592 results on '"Hershberger, Ray E."'
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2. Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
3. The DCM Project Portal: A direct-to-participant platform of The DCM Research Project
4. Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
5. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
6. ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
7. Abstract 14241: Alcohol Exposure Among Patients With Dilated Cardiomyopathy: A Report From the DCM Precision Medicine Study
8. Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study
9. TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study
10. Bidirectional Risk Modulator and Modifier Variant of Dilated and Hypertrophic Cardiomyopathy in BAG3.
11. Dilated Cardiomyopathy
12. ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
13. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
14. Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert Panel
15. Abstract 14707: Electrocardiographic Abnormalities Are Common in DCM Patients’ Family Members With Early Manifestations of DCM
16. Familial Dilated Cardiomyopathy
17. Monoallelic TTN Truncation Variants Identified in Individuals With DCM May Cause a Mild Skeletal Myopathy
18. Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
19. Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the future
20. The DCM Project Portal: A direct-to-participant platform of The DCM Research Project
21. Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
22. Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline
23. Author response: A human mitofusin 2 mutation can cause mitophagic cardiomyopathy
24. Differences in Cardiac Mechanics among Genetically At-Risk First-Degree Relatives: The DCM Precision Medicine Study
25. Screening for Dilated Cardiomyopathy in At-Risk First-Degree Relatives
26. Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
27. Transcriptomics and Beyond in Dilated Cardiomyopathy
28. Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
29. Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
30. Reappraisal of Reported Genes for Sudden Arrhythmic Death: An Evidence-Based Evaluation of Gene Validity for Brugada Syndrome
31. Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy
32. Dilated cardiomyopathy
33. A human mitofusin 2 mutation can cause mitophagic cardiomyopathy.
34. Efficacy and Safety of ARRY-371797 in LMNA -Related Dilated Cardiomyopathy: A Phase 2 Study
35. Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene
36. 2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis
37. Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy
38. The Rationale and Timing of Molecular Genetic Testing for Dilated Cardiomyopathy
39. Heart Failure in Non-Caucasians, Women, and Older Adults: A White Paper on Special Populations From the Heart Failure Society of America Guideline Committee
40. Advanced (Stage D) Heart Failure: A Statement From the Heart Failure Society of America Guidelines Committee
41. A human mitofusin 2 mutation causes mitophagic cardiomyopathy
42. Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome
43. ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
44. TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study
45. Acute Decompensated Heart Failure: Update on New and Emerging Evidence and Directions for Future Research
46. Temporal Relationship of Conduction System Disease and Ventricular Dysfunction in LMNA Cardiomyopathy
47. Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
48. Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study
49. Is Left Ventricular Noncompaction a Trait, Phenotype, or Disease?: The Evidence Points to Phenotype
50. Update on Aldosterone Antagonists Use in Heart Failure With Reduced Left Ventricular Ejection Fraction Heart Failure Society of America Guidelines Committee
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