| 36723951 | Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease. | JAMA Cardiol | 2023 |
| 38028628 | Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci. | Front Genet | 2023 |
| 38014529 | Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis. | Circ Genom Precis Med | 2023 |
| 37648373 | Ancestral diversity in lipoprotein(a) studies helps address evidence gaps. | Open Heart | 2023 |
| 37986948 | Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure. | medRxiv | 2023 |
| 37802043 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. | Am J Hum Genet | 2023 |
| 37886448 | A new Approach to Identify Gene-Environment Interactions and Reveal New Biological Insight in Complex traits. | Res Sq | 2023 |
| 37961350 | A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. | bioRxiv | 2023 |
| 37770635 | Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. | Nat Genet | 2023 |
| 36716967 | DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood. | J Thromb Haemost | 2023 |
| 37398003 | Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. | medRxiv | 2023 |
| 36759176 | Polygenic risk, lifestyle and the lifetime risk of coronary artery disease. | | 2023 |
| 37327218 | Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study. | PLoS One | 2023 |
| 36696182 | Novel genetic regulators of fibrinogen synthesis identified by an in vitro experimental platform. | J Thromb Haemost | 2023 |
| 37425772 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. | medRxiv | 2023 |
| 37546893 | Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus. | medRxiv | 2023 |
| 35285134 | Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. | J Thromb Haemost | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 35388009 | Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. | Nat Commun | 2022 |
| 36220816 | Whole genome sequence analysis of blood lipid levels in >66,000 individuals. | Nat Commun | 2022 |
| 36154123 | Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. | Circulation | 2022 |
| 35995843 | Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations. | Commun Biol | 2022 |
| 36513073 | Correlations between complex human phenotypes vary by genetic background, gender, and environment. | Cell Rep Med | 2022 |
| 36481753 | Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. | Nat Commun | 2022 |
| 36544485 | Multi-omics insights into the biological mechanisms underlying statistical gene-by-lifestyle interactions with smoking and alcohol consumption. | Front Genet | 2022 |
| 34788810 | Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues. | Hum Mol Genet | 2022 |
| 35264566 | Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. | Nat Commun | 2022 |
| 35022422 | A multi-omics study of circulating phospholipid markers of blood pressure. | Sci Rep | 2022 |
| 35094551 | American Heart Association's Life's Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease. | Circulation | 2022 |
| 34582791 | Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 33859359 | Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure. | Mol Psychiatry | 2021 |
| 33795393 | Association Between Hemostatic Profile and Migraine: A Mendelian Randomization Analysis. | Neurology | 2021 |
| 33846329 | Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. | Nat Commun | 2021 |
| 33887194 | Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 33512453 | Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation. | Blood | 2021 |
| 34039022 | <i>APOL1</i> Genetic Variants Are Associated With Increased Risk of Coronary Atherosclerotic Plaque Rupture in the Black Population. | Arterioscler Thromb Vasc Biol | 2021 |
| 33876560 | FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimer. | J Thromb Haemost | 2021 |
| 33500576 | Lifestyle Risk Score: handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions. | Eur J Hum Genet | 2021 |
| 34087167 | Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 34245042 | Genetic susceptibility, obesity and lifetime risk of type 2 diabetes: The ARIC study and Rotterdam Study. | Diabet Med | 2021 |
| 34081724 | Leveraging a health information exchange for analyses of COVID-19 outcomes including an example application using smoking history and mortality. | PLoS One | 2021 |
| 32847391 | Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief Report. | Arterioscler Thromb Vasc Biol | 2021 |
| 34409733 | No prospective association of a polygenic risk score for coronary artery disease with venous thromboembolism incidence. | Journal of Thrombosis and Haemostasis | 2021 |
| 34387095 | Progress and Research Priorities in Imaging Genomics for Heart and Lung Disease: Summary of an NHLBI Workshop. | Circ Cardiovasc Imaging | 2021 |
| 34363016 | Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications. | Genet Med | 2021 |
| 32552674 | Deriving stratified effects from joint models investigating gene-environment interactions. | BMC Bioinformatics | 2020 |
| 33367543 | A Mendelian randomization of γ' and total fibrinogen levels in relation to venous thromboembolism and ischemic stroke. | Blood | 2020 |
| 33186364 | 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. | PLoS One | 2020 |
| 32510982 | Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels. | Circ Genom Precis Med | 2020 |
| 32661250 | The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function. | Nature Communications | 2020 |