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

2. Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program

4. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

5. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

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

7. Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study

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

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

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

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

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

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

16. peri -Adventitial delivery of smooth muscle cells in porous collagen scaffolds for treatment of experimental abdominal aortic aneurysm

17. Genetics of varicose veins reveals polygenic architecture and genetic overlap with arterial and venous disease

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

19. 2022 ACC/AHA guideline for the diagnosis and management of aortic disease: A report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines

20. E-Cigarettes and Cardiopulmonary Health

27. Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease

28. Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility

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

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

31. Genome-Wide Association Study of CKD Progression

32. Deep learning modeling of rare noncoding genetic variants in human motor neurons definesCCDC146as a therapeutic target for ALS

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

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

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

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

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

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

40. Alcohol Consumption and Risk of Coronary Artery Disease (from the Million Veteran Program)

41. DASH Score and Subsequent Risk of Coronary Artery Disease: The Findings From Million Veteran Program

42. GWAS of epigenetic aging rates in blood reveals a critical role for TERT.

44. 2022 ACC/AHA Guideline for the Diagnosis and Management of Aortic Disease: A Report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines

47. MicroRNA miR-29b regulates diabetic aortic remodeling and stiffening

48. A Pilot Study: The Beneficial Effects of Combined Statin-exercise Therapy on Cognitive Function in Patients with Coronary Artery Disease and Mild Cognitive Decline

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

50. An epigenetic clock analysis of race/ethnicity, sex, and coronary heart disease

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