De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism.
Research Articles
Monosynaptic tracing maps brain-wide afferent oligodendrocyte precursor cell connectivity.
Nucleosome turnover regulates histone methylation patterns over the genome.
Sex-specific gene-environment interactions underlying ASD-like behaviors.
Predicting imminent aggression onset in minimally-verbal youth with autism spectrum disorder using preceding physiological signals.
The immune signaling adaptor LAT contributes to the neuroanatomical phenotype of 16p11.2 BP2-BP3 CNVs.
Altered synaptic transmission and maturation of hippocampal CA1 neurons in a mouse model of human chr16p11.2 microdeletion.
Neuroligin-1-dependent competition regulates cortical synaptogenesis and synapse number.
Focal cortical anomalies and language impairment in 16p11.2 deletion and duplication syndrome.
T-lymphocytes and cytotoxic astrocyte blebs correlate across autism brains.
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