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

2. Identification of proteins associated with type 2 diabetes risk in diverse racial and ethnic populations

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

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

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

6. Genome-wide association identifies novel ROP risk loci in a multiethnic cohort

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

8. Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk.

9. Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

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

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

12. Multivariate adaptive shrinkage improves cross-population transcriptome prediction and association studies in underrepresented populations

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

14. The functional impact of rare variation across the regulatory cascade

15. Myocardial Fibrosis and Cardiomyopathy Risk: A Genetic Link in the MESA

16. Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma

17. Lac-Phe mediates the effects of metformin on food intake and body weight

18. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

19. Multiset correlation and factor analysis enables exploration of multi-omics data

20. Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake

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

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

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

24. Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis

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

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

27. Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA

28. Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS)

29. Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

30. Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

31. Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis

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

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

34. Nontargeted and Targeted Metabolomic Profiling Reveals Novel Metabolite Biomarkers of Incident Diabetes in African Americans

35. Rare genetic variants explain missing heritability in smoking.

36. Differences in Metabolomic Profiles Between Black and White Women and Risk of Coronary Heart Disease: an Observational Study of Women From Four US Cohorts

37. Association of polygenic risk scores with incident atherosclerotic cardiovascular disease events among individuals with coronary artery calcium score of zero: The multi-ethnic study of atherosclerosis

38. Proteomic Profile of the ICAM1 p.K56M HFpEF Risk Variant

39. Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

40. Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease

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

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

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

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

46. Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

47. A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

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

50. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

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