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

2. Rare variant contribution to the heritability of coronary artery disease

4. Polygenic Risk Scores and Extreme Coronary Artery Calcium Phenotypes (CAC=0 and CAC≥1000) in Adults ≥75 Years Old: The ARIC Study

5. Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.

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

7. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

8. Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study.

9. Correlations between complex human phenotypes vary by genetic background, gender, and environment

10. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

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

12. Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

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

15. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

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

17. Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

18. Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

19. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

20. A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

21. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

22. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

23. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

24. Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

25. Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

26. A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

27. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

29. FGL1 as a modulator of plasma D‐dimer levels: Exome‐wide marker analysis of plasma tPA, PAI‐1, and D‐dimer

30. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.

31. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

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

33. Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

34. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

35. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

36. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

37. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.

38. Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

39. DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood

41. Gene-lifestyle interactions in the genomics of human complex traits

42. Antithrombin, PC (Protein C), and PS (Protein S): Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

43. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

44. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

45. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

46. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

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

48. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

49. Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

50. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.

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