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A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder.

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Title: A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder.
Authors: Arutiunian V; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA., Santhosh M; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA., Neuhaus E; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.; Department of Psychiatry and Behavioral Science, University of Washington, Seattle, Washington, USA., Sullivan CAW; Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA., Bernier RA; Department of Psychiatry and Behavioral Science, University of Washington, Seattle, Washington, USA., Bookheimer SY; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA., Dapretto M; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA., Geschwind DH; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA., Jack A; Department of Psychology, George Mason University, Fairfax, Virginia, USA., McPartland JC; Yale Child Study Center, Yale School of Medicine, New Haven, Connecticut, USA., Van Horn JD; Department of Psychology, University of Virginia, Charlottesville, Virginia, USA.; School of Data Science, University of Virginia, Charlottesville, Virginia, USA., Pelphrey KA; Department of Neurology, School of Medicine, University of Virginia, Virginia, USA., Gupta AR; Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA.; Yale Child Study Center, Yale School of Medicine, New Haven, Connecticut, USA.; Department of Neuroscience, Yale School of Medicine, New Haven, Connecticut, USA., Webb SJ; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.; Department of Psychiatry and Behavioral Science, University of Washington, Seattle, Washington, USA.
Corporate Authors: ACE GENDAAR Network
Source: Autism research : official journal of the International Society for Autism Research [Autism Res] 2025 May; Vol. 18 (5), pp. 898-908. Date of Electronic Publication: 2024 Jul 10.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101461858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1939-3806 (Electronic) Linking ISSN: 19393806 NLM ISO Abbreviation: Autism Res Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder.
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