Aaron D. Besterman

This study shows that long-read genome sequencing improves detection of structural and repeat variants in autism and links them to functional consequences.

This study examines common and rare variant genetic contributions to autism in African Americans, highlighting differences in genetic effects and polygenic score transferability between European and African ancestries.

The paper compares neurobehavioral profiles of Smith-Kingsmore Syndrome and PTEN Hamartoma Tumor Syndrome, identifying distinct features and diagnostic markers.

This study evaluates a genomics-informed multidisciplinary clinic for neurodevelopmental disorders, finding that genetic diagnoses lead to significant clinical management changes in most patients.

This study evaluates the impact of genetic testing on an inpatient child and adolescent psychiatry service, finding increased testing rates and higher representation of underrepresented minorities.