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Genetic studies of body mass index yield new insights for obesity biologyMeta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsDirectional dominance on stature and cognition in diverse human populationsRare and low-frequency coding variants alter human adult heightCystatin C and Cardiovascular Disease: A Mendelian Randomization Study.Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Human Validation of Genes Associated With a Murine Atherosclerotic Phenotype.Genetic loci associated with heart rate variability and their effects on cardiac disease risk.Genome-wide analysis identifies 12 loci influencing human reproductive behavior.Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Common coding variant in SERPINA1 increases the risk for large artery stroke.Fine mapping the CETP region reveals a common intronic insertion associated to HDL-CDefining the role of common variation in the genomic and biological architecture of adult human height.The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesityLeukotriene B4 levels in human atherosclerotic plaques and abdominal aortic aneurysms.Taking risk prediction to the next level. Advances in biomarker research for atherosclerosis.Loss of Y Chromosome in Blood Is Associated With Major Cardiovascular Events During Follow-Up in Men After Carotid Endarterectomy.Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization.Genetic variation within the Y chromosome is not associated with histological characteristics of the atherosclerotic carotid artery or aneurysmal wall.Common variants associated with blood lipid levels do not affect carotid plaque composition.Variants in ALOX5, ALOX5AP and LTA4H are not associated with atherosclerotic plaque phenotypes: the Athero-Express Genomics Study.Impaired kidney function is associated with intraplaque hemorrhage in patients undergoing carotid endarterectomy.Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets.Lack of association between connexin40 polymorphisms and coronary artery disease.Deficiency of the stroke relevant HDAC9 gene attenuates atherosclerosis in accord with allele-specific effects at 7p21.1.Impact of carotid atherosclerosis loci on cardiovascular events.Testosterone to estradiol ratio reflects systemic and plaque inflammation and predicts future cardiovascular events in men with severe atherosclerosisTime-Dependent Changes in Atherosclerotic Plaque Composition in Patients Undergoing Carotid Surgery[Genome-wide association studies: methodology and interpretation for clinicians]Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic PlaquesSmoking is Associated to DNA Methylation in Atherosclerotic Carotid LesionsFrom lipid locus to drug target through human genomicsAlternate approach to stroke phenotyping identifies a genetic risk locus for small vessel strokeCirculating CD14+CD16- classical monocytes do not associate with a vulnerable plaque phenotype, and do not predict secondary events in severe atherosclerotic patientsAssociations of autozygosity with a broad range of human phenotypesPlatelet RNA modules point to coronary calcification in asymptomatic women with former preeclampsiaPolygenic Susceptibility of Aortic Aneurysms Associates to the Diameter of the Aneurysm Sac: the Aneurysm-Express Biobank CohortPublisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypesSubsequent Event Risk in Individuals With Established Coronary Heart Disease
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