898 results on '"Bezzina, Connie"'
Search Results
2. Knock-in swine model reveals new arrhythmia mechanism in Timothy syndrome
3. Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies.
4. A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population
5. Causal inference in the field of arrhythmia: An introduction to mendelian randomization
6. Novelties in Brugada Syndrome: Complex Genetics, Risk Stratification, and Catheter Ablation
7. Common genetic variants improve risk stratification after the atrial switch operation for transposition of the great arteries
8. Cardiac Repolarization in Health and Disease
9. Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci
10. Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assay
11. A comprehensive evaluation of the genetic architecture of sudden cardiac arrest
12. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
13. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
14. Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
15. A deep learning approach identifies new ECG features in congenital long QT syndrome
16. Genetic testing in early-onset atrial fibrillation.
17. Genetics and genomics of arrhythmic risk: current and future strategies to prevent sudden cardiac death
18. The Role of MAPRE2 and Microtubules in Maintaining Normal Ventricular Conduction
19. A Genotype-phenotype Taxonomy of Hypertrophic Cardiomyopathy
20. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
21. Novel pathogenic role for galectin-3 in early disease stages of arrhythmogenic cardiomyopathy
22. Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
23. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand
24. Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
25. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
26. Genetic background determines the severity of age-dependent cardiac structural abnormalities and arrhythmia susceptibility in Scn5a-1798insD mice.
27. SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes
28. A rare non-coding enhancer variant in SCN5A contributes to the high prevalence of Brugada syndrome in Thailand
29. Knock-in swine model reveals new arrhythmia mechanism in Timothy syndrome
30. Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy
31. A validated heart-specific model for splice-disrupting variants in childhood heart disease
32. Integrating metabolomics and proteomics to identify novel drug targets for heart failure and atrial fibrillation
33. Clinical interpretation ofKCNH2variants using a robust PS3/BS3 functional patch clamp assay
34. Top stories on genome-wide association studies.
35. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries
36. Epidemiology of inherited arrhythmias
37. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy
38. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
39. Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias
40. Genome-wide association studies of cardiovascular disease
41. Enhanced late sodium current underlies pro-arrhythmic intracellular sodium and calcium dysregulation in murine sodium channelopathy
42. Inherited cardiac arrhythmias
43. Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families
44. CMR 3-104 - A Genotype-phenotype Taxonomy of Hypertrophic Cardiomyopathy
45. Associations of schizophrenia with arrhythmic disorders and electrocardiogram traits: an in-depth genetic exploration of population samples
46. PO-02-153 THE ROLE OF AND MICROTUBULES IN CARDIAC ELECTROPHYSIOLOGY AND BRUGADA SYNDROME
47. Abstract 16685: Shared Genetic Pathways Contribute to Risk of Hypertrophic and Dilated Cardiomyopathies With Opposite Directions of Effect
48. Animal models and animal-free innovations for cardiovascular research
49. Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation
50. Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies.
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