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

Polymorphisms in the CTNND2 gene and 11q24.1 genomic region are associated with pathological myopia in a Chinese population.

Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde - 1 Jan 2012

Yu Zhiqiang, Zhou Jiaqi, Chen Xueli, Zhou Xingtao, Sun Xinghuai, Chu Renyuan

Abstract excerpt

Pathological myopia is a refractive error that can result in legal blindness and is prevalent in China. A number of genomic loci have been associated with pathological myopia, but only a few have been validated. This study further evaluated the association of polymorphisms in the CTNND2 gene and the 11q24.1 genomic region with pathological myopia. Both regions had previously been implicated in carrying...

Read the complete abstract on PubMed

Topics

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

Share to Catenins
Share to Chromosomes, Human, Pair 11

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Delta Catenin

Share to Genomic Islands

Share to Genotyping Techniques

Share to Myopia, Degenerative

Share to Spectrometry, Mass, Electrospray Ionization

Share to Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Source

Identifiers

PMID: 22759899
DOI: 10.1159/000338188

Genes

CTNND2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polymorphisms in the CTNND2 gene and 11q24.1 genomic region are associated with pathological myopia in a Chinese population.PMID 22759899Read ↗

Polymorphism in the 11q24.1 genomic region is associated with myopia: a comprehensive genetic study in Chinese and Japanese populations.Semantic proximity Read ↗

Replication study supports CTNND2 as a susceptibility gene for high myopia.Semantic proximity Read ↗

Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.Semantic proximity Read ↗

A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1.Semantic proximity Read ↗

[Association of ZNF644, GRM6 and CTNND2 genes polymorphisms with high myopia].Semantic proximity Read ↗

Association of ZNF644, GRM6, and CTNND2 genes with high myopia in the Han Chinese population: Jiangsu Eye Study.Semantic proximity Read ↗

Screening of genes interacting with high myopia and neuropsychiatric disorders.Semantic proximity Read ↗

Evaluating the association between pathological myopia and SNPs in RASGRF1. ACTC1 and GJD2 genes at chromosome 15q14 and 15q25 in a Chinese population.Semantic proximity Read ↗

Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis.Semantic proximity Read ↗

Evaluation of myopia-associated genes in a Han Chinese population with high myopia.Semantic proximity Read ↗

Association Between Polymorphisms of 4 Common Genes and High Myopia Risk: A Comprehensive Analysis.Semantic proximity Read ↗

Evaluation of 12 myopia-associated genes in Chinese patients with high myopia.Semantic proximity Read ↗

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