Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder - ScienceDirect
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
Transcriptional regulation network of CNTNAP2 (A) and the Caspr2... | Download Scientific Diagram
The Autism Related Protein Contactin-Associated Protein-Like 2 (CNTNAP2) Stabilizes New Spines: An In Vivo Mouse Study | PLOS ONE
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts
Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment | BMC Medical Genetics | Full Text
Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variants
JCM | Free Full-Text | Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
Contactinâ•'associated proteinâ•'like 2, a protein of the neurexin family involved in several human diseases
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
What does CNTNAP2 reveal about autism spectrum disorder? - ScienceDirect
CNTNAP2 Mutations in Autism - ScienceDirect
PTPRD and CNTNAP2 as markers of tumor aggressiveness in oligodendrogliomas | Scientific Reports
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 | BMC Medical Genetics | Full Text
Genetics of structural and functional brain changes in autism spectrum disorder | Translational Psychiatry
Shining a light on CNTNAP2: complex functions to complex disorders | European Journal of Human Genetics
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 | PLOS Genetics
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
Location of all mutations of interest, i.e. rare and exclusive to cases... | Download Scientific Diagram
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
