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Times Cited: 157
Times Cited: 157
Times Cited
Times Co-cited
Similarity
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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Synaptic, transcriptional and chromatin genes disrupted in autism.
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Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014.
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Patterns and rates of exonic de novo mutations in autism spectrum disorders.
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Strong association of de novo copy number mutations with autism.
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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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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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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
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A de novo convergence of autism genetics and molecular neuroscience.
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From the genetic architecture to synaptic plasticity in autism spectrum disorder.
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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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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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Common genetic variants on 5p14.1 associate with autism spectrum disorders.
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Common genetic variants, acting additively, are a major source of risk for autism.
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
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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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Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain.
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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
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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.