Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants.
Research Articles
Developmental diversification of cortical inhibitory interneurons
Rbfox splicing factors promote neuronal maturation and axon initial segment assembly
Genetic analysis of very obese children with autism spectrum disorder.
Differential attention to faces in infant siblings of children with autism spectrum disorder and associations with later social and language ability.
A unified genetic theory for sporadic and inherited autism.
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.
Enhanced operant extinction and prefrontal excitability in a mouse model of Angelman syndrome.
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion.
Damaging de novo mutations diminish motor skills in children on the autism spectrum.
- Previous Page
- Viewing
- Next Page