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성함이나 학술지명, PMID로 찾아보십시오.
Stefansson K에 대해
207건, 그중 20건 표시.
Mutations in BRIP1 confer high risk of ovarian cancer
Rafnar T,
Gudbjartsson DF,
Sulem P,
Jonasdottir A,
Sigurdsson A,
Jonasdottir A,
Besenbacher S,
Lundin P,
Stacey SN,
Gudmundsson J,
Magnusson OT,
le Roux L
외 33명 — 모두 보기
Orlygsdottir G,
Helgadottir HT,
Johannsdottir H,
Gylfason A,
Tryggvadottir L,
Jonasson JG,
de Juan A,
Ortega E,
Ramon-Cajal JM,
García-Prats MD,
Mayordomo C,
Panadero A,
Rivera F,
Aben KK,
van Altena AM,
Massuger LF,
Aavikko M,
Kujala PM,
Staff S,
Aaltonen LA,
Olafsdottir K,
Bjornsson J,
Kong A,
Salvarsdottir A,
Saemundsson H,
Olafsson K,
Benediktsdottir KR,
Gulcher J,
Masson G,
Kiemeney LA,
Mayordomo JI,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2011 · PMID 21964575
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,
Talbert ME,
Lewis JP
외 379명 — 모두 보기
Ferrara A,
Lu L,
Ziegler JT,
Sale MM,
Divers J,
Shriner D,
Adeyemo A,
Rotimi CN,
Ng MC,
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Freedman BI,
Bowden DW,
Voight BF,
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Steinthorsdottir V,
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DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
페이지 1개
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Voight BF,
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외 114명 — 모두 보기
Clarke R,
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Lancet (London, England) · 2012 · PMID 22607825 · open access
페이지 1개
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
Perry JR,
Voight BF,
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Amin N,
Dupuis J,
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외 63명 — 모두 보기
Almgren P,
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MAGIC · DIAGRAM Consortium 외 컨소시엄 1곳
PLoS genetics · 2012 · PMID 22693455 · open access
페이지 1개
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Zeggini E,
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Day-Williams AG,
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외 64명 — 모두 보기
Jonsdottir I,
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arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
페이지 1개
FTO genotype is associated with phenotypic variability of body mass index
Yang J,
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외 160명 — 모두 보기
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Nature · 2012 · PMID 22982992
페이지 1개
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
Dichgans M,
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외 27명 — 모두 보기
Thorsteinsdottir U,
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METASTROKE Consortium · CARDIoGRAM Consortium 외 컨소시엄 2곳
Stroke · 2014 · PMID 24262325
페이지 1개
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
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외 71명 — 모두 보기
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Nature genetics · 2014 · PMID 24880342 · open access
페이지 1개
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Power RA,
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Cohen-Woods S,
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외 64명 — 모두 보기
Wray NR,
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페이지 1개
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
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외 10명 — 모두 보기
Nature genetics · 2017 · PMID 27918536
페이지 1개
Genetic variation at 16q24.2 is associated with small vessel stroke
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외 55명 — 모두 보기
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METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
페이지 1개
A genome-wide association study yields five novel thyroid cancer risk loci
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외 28명 — 모두 보기
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페이지 1개
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
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LifeLines Cohort Study · InterAct Consortium 외 컨소시엄 4곳
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페이지 1개
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
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외 30명 — 모두 보기
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iPSYCH-SSI-Broad Group
Nature communications · 2017 · PMID 28537267 · open access
페이지 1개
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
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외 163명 — 모두 보기
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DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
페이지 1개
The nature of nurture: Effects of parental genotypes
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외 3명 — 모두 보기
Science (New York, N.Y.) · 2018 · PMID 29371463
페이지 1개
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin
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외 11명 — 모두 보기
Arnadottir GA,
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Communications biology · 2018 · PMID 30271932 · open access
페이지 1개
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy
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Helgadottir A,
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Jonsdottir I
외 21명 — 모두 보기
Kristinsdottir AM,
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Nature communications · 2019 · PMID 30992453 · open access
페이지 1개
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk
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외 14명 — 모두 보기
Chen YE,
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Regeneron Genetics Center
Nature communications · 2020 · PMID 33097703 · open access
페이지 1개
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
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McGinnis R,
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Stefansdottir L,
Thorleifsson G,
Shooter S,
Fadista J,
Sigurdsson JK,
Auro KM,
Berezina G,
Borges MC,
Bumpstead S
외 63명 — 모두 보기
Bybjerg-Grauholm J,
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Dolby VA,
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Nishanova F,
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Pipkin FB,
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Saevarsdottir S,
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Scaife PJ,
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Stefansson OA,
Sørensen KM,
Thomsen LCV,
Tragante V,
Trogstad L,
Simpson NAB,
Aripova T,
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Dominiczak AF,
Walker JJ,
Thorsteinsdottir U,
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FINNPEC Consortium · GOPEC Consortium
Nature communications · 2020 · PMID 33239696 · open access
페이지 1개
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