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1. Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

2. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

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

4. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

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

6. Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential.

7. Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease

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

9. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

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

11. Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.

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

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

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

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

17. FixItFelix: improving genomic analysis by fixing reference errors

18. Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

19. Rare genetic variants explain missing heritability in smoking.

21. Interpreting NMR dynamic parameters via the separation of reorientational motion in MD simulation

22. TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

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

24. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

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

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

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

29. Gene Set Enrichment Analsyes Identiify Pathways Involved in Genetic Risk for Diabetic Retinopathy

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

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

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

36. A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

37. Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

38. Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer’s disease and myocardial infarction

40. Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

41. Unraveling motion in proteins by combining NMR relaxometry and molecular dynamics simulations: A case study on ubiquitin.

42. Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

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

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

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

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

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

50. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

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