Author: Vilmundur Gudnason

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Preprints

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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The genetic architecture of the human cerebral cortex

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Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis

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Deep serum proteomics reveal biomarkers and causal candidates for type 2 diabetes

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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Discovering patterns of pleiotropy in genome-wide association studies

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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Molecular Screening of Familial Hypercholesterolemia in the Icelandic Population

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Large Meta-Analysis in the CHARGE Consortium Provides Evidence For an Association of Serum Vitamin D With Pulmonary Function

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Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities

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Human serum proteome profoundly overlaps with genetic signatures of disease

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Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

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