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Times Cited: 1529
Times Cited
Times Co-cited
Similarity
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Most genetic risk for autism resides with common variation.
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The contribution of de novo coding mutations to autism spectrum disorder.
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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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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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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Strong association of de novo copy number mutations with autism.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
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Patterns and rates of exonic de novo mutations in autism spectrum disorders.
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Identification of common genetic risk variants for autism spectrum disorder.
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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
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De novo gene disruptions in children on the autistic spectrum.
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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
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Individual common variants exert weak effects on the risk for autism spectrum disorders.
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Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
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A genome-wide linkage and association scan reveals novel loci for autism.
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Common genetic variants, acting additively, are a major source of risk for autism.
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
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Disruptive CHD8 mutations define a subtype of autism early in development.
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Common genetic variants on 5p14.1 associate with autism spectrum disorders.
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Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits.
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6
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.