Multiple autism-linked genes mediate synapse elimination via proteasomal degradation of a synaptic scaffold PSD-95.
Research Articles
Maternal loss of Ube3a produces an excitatory/inhibitory imbalance through neuron type-specific synaptic defects.
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum.
Tympanostomy tube placement in children with autism.
Age-associated DNA methylation in pediatric populations.
Relationship between the social functioning of children with autism spectrum disorders and their siblings’ competencies/problem behaviors.
Networks of neuronal genes affected by common and rare variants in autism spectrum disorders.
Emotional and behavioral adjustment in typically developing siblings of children with autism spectrum disorders.
Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Application of DSM-5 criteria for autism spectrum disorder to three samples of children with DSM-IV diagnoses of pervasive developmental disorders.
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