Simons Searchlight

Neurodevelopmental profile of HIVEP2-related disorder.

Characterizing sleep problems in 16p11.2 deletion and duplication.

Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism.

Patterns of delay in early gross motor and expressive language milestone attainment in probands with genetic conditions versus idiopathic ASD from SFARI registries.

Neurodevelopmental phenotypes in individuals with pathogenic variants in CHAMP1.

Effects of eight neuropsychiatric copy number variants on human brain structure.

Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions.

Neurodevelopmental phenotypes associated with pathogenic variants in SLC6A1.

Overexpression of CD47 is associated with brain overgrowth and 16p11.2 deletion syndrome.

Availability of services and caregiver burden: Supporting individuals with neurogenetic conditions during the COVID-19 pandemic.