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Times Co-cited
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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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Synaptic, transcriptional and chromatin genes disrupted in autism.
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Identification of common genetic risk variants for autism spectrum disorder.
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
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Association between microdeletion and microduplication at 16p11.2 and autism.
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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
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Genetic heritability and shared environmental factors among twin pairs with 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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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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Excess of rare, inherited truncating mutations in autism.
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Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
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Paternally inherited cis-regulatory structural variants are associated with autism.
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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.