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1. Rare coding variant analysis for human diseases across biobanks and ancestries

9. Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci

10. A comprehensive evaluation of the genetic architecture of sudden cardiac arrest

11. 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

12. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

14. Genetic testing in early-onset atrial fibrillation.

16. Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assay

17. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

19. Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

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

22. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

23. Genetic background determines the severity of age-dependent cardiac structural abnormalities and arrhythmia susceptibility in Scn5a-1798insD mice.

25. The Role of MAPRE2 and Microtubules in Maintaining Normal Ventricular Conduction

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

28. Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy

29. A validated heart-specific model for splice-disrupting variants in childhood heart disease

31. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy

32. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

33. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

35. Clinical interpretation ofKCNH2variants using a robust PS3/BS3 functional patch clamp assay

36. Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

38. Inherited cardiac arrhythmias

41. Associations of schizophrenia with arrhythmic disorders and electrocardiogram traits: an in-depth genetic exploration of population samples

45. Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies.

46. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

47. Associations of schizophrenia with arrhythmic disorders and electrocardiogram traits: an in-depth genetic exploration of population samples

48. Animal models and animal-free innovations for cardiovascular research

49. Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

50. Reclassification of a likely pathogenic Dutch founder variant in KCNH2:implications of reduced penetrance

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