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

Association of DNMT1 Gene Polymorphisms with Congenital Heart Disease in Child Patients.

Pediatric cardiology - 1 Jun 2015

Wang FengYu, Zhou ShiYuan, Wang YanLi, Wang LiNa, Zhou JiPing, Wang HaiLi, Li CongMin, Chang MingXiu

Abstract excerpt

To reveal the association between DNMT1 polymorphisms and congenital heart disease (CHD) in child patients, a total of 224 CHD child patients as well as 199 healthy individuals were enrolled in the present study. The DNA was extracted from whole blood, and four SNPs including rs16999593, rs2228612, rs2288349 and rs10420321 were selected for the gene polymorphism investigation via ligase detection reaction (LDR)...

Read the complete abstract on PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Topics

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

Share to Alleles
Share to Child
Share to Child, Preschool
Share to Genes, Dominant
Share to Heart Defects, Congenital
Share to Heterozygote
Share to Homozygote
Share to Repressor Proteins

Source

Identifiers

PMID: 25596970
DOI: 10.1007/s00246-015-1093-9

Genes

DNMT1

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

Association of DNMT1 Gene Polymorphisms with Congenital Heart Disease in Child Patients.PMID 25596970Read ↗

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

Association of Maternal Betaine-Homocysteine Methyltransferase (BHMT) and BHMT2 Genes Polymorphisms with Congenital Heart Disease in Offspring.Semantic proximity Read ↗

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

Two Common MTHFR Gene Polymorphisms (C677T and A1298C) and Fetal Congenital Heart Disease Risk: An Updated Meta-Analysis with Trial Sequential Analysis.Semantic proximity Read ↗

Association of maternal folic acid supplementation and offspring MTRR gene polymorphism with congenital heart disease: a hospital-based case-control study in Han populationSemantic proximity Read ↗

Association between maternal MTHFR and MTRR gene polymorphisms and the risk of congenital heart disease in newbornsSemantic proximity Read ↗

Association analysis of maternal MTHFR gene polymorphisms and the occurrence of congenital heart disease in offspring.Semantic proximity Read ↗

Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study.Semantic proximity Read ↗

Maternal MTHFR A1298C polymorphism and risk of congenital heart disease in fetusSemantic proximity Read ↗

[Case-control study on the association between four single nucleotide polymorphisms in folate metabolism way and the risk of congenital heart disease].Semantic proximity Read ↗

Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls.Semantic proximity Read ↗

Association between maternal MTHFR and MTRR gene polymorphisms and the risk of congenital heart disease in newborns.Semantic proximity Read ↗

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