HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS)…

By M. Ackerman, S. Priori, S. Willems, C. Berul, R. Brugada, H. Calkins, A. Camm, P. Ellinor, M. Gollob, R. Hamilton and 11 more. Heart Rhythm, 2011

872 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine

View Paper: https://www.semanticscholar.org/paper/200c03d47ce7d585fd21e3b90546e61a7e5ba7aa

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Citations in the corpus

• Exercise Increases Age-Related Penetrance and Arrhythmic Risk in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated Desmosomal Mutation Carriers (2013, background): “Clinical genetic testing for ARVD/C is now routinely performed (19).”
• 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the preventionof sudden cardiac death (2015, neutral): “variant due to mutations in the gene encoding for the cardiac ryanodine receptor gene (RyR2) and a rare recessive variant caused by mutation in the cardiac calsequestrin gene (CASQ2).(52) Mutations”