Clinical

Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.

Model’ or ‘tool’? New definitions for translational research.

EEG complexity as a biomarker for autism spectrum disorder risk.

Neuron number and size in prefrontal cortex of children with autism.

Translating glutamate: from pathophysiology to treatment.

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.

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