Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.
Research Articles
An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development.
Testing sensory and multisensory function in children with autism spectrum disorder.
Atypical processing of voice sounds in infants at risk for autism spectrum disorder.
Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model.
Comprehensive analysis of the 16p11.2 deletion and null CNTNAP2 mouse models of autism spectrum disorder.
Arginine vasopressin is a blood-based biomarker of social functioning in children with autism.
Genotype to phenotype relationships in autism spectrum disorders.
PTEN mutations alter brain growth trajectory and allocation of cell types through elevated beta-catenin signaling.
Eye-tracking measurements of language processing: Developmental differences in children at high risk for ASD.
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