Michael Ronemus, Ivan Iossifov, Dan Levy, Michael Wigler. Nat Rev Genet 2014
Times Cited: 208
Times Cited: 208
Times Cited
Times Co-cited
Similarity
The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
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Synaptic, transcriptional and chromatin genes disrupted in autism.
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
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De novo mutations revealed by whole-exome sequencing 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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Most genetic risk for autism resides with common variation.
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Strong association of de novo copy number mutations with autism.
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Whole genome sequencing resource identifies 18 new candidate genes for 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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Patterns and rates of exonic de novo mutations in autism spectrum disorders.
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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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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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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
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Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
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Identification of common genetic risk variants for autism spectrum disorder.
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Rate of de novo mutations and the importance of father's age to disease risk.
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13
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.
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Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
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Analysis of protein-coding genetic variation in 60,706 humans.
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Whole-genome sequencing of quartet families with autism spectrum disorder.
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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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Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
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Common genetic variants, acting additively, are a major source of risk for autism.
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10
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.