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1. A methylation risk score for chronic kidney disease: a HyperGEN study

2. Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

3. Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

5. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.

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

7. The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

8. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.

9. Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

10. Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.

11. Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

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

13. Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

14. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

15. Genetic diversity fuels gene discovery for tobacco and alcohol use

16. Association of a Multiancestry Genome-Wide Blood Pressure Polygenic Risk Score With Adverse Cardiovascular Events

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

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

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

22. Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study

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

24. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

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

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

27. Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci

28. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

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

30. Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

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

32. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

33. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

34. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

35. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.

36. A lipidome-wide association study of the lipoprotein insulin resistance index

37. Inherited causes of clonal haematopoiesis in 97,691 whole genomes

38. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.

39. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

40. Returning integrated genomic risk and clinical recommendations: The eMERGE study

41. Stroke genetics informs drug discovery and risk prediction across ancestries

42. Integrating Hypertension Phenotype and Genotype with Hybrid Non-negative Matrix Factorization

43. APOL1 Nephropathy Risk Alleles and Mortality in African American Adults: A Cohort Study

44. 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.

45. Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group

48. Genome-wide polygenic score to predict chronic kidney disease across ancestries

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

50. Novel risk loci encompassing genes influencing STAT3, GPCR, and oxidative stress signaling are associated with co-morbid GERD and COPD.

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