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Times Cited: 12
Times Cited: 12
Times Cited
Times Co-cited
Similarity
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
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Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
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Loss of cadherin-11 adhesion receptor enhances plastic changes in hippocampal synapses and modifies behavioral responses.
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Cadherins and catenins in dendrite and synapse morphogenesis.
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Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.
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Patterns and rates of exonic de novo mutations in autism spectrum disorders.
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Cadherin-9 regulates synapse-specific differentiation in the developing hippocampus.
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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.
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Synaptic proteins and receptors defects in autism spectrum disorders.
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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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Cadherin-8 expression, synaptic localization, and molecular control of neuronal form in prefrontal corticostriatal circuits.
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Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism.
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Disentangling the heterogeneity of autism spectrum disorder through genetic findings.
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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
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Synaptic, transcriptional and chromatin genes disrupted in autism.
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Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities.
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Structural variation of chromosomes in autism spectrum disorder.
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The contribution of de novo coding mutations to autism spectrum disorder.
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Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
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Loss of Tsc2 in Purkinje cells is associated with autistic-like behavior in a mouse model of tuberous sclerosis complex.
R Michelle Reith, James McKenna, Henry Wu, S Shahrukh Hashmi, Seo-Hee Cho, Pramod K Dash, Michael J Gambello. Neurobiol Dis 2013
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Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses.
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Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
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Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
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Excess of rare, inherited truncating mutations in autism.
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Contribution of SHANK3 mutations to autism spectrum disorder.
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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N-cadherin mediates cortical organization in the mouse brain.
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Neural (N)-cadherin at developing thalamocortical synapses provides an adhesion mechanism for the formation of somatopically organized connections.
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Rab GTPases-dependent endocytic pathways regulate neuronal migration and maturation through N-cadherin trafficking.
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Neuronal circuits are subdivided by differential expression of type-II classic cadherins in postnatal mouse brains.
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Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition.
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Molecular evolution of the cadherin superfamily.
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Cadherin regulates dendritic spine morphogenesis.
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Cognitive and behavioral profile in females with epilepsy with PDCH19 mutation: two novel mutations and review of the literature.
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The classic cadherins in synaptic specificity.
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Identifying autism loci and genes by tracing recent shared ancestry.
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An RNAi-based approach identifies molecules required for glutamatergic and GABAergic synapse development.
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Cadherin-8 and N-cadherin differentially regulate pre- and postsynaptic development of the hippocampal mossy fiber pathway.
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
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Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.
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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.