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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. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

8. Determinants of mosaic chromosomal alteration fitness

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

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

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

13. Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve KCNH2-LQTS Variant Classification and Cardiac Event Risk Stratification

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

15. Clinical Characteristics and Outcomes in Patients With Atrial Fibrillation and Pathogenic TTN Variants

16. Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia Genes

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

43. Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia

44. ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia

45. The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network

46. Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort

47. Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease.

48. PheMIME: an interactive web app and knowledge base for phenome-wide, multi-institutional multimorbidity analysis.

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

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