Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
![CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018 CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018](https://journals.sagepub.com/cms/10.1177/1179069518809666/asset/images/large/10.1177_1179069518809666-fig2.jpeg)
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018
![Abnormal excitatory synaptic transmission in the neocortex of Cntnap2... | Download Scientific Diagram Abnormal excitatory synaptic transmission in the neocortex of Cntnap2... | Download Scientific Diagram](https://www.researchgate.net/profile/Hilgo-Bruining/publication/322146825/figure/fig3/AS:577319259435008@1514655045423/Abnormal-excitatory-synaptic-transmission-in-the-neocortex-of-Cntnap2-mutant-mice-A-B_Q640.jpg)
Abnormal excitatory synaptic transmission in the neocortex of Cntnap2... | Download Scientific Diagram
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
A common variant of CNTNAP2 is associated with sub-threshold autistic traits and intellectual disability | PLOS ONE
![CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018 CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018](https://journals.sagepub.com/cms/10.1177/1179069518809666/asset/images/large/10.1177_1179069518809666-fig3.jpeg)
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018
A common variant of CNTNAP2 is associated with sub-threshold autistic traits and intellectual disability | PLOS ONE
![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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41380-022-01822-1/MediaObjects/41380_2022_1822_Fig4_HTML.png)
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
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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 Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs43042-021-00138-z/MediaObjects/43042_2021_138_Fig1_HTML.png)
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
![Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs43042-021-00138-z/MediaObjects/43042_2021_138_Fig3_HTML.png)
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
![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](https://media.springernature.com/w136h75/springer-static/image/art%3A10.1038%2Fs41467-021-26131-z/MediaObjects/41467_2021_26131_Fig1_HTML.png)
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-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry](https://media.springernature.com/w136h75/springer-static/image/art%3A10.1038%2Fs41380-020-0669-9/MediaObjects/41380_2020_669_Fig1_HTML.png)
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
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
![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 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](https://onlinelibrary.wiley.com/cms/asset/ec4ff0ad-e90a-4f41-8bb1-fc2a46266c8d/ejn14081-fig-0003-m.jpg)
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
![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](https://media.springernature.com/w136h75/springer-static/image/art%3A10.1038%2Fs41398-021-01578-2/MediaObjects/41398_2021_1578_Fig1_HTML.png)
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 Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs43042-021-00138-z/MediaObjects/43042_2021_138_Fig2_HTML.png)
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
![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](https://media.springernature.com/w136h75/springer-static/image/art%3A10.1038%2Fs41598-019-49533-y/MediaObjects/41598_2019_49533_Fig1_HTML.png)
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
![CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018 CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018](https://journals.sagepub.com/cms/10.1177/1179069518809666/asset/images/large/10.1177_1179069518809666-fig1.jpeg)