Research Articles

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.

Emerging executive functioning and motor development in infants at high and low risk for autism spectrum disorder.

Histone acetylome-wide association study of autism spectrum disorder.

Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.

Negative allosteric modulation of mGluR5 partially corrects pathophysiology in a mouse model of Rett syndrome.

Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder.