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

Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.

Circulation. Cardiovascular genetics - 1 Feb 2012

Pasquale Ferdinando, Syrris Petros, Kaski Juan Pablo, Mogensen Jens, McKenna William J, Elliott Perry

Abstract excerpt

BACKGROUND: Hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene (TNNT2) has been associated with a high risk of sudden cardiac death (SCD) and mild left ventricular hypertrophy. However, previous studies are limited by sample size, cross-sectional design, and few data in relatives. METHODS AND RESULTS: Five hundred fifty-two unrelated hypertrophic cardiomyopathy probands were screened...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy, Hypertrophic
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Death, Sudden, Cardiac

Share to Electrocardiography

Share to Follow-Up Studies

Share to Kaplan-Meier Estimate

Share to Pedigree

Share to Troponin T

Source

Identifiers

PMID: 22144547
DOI: 10.1161/CIRCGENETICS.111.959973

Genes

SCD
TNNT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.PMID 22144547Read ↗

Value of Genetic Testing for the Prediction of Long-Term Outcome in Patients With Hypertrophic Cardiomyopathy.Semantic proximity Read ↗

Clinical and Prognostic Profiles of Cardiomyopathies Caused by Mutations in the Troponin T Gene.Semantic proximity Read ↗

Genotype-phenotype Correlations of Hypertrophic Cardiomyopathy When Diagnosed in Children, Adolescents, and Young Adults.Semantic proximity Read ↗

Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.Semantic proximity Read ↗

Sudden death due to troponin T mutations.Semantic proximity Read ↗

Long-Term Outcomes of Childhood Left Ventricular Noncompaction Cardiomyopathy: Results From a National Population-Based Study.Semantic proximity Read ↗

Cardiomyopathy Phenotypes and Outcomes for Children With Left Ventricular Myocardial Noncompaction: Results From the Pediatric Cardiomyopathy Registry.Semantic proximity Read ↗

Lifelong Clinical Impact of the Presence of Sarcomere Gene Mutation in Japanese Patients With Hypertrophic Cardiomyopathy.Semantic proximity Read ↗

Low prevalence and variable clinical presentation of troponin I and troponin T gene mutations in hypertrophic cardiomyopathy.Semantic proximity Read ↗

Penetrance of Hypertrophic Cardiomyopathy in Children Who Are Mutation Positive.Semantic proximity Read ↗

Phenotype and Clinical Outcomes of Titin Cardiomyopathy.Semantic proximity Read ↗

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective.Semantic proximity Read ↗

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