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1. Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

2. Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings

3. Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

6. Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

7. A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand

9. Catheter Ablation for Ventricular Tachycardia in Patients With Desmoplakin Cardiomyopathy

10. Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome

14. A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

17. A Rare Noncoding Enhancer Variant in SCN5AContributes to the High Prevalence of Brugada Syndrome in Thailand

19. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

20. Computer versus cardiologist: Is a machine learning algorithm able to outperform an expert in diagnosing a phospholamban p.Arg14del mutation on the electrocardiogram?

21. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand

22. Catheter Ablation for Ventricular Tachycardia in Patients With Desmoplakin Cardiomyopathy

23. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study

24. Tropomyosin–troponin complex in inherited cardiomyopathies

26. A rare non-coding enhancer variant in SCN5A contributes to the high prevalence of Brugada syndrome in Thailand

27. Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic review

31. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies

33. Prognostic significance of fever-induced Brugada syndrome

35. An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

36. Variant Location Is a Novel Risk Factor for Individuals with Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant

37. Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy

38. Variant Location Is a Novel Risk Factor for Individuals with Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant

39. Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy

42. Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant

43. Multimodality Screening For (Peri)Myocarditis In Newly Diagnosed Idiopathic Inflammatory Myopathies: A Cross-Sectional Study

44. Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy

46. Contributors

48. Penetrance and Prognosis of MYH7Variant-Associated Cardiomyopathies

49. KBTBD13 is a novel cardiomyopathy gene

50. Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy

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