Genetic Evaluation of Dilated Cardiomyopathy

Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated Cardiomyopathy

(2013) Nadine Norton et al.   Circulation-Cardiovascular Genetics

The changing spectrum of arrhythmogenic (right ventricular) cardiomyopathy

(2012) Stefania Rizzo et al.   CELL AND TISSUE RESEARCH

Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era

(2012) Nadine Norton et al.   Circulation-Cardiovascular Genetics

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

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

Dominant missense mutations in ABCC9 cause Cantú syndrome

(2012) Magdalena Harakalova et al.   NATURE GENETICS

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

(2012) Wei Guo et al.   NATURE MEDICINE

Truncations of Titin Causing Dilated Cardiomyopathy

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

Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy

(2011) Nadine Norton et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Psychological Issues in Genetic Testing for Inherited Cardiovascular Diseases

(2011) Rajani D. Aatre et al.   Circulation-Cardiovascular Genetics

Homozygosity Mapping and Exome Sequencing Reveal GATAD1 Mutation in Autosomal Recessive Dilated Cardiomyopathy

(2011) Jeanne L. Theis et al.   Circulation-Cardiovascular Genetics

Assessment of LMNA Copy Number Variation in 58 Probands with Dilated Cardiomyopathy

(2011) Nadine Norton et al.   CTS-Clinical and Translational Science

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

(2011) P. Garcia-Pavia et al.   HEART

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

(2011) Michael J. Ackerman et al.   HEART RHYTHM

Clinical Characteristics of Peripartum Cardiomyopathy in the United States

(2011) Uri Elkayam   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy

(2011) Ray E. Hershberger et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

(2010) Pallavi Gupta et al.   BASIC RESEARCH IN CARDIOLOGY

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

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

Coding Sequence Rare Variants Identified in MYBPC3 , MYH6 , TPM1 , TNNC1 , and TNNI3 From 312 Patients With Familial or Idiopathic Dilated Cardiomyopathy

(2010) Ray E. Hershberger et al.   Circulation-Cardiovascular Genetics

Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T Mutation

(2010) Ana Morales et al.   CTS-Clinical and Translational Science

Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy

(2010) Duanxiang Li et al.   CTS-Clinical and Translational Science

Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny

(2010) Michael V Zaragoza et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals

(2010) Ray E Hershberger et al.   GENETICS IN MEDICINE

A Glimpse Into Multigene Rare Variant Genetics

(2010) Ray E. Hershberger   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy

(2009) Ray E. Hershberger et al.   Circulation-Cardiovascular Genetics

Multiple Mutations in Genetic Cardiovascular Disease

(2009) Matthew Kelly et al.   Circulation-Cardiovascular Genetics

Progress With Genetic Cardiomyopathies

(2009) Ray E. Hershberger et al.   Circulation-Heart Failure

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

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

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

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

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

(2009) Katharine M. Brauch et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Mutation in BAG3 causes severe dominant childhood muscular dystrophy

(2008) Duygu Selcen et al.   ANNALS OF NEUROLOGY

Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

(2008) Ray E. Hershberger et al.   CTS-Clinical and Translational Science

Left-Dominant Arrhythmogenic Cardiomyopathy

(2008) Srijita Sen-Chowdhry et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy

(2008) Maximilian G. Posch et al.   MOLECULAR GENETICS AND METABOLISM