De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference40 articles.
1. De novo mutations in epileptic encephalopathies;Allen;Nature,2013
2. ToppGene Suite for gene list enrichment analysis and candidate gene prioritization;Chen;Nucleic Acids Res.,2009
3. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment;Cotney;Nat. Commun.,2015
4. Synaptic, transcriptional and chromatin genes disrupted in autism;De Rubeis;Nature,2014
5. An integrated encyclopedia of DNA elements in the human genome;Nature,2012
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