The contribution of de novo coding mutations to autism spectrum disorder
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Cites background or methods from "The contribution of de novo coding ..."
...Applying this model to the entire SSC cohort identified eight ASD genes (Table S6) in addition to the 27 identified previously at an FDR of % 0.1 (Iossifov et al., 2014)....
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..., 2014) alongside exome data from 3,982 probands in the SSC (Iossifov et al., 2014) and ASC (De Rubeis et al....
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...1220 Neuron 87, 1215–1233, September 23, 2015 ª2015 Elsevier Inc. LoF (dnLoF) mutation (Iossifov et al., 2014; Robinson et al., 2014; Samocha et al., 2014)....
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...Recent collaborative efforts have applied exome sequencing technology to the entire SSC cohort (Iossifov et al., 2014) identifying 27 ASD associated genes (FDR of % 0.1)....
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...…PA 15213, USA *Correspondence: stephan.sanders@ucsf.edu (S.J.S.), matthew.state@ucsf.edu (M.W.S.) http://dx.doi.org/10.1016/j.neuron.2015.09.016 2014; Iossifov et al., 2012, 2014; Neale et al., 2012; O’Roak et al., 2012; Sanders et al., 2012), as well as yielding important insights into the…...
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