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Times Cited
Times Co-cited
Similarity
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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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Identification of common genetic risk variants for autism spectrum disorder.
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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
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Genotype to phenotype relationships in autism spectrum disorders.
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SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).
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FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders.
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Prenatal valproate exposure and risk of autism spectrum disorders and childhood autism.
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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STAR: ultrafast universal RNA-seq aligner.
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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
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Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses.
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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.