Familial dilated cardiomyopathy

Next-generation sequencing to identify genetic causes of cardiomyopathies

(2012) Nadine Norton et al.   CURRENT OPINION IN CARDIOLOGY

Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases

(2012) C. Rapezzi et al.   EUROPEAN HEART JOURNAL

Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

(2012) Paul A. van der Zwaag et al.   EUROPEAN JOURNAL OF HEART FAILURE

Genetics and metabolic cardiomyopathies

(2012) E.C. Wicks et al.   HERZ

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

(2012) Neal K. Lakdawala et al.   JOURNAL OF CARDIAC FAILURE

Return of Genetic Results in the Familial Dilated Cardiomyopathy Research Project

(2012) Jill D. Siegfried et al.   Journal of Genetic Counseling

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

(2012) Ingrid A.W. van Rijsingen et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Where Genome Meets Phenome: Rationale for Integrating Genetic and Protein Biomarkers in the Diagnosis and Management of Dilated Cardiomyopathy and Heart Failure

(2012) Sanaz Piran et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Dominant missense mutations in ABCC9 cause Cantú syndrome

(2012) Magdalena Harakalova et al.   NATURE GENETICS

Truncations of Titin Causing Dilated Cardiomyopathy

(2012) Daniel S. Herman et al.   NEW ENGLAND JOURNAL OF MEDICINE

Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of Cardiomyopathies

(2011) Benjamin Meder et al.   Circulation-Cardiovascular Genetics

Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological study

(2011) P. Garcia-Pavia et al.   HEART

Diagnostic Work-Up and Risk Stratification in X-Linked Dilated Cardiomyopathies Caused by Dystrophin Defects

(2011) Marta Diegoli et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

(2010) Frank I. Marcus et al.   CIRCULATION

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

(2010) Perry Elliott et al.   Circulation-Cardiovascular Genetics

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

(2010) P. Charron et al.   EUROPEAN HEART JOURNAL

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy

(2009) Daniel Vega Møller et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Ventricular dysfunction in type 1 myotonic dystrophy: Electrical, mechanical, or both?

(2009) P. Lindqvist et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

(2009) Ray E. Hershberger et al.   JOURNAL OF CARDIAC FAILURE

Mutations in Troponin that cause HCM, DCM AND RCM: What can we learn about thin filament function?

(2009) Ruth H. Willott et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Sudden Death in Hypertrophic Cardiomyopathy

(2009) Barry J. Maron   Journal of Cardiovascular Translational Research

Re-examination of the Electrocardiogram in Boys With Duchenne Muscular Dystrophy and Correlation With Its Dilated Cardiomyopathy

(2008) Philip T. Thrush et al.   AMERICAN JOURNAL OF CARDIOLOGY

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

(2008) Michele Pasotti et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY