A framework for the interpretation of de novo mutation in human disease.
Research Articles
NPAS1 represses the generation of specific subtypes of cortical interneurons.
The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder.
Brief report: Impact of child problem behaviors and parental broad autism phenotype traits on substance use among parents of children with ASD.
Soy infant formula and seizures in children with autism: A retrospective study.
Investigation of maternal genotype effects in autism by genome-wide association.
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
Eating in the absence of hunger but not loss of control behaviors are associated with 16p11.2 deletions.
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
Chromatin regulators, phenotypic robustness, and autism risk.
- Previous Page
- Viewing
- Next Page