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 between RNF41 gene c.-206 T > A genetic polymorphism and risk of congenital heart diseases in the Chinese Mongolian population.

Genetics and molecular research : GMR - 17 Jun 2016

Zhang Y, Jin S Q, Li W X, Gao G Q, Zhang K, Huang J L

Abstract excerpt

This study aimed to explore the association between ring finger protein 41 (RNF41) c.-206 T > A variant and susceptibility to congenital heart disease (CHD) in the Chinese Mongolian population. The association between RNF41 gene c.-206 T > A polymorphism and CHD was examined in two independent case-control studies consisting of 219 CHD patients and 208 healthy controls. Genotype was determined by direct...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Heart Defects, Congenital

Share to Mongolia

Share to Risk Factors

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 27323192
DOI: 10.4238/gmr.15028089

Genes

RNF41

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association between RNF41 gene c.-206 T > A genetic polymorphism and risk of congenital heart diseases in the Chinese Mongolian population.PMID 27323192Read ↗

Association analysis between MTHFR genetic polymorphisms and the risk of congenital heart diseases in Chinese Han population.Semantic proximity Read ↗

Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population.Semantic proximity Read ↗

The association of the MTHFR c.1625A>C genetic variant with the risk of congenital heart diseases in the Chinese.Semantic proximity Read ↗

Association of genetic polymorphisms of de novo nucleotide biosynthesis with increased CHD susceptibility in the northern Chinese population.Semantic proximity Read ↗

A66G and C524T polymorphisms of the methionine synthase reductase gene are associated with congenital heart defects in the Chinese Han population.Semantic proximity Read ↗

Association of TBX20 gene polymorphism with congenital heart disease in Han Chinese neonates.Semantic proximity Read ↗

Association between TGFBR2 gene polymorphisms and congenital heart defects in Han Chinese population.Semantic proximity Read ↗

Association Analysis of Nonsyndromic Congenital Heart Disease and Tag Single Nucleotide Polymorphisms of TBX20 and Genes in the Ras-MAPK Pathway.Semantic proximity Read ↗

Relationship between polymorphism of methylenetetrahydrofolate dehydrogenase and congenital heart defect.Semantic proximity Read ↗

Connection of GLI1 variants to congenital heart disease susceptibility: A case-control study.Semantic proximity Read ↗

Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population.Semantic proximity Read ↗

No association of functional variant in pri-miR-218 and risk of congenital heart disease in a Chinese population.Semantic proximity Read ↗

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