• "Inherited cardiovascular disease mindset" can identify concealed inherited conditions at cardio-oncology evaluation: An opportunistic screening
• A case of Carvajal syndrome presenting with dilated cardiomyopathy
• A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weakness
• A prospective multicenter feasibility study of a miniaturized implantable continuous flow ventricular assist device in smaller children with heart failure
• A Rare Treatable Cause of Cardiomyopathy: Primary Carnitine Deficiency
• A Review of Pediatric Cardiomyopathy
• AAV9:PKP2 improves heart function and survival in a Pkp2-deficient mouse model of arrhythmogenic right ventricular cardiomyopathy
• Altered myocardial lipid regulation in junctophilin-2-associated familial cardiomyopathies
• Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown-Rahman syndrome
• Arrhythmogenic or dilated or desmoplakin cardiomyopathy? A challenging case managed by our multidisciplinary cardiogenetic team
• Atypical Progeria Primarily Manifesting as Premature Cardiac Valvular Disease Segregates with <em>LMNA</em>-Gene Variants
• CaMK II in Cardiovascular Diseases, Especially CaMK II-δ: Friends or Enemies
• Cardiac genetic test yields and genotype-phenotype correlations from large cohort investigated by medical examiner's office
• Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry
• Cardiomyopathy in children: a single-centre, retrospective study of genetic and clinical characteristics
• Cardiomyopathy in First-Degree Relatives of Patients Presenting With Acute Myocarditis: Prevalence and Prognostic Significance
• Challenging Case: A Multidisciplinary Approach to Demystifying Chronic Sleep Impairment in an Infant with a Complex Medical and Behavioral Profile
• Characterization of cardiac involvement in patients with LMNA splice-site mutation-related dilated cardiomyopathy and sudden cardiac death
• Clinical and genetic yield of familial screening after a sudden unexplained death at a young age
• Clinical and imaging characteristics of patients with cardiac amyloidosis- a single center observational study
• Clinical Insights in RNA-Binding Protein Motif 20 Cardiomyopathy: A Systematic Review
• Cocaine, amphetamine, or titin: Unraveling the genetic underpinnings of dilated cardiomyopathy
• COQ7 defect causes prenatal onset of mitochondrial CoQ(10) deficiency with cardiomyopathy and gastrointestinal obstruction
• Correction to: Screening for dilated cardiomyopathy in immediate family members: to whom, how, when (and where)
• De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis
• Diagnosis and management of arrhythmogenic cardiomyopathy: a case report
• Diagnostic Value of Late Gadolinium Enhancement at Cardiac Magnetic Resonance to distinguish Arrhythmogenic Right Ventricular Cardiomyopathy from Differentials
• Diagnostic value of late gadolinium enhancement at cardiovascular magnetic resonance to distinguish arrhythmogenic right ventricular cardiomyopathy from differentials
• Dilated cardiomyopathy due to a novel combination of TTN and BAG3 genetic variants: From acute heart failure to subclinical phenotypes
• Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous RRAGD Gene Variant
• Dilated cardiomyopathy-associated skeletal muscle actin (ACTA1) mutation R256H disrupts actin structure and function and causes cardiomyocyte hypocontractility
• Emerging Concepts of Mechanisms Controlling Cardiac Tension: Focus on Familial Dilated Cardiomyopathy (DCM) and Sarcomere-Directed Therapies
• Endoplasmic reticulum stress-related gene expression causes the progression of dilated cardiomyopathy by inducing apoptosis
• Establishment of a human induced pluripotent stem cell line from a patient with dilated cardiomyopathy
• Ethanol Ablation of Refractory Premature Ventricular Complex Originating from a Left Ventricular Summit Communicating Vein after Radiofrequency Catheter Ablation Failed in a Dilated Cardiomyopathy Patient
• Expert consensus on the genetic counseling for Dystrophinopathies
• Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene
• Familial dilated cardiomyopathy in a child: a case report
• Familial Dilated Cardiomyopathy: A Novel MED9 Short Isoform Identification
• Familial Profile of Pediatric and Adult Patients With Congenital Heart Disease in Heart Transplantation
• Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models
• Generation of a homozygous DNAJC19 knockout human embryonic stem cell line by CRISPR/Cas9 system
• Generation of a TBX20 homozygous knockout stem cell line (WAe009-A-1E) by episomal vector-based CRISPR/Cas9 system
• Generation of human induced pluripotent stem cell (hiPSC) lines derived from three patients carrying the pathogenic CRYAB (A527G) mutation and one non-carrier family member
• Genetic analysis and family screening for dilated cardiomyopathy: a retrospective analysis of the stepwise pedigree approach
• Genetic Characterization of Dilated Cardiomyopathy in Romanian Adult Patients
• Genotype is associated with left ventricular reverse remodelling and early events in recent-onset dilated cardiomyopathy
• Genotype-Phenotype Insights of Inherited Cardiomyopathies-A Review
• Harnessing molecular mechanism for precision medicine in dilated cardiomyopathy caused by a mutation in troponin T
• Heart in Disguise: Unmasking a Novel Gene Deletion in Dilated Cardiomyopathy
• Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy
• How Normal Is Low-Normal Left Ventricular Ejection Fraction in Familial Dilated Cardiomyopathy?
• Human disease-causing mutations result in loss of leiomodin 2 through nonsense-mediated mRNA decay
• Identification and development of Tetra-ARMS PCR-based screening test for a genetic variant of OLA1 (Tyr254Cys) in the human failing heart
• Identification of a SCN5A Genetic Variant Associated With Type 1 Brugada Syndrome (BrS) in a Family
• Identification of novel TTN gene variant in a patient exhibiting severe dilated cardiomyopathy co-occurring with acute fibrinoid organizing pneumonia
• Imaging Features of Arrhythmogenic Cardiomyopathies
• Impact of DCM-Causing Genetic Background on Long-Term Response to Cardiac Resynchronization Therapy
• Impella RP Flex: Rescue for the Failing Right Ventricle After Heart Transplantation-Case Report
• Implementing a clinical scientist-led screening clinic for hypertrophic and dilated cardiomyopathies
• Investigation of mutation spectrum amongst patients with familial primary cardiomyopathy using targeted NGS in Indian population
• Krupple-like factors in cardiomyopathy: emerging player and therapeutic opportunities
• LMNA -Related Dilated Cardiomyopathy: Single-Cell Transcriptomics during Patient-derived iPSC Differentiation Support Cell type and Lineage-specific Dysregulation of Gene Expression and Development for Cardiomyocytes and Epicardium-Derived Cells with Lami
• Localized translation and sarcomere maintenance requires ribosomal protein SA in mice
• Magnetic Resonance Imaging Characterization and Clinical Outcomes of Dilated and Arrhythmogenic Left Ventricular Cardiomyopathies
• Mechanisms of RBM20 Cardiomyopathy: Insights From Model Systems
• Missense variants in phospholamban and cardiac myosin binding protein identified in patients with a family history and clinical diagnosis of dilated cardiomyopathy
• NASCI case of the month: desmoplakin cardiomyopathy masquerading as acute myocarditis
• Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomere
• Nuclear Abnormalities in <em>LMNA</em> p.(Glu2Lys) Variant Segregating with <em>LMNA</em>-Associated Cardiocutaneous Progeria Syndrome
• Nuclear envelope lamin-related dilated cardiomyopathy: a case series including histopathology
• Pathogenic mutations of human phosphorylation sites affect protein-protein interactions
• Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives
• Phospholamban Cardiomyopathy Leading to Advanced Heart Failure in an Active Duty Service Member
• Plekhm2 acts as an autophagy modulator in murine heart and cardiofibroblasts
• PLEKHM2 deficiency induces impaired mitochondrial clearance and elevated ROS levels in human iPSC-derived cardiomyocytes
• Predicting the Development of Dilated Cardiomyopathy in Kindred With Genetic Risk: Family Matters
• Protein phosphatase 2A anchoring disruptor gene therapy for familial dilated cardiomyopathy
• Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardia
• Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India
• Right ventricular assessment of the adolescent footballer's heart
• Role of CAMK2D in neurodevelopment and associated conditions
• Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction
• Role of the Alpha-B-Crystallin Protein in Cardiomyopathic Disease
• Screening for dilated cardiomyopathy in immediate family members: to whom, how, when (and where)
• Targeting calpain-2-mediated junctophilin-2 cleavage delays heart failure progression following myocardial infarction
• TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant
• The causal effect of Alzheimer's disease and family history of Alzheimer's disease on non-ischemic cardiomyopathy and left ventricular structure and function: a Mendelian randomization study
• The DCM Project Portal: A direct-to-participant platform of The DCM Research Project
• The Hippo Signaling Pathway as a Drug Target in Familial Dilated Cardiomyopathy
• The Impact of Integration of a Genetic Clinic Into a Pediatric Cardiac Unit
• The role of detailed medical history for the early diagnosis of familial bradycardia in a patient with associated atrial fibrillation: case report
• The Role of Genetics in Risk Stratification Strategy of Dilated Cardiomyopathy
• Titin: The Missing Link in Cardiac Physiology
• TTN novel splice variant in familial dilated cardiomyopathy and splice variants review: a case report
• Unexpected Genetic Twists in Patients with Cardiac Devices
• Variable clinical expression of a novel FLNC truncating variant in a large family
• Variable Penetrance and Expressivity of a Rare Pore Loss-of-Function Mutation (p.L889V) of Nav1.5 Channels in Three Spanish Families
• Variants in structural cardiac genes in patients with cancer therapy-related cardiac dysfunction after anthracycline chemotherapy: a case control study
• Ventricular Angiography: A Forgotten Diagnostic Tool?