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

Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.

Molecular psychiatry - 1 Jul 2015

Chiocchetti A G, Kopp M, Waltes R, Haslinger D, Duketis E, Jarczok T A, Poustka F, Voran A, Graab U, Meyer J, Klauck S M, Fulda S, Freitag C M

Abstract excerpt

Contactin-associated protein-like 2 gene (CNTNAP2), a member of the Neurexin gene superfamily, is one of the best-replicated risk genes for autism spectrum disorders (ASD). ASD are predominately genetically determined neurodevelopmental disorders characterized by impairments of language development, social interaction and communication, as well as stereotyped behavior and interests. Although CNTNAP2 expression...

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder
Share to Cell Line, Tumor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Germany

Share to HEK293 Cells

Share to Language Development

Share to Nerve Tissue Proteins

Share to Neurogenesis

Share to White People

Source

Identifiers

PMID: 25224256
DOI: 10.1038/mp.2014.103

Genes

CNTNAP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.PMID 25224256Read ↗

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

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.Semantic proximity Read ↗

Defining the contribution of CNTNAP2 to autism susceptibility.Semantic proximity Read ↗

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.Semantic proximity Read ↗

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

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

An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder.Semantic proximity Read ↗

Shining a light on CNTNAP2: complex functions to complex disorders.Semantic proximity Read ↗

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

A common variant of CNTNAP2 is associated with sub-threshold autistic traits and intellectual disability.Semantic proximity Read ↗

A Protective Super-Enhancer Variant Regulating SLC7A7 Modulates Autism Spectrum Disorder Risk: A Cross-Population Study.Semantic proximity Read ↗

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.Semantic proximity Read ↗

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