Cardiomyopathies are a heterogeneous group of heart muscle diseases associated with
heart failure, arrhythmias, and death. Genetic variation has a critical role in the pathogenesis …

Cardiomyopathies are primarily genetic disorders of the myocardium associated with higher
risk of life-threatening cardiac arrhythmias, heart failure, and sudden cardiac death. The …

Over the last quarter-century, there has been tremendous progress in genetics research that
has defined molecular causes for cardiomyopathies. More than a thousand mutations have …

With the wider deployment of massively-parallel, next-generation sequencing, it is now
possible to survey human genome data for research and clinical purposes. The reduced …

Background Cardiomyopathies are a leading cause of progressive heart failure and sudden
cardiac death; however, their genetic aetiology remains poorly understood. We …

Inherited cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy,
arrhythmogenic right ventricular cardiomyopathy, left ventricular noncompaction, and …

Despite the striking advances in medical and surgical therapy, the morbidity, mortality, and
economic burden of heart failure (HF) remain unacceptably high. There is increasing …

Cardiomyopathies are the most common disorders resulting in heart failure, with dilated
cardiomyopathy being responsible for the majority of cases. Other forms of cardiomyopathy …

The Genetic Basis for Cardiomyopathy: Cell Skip to Main Content Advertisement Cell This
journal offers authors two options (open access or subscription) to publish research This …

Next-generation sequencing to identify genetic causes of car... : Current Opinion in
Cardiology Next-generation sequencing to identify genetic causes of cardiomyopathies …