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

Genetic basis of familial dilated cardiomyopathy patients undergoing heart transplantation.

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation - 1 May 2016

Cuenca Sofia, Ruiz-Cano Maria J, Gimeno-Blanes Juan Ramón, Jurado Alfonso, Salas Clara, Gomez-Diaz Iria, Padron-Barthe Laura, Grillo Jose Javier, Vilches Carlos, Segovia Javier, Pascual-Figal Domingo, Lara-Pezzi Enrique, Monserrat Lorenzo, Alonso-Pulpon Luis, Garcia-Pavia Pablo

Abstract excerpt

BACKGROUND: Dilated cardiomyopathy (DCM) is the most frequent cause of heart transplantation (HTx). The genetic basis of DCM among patients undergoing HTx has been poorly characterized. We sought to determine the genetic basis of familial DCM HTx and to establish the yield of modern next generation sequencing (NGS) technologies in this setting. METHODS: Fifty-two heart-transplanted patients due to familial DCM...

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiomyopathy, Dilated

Share to Heart Transplantation

Share to High-Throughput Nucleotide Sequencing

Share to Mutation

Share to Neurogenetic and Muscular Disorders Research

Share to Viral Infections and Immunology Research

Source

Identifiers

PMID: 26899768
DOI: 10.1016/j.healun.2015.12.014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic basis of familial dilated cardiomyopathy patients undergoing heart transplantation.PMID 26899768Read ↗

Clinical utility of genetic testing in patients with dilated cardiomyopathy.Semantic proximity Read ↗

Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing.Semantic proximity Read ↗

Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patientsSemantic proximity Read ↗

Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy.Semantic proximity Read ↗

Implications of Genetic Testing in Dilated Cardiomyopathy.Semantic proximity Read ↗

Novel combination of TTN and CTNNA3 Pathogenic variant leading to Familial Dilated Cardiomyopathy: From acute heart failure to subclinical phenotypes.Semantic proximity Read ↗

Familial dilated cardiomyopathy secondary to dystrophin splice site mutation.Semantic proximity Read ↗

Clinical and Genetic Investigations of 109 Index Patients With Dilated Cardiomyopathy and 445 of Their Relatives.Semantic proximity Read ↗

Genetic Basis and Genotype–Phenotype Correlations in Han Chinese Patients with Idiopathic Dilated CardiomyopathySemantic proximity Read ↗

Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological study.Semantic proximity Read ↗

Next-Generation Sequencing Reveals Novel Genetic Variants for Dilated Cardiomyopathy in Pediatric Chinese Patients.Semantic proximity Read ↗

Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy‐Associated GenesSemantic proximity Read ↗

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