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Author Details

Paul S de Vries
2014
88
26
PMIDPaper TitleJournal TitlePublished Year
36723951Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease.JAMA Cardiol2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
38014529Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.Circ Genom Precis Med2023
37648373Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.Open Heart2023
37986948Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure.medRxiv2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37886448A new Approach to Identify Gene-Environment Interactions and Reveal New Biological Insight in Complex traits.Res Sq2023
37961350A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.bioRxiv2023
37770635Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.Nat Genet2023
36716967DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.J Thromb Haemost2023
37398003Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.medRxiv2023
36759176Polygenic risk, lifestyle and the lifetime risk of coronary artery disease.2023
37327218Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study.PLoS One2023
36696182Novel genetic regulators of fibrinogen synthesis identified by an in vitro experimental platform.J Thromb Haemost2023
37425772Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.medRxiv2023
37546893Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.medRxiv2023
35285134Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.J Thromb Haemost2022
35652341Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.Hypertension2022
35388009Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.Nat Commun2022
36220816Whole genome sequence analysis of blood lipid levels in >66,000 individuals.Nat Commun2022
36154123Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.Circulation2022
35995843Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations.Commun Biol2022
36513073Correlations between complex human phenotypes vary by genetic background, gender, and environment.Cell Rep Med2022
36481753Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.Nat Commun2022
36544485Multi-omics insights into the biological mechanisms underlying statistical gene-by-lifestyle interactions with smoking and alcohol consumption.Front Genet2022
34788810Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.Hum Mol Genet2022
35264566Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.Nat Commun2022
35022422A multi-omics study of circulating phospholipid markers of blood pressure.Sci Rep2022
35094551American Heart Association's Life's Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease.Circulation2022
34582791Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.Am J Hum Genet2021
33859359Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.Mol Psychiatry2021
33795393Association Between Hemostatic Profile and Migraine: A Mendelian Randomization Analysis.Neurology2021
33846329Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.Nat Commun2021
33887194Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
33512453Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation.Blood2021
34039022<i>APOL1</i> Genetic Variants Are Associated With Increased Risk of Coronary Atherosclerotic Plaque Rupture in the Black Population.Arterioscler Thromb Vasc Biol2021
33876560FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimer.J Thromb Haemost2021
33500576Lifestyle Risk Score: handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions.Eur J Hum Genet2021
34087167Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
34245042Genetic susceptibility, obesity and lifetime risk of type 2 diabetes: The ARIC study and Rotterdam Study.Diabet Med2021
34081724Leveraging a health information exchange for analyses of COVID-19 outcomes including an example application using smoking history and mortality.PLoS One2021
32847391Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief Report.Arterioscler Thromb Vasc Biol2021
34409733No prospective association of a polygenic risk score for coronary artery disease with venous thromboembolism incidence.Journal of Thrombosis and Haemostasis2021
34387095Progress and Research Priorities in Imaging Genomics for Heart and Lung Disease: Summary of an NHLBI Workshop.Circ Cardiovasc Imaging2021
34363016Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications.Genet Med2021
32552674Deriving stratified effects from joint models investigating gene-environment interactions.BMC Bioinformatics2020
33367543A Mendelian randomization of γ' and total fibrinogen levels in relation to venous thromboembolism and ischemic stroke.Blood2020
33186364Genetic 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.PLoS One2020
32510982Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels.Circ Genom Precis Med2020
32661250The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function.Nature Communications2020
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