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Times Cited
Times Co-cited
Similarity
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.
Kevin A Strauss, Erik G Puffenberger, Matthew J Huentelman, Steven Gottlieb, Seth E Dobrin, Jennifer M Parod, Dietrich A Stephan, D Holmes Morton. N Engl J Med 2006
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Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
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Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Maricela Alarcón, Brett S Abrahams, Jennifer L Stone, Jacqueline A Duvall, Julia V Perederiy, Jamee M Bomar, Jonathan Sebat, Michael Wigler, Christa L Martin, David H Ledbetter,[...]. Am J Hum Genet 2008
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Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2.
Geoffrey C Y Tan, Thomas F Doke, John Ashburner, Nicholas W Wood, Richard S J Frackowiak. Neuroimage 2010
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A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Dan E Arking, David J Cutler, Camille W Brune, Tanya M Teslovich, Kristen West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H Cook,[...]. Am J Hum Genet 2008
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Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2.
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Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.
Heather C Whalley, Garret O'Connell, Jessika E Sussmann, Anna Peel, Andrew C Stanfield, Marianna E Hayiou-Thomas, Eve C Johnstone, Stephen M Lawrie, Andrew M McIntosh, Jeremy Hall. Am J Med Genet B Neuropsychiatr Genet 2011
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Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
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Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1.
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The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism.
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A functional genetic link between distinct developmental language disorders.
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Shining a light on CNTNAP2: complex functions to complex disorders.
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Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development.
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Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels.
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CNTNAP2 polymorphisms and structural brain connectivity: a diffusion-tensor imaging study.
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Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
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Homozygous Loss of Autism-Risk Gene CNTNAP2 Results in Reduced Local and Long-Range Prefrontal Functional Connectivity.
Adam Liska, Alice Bertero, Ryszard Gomolka, Mara Sabbioni, Alberto Galbusera, Noemi Barsotti, Stefano Panzeri, Maria Luisa Scattoni, Massimo Pasqualetti, Alessandro Gozzi. Cereb Cortex 2018
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Autism-associated promoter variant in MET impacts functional and structural brain networks.
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CNTNAP2 variants affect early language development in the general population.
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Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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Individual common variants exert weak effects on the risk for autism spectrum disorders.
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12
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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12
Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection.
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Autism spectrum disorders: developmental disconnection syndromes.
Daniel H Geschwind, Pat Levitt. Curr Opin Neurobiol 2007
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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
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11
Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
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11
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.
Beate Peter, Wendy H Raskind, Mark Matsushita, Mark Lisowski, Tiffany Vu, Virginia W Berninger, Ellen M Wijsman, Zoran Brkanac. J Neurodev Disord 2011
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Brain hyperconnectivity in children with autism and its links to social deficits.
Kaustubh Supekar, Lucina Q Uddin, Amirah Khouzam, Jennifer Phillips, William D Gaillard, Lauren E Kenworthy, Benjamin E Yerys, Chandan J Vaidya, Vinod Menon. Cell Rep 2013
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Autism as a neural systems disorder: a theory of frontal-posterior underconnectivity.
Marcel Adam Just, Timothy A Keller, Vicente L Malave, Rajesh K Kana, Sashank Varma. Neurosci Biobehav Rev 2012
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Genetic heritability and shared environmental factors among twin pairs with autism.
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A genome-wide linkage and association scan reveals novel loci for autism.
Lauren A Weiss, Dan E Arking, Mark J Daly, Aravinda Chakravarti. Nature 2009
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Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.
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Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
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The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
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Reconceptualizing functional brain connectivity in autism from a developmental perspective.
Lucina Q Uddin, Kaustubh Supekar, Vinod Menon. Front Hum Neurosci 2013
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The amygdala is enlarged in children but not adolescents with autism; the hippocampus is enlarged at all ages.
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Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study.
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Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.
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Common genetic variants on 5p14.1 associate with autism spectrum disorders.
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Advances in autism genetics: on the threshold of a new neurobiology.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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What does CNTNAP2 reveal about autism spectrum disorder?
Olga Peñagarikano, Daniel H Geschwind. Trends Mol Med 2012
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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
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Neocortical excitation/inhibition balance in information processing and social dysfunction.
Ofer Yizhar, Lief E Fenno, Matthias Prigge, Franziska Schneider, Thomas J Davidson, Daniel J O'Shea, Vikaas S Sohal, Inbal Goshen, Joel Finkelstein, Jeanne T Paz,[...]. Nature 2011
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The emerging picture of autism spectrum disorder: genetics and pathology.
Jason A Chen, Olga Peñagarikano, T Grant Belgard, Vivek Swarup, Daniel H Geschwind. Annu Rev Pathol 2015
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Gene hunting in autism spectrum disorder: on the path to precision medicine.
Daniel H Geschwind, Matthew W State. Lancet Neurol 2015
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Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons.
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11
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.