• A bibliometric review of peripartum cardiomyopathy compared to other cardiomyopathies using artificial intelligence and machine learning
• A Family with Myh7 Mutation and Different Forms of Cardiomyopathies
• A novel causative functional mutation in GATA6 gene is responsible for familial dilated cardiomyopathy as supported by in silico functional analysis
• A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencing
• A Novel Titin Truncation Variant Linked to Familial Dilated Cardiomyopathy Found in a Japanese Family and Its Functional Analysis in Genome-Edited Model Cells
• A Rare Cause of Left Ventricular Dysfunction and Familial Dilated Cardiomyopathy in Children; Emery-Dreifuss Type 2: A Case Report
• Aortic valve insufficiency after Impella device insertion that required aortic valve replacement after Heart Mate III left ventricular assist device implantation: a case report
• Association between SCN5A R225Q variant and dilated cardiomyopathy: potential role of intracellular pH and WNT/β-catenin pathway
• Becker dystrophy induced familial dilated cardiomyopathy: two cases report
• Bi-allelic variants in FLII cause pediatric cardiomyopathy by disrupting cardiomyocyte cell adhesion and myofibril organization
• Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy
• Cardiac MRI after Sudden Cardiac Arrest in a Young Woman Prompts Diagnosis of Familial Dilated Cardiomyopathy
• Cardiac MRI of Hereditary Cardiomyopathy
• Cardiovascular Magnetic Resonance Imaging in Familial Dilated Cardiomyopathy
• Care and Monitoring of Pregnant Patients With Left Ventricular Assist Devices
• Case Report: A novel desmoplakin mutation in a taiwanese woman with familial dilated cardiomyopathy that necessitated heart transplantation
• Circulating circRNA as biomarkers for dilated cardiomyopathy etiology
• Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel <em>TTN</em> Frameshift Mutation
• Clinical manifestations and MRI features of Danon disease: a case series
• Comparison of and Frequency of Mortality, Left Ventricular Assist Device Implantation, Ventricular Arrhythmias, and Heart Transplantation in Patients With Familial Versus Nonfamilial Idiopathic Dilated Cardiomyopathy
• Compound Heterozygous Missense Variants in <em>RPL3L</em> Genes Associated with Severe Forms of Dilated Cardiomyopathy: A Case Report and Literature Review
• Continuous Spinal Anesthesia for Labor Analgesia and Cesarean Delivery in a Parturient With Familial Dilated Cardiomyopathy: A Case Report
• Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy
• Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients
• Emerging Concepts of Mechanisms Controlling Cardiac Tension: Focus on Familial Dilated Cardiomyopathy (DCM) and Sarcomere-Directed Therapies
• Establishment of an iPSC line (JSPHi001-A) from a patient with familial dilated cardiomyopathy and atrial fibrillation caused by LMNA missense mutation (c.1003C > T)
• Exosomes mediated fibrogenesis in dilated cardiomyopathy through a MicroRNA pathway
• FAM210A regulates mitochondrial translation and maintains cardiac mitochondrial homeostasis
• Familial Dilated Cardiomyopathy and Sudden Cardiac Arrest: New Association with a <em>SCN5A</em> Mutation
• Familial Dilated Cardiomyopathy and Sudden Cardiac Arrest: New Association with a SCN5A Mutation
• Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report
• Familial dilated cardiomyopathy in a child: a case report
• Familial dilated cardiomyopathy with a novel LMNA mutation (p.R429C): a case report
• Familial dilated cardiomyopathy with RBM20 mutation in an Indian patient: a case report
• Familial Dilated Cardiomyopathy: A Novel MED9 Short Isoform Identification
• Family Screening in Dilated Cardiomyopathy: Prevalence, Incidence, and Potential for Limiting Follow-Up
• Further Evidence of Autosomal Recessive Inheritance of <em>RPL3L</em> Pathogenic Variants with Rapidly Progressive Neonatal Dilated Cardiomyopathy
• Generation of human induced pluripotent stem cell lines carrying heterozygous PLN mutation from dilated cardiomyopathy patients
• Genetic analysis and family screening for dilated cardiomyopathy: a retrospective analysis of the stepwise pedigree approach
• Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry
• Genetic Testing as a Guide for Treatment in Dilated Cardiomyopathies
• Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study
• Genetics of Peripartum Cardiomyopathy: Current Knowledge, Future Directions and Clinical Implications
• Genotype-Phenotype Correlation in Familial <em>BAG3</em> Mutation Dilated Cardiomyopathy
• GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy
• Harnessing molecular mechanism for precision medicine in dilated cardiomyopathy caused by a mutation in troponin T
• Heart Failure with Recovered Ejection Fraction in Patients with Vinculin Loss-of-function Variants
• Heterozygous desmin gene (DES) mutation contributes to familial dilated cardiomyopathy
• How Normal Is Low-Normal Left Ventricular Ejection Fraction in Familial Dilated Cardiomyopathy?
• Identification and development of Tetra-ARMS PCR-based screening test for a genetic variant of OLA1 (Tyr254Cys) in the human failing heart
• Identification and development of Tetra-ARMS PCR-based screening test for a genetic variant of OLA1 (Tyr254Cys) in the human failing heart
• Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
• Identification of <em>SCN5a</em> p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease
• Impella RP Flex: Rescue for the Failing Right Ventricle After Heart Transplantation-Case Report
• Interaction of Filamin C With Actin Is Essential for Cardiac Development and Function
• Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
• Jmjd4 Facilitates Pkm2 Degradation in Cardiomyocytes and Is Protective Against Dilated Cardiomyopathy
• Juvenile-onset multifocal atrial arrhythmias, atrial standstill and compound heterozygosity of genetic variants in <em>TAF1A</em>: sentinel event for evolving dilated cardiomyopathy-a case report
• KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy
• Late gadolinium enhancement distribution patterns in non-ischemic dilated cardiomyopathy: Genotype-phenotype correlation
• Lem2 is essential for cardiac development by maintaining nuclear integrity
• Machine Learning and Bioinformatics Framework Integration to Potential Familial DCM-Related Markers Discovery
• Machine-learning-based exploration to identify remodeling patterns associated with death or heart-transplant in pediatric-dilated cardiomyopathy
• Malignant Arrhythmogenic Role Associated with <em>RBM20</em>: A Comprehensive Interpretation Focused on a Personalized Approach
• Maternal Outcomes in Women with Peripartum Cardiomyopathy versus Age and Race-Matched Peers in an Urban US Community
• Mechanical Circulatory Support Devices Among Patients With Familial Dilated Cardiomyopathy: Insights From the INTERMACS
• Modulation of Structure and Dynamics of Cardiac Troponin by Phosphorylation and Mutations Revealed by Molecular Dynamics Simulations
• Molecular studies in familial dilated cardiomyopathy - A pilot study
• Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
• Personalized Medicine Approach in a DCM Patient with <em>LMNA</em> Mutation Reveals Dysregulation of mTOR Signaling
• Phenotypic variability of filamin C-related cardiomyopathy: Insights from a novel Dutch founder variant
• Precise genomic editing of pathogenic mutations in <em>RBM20</em> rescues dilated cardiomyopathy
• Protective mechanism of tetramethylpyrazine on cardiovascular system
• Protein phosphatase 2A anchoring disruptor gene therapy for familial dilated cardiomyopathy
• Quantitative Profiling of Serum Carnitines Facilitates the Etiology Diagnosis and Prognosis Prediction in Heart Failure
• Rate of Heart Failure Following Atrial Fibrillation According to Presence of Family History of Dilated Cardiomyopathy or Heart Failure: A Nationwide Study
• Recommendations for the Management of Cardiomyopathy Mutation Carriers: Evidence, Doubts, and Intentions
• Restoration of Cardiac Myosin Light Chain Kinase Ameliorates Systolic Dysfunction by Reducing Superrelaxed Myosin
• Risks of Ventricular Arrhythmia and Heart Failure in Carriers of <em>RBM20</em> Variants
• SARS-CoV-2 Infection and Emery-Dreifuss Syndrome in a Young Patient with a Family History of Dilated Cardiomyopathy
• Second-degree AV block type Mobitz I (Wenckebach) in a 49-year-old man with dilative cardiomyopathy
• Sex Differences, Genetic and Environmental Influences on Dilated Cardiomyopathy
• Skeletal Muscle Involvement in Patients With Truncations of Titin and Familial Dilated Cardiomyopathy
• Splicing factors in the heart: Uncovering shared and unique targets
• Structures of PKA-phospholamban complexes reveal a mechanism of familial dilated cardiomyopathy
• Study of pathogenic genes in a pedigree with familial dilated cardiomyopathy
• Teen pregnancy in the setting of familial dilated cardiomyopathy: a case report
• The genetic basis for adult-onset idiopathic dilated cardiomyopathy in people of African descent
• The Hippo Signaling Pathway as a Drug Target in Familial Dilated Cardiomyopathy
• The phenotypic characteristic observed by cardiac magnetic resonance in a PLN-R14del family
• Therapeutic targeting of BAG3: considering its complexity in cancer and heart disease
• Titin Missense Variants as a Cause of Familial Dilated Cardiomyopathy
• Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI
• TTN novel splice variant in familial dilated cardiomyopathy and splice variants review: a case report
• UEDA Heart Awards for 2022
• VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy
• Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in <em>DSP</em> Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy
• Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy
• Yield of family screening in dilated cardiomyopathy within low-income setting: Tanzanian experience
• Young Child With Dyspnea and Vomiting