Research Articles

Using rare genetic mutations to revisit structural brain asymmetry.

Structural models of genome-wide covariance identify multiple common dimensions in autism.

Interpreting polygenic score effects in sibling analysis.

Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk.

HAT: de novo variant calling for highly accurate short-read and long-read sequencing data.

B56δ long-disordered arms form a dynamic PP2A regulation interface coupled with global allostery and Jordan’s syndrome mutations

Receptive language and receptive-expressive discrepancy in minimally verbal autistic children and adolescents.

ANKS1B encoded AIDA-1 regulates social behaviors by controlling oligodendrocyte function.

Wearable biosensing to predict imminent aggressive behavior in psychiatric inpatient youths with autism.

Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.