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1. Clinical and genetic risk factors for progressive fibrosis in metabolic dysfunction-associated steatotic liver disease.

2. Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis.

3. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

4. Characteristics of Older Patients With Immunotolerant Chronic Hepatitis B Virus Infection

5. A MUC5B Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality

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

7. Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis

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

9. A missense variant in human perilipin 2 (PLIN2 Ser251Pro) reduces hepatic steatosis in mice

10. Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes

11. Large-scale identification of undiagnosed hepatic steatosis using natural language processing

13. A roadmap for serum biomarkers for hepatitis B virus: current status and future outlook

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

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

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

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

19. Gender Differences in Demographic and Health Characteristics of the Million Veteran Program Cohort

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

21. The power of genetic diversity in genome-wide association studies of lipids

22. Virus-associated Inflammation Imprints an Inflammatory Profile on Long-lived Monocyte-derived Macrophages in the Human Liver

24. Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19

26. Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry

28. Improved Survival Among all Interferon-α-Treated Patients in HCV-002, a Veterans Affairs Hepatitis C Cohort of 2211 Patients, Despite Increased Cirrhosis Among Nonresponders

29. CXCL12 regulates coronary artery dominance in diverse populations and links development to disease

30. A Missense Variant in Human Perilipin 2 (Plin2 Ser251pro) Reduces Hepatic Steatosis In Mice

31. Heterogeneous effects on type 2 diabetes and cardiovascular outcomes of genetic variants and traits associated with fasting insulin.

33. Association Between Severe Serum Alanine Aminotransferase Flares and Hepatitis B e Antigen Seroconversion and HBV DNA Decrease in Untreated Patients With Chronic HBV Infection

34. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

35. Characteristics of Adults in the Hepatitis B Research Network in North America Reflect Their Country of Origin and Hepatitis B Virus Genotype

36. Gender Differences in Demographic and Health Characteristics of the Million Veteran Program Cohort

39. Risk of Hepatocellular Carcinoma After Spontaneous Clearance of Hepatitis C Virus and in Noncirrhosis Chronic Hepatitis C Patients With Sustained Virological Response: A Systematic Review

40. Dissecting the Genetic Architecture of Intracranial Aneurysms

41. A Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization

42. Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease

43. Genome-wide association study of peripheral artery disease in the Million Veteran Program

44. Abstract 560: Genetics Of Physical Activity And Risk Of Cardiovascular Disease

46. Abstract 16710: CYP2C19 Polymorphisms and Clinical Outcomes Following Percutaneous Coronary Intervention (PCI) in the Million Veterans Program (MVP)

48. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program

50. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

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