Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality

11 May 2022

Abstract excerpt

Importance: Pathogenic variants associated with inherited cardiomyopathy are recognized as important and clinically actionable when identified, leading some clinicians to recommend population-wide genomic screening. Objective: To determine the prevalence and clinical importance of pathogenic variants associated with inherited cardiomyopathy within the context of contemporary clinical care. Design, Setting, and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiomyopathy and Myosin Studies
Share to Cardiovascular Effects of Exercise
Share to Genomics and Rare Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35544052
DOI: 10.1001/jamacardio.2022.0901

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause MortalityPMID 35544052Read ↗

Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank.Semantic proximity Read ↗

Prevalence, Penetrance, and Phenotypic Manifestation of Cardiomyopathy-Associated Genetic Variants in the General Population: Insights from a Mayo Clinic Biobank Study.Semantic proximity Read ↗

Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in the UK Biobank.Semantic proximity Read ↗

Prevalence and Clinical Impact of Pathogenic Variants in Cardiomyopathy Genes Among Individuals with Cardiac Conduction DisordersSemantic proximity Read ↗

Screening for Pathogenic Variants in Cardiomyopathy Genes Predicts Mortality and Composite Outcomes in UK BiobankSemantic proximity Read ↗

Association of Pathogenic/Likely Pathogenic Inherited Cardiomyopathy Variants With Heart Failure: A TOPMed Multiancestry Analysis.Semantic proximity Read ↗

Assessing the Role of Rare Genetic Variation in Patients With Heart Failure.Semantic proximity Read ↗

Genetic, Clinical, and Sociodemographic Profile in Individuals with Diagnosis or Family History of Hypertrophic Cardiomyopathy: Insights from a Prospective CohortSemantic proximity Read ↗

Cardiomyopathy-Associated Gene Variants in Atrial Fibrillation.Semantic proximity Read ↗

Cardiac genetic test yields and genotype-phenotype correlations from large cohort investigated by medical examiner's office.Semantic proximity Read ↗

Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service.Semantic proximity Read ↗

Monogenic and Polygenic Contributions to Cardiomyopathy and Heart Failure Across Diverse PopulationsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.