PDF) Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
Contactinâ•'associated proteinâ•'like 2, a protein of the neurexin family involved in several human diseases
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse
Contactin‐associated protein‐like 2, a protein of the neurexin family involved in several human diseases - Saint‐Martin - 2018 - European Journal of Neuroscience - Wiley Online Library
![PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution](https://www.researchgate.net/publication/364473606/figure/fig2/AS:11431281091271320@1666364690703/figure-fig2_Q320.jpg "PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution")
PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution
PTPRD and CNTNAP2 as markers of tumor aggressiveness in oligodendrogliomas | Scientific Reports
Location of all mutations of interest, i.e. rare and exclusive to cases... | Download Scientific Diagram
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
JCM | Free Full-Text | Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model
![PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution](https://www.researchgate.net/publication/364473606/figure/fig1/AS:11431281091285061@1666364690604/Location-and-structure-of-the-contactin-associated-protein-like-2-CNTNAP2-gene-and_Q320.jpg "PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution")
PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts
Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts. - Abstract - Europe PMC
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
A meta-analysis of areas of structural variation in grey matter in individuals with Autism Spectrum Disorder (ASD) in relation to gene expression of candidate ASD genes | bioRxiv
Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder - ScienceDirect
Gene: cntnap2 -
Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variants | Italian Journal of Pediatrics | Full Text
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
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018
