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

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia - 1 May 2017

Zare Sahar, Mashayekhi Farhad, Bidabadi Elham

Abstract excerpt

Autism is a heterogeneous and multifactorial disease that results from the interaction between genetic vulnerability and environmental factors. Several studies showed that many of genes that play role in autism are component of signaling networks that regulate growth and synaptic plasticity, play an important role in the etiology of autism. Contactin associated-like 2 (CNTNAP2) gene is a member of the superfamily...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Membrane Proteins

Share to Nerve Tissue Proteins

Share to Population Surveillance

Source

Identifiers

PMID: 28284582
DOI: 10.1016/j.jocn.2017.01.008

Genes

CNTNAP2

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

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.PMID 28284582Read ↗

CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case-control study combined with a meta-analysis.Semantic proximity Read ↗

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.Semantic proximity Read ↗

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.Semantic proximity Read ↗

Genetic Risk of Autism Spectrum Disorder in a Pakistani Population.Semantic proximity Read ↗

CNTNAP2 gene in high functioning autism: no association according to family and meta-analysis approaches.Semantic proximity Read ↗

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.Semantic proximity Read ↗

Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorderSemantic proximity Read ↗

Neuropilin-2 rs849563 gene variations and susceptibility to autism in Iranian population: A case-control study.Semantic proximity Read ↗

Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder.Semantic proximity Read ↗

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.Semantic proximity Read ↗

Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case-control association study reveals potential biomarkers.Semantic proximity Read ↗

Contact in the genetics of autism and schizophrenia.Semantic proximity Read ↗

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