|
| 37351609 | Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts. | Ann Am Thorac Soc | 2023 |
| 37848499 | Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA. | | 2023 |
| 37601969 | Multiset correlation and factor analysis enables exploration of multi-omics data. | Cell Genom | 2023 |
| 37745480 | Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium. | bioRxiv | 2023 |
| 37662416 | Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies. | bioRxiv | 2023 |
| 37582364 | Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma. | Cell Metab | 2023 |
| 37869564 | Multivariate adaptive shrinkage improves cross-population transcriptome prediction and association studies in underrepresented populations. | HGG Adv | 2023 |
| 37216410 | Canonical correlation analysis for multi-omics: Application to cross-cohort analysis. | PLoS Genet | 2023 |
| 36698131 | Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis. | Respir Res | 2023 |
| 36798214 | Multivariate adaptive shrinkage improves cross-population transcriptome prediction for transcriptome-wide association studies in underrepresented populations. | bioRxiv | 2023 |
| 36463326 | Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis. | Int J Obes (Lond) | 2023 |
| 37425716 | Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects. | bioRxiv | 2023 |
| 37502922 | Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA. | Res Sq | 2023 |
| 35087136 | Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study. | Sci Rep | 2022 |
| 36314488 | Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study. | Journal of the American Heart Association | 2022 |
| 35658476 | Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease. | Circ Res | 2022 |
| 35657918 | Telomere shortening and the transition to family caregiving in the Reasons for Geographic and Racial Differences in Stroke (REGARDS) study. | PLoS One | 2022 |
| 36240095 | Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke. | Neurology | 2022 |
| 36052690 | Differences in Metabolomic Profiles Between Black and White Women and Risk of Coronary Heart Disease: an Observational Study of Women From Four US Cohorts. | Circ Res | 2022 |
| 35716666 | Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits. | Am J Hum Genet | 2022 |
| 36526671 | Development and validation of a metabolite index for obstructive sleep apnea across race/ethnicities. | Sci Rep | 2022 |
| 34814699 | Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. | Circulation | 2022 |
| 33931109 | Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci. | Genome Med | 2021 |
| 34015820 | Benchmarking association analyses of continuous exposures with RNA-seq in observational studies. | Brief Bioinform | 2021 |
| 34050697 | Clonal hematopoiesis associated with epigenetic aging and clinical outcomes. | Aging Cell | 2021 |
| 33517400 | Genome-wide association study of circulating interleukin 6 levels identifies novel loci. | Hum Mol Genet | 2021 |
| 33057025 | Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants. | Nat Commun | 2020 |
| 31630377 | Transitions to family caregiving: enrolling incident caregivers and matched non-caregiving controls from a population-based study. | Aging clinical and experimental research | 2020 |
| 31883642 | Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts. | Am J Hum Genet | 2020 |
| 32155316 | Association of soluble interleukin-2 receptor α and tumour necrosis factor receptor 1 with heart failure: The Multi-Ethnic Study of Atherosclerosis. | ESC heart failure | 2020 |
| 32386347 | Comparison of Proteomic Assessment Methods in Multiple Cohort Studies. | Proteomics | 2020 |
| 32581123 | The transition to family caregiving and its effect on biomarkers of inflammation. | Proceedings of the National Academy of Sciences of the United States of America | 2020 |
| 29321517 | Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study. | J Hum Genet | 2018 |
| 28630896 | The GH receptor exon 3 deletion is a marker of male-specific exceptional longevity associated with increased GH sensitivity and taller stature. | Sci Adv | 2017 |
| 28912365 | D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study. | Arterioscler Thromb Vasc Biol | 2017 |
| 26293465 | Plasma Levels of Soluble Interleukin-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan. | Arterioscler Thromb Vasc Biol | 2015 |
| 25896652 | Platelets and platelet-derived factor Va confer hemostatic competence in complete factor V deficiency. | Blood | 2015 |
| 26442836 | A genetic risk score comprising known venous thromboembolism loci is associated with chronic venous disease in a multi-ethnic cohort. | Thromb Res | 2015 |
| 25065297 | A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans. | J Cardiovasc Electrophysiol | 2014 |
| 24622110 | Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study. | Circ Cardiovasc Genet | 2014 |
| 24643644 | Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans. | Hum Genet | 2014 |
| 24507775 | Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. | Am J Hum Genet | 2014 |
| 23022100 | Discovery and fine mapping of serum protein loci through transethnic meta-analysis. | Am J Hum Genet | 2012 |
| 21386754 | Cerivastatin, genetic variants, and the risk of rhabdomyolysis. | Pharmacogenet Genomics | 2011 |
| 20167578 | Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. | Hum Mol Genet | 2010 |
| 20040767 | Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators. | Blood | 2010 |
| 18439552 | Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. | Am J Hum Genet | 2008 |
| 18278190 | Associations between common fibrinogen gene polymorphisms and cardiovascular disease in older adults. The Cardiovascular Health Study. | Thromb Haemost | 2008 |
| 17885212 | USF1 gene variants, cardiovascular risk, and mortality in European Americans: analysis of two US cohort studies. | Arterioscler Thromb Vasc Biol | 2007 |
| 17851695 | IL-6 gene variation is associated with IL-6 and C-reactive protein levels but not cardiovascular outcomes in the Cardiovascular Health Study. | Human Genetics | 2007 |