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

Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.

Cardiovascular research - 1 Oct 2016

Grunert Marcel, Dorn Cornelia, Cui Huanhuan, Dunkel Ilona, Schulz Kerstin, Schoenhals Sophia, Sun Wei, Berger Felix, Chen Wei, Sperling Silke R

Abstract excerpt

AIMS: For the majority of congenital heart diseases (CHDs), the full complexity of the causative molecular network, which is driven by genetic, epigenetic, and environmental factors, is yet to be elucidated. Epigenetic alterations are suggested to play a pivotal role in modulating the phenotypic expression of CHDs and their clinical course during life. Candidate approaches implied that DNA methylation might have...

Read the complete abstract on PubMed

Topics

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

Share to CpG Islands
Share to Heart Septal Defects, Ventricular

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemodynamics

Share to Mitochondrial Proteins

Share to Molecular Chaperones

Share to Principal Component Analysis

Share to RNA Splicing

Share to Tetralogy of Fallot

Source

Identifiers

PMID: 27496870
DOI: 10.1093/cvr/cvw195

Genes

SCO2

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

Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.PMID 27496870Read ↗

Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of FallotSemantic proximity Read ↗

The role of DNA methylation in syndromic and non-syndromic congenital heart diseaseSemantic proximity Read ↗

The Role of Epigenetics in Congenital Heart DiseaseSemantic proximity Read ↗

DNA methylation abnormalities in congenital heart diseaseSemantic proximity Read ↗

Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD)Semantic proximity Read ↗

DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Congenital Heart DiseasesSemantic proximity Read ↗

Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular septal defect (VSD)Semantic proximity Read ↗

Distinct epigenetic programs regulate cardiac myocyte development and disease in the human heart <i>in vivo</i>Semantic proximity Read ↗

Genome-wide DNA methylation analysis of discordant monozygotic twins reveals consistent sites of differential methylation associated with congenital heart diseaseSemantic proximity Read ↗

Epigenetics in Congenital Heart Disease.Semantic proximity Read ↗

Congenital Heart Diseases: Recent Insights into Epigenetic MechanismsSemantic proximity Read ↗

Epigenetics and Congenital Heart DiseasesSemantic proximity Read ↗

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