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Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesAttenuated familial adenomatous polyposis manifests as autosomal dominant late-onset colorectal cancer.Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathwaysNo interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels.Impact of common variation in bone-related genes on type 2 diabetes and related traitsA genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistanceFunctional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate CancerTrans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.Unravelling modifiers of breast and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers: update on genetic modifiers.Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.Exome array analysis identifies ETFB as a novel susceptibility gene for anthracycline-induced cardiotoxicity in cancer patients.Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.Prediction of measured weight from self-reported weight was not improved after stratification by body mass index.Exome array analysis identifies GPR35 as a novel susceptibility gene for anthracycline-induced cardiotoxicity in childhood cancer.Evaluation of association methods for analysing modifiers of disease risk in carriers of high-risk mutations.No evidence for a causal link between uric acid and type 2 diabetes: a Mendelian randomisation approachPublisher Correction: Shared heritability and functional enrichment across six solid cancersEpidemiology of ATTRV30M neuropathy in Cyprus and the modifier effect of complement C1q on the age of disease onsetAssociation of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and AggressivenessFine-mapping of 150 breast cancer risk regions identifies 191 likely target genesCandidate Causal Variants at the 8p12 Breast Cancer Risk Locus Regulate DUSP4Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
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description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Daniel Barnes
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Daniel Barnes
@en
Daniel Barnes
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Daniel Barnes
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Daniel Barnes
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type
label
Daniel Barnes
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Daniel Barnes
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Daniel Barnes
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Daniel Barnes
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Daniel Barnes
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altLabel
Daniel R Barnes
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prefLabel
Daniel Barnes
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Daniel Barnes
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Daniel Barnes
@es
Daniel Barnes
@nl
Daniel Barnes
@sl
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36717400000
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0000-0002-3781-7570