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

Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.

European heart journal - 7 Sept 2015

Akinrinade Oyediran, Ollila Laura, Vattulainen Sanna, Tallila Jonna, Gentile Massimiliano, Salmenperä Pertteli, Koillinen Hannele, Kaartinen Maija, Nieminen Markku S, Myllykangas Samuel, Alastalo Tero-Pekka, Koskenvuo Juha W, Heliö Tiina

Abstract excerpt

AIMS: Despite our increased understanding of the genetic basis of dilated cardiomyopathy (DCM), the clinical utility and yield of clinically meaningful findings of comprehensive next-generation sequencing (NGS)-based genetic diagnostics in DCM has been poorly described. We utilized a high-quality...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy, Dilated
Share to Finland

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Frameshift Mutation

Share to Kaplan-Meier Estimate

Share to Mutation, Missense

Share to Oligonucleotide Array Sequence Analysis

Share to Recurrence

Source

Open in PubMed Open full text

Identifiers

PMID: 26084686
DOI: 10.1093/eurheartj/ehv253
PMCID: PMC4561350

Genes

TTN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-26084686-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.PMID 26084686Read ↗

Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated CardiomyopathySemantic proximity Read ↗

Relevance of truncating titin mutations in dilated cardiomyopathy.Semantic proximity Read ↗

Atlas of the clinical genetics of human dilated cardiomyopathy.Semantic proximity Read ↗

Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated CardiomyopathySemantic proximity Read ↗

Truncations of titin causing dilated cardiomyopathy.Semantic proximity Read ↗

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.Semantic proximity Read ↗

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

Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.Semantic proximity Read ↗

Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy.Semantic proximity Read ↗

The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases.Semantic proximity Read ↗

Genetics and genomics of dilated cardiomyopathy and systolic heart failure.Semantic proximity Read ↗

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

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