Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals

Relevance of truncating titin mutations in dilated cardiomyopathy

(2016) O. Akinrinade et al.   CLINICAL GENETICS

Deception in simplicity: Hereditary phospholamban mutations in dilated cardiomyopathy

(2015) Howard S. Young et al.   Biochemistry and Cell Biology

A study in Polish patients with cardiomyopathy emphasizes pathogenicity of phospholamban (PLN) mutations at amino acid position 9 and low penetrance of heterozygous null PLN mutations

(2015) Grażyna T Truszkowska et al.   BMC Medical Genetics

Genetic advances in sarcomeric cardiomyopathies: state of the art

(2015) C. Y. Ho et al.   CARDIOVASCULAR RESEARCH

A novel human R25C-phospholamban mutation is associated with super-inhibition of calcium cycling and ventricular arrhythmia

(2015) Guan-Sheng Liu et al.   CARDIOVASCULAR RESEARCH

Prolonged dual antiplatelet therapy after drug-eluting stenting: meta-analysis of randomized trials

(2015) Salvatore Cassese et al.   Clinical Research in Cardiology

Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy

(2015) M. Gramlich et al.   EMBO Molecular Medicine

Genetics and genotype–phenotype correlations in Finnish patients with dilated cardiomyopathy

(2015) Oyediran Akinrinade et al.   EUROPEAN HEART JOURNAL

A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genes

(2015) Magdalena Harakalova et al.   EUROPEAN JOURNAL OF HEART FAILURE

Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies

(2015) Stephan Waldmüller et al.   MOLECULAR AND CELLULAR PROBES

Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease

(2015) Angharad M. Roberts et al.   Science Translational Medicine

Outcome in Phospholamban R14del Carriers: Results of a Large Multicentre Cohort Study

(2014) I. A. W. van Rijsingen et al.   Circulation-Cardiovascular Genetics

Investigating the role of acute mental stress on endothelial dysfunction: a systematic review and meta-analysis

(2014) Yi-Tao Xue et al.   Clinical Research in Cardiology

Atlas of the clinical genetics of human dilated cardiomyopathy

(2014) Jan Haas et al.   EUROPEAN HEART JOURNAL

Normal and aberrant splicing ofLMNA

(2014) Yue-Bei Luo et al.   JOURNAL OF MEDICAL GENETICS

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies

(2013) Michal Saj et al.   BMC Medical Genetics

Whole Exome Sequencing Identifies a Causal RBM20 Mutation in a Large Pedigree With Familial Dilated Cardiomyopathy

(2013) Quinn S. Wells et al.   Circulation-Cardiovascular Genetics

The Genetics of Dilated Cardiomyopathy: A Prioritized Candidate Gene Study ofLMNA,TNNT2,TCAP, andPLN

(2013) Marika Hirtle-Lewis et al.   CLINICAL CARDIOLOGY

Poor Prognosis of Rare Sarcomeric Gene Variants in Patients with Dilated Cardiomyopathy

(2013) Marco Merlo et al.   CTS-Clinical and Translational Science

Alterations in cardiac DNA methylation in human dilated cardiomyopathy

(2013) Jan Haas et al.   EMBO Molecular Medicine

Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects

(2013) Nina E. Hasselberg et al.   EUROPACE

Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience

(2013) Karin Y. van Spaendonck-Zwarts et al.   EUROPEAN JOURNAL OF HEART FAILURE

Implantable cardioverter-defibrillators in lamin A/C mutation carriers with cardiac conduction disorders

(2013) Frédéric Anselme et al.   HEART RHYTHM

Temporal Relationship of Conduction System Disease and Ventricular Dysfunction in LMNA Cardiomyopathy

(2013) Chad Brodt et al.   JOURNAL OF CARDIAC FAILURE

Genetic mutations and mechanisms in dilated cardiomyopathy

(2013) Elizabeth M. McNally et al.   JOURNAL OF CLINICAL INVESTIGATION

Recurrent and founder mutations in the Netherlands—Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy

(2013) P. A. van der Zwaag et al.   Netherlands Heart Journal

Cardiac Myosin Binding Protein-C Mutations in Families With Hypertrophic Cardiomyopathy

(2012) Stephen P. Page et al.   Circulation-Cardiovascular Genetics

Subtle Abnormalities in Contractile Function Are an Early Manifestation of Sarcomere Mutations in Dilated Cardiomyopathy

(2012) Neal K. Lakdawala et al.   Circulation-Cardiovascular Genetics

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

Identification of Novel Mutations in LMNA Associated with Familial Forms of Dilated Cardiomyopathy

(2012) Birgit Stallmeyer et al.   Genetic Testing and Molecular Biomarkers

Hydrophobic Imbalance in the Cytoplasmic Domain of Phospholamban Is a Determinant for Lethal Dilated Cardiomyopathy

(2012) Delaine K. Ceholski et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

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

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

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

Mutations in the human phospholamban gene in patients with heart failure

(2011) Alessandra Medeiros et al.   AMERICAN HEART JOURNAL

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

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

Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure

(2011) Stephan Waldmüller et al.   EUROPEAN JOURNAL OF HEART FAILURE

Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy

(2011) Gilles Millat et al.   European Journal of Medical Genetics

Inherited Cardiomyopathies

(2011) Hugh Watkins et al.   NEW ENGLAND JOURNAL OF MEDICINE

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

Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy

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

Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3gene

(2009) Philipp Ehlermann et al.   BMC Medical 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 deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes

(2009) Maximilian G. Posch et al.   HEART RHYTHM

Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement

(2009) David Moher et al.   JOURNAL OF CLINICAL EPIDEMIOLOGY

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

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

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

(2008) Sharie B. Parks et al.   AMERICAN HEART JOURNAL

Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy

(2008) Andreas Perrot et al.   BASIC RESEARCH IN CARDIOLOGY

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

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

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

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy

(2008) Taranjit Singh Rai et al.   MOLECULAR AND CELLULAR BIOCHEMISTRY