Search

Your search keyword '"Smith, Nicholas L."' showing total 1,206 results

Search Constraints

Start Over You searched for: Author "Smith, Nicholas L." Remove constraint Author: "Smith, Nicholas L."
1,206 results on '"Smith, Nicholas L."'

Search Results

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

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

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

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

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

7. Circulating Androgen Concentrations and Risk of Incident Heart Failure in Older Men: The Cardiovascular Health Study

8. Rare genetic variants explain missing heritability in smoking.

11. Genome-wide investigation of exogenous female hormones, genetic variation, and venous thromboembolism risk

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

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

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

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

16. Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

17. Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

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

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

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

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

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

23. Development and validation of a risk model for hospital-acquired venous thrombosis: the Medical Inpatients Thrombosis and Hemostasis study

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

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

27. BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion

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

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

30. Genome-wide analysis identifies novel susceptibility loci for myocardial infarction

31. Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism

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

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

35. Stroke genetics informs drug discovery and risk prediction across ancestries

37. DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood

38. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

39. 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.

42. Antithrombin, PC (Protein C), and PS (Protein S): Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

43. Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

44. A large‐scale exome array analysis of venous thromboembolism

45. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

46. Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

47. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

49. Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

50. Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain.

Catalog

Books, media, physical & digital resources