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Article

The Human Contactin-Associated Protein-like 2 Gene (CNTNAP2) Spans over 2 Mb of DNA at Chromosome 7q35

1 Apr 2001

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11352571
DOI: 10.1006/geno.2001.6517

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Human Contactin-Associated Protein-like 2 Gene (CNTNAP2) Spans over 2 Mb of DNA at Chromosome 7q35PMID 11352571Read ↗

Molecular Cloning and in Situ Localization of the Human Contactin Gene (CNTN1) on Chromosome 12q11-q12Semantic proximity Read ↗

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

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

Third-generation whole-genome sequencing reveals the role of CNTNAP2 as a tumor suppressor gene in high-risk neuroblastomas.Semantic proximity Read ↗

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

The role of CNTNAP2 in the development & evolution of the human cerebral cortexSemantic 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 ↗

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

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

Disruption of Contactin 4 in two subjects with autism in Chinese population.Semantic proximity Read ↗

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

Contactin-associated protein-like (CNTNAP) 2 gene mutation in a patient with bilateral schizencephaly.Semantic proximity Read ↗

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