Increased expression of the PI3K catalytic subunit p110-delta underlies elevated S6 phosphorylation and protein synthesis in an individual with autism from a multiplex family.
Research Articles
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Language ability predicts cortical structure and covariance in boys with autism spectrum disorder.
Genome sequencing of autism-affected families reveals disruption of putative noncoding regulatory DNA.
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.
Genetic evidence for elevated pathogenicity of mitochondrial DNA heteroplasmy in autism spectrum disorder.
Characterizing cognitive control abilities in children with 16p11.2 deletion using adaptive ‘video game’ technology: A pilot study.
Relationship between M100 auditory evoked response and auditory radiation microstructure in 16p11.2 deletion and duplication carriers.
Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications.
Defining the effect of the 16p11.2 duplication on cognition, behavior, and medical comorbidities.
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