Dilated cardiomyopathy: the complexity of a diverse genetic architecture

By R. Hershberger, D. Hedges, A. Morales. Nature Reviews Cardiology, 2013

916 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/f3a5a432f8e98cef42ea0c347a085ae95c787c9e

Citations in the corpus

• Dilated Cardiomyopathy: Genetic Determinants and Mechanisms (2017, neutral): “DCM Genetics The majority of genetic DCM is inherited in an autosomal dominant pattern with variable expressivity and penetrance (Figure 4) although specific forms of autosomal recessive, X-linked recessive, and mitochondrial inheritance each occur.(14,19,60) De novo mutations also contribute to gen”
• Adaptation and Validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: Recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel (2018, neutral): “These disorders include hypertrophic, dilated and restrictive cardiomyopathy (HCM, DCM, and RCM), which are collectively among the most prevalent Mendelian conditions and affect 1 in 200–500 individuals 12,13 .”