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(101 - 120 of 188)

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Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Genetic Risk Prediction of Atrial Fibrillation
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function
Cross-sectional association of endogenous steroid hormone, sex hormone-binding globulin, and precursor steroid levels with hemostatic factor levels in postmenopausal women
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study
Novel genetic loci associated with hippocampal volume
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Novel genetic loci underlying human intracranial volume identified through genome-wide association
Thyroid Function Within the Reference Range and the Risk of Stroke: An Individual Participant Data Analysis
Gene-gene Interaction Analyses for Atrial Fibrillation
Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits
Rooted in risk: genetic predisposition for low-density lipoprotein cholesterol level associates with diminished low-density lipoprotein cholesterol response to statin treatment
52 Genetic Loci Influencing Myocardial Mass
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
The association of statin therapy with the risk of recurrent venous thrombosis
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

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