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1. Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

2. The Relationship of Duffy Gene Polymorphism with High-Sensitivity C-Reactive Protein, Mortality, and Cardiovascular Outcomes in Black Individuals

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

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

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

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

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

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

9. Determinants of mosaic chromosomal alteration fitness

10. Demographic and Clinical Factors Associated With SARS-CoV-2 Spike 1 Antibody Response Among Vaccinated US Adults: the C4R Study

12. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

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

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

15. Proteogenomic analysis integrated with electronic health records data reveals disease-associated variants in Black Americans

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

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

18. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

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

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

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

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

24. The PRIMED Consortium: Reducing disparities in polygenic risk assessment

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

26. Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

43. Association of mitochondrial DNA copy number with cardiometabolic diseases

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

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

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

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

49. Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study

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

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