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1. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program

2. A scoping review of using Large Language Models (LLMs) to investigate Electronic Health Records (EHRs)

3. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

4. Cardiovascular Disease and Mortality in Black Women Carrying the Amyloidogenic V122I Transthyretin Gene Variant.

5. Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers

6. Epigenome-wide meta-analysis of BMI in nine cohorts: Examining the utility of epigenetically predicted BMI.

7. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program.

8. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification

9. Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts

10. Rare coding variants in RCN3 are associated with blood pressure

11. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

12. Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits

14. A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease

15. A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

16. Design and pilot results from the Million Veteran Program Return Of Actionable Results (MVP-ROAR) Study

17. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

18. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

20. Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases

21. Genetic insights into resting heart rate and its role in cardiovascular disease

22. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

23. Broad clinical manifestations of polygenic risk for coronary artery disease in the Women’s Health Initiative

24. Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program

25. Identifying a stable and generalizable factor structure of major depressive disorder across three large longitudinal cohorts

27. Multi-trait association studies discover pleiotropic loci between Alzheimer’s disease and cardiometabolic traits

28. Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes

29. Clonal hematopoiesis associated with epigenetic aging and clinical outcomes

30. Epigenome-wide association study of diet quality in the Women's Health Initiative and TwinsUK cohort.

31. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

32. Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

34. A saturated map of common genetic variants associated with human height

37. Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies

39. Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

41. High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease

42. Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease

43. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

44. An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis

45. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

46. Integration of rare expression outlier-associated variants improves polygenic risk prediction

47. A translational genomics approach identifies IL10RB as the top candidate gene target for COVID-19 susceptibility

48. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

49. Genomics and phenomics of body mass index reveals a complex disease network

50. Mendelian randomization analyses clarify the effects of height on cardiovascular diseases.

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