Related references
Note: Only part of the references are listed.Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
Andrew R. Harper et al.
NATURE GENETICS (2021)
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Rafik Tadros et al.
NATURE GENETICS (2021)
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
Francesco Mazzarotto et al.
CIRCULATION (2020)
The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski et al.
NATURE (2020)
The Broad Spectrum ofLMNACardiac Diseases: From Molecular Mechanisms to Clinical Phenotype
Silvia Crasto et al.
FRONTIERS IN PHYSIOLOGY (2020)
Gene specific therapies - the next therapeutic milestone in neurology
David Brenner et al.
NEUROLOGICAL RESEARCH AND PRACTICE (2020)
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy
Andre E. Minoche et al.
GENETICS IN MEDICINE (2019)
Gene therapy strategies in the treatment of hypertrophic cardiomyopathy
Maksymilian Prondzynski et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2019)
Combinatorial interactions of genetic variants in human cardiomyopathy
Dekker C. Deacon et al.
NATURE BIOMEDICAL ENGINEERING (2019)
Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood
Amit Khera et al.
CELL (2019)
Polygenic risk scores in coronary artery disease
Abhiram S. Rao et al.
CURRENT OPINION IN CARDIOLOGY (2019)
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy
Jeffrey A. Towbin et al.
HEART RHYTHM (2019)
Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies
Karim Wahbi et al.
CIRCULATION (2019)
Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Attributable to a Human Myosin Regulatory Light Chain Mutation
Kathia Zaleta-Rivera et al.
CIRCULATION (2019)
Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield
Kate L. Thomson et al.
GENETICS IN MEDICINE (2019)
Heritability in genetic heart disease: the role of genetic background
Joeri A. Jansweijer et al.
OPEN HEART (2019)
Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes
Jodie Ingles et al.
CIRCULATION-GENOMIC AND PRECISION MEDICINE (2019)
Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation
Nina Eide Hasselberg et al.
EUROPEAN HEART JOURNAL (2018)
Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology
Antoine Bondue et al.
CARDIOVASCULAR RESEARCH (2018)
Prevalence of Pathogenic Gene Mutations and Prognosis Do Not Differ in Isolated Left Ventricular Dysfunction Compared With Dilated Cardiomyopathy
Mark R. Hazebroek et al.
CIRCULATION-HEART FAILURE (2018)
Titin cardiomyopathy leads to altered mitochondrial energetics, increased fibrosis and long-termlife-threatening arrhythmias
Job A. J. Verdonschot et al.
EUROPEAN HEART JOURNAL (2018)
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E. Hershberger et al.
GENETICS IN MEDICINE (2018)
Genetic Etiology for Alcohol-Induced Cardiac Toxicity
James S. Ware et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2018)
Putative functional genes in idiopathic dilated cardiomyopathy
Nishanth Ulhas Nair et al.
SCIENTIFIC REPORTS (2018)
Association of Racial/Ethnic Categories With the Ability of Genetic Tests to Detect a Cause of Cardiomyopathy
Latrice G. Landry et al.
JAMA CARDIOLOGY (2018)
Genomic structural variations lead to dysregulation of important coding and non-coding RNA species in dilated cardiomyopathy
Jan Haas et al.
EMBO MOLECULAR MEDICINE (2018)
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
Roddy Walsh et al.
GENETICS IN MEDICINE (2017)
Titin-truncating variants affect heart function in disease cohorts and the general population
Sebastian Schafer et al.
NATURE GENETICS (2017)
PREIMPLANTATION GENETIC DIAGNOSIS (PGD) FOR BORDERLINE INDICATIONS INCLUDING HUMAN LEUKOCYTE ANTIGENS (HLA) MATCHING, CANCER PREDISPOSITION, CARDIAC DISEASE AND THEIR PROPORTION IN OVERALL PGD CASES FOR SINGLE GENE DISORDERS.
D. S. Baxi et al.
FERTILITY AND STERILITY (2017)
Genetics and genomics of dilated cardiomyopathy and systolic heart failure
Upasana Tayal et al.
GENOME MEDICINE (2017)
Effects of myosin variants on interacting heads motif explain distinct hypertrophic and dilated cardiomyopathy phenotypes
Lorenzo Alamo et al.
ELIFE (2017)
Genetics of paediatric cardiomyopathies
Stephanie M. Ware
CURRENT OPINION IN PEDIATRICS (2017)
ClinVar: public archive of interpretations of clinically relevant variants
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2016)
Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association
Biykem Bozkurt et al.
CIRCULATION (2016)
Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases
Yigal M. Pinto et al.
EUROPEAN HEART JOURNAL (2016)
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers
Saurabh Kumar et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies
James S. Ware et al.
NEW ENGLAND JOURNAL OF MEDICINE (2016)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Prognostic Relevance of Gene-Environment Interactions in Patients With Dilated Cardiomyopathy Applying the MOGE(S) Classification
Mark R. Hazebroek et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2015)
Atlas of the clinical genetics of human dilated cardiomyopathy
Jan Haas et al.
EUROPEAN HEART JOURNAL (2015)
The role of the genetic counsellor: a systematic review of research evidence
Heather Skirton et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2015)
ClinVar: public archive of relationships among sequence variation and human phenotype
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2014)
Genetic causes of dilated cardiomyopathy
Luisa Mestroni et al.
PROGRESS IN PEDIATRIC CARDIOLOGY (2014)
Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy
Roberta Roncarati et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Dilated cardiomyopathy: the complexity of a diverse genetic architecture
Ray E. Hershberger et al.
NATURE REVIEWS CARDIOLOGY (2013)
Abnormal p38 mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation
Antoine Muchir et al.
HUMAN MOLECULAR GENETICS (2012)
Pediatric Cardiomyopathy: Importance of Genetic and Metabolic Evaluation
Steven J. Kindel et al.
JOURNAL OF CARDIAC FAILURE (2012)
Genetic Testing for Dilated Cardiomyopathy in Clinical Practice
Neal K. Lakdawala et al.
JOURNAL OF CARDIAC FAILURE (2012)
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers A European Cohort Study
Ingrid A. W. van Rijsingen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2012)
PGD for inherited cardiac diseases
Anver Kuliev et al.
REPRODUCTIVE BIOMEDICINE ONLINE (2012)
Review and Metaanalysis of the Frequency of Familial Dilated Cardiomyopathy
Mario Petretta et al.
AMERICAN JOURNAL OF CARDIOLOGY (2011)
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
Michael J. Ackerman et al.
EUROPACE (2011)
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
Philippe Charron et al.
EUROPEAN HEART JOURNAL (2010)
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
Sharie B. Parks et al.
AMERICAN HEART JOURNAL (2008)
Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease
E Arbustini et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)
The complexities of predictive genetic testing
JP Evans et al.
BMJ-BRITISH MEDICAL JOURNAL (2001)
Share Paper
