Discover Community Create You

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

Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in the UK Biobank.

JACC. Heart failure - 1 May 2024

Asatryan Babken, Shah Ravi A, Sharaf Dabbagh Ghaith, Landstrom Andrew P, Darbar Dawood, Khanji Mohammed Y, Lopes Luis R, van Duijvenboden Stefan, Muser Daniele, Lee Aaron Mark, Haggerty Christopher M, Arora Pankaj, Semsarian Christopher, Reichlin Tobias, Somers Virend K, Owens Anjali T, Petersen Steffen E, Deo Rajat, Munroe Patricia B, Aung Nay, Chahal C Anwar A

Abstract excerpt

BACKGROUND: Inherited cardiomyopathies present with broad variation of phenotype. Data are limited regarding genetic screening strategies and outcomes associated with predicted deleterious variants in cardiomyopathy-associated genes in the general population. OBJECTIVES: The authors aimed to determine the risk of mortality and composite cardiomyopathy-related outcomes associated with predicted deleterious...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Cardiomyopathies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exome Sequencing

Share to Genetic Testing

Share to Genotype

Share to Prognosis

Share to UK Biobank

Share to United Kingdom

Source

Identifiers

PMID: 37715771
DOI: 10.1016/j.jchf.2023.07.023

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in the UK Biobank.PMID 37715771Read ↗

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

Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General PopulationSemantic proximity Read ↗

Prevalence and disease expression of pathogenic and likely pathogenic variants associated with inherited cardiomyopathies in the general populationSemantic proximity Read ↗

The Frequency, Penetrance and Variable Expressivity of Dilated Cardiomyopathy-Associated Putative Pathogenic Gene Variants in UK Biobank ParticipantsSemantic proximity Read ↗

Frequency, Penetrance, and Variable Expressivity of Dilated Cardiomyopathy–Associated Putative Pathogenic Gene Variants in UK Biobank ParticipantsSemantic 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 ↗

Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variantsSemantic proximity Read ↗

Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variantsSemantic proximity Read ↗

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

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

Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing.Semantic proximity Read ↗

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

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