Postsynaptic FMRP bidirectionally regulates excitatory synapses as a function of developmental age and MEF2 activity.
Research Articles
Epilepsy in simplex autism pedigrees is much lower than the rate in multiplex autism pedigrees.
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder.
Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism.
The role of imitation in the observed heterogeneity in EEG mu rhythm in autism and typical development.
Subcategories of restricted and repetitive behaviors in children with autism spectrum disorders.
Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome.
An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.
The disruption of CELF6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.
Intellectual disability is associated with increased runs of homozygosity in simplex autism.
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