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Times Co-cited
Similarity
Synaptic, transcriptional and chromatin genes disrupted in autism.
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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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Excess of rare, inherited truncating mutations in autism.
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FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
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Disruptive CHD8 mutations define a subtype of autism early in development.
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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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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum 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.