Clinical

Facilitating the iterative design of informatics tools to advance the science of autism.

Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities.

Toward fulfilling the promise of molecular medicine in fragile X syndrome.

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.

A multisite study of the clinical diagnosis of different autism spectrum disorders.

Predicting improvement in social-communication symptoms of autism spectrum disorders using retrospective treatment data.

The behavioral phenotype in MeCP2 duplication syndrome: A comparison to idiopathic autism.

Neurocognitive and behavioral outcomes of younger siblings of children with autism spectrum disorder at age five.

Accuracy of phenotyping children with autism based on parent report: What specifically do we gain phenotyping ‘rapidly’?

Tympanostomy tube placement in children with autism.