The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Recent studies implicate chromatin modifiers in autism spectrum disorder (ASD) through the identification of recurrent de novo loss of function mutations in affected individuals. ASD risk genes are co-expressed in human midfetal cortex, suggesting that ASD risk genes converge in specific regulatory...
Main Authors: | Cotney, Justin, Muhle, Rebecca A., Sanders, Stephan J., Liu, Li, Willsey, A. Jeremy, Niu, Wei, Liu, Wenzhong, Klei, Lambertus, Lei, Jing, Yin, Jun, Reilly, Steven K., Tebbenkamp, Andrew T., Bichsel, Candace, Pletikos, Mihovil, Sestan, Nenad, Roeder, Kathryn, State, Matthew W., Devlin, Bernie, Noonan, James P. |
---|---|
Format: | Online |
Language: | English |
Published: |
Nature Pub. Group
2015
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4355952/ |
Similar Items
-
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
by: Liu, Li, et al.
Published: (2014) -
CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment
by: Wang, Ping, et al.
Published: (2015) -
ANS: Aberrant Neurodevelopment of the Social Cognition Network in Adolescents with Autism Spectrum Disorders
by: Cheng, Yawei, et al.
Published: (2011) -
Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology
by: Barnard, Rebecca A., et al.
Published: (2015) -
Common genetic variants, acting additively, are a major source of risk for autism
by: Klei, Lambertus, et al.
Published: (2012)