De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Research Articles
The emerging biology of autism spectrum disorders.
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.
Microglia in the cerebral cortex in autism.
Developmental trajectories of resting EEG power: An endophenotype of autism spectrum disorder.
Multiple autism-linked genes mediate synapse elimination via proteasomal degradation of a synaptic scaffold PSD-95.
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.
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