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New common variants affecting susceptibility to basal cell carcinomaAbdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Localization of a susceptibility gene for common forms of stroke to 5q12Genome-wide association yields new sequence variants at seven loci that associate with measures of obesityNew sequence variants associated with bone mineral densityA rare variant in MYH6 is associated with high risk of sick sinus syndromeThe role of adiposity in cardiometabolic traits: a Mendelian randomization analysisEuropean bone mineral density loci are also associated with BMD in East-Asian populationsGenome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysmLarge-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.Genetic variation at 16q24.2 is associated with small vessel stroke.Variants conferring risk of atrial fibrillation on chromosome 4q25.ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries.A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.Large-scale whole-genome sequencing of the Icelandic population.A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.Genes contributing to risk for common forms of stroke.A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.Ischemic stroke is associated with the ABO locus: the EuroCLOT studyA sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysmMeta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease.
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