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70 results on '"Raffield, Laura M"'

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

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

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

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

5. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

6. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

7. The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes

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

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

10. A saturated map of common genetic variants associated with human height

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

12. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

13. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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

15. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

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

17. Additional file 3 of Rare coding variants in RCN3 are associated with blood pressure

18. Additional file 5 of Rare coding variants in RCN3 are associated with blood pressure

19. Additional file 1 of Rare coding variants in RCN3 are associated with blood pressure

20. Additional file 7 of Rare coding variants in RCN3 are associated with blood pressure

21. Additional file 8 of Rare coding variants in RCN3 are associated with blood pressure

22. Additional file 9 of Rare coding variants in RCN3 are associated with blood pressure

23. Additional file 2 of Rare coding variants in RCN3 are associated with blood pressure

24. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

25. Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in African Americans: Olson; suPAR genetic variation and CVD risk in JHS

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

27. Association of mitochondrial DNA copy number with cardiometabolic diseases

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

29. Clonal hematopoiesis associated with epigenetic aging and clinical outcomes

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

31. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

32. Additional file 6 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

33. Additional file 1 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

34. Additional file 5 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

35. Additional file 3 of DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function

36. Additional file 5 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

37. Additional file 6 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

38. DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function

39. Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study

40. Additional file 4 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

41. Additional file 3 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

42. Additional file 2 of DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function

43. DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function

44. The Polygenic and Monogenic Basis of Blood Traits and Diseases

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

46. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

47. Additional file 1 of Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics

48. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

49. 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

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

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