
외 86명 — 모두 보기
Surakka I,
Nolte IM,
Zhang W,
Mbarek H,
Li-Gao R,
Trompet S,
Verweij N,
Evangelou E,
Lyytikäinen LP,
Tayo BO,
Deelen J,
van der Most PJ,
van der Laan SW,
Arking DE,
Morrison A,
Dehghan A,
Franco OH,
Hofman A,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Mychaleckyj JC,
Campbell A,
Hocking LJ,
Padmanabhan S,
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Rice KM,
White CC,
Harris T,
Isaacs A,
Campbell H,
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Rudan I,
Kolcic I,
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Zemunik T,
Salomaa V,
Kooner AS,
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Lehne B,
Scott WR,
Tan ST,
de Geus EJ,
Milaneschi Y,
Penninx BW,
Willemsen G,
de Mutsert R,
Ford I,
Gansevoort RT,
Segura-Lepe MP,
Raitakari OT,
Viikari JS,
Nikus K,
Forrester T,
McKenzie CA,
de Craen AJ,
de Ruijter HM,
Pasterkamp G,
Snieder H,
Oldehinkel AJ,
Slagboom PE,
Cooper RS,
Kähönen M,
Lehtimäki T,
Elliott P,
van der Harst P,
Jukema JW,
Mook-Kanamori DO,
Boomsma DI,
Chambers JC,
Swertz M,
Ripatti S,
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Vitart V,
Polasek O,
Hayward C,
Wilson JG,
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Gudnason V,
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Boerwinkle E,
Rotter JI,
Cupples LA,
van Duijn CM
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
페이지 2개
Variants in MTNR1B influence fasting glucose levels
Prokopenko I,
Langenberg C,
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Saxena R,
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Thorleifsson G,
Loos RJ,
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Potter SC,
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외 96명 — 모두 보기
Sanna S,
Hottenga JJ,
Wheeler E,
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Scuteri A,
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Song K,
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Stringham HM,
Tuomi T,
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Uitterlinden AG,
Voight BF,
Waterworth D,
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Witteman JC,
Yuan X,
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Nature genetics · 2009 · PMID 19060907
페이지 1개
Sequence variants in three loci influence monocyte counts and erythrocyte volume
Ferreira MA,
Hottenga JJ,
Warrington NM,
Medland SE,
Willemsen G,
Lawrence RW,
Gordon S,
de Geus EJ,
Henders AK,
Smit JH,
Campbell MJ,
Wallace L
외 11명 — 모두 보기
Evans DM,
Wright MJ,
Nyholt DR,
James AL,
Beilby JP,
Penninx BW,
Palmer LJ,
Frazer IH,
Montgomery GW,
Martin NG,
Boomsma DI
American journal of human genetics · 2009 · PMID 19853236
페이지 1개
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
외 82명 — 모두 보기
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
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Hofman A,
Tönjes A,
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De Diego V,
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Salomaa V,
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Metspalu A,
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ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
페이지 1개
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma
Ferreira MA,
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Marks GB,
Hui J,
Le Souëf P,
Danoy P,
Baltic S,
Nyholt DR,
Jenkins M,
Hayden C,
Willemsen G
외 28명 — 모두 보기
Ang W,
Kuokkanen M,
Beilby J,
Cheah F,
de Geus EJ,
Ramasamy A,
Vedantam S,
Salomaa V,
Madden PA,
Heath AC,
Hopper JL,
Visscher PM,
Musk B,
Leeder SR,
Jarvelin MR,
Pennell C,
Boomsma DI,
Hirschhorn JN,
Walters H,
Martin NG,
James A,
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Abramson MJ,
Robertson CF,
Dharmage SC,
Brown MA,
Montgomery GW,
Thompson PJ
Australian Asthma Genetics Consortium
Lancet (London, England) · 2011 · PMID 21907864
페이지 1개
A genome-wide association search for type 2 diabetes genes in African Americans
Palmer ND,
McDonough CW,
Hicks PJ,
Roh BH,
Wing MR,
An SS,
Hester JM,
Cooke JN,
Bostrom MA,
Rudock ME,
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외 379명 — 모두 보기
Ferrara A,
Lu L,
Ziegler JT,
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Shriner D,
Adeyemo A,
Rotimi CN,
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Voight BF,
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Zeggini E,
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Thorleifsson G,
McCulloch LJ,
Ferreira T,
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Segrè AV,
van Hoek M,
Navarro P,
Ardlie K,
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Boerwinkle E,
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Charpentier G,
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Couper DJ,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
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Jackson AU,
Johnson PR,
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Kao WH,
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Kong A,
Kraft P,
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Lauritzen T,
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DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
페이지 1개
FTO genotype is associated with phenotypic variability of body mass index
Yang J,
Loos RJ,
Powell JE,
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Chasman DI,
Rose LM,
Thorleifsson G,
Steinthorsdottir V,
Mägi R,
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외 160명 — 모두 보기
Yerges-Armstrong LM,
Monda KL,
Hadley D,
Mahajan A,
Li G,
Kapur K,
Vitart V,
Huffman JE,
Wang SR,
Palmer C,
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Fischer K,
Zhao JH,
Demirkan A,
Isaacs A,
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Luan J,
Heard-Costa NL,
White C,
Jackson AU,
Preuss M,
Ziegler A,
Eriksson J,
Kutalik Z,
Frau F,
Nolte IM,
Van Vliet-Ostaptchouk JV,
Hottenga JJ,
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Verweij N,
Goel A,
Medina-Gomez C,
Estrada K,
Bragg-Gresham JL,
Sanna S,
Sidore C,
Tyrer J,
Teumer A,
Prokopenko I,
Mangino M,
Lindgren CM,
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Shuldiner AR,
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Nature · 2012 · PMID 22982992
페이지 1개
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Gottlieb DJ,
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Watson NF,
Eiriksdottir G,
Byrne EM,
Cornelis M,
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외 74명 — 모두 보기
Lahti J,
Li M,
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Molecular psychiatry · 2015 · PMID 25469926 · open access
페이지 1개
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility
Mbarek H,
Steinberg S,
Nyholt DR,
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Miller MB,
McRae AF,
Hottenga JJ,
Day FR,
Willemsen G,
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외 25명 — 모두 보기
Penninx BW,
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American journal of human genetics · 2016 · PMID 27132594
페이지 1개
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
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Finucane H,
Sulem P,
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