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

6. Determinants of mosaic chromosomal alteration fitness

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41. Neptune: an environment for the delivery of genomic medicine

45. Abstract 10822: Familial Hypercholesterolemia in the EMERGE Network: 1-Year Outcomes After Return of Results

46. Genetic testing in early-onset atrial fibrillation.

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

50. Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome

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