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

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

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

4. Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

5. Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function

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

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

10. Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups

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

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

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

14. Rare genetic variants explain missing heritability in smoking.

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

16. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

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

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

19. A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

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

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

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

23. Population sequencing data reveal a compendium of mutational processes in the human germ line.

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

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

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

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

28. Bending the Curve in Cardiovascular Disease Mortality

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

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

31. Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

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

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

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

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

36. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

37. Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

38. 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.

39. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

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

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

42. 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease

43. Correction to: 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines

44. Correction to: 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines

45. 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines

46. 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.

47. Systematic Error Removal Using Random Forest for Normalizing Large-Scale Untargeted Lipidomics Data

48. Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry

49. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

50. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.

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