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

Genome-wide DNA methylation analysis of discordant monozygotic twins reveals consistent sites of differential methylation associated with congenital heart disease

20 Jan 2023

Abstract excerpt

BACKGROUND: Despite being essentially genetically identical, monozygotic (MZ) twins can be discordant for congenital heart disease (CHD), thus highlighting the importance of in utero environmental factors for CHD pathogenesis. This study aimed to identify the epigenetic variations between discordant MZ twin pairs that are associated with CHD at birth. METHODS: Cord blood of CHD-discordant MZ twins from the...

Read the complete abstract on PubMed

Topics

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

Share to Congenital heart defects research
Share to Congenital Heart Disease Studies
Share to Epigenetics and DNA Methylation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36690264
DOI: 10.1016/j.ygeno.2023.110565

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide DNA methylation analysis of discordant monozygotic twins reveals consistent sites of differential methylation associated with congenital heart diseasePMID 36690264Read ↗

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

Genome and epigenome analysis of monozygotic twins discordant for congenital heart diseaseSemantic proximity Read ↗

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

Maternal Genome-Wide DNA Methylation Patterns and Congenital Heart DefectsSemantic proximity Read ↗

DNA methylation abnormalities in congenital heart diseaseSemantic proximity Read ↗

Epigenomic signature of major congenital heart defects in newborns with Down syndromeSemantic proximity Read ↗

Epigenomic signature of major congenital heart defects in newborns with Down syndromeSemantic proximity Read ↗

Genome-Wide Methylation Analysis Identifies Novel Cpg Loci For Perimembranous Ventricular Septal Defects In HumanSemantic proximity Read ↗

The Role of Epigenetics in Congenital Heart DiseaseSemantic proximity Read ↗

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

Genetic and epigenetic mechanisms in the development of congenital heart diseasesSemantic proximity Read ↗

Multiomic Investigation of Shared Genetic Pathways in Paediatric Congenital Heart Disease and Neurodevelopmental Disorders.Semantic proximity Read ↗

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