The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
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Title
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Authors
Keywords
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Journal
Nature Communications
Volume 6, Issue 1, Pages -
Publisher
Springer Nature
Online
2015-03-10
DOI
10.1038/ncomms7404
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Note: Only part of the references are listed.- Psychiatric Disorders: Diagnosis to Therapy
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- (2014) Li Liu et al. Molecular Autism
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- (2013) A. Jeremy Willsey et al. CELL
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- (2013) Alicia Subtil-Rodríguez et al. NUCLEIC ACIDS RESEARCH
- Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes
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- Genetic architecture in autism spectrum disorder
- (2012) Bernie Devlin et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
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- (2012) Benjamin M. Neale et al. NATURE
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- (2012) Brian J. O’Roak et al. NATURE
- De Novo Gene Disruptions in Children on the Autistic Spectrum
- (2012) Ivan Iossifov et al. NEURON
- Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
- (2012) B. J. O'Roak et al. SCIENCE
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- (2012) Lisa Helbling Chadwick Epigenomics
- Spatio-temporal transcriptome of the human brain
- (2011) Hyo Jung Kang et al. NATURE
- Computational methods for transcriptome annotation and quantification using RNA-seq
- (2011) Manuel Garber et al. NATURE METHODS
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- (2011) Matthew W State et al. NATURE NEUROSCIENCE
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- BEDTools: a flexible suite of utilities for comparing genomic features
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