Jessica van Setten
occupation: researcher
Articles 26
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Rare and low-frequency coding variants alter human adult height
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Discovery of novel heart rate-associated loci using the Exome Chip
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Loss of Y Chromosome in Blood Is Associated With Major Cardiovascular Events During Follow-Up in Men After Carotid Endarterectomy
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Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization
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Genetic variation within the Y chromosome is not associated with histological characteristics of the atherosclerotic carotid artery or aneurysmal wall
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Association between a Single Donor TARC/CCL17 Promotor Polymorphism and Obstructive Chronic Lung Allograft Dysfunction after Lung Transplantation
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Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk
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Human Validation of Genes Associated With a Murine Atherosclerotic Phenotype
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52 Genetic Loci Influencing Myocardial Mass
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Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population
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Exome Array Analysis of Susceptibility to Pneumococcal Meningitis
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Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
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Genetic studies of body mass index yield new insights for obesity biology
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Directional dominance on stature and cognition in diverse human populations
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The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
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Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies
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Variants in ALOX5, ALOX5AP and LTA4H are not associated with atherosclerotic plaque phenotypes: the Athero-Express Genomics Study
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Serum lipid levels, body mass index, and their role in coronary artery calcification: a polygenic analysis
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The Genome of the Netherlands: design, and project goals
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Defining the role of common variation in the genomic and biological architecture of adult human height
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Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'.
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Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction
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No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
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Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci
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Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci
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Composition of carotid atherosclerotic plaque is associated with cardiovascular outcome: a prognostic study
Human - wd:Q42170904