|
| 36721044 | An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signaling. | Commun Biol | 2023 |
| 35567697 | Assay-related differences in SuPAR levels: implications for measurement and data interpretation. | Journal of Nephrology | 2023 |
| 36414227 | Risk factors for clonal hematopoiesis of indeterminate potential and mosaic chromosomal alterations. | | 2023 |
| 36444934 | Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease. | Hum Mol Genet | 2023 |
| 36116031 | An empirical Bayes approach to improving population-specific genetic association estimation by leveraging cross-population data. | Genetic Epidemiology | 2023 |
| 37756531 | Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk. | Diabetes Care | 2023 |
| 37745480 | Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium. | bioRxiv | 2023 |
| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 37905118 | Determinants of mosaic chromosomal alteration fitness. | medRxiv | 2023 |
| 37904051 | Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing. | Nat Genet | 2023 |
| 37804200 | Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk. | J Am Heart Assoc | 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 |
| 37558590 | Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19. | Blood Cells Mol Dis | 2023 |
| 38061917 | Individual and Neighborhood-level Socioeconomic Status and Somatic Mutations Associated With Increased Risk of Cardiovascular Disease and Mortality: A Cross-Sectional Analysis in the Women's Health Initiative. | | 2023 |
| 37777527 | Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality. | Nat Commun | 2023 |
| 37961350 | A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. | bioRxiv | 2023 |
| 37609271 | The Relationship of Duffy Gene Polymorphism, High Sensitivity C-Reactive Protein, and Long-term Outcomes. | medRxiv | 2023 |
| 37034613 | Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders. | Res Sq | 2023 |
| 36964402 | Centenarian clocks: epigenetic clocks for validating claims of exceptional longevity. | Geroscience | 2023 |
| 37466697 | Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential. | Cancer Epidemiol Biomarkers Prev | 2023 |
| 37333361 | Association of Clonal Hematopoiesis of Indeterminate Potential with Incident Heart Failure with Preserved Ejection Fraction. | | 2023 |
| 36824751 | Genetic mechanisms of 184 neuro-related proteins in human plasma. | medRxiv | 2023 |
| 36812475 | DNAmFitAge: biological age indicator incorporating physical fitness. | Aging (Albany NY) | 2023 |
| 37118842 | Assessment of immune cell profiles among post-menopausal women in the Women's Health Initiative using DNA methylation-based methods. | Clin Epigenetics | 2023 |
| 36791419 | Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits. | Diabetes | 2023 |
| 37533140 | Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait. | Clin J Am Soc Nephrol | 2023 |
| 37489536 | Age at Menopause, Leukocyte Telomere Length, and Coronary Artery Disease in Postmenopausal Women. | | 2023 |
| 37163084 | Gene Expression and Splicing QTL Analysis of Blood Cells in African American Participants from the Jackson Heart Study. | | 2023 |
| 35138379 | Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits. | Hum Mol Genet | 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 |
| 35592775 | The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. | Front Endocrinol (Lausanne) | 2022 |
| 35588732 | Integration of rare expression outlier-associated variants improves polygenic risk prediction. | Am J Hum Genet | 2022 |
| 35835498 | Contributions of the Women's Health Initiative to Cardiovascular Research: JACC State-of-the-Art Review. | J Am Coll Cardiol | 2022 |
| 35387486 | Genetic Landscape of the ACE2 Coronavirus Receptor. | Circulation | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 36220816 | Whole genome sequence analysis of blood lipid levels in >66,000 individuals. | Nat Commun | 2022 |
| 35504290 | TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data. | Am J Hum Genet | 2022 |
| 36154123 | Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. | Circulation | 2022 |
| 35948364 | Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney Disease. | Clin J Am Soc Nephrol | 2022 |
| 35552711 | Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. | Hum Mol Genet | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 35610705 | Longitudinal profiling of clonal hematopoiesis provides insight into clonal dynamics. | Immunity and Ageing | 2022 |
| 35357453 | Intake and Sources of Dietary Fiber, Inflammation, and Cardiovascular Disease in Older US Adults. | JAMA Netw Open | 2022 |
| 36193739 | Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney Function. | Hypertension | 2022 |
| 36050321 | Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. | Nat Commun | 2022 |
| 36516495 | DNA methylation GrimAge version 2. | Aging (Albany NY) | 2022 |
| 36568030 | Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. | HGG Adv | 2022 |
| 36481753 | Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. | Nat Commun | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 34990411 | Clonal hematopoiesis in sickle cell disease. | J Clin Invest | 2022 |