<p>Autism spectrum disorder (ASD) is a collection of neurodevelopmental disorders manifested by impaired social communication, repetitive behaviors, and restricted interests. We performed whole exome sequencing (WES) on a total of 754 individuals from 195 families, including 222 probands with ASD, from diverse ancestral backgrounds. We identified potentially pathogenic variants in known and novel ASD or neurodevelopmental disease genes.</p>

Exome Sequencing in an Ancestrally Diverse Autism Cohort

Autism Spectrum Disorder study with SNP/CNV Genotypes (NGS) data on dbGaP (754 participants)