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

Positive association of CC2D1A and CC2D2A gene haplotypes with mental retardation in a Han Chinese population.

DNA and cell biology - 1 Jan 2012

Shi Zhang-Yan, Li Ya-Jing, Zhang Ke-Jin, Gao Xiao-Cai, Zheng Zi-Jian, Han Ning, Zhang Fu-Chang

Abstract excerpt

The CC2D1A and CC2D2A genes are involved in Ca(2+)-regulated signaling pathways and have recently been implicated in the etiology of mental retardation (MR). The aim of this study was to investigate whether CC2D1A and CC2D2A polymorphisms are associated with susceptibility to MR in a Han Chinese population using a family based association approach. The sample included 172 trios (parents and offspring), and all...

Read the complete abstract on PubMed

Topics

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

Share to Cytoskeletal Proteins
Share to Family Health

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intellectual Disability

Share to Linkage Disequilibrium

Share to Nuclear Family

Share to Odds Ratio

Share to Polymorphism, Single-Stranded Conformational

Share to Proteins

Source

Identifiers

PMID: 22023432
DOI: 10.1089/dna.2011.1253

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

Positive association of CC2D1A and CC2D2A gene haplotypes with mental retardation in a Han Chinese population.PMID 22023432Read ↗

A family-based association study of dopamine receptor D4 and mental retardation in Qinba region of China.Semantic proximity Read ↗

The <i>CC2D1A</i>, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationSemantic proximity Read ↗

Evaluation of genetic susceptibility of common variants in CACNA1D with schizophrenia in Han Chinese.Semantic proximity Read ↗

CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis PigmentosaSemantic proximity Read ↗

A family-based association study of DIO2 and children mental retardation in the Qinba region of China.Semantic proximity Read ↗

An association study of the SLC26A4 gene in children with mental retardation.Semantic proximity Read ↗

Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.Semantic proximity Read ↗

Transmission disequilibrium test provides evidence of association between promoter polymorphisms in 22q11 gene DGCR14 and schizophrenia.Semantic proximity Read ↗

Positive association of the DIO2 (deiodinase type 2) gene with mental retardation in the iodine-deficient areas of China.Semantic proximity Read ↗

A genetic study of two calcium-independent cytosolic PLA2 genes in schizophrenia.Semantic proximity Read ↗

An association study between the transthyretin (TTR) gene and mental retardation.Semantic proximity Read ↗

Positive association between POU1F1 and mental retardation in young females in the Chinese Han population.Semantic proximity Read ↗

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