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1. Invasive Assessment of Coronary Artery Disease in Clonal Hematopoiesis of Indeterminate Potential.

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

3. Determinants of mosaic chromosomal alteration fitness.

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

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

8. Clinical associations with a polygenic predisposition to benign lower white blood cell counts

10. The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

11. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

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

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

14. Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

15. The All of Us Research Program: Data quality, utility, and diversity

16. Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.

17. The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and Statin‐Associated Musculoskeletal Symptoms

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

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

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

23. Returning integrated genomic risk and clinical recommendations: The eMERGE study

24. Anticancer drug-induced life-threatening ventricular arrhythmias: a World Health Organization pharmacovigilance study.

26. Clinical Management of Brugada Syndrome: Commentary From the Experts

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

28. The All of Us Research Program: Data quality, utility, and diversity

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

30. Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant

32. Abstract 15689: Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia Genes

35. Pulmonary Vein Myocardial Sleeve Length and its Association With Sex and 4q25/PITX2 Genotype

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

40. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

41. An International Multicenter Evaluation of Type 5 Long QT Syndrome

44. Large language models facilitate the generation of electronic health record phenotyping algorithms

45. Androgenic Effects on Ventricular Repolarization: A Translational Study From the International Pharmacovigilance Database to iPSC-Cardiomyocytes.

46. Genome‐Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol

47. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

48. Cardiovascular toxicities associated with immune checkpoint inhibitors: an observational, retrospective, pharmacovigilance study.

49. Increased long QT and torsade de pointes reporting on tamoxifen compared with aromatase inhibitors.

50. LPA Variants are Associated with Residual Cardiovascular Risk in Patients Receiving Statins

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