Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Research Articles
A genome-wide linkage and association scan reveals novel loci for autism.
Cell type-specific regulation of DARPP-32 phosphorylation by psychostimulant and antipsychotic drugs.
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
I can see you better if I can hear you coming: action-consistent sounds facilitate the visual detection of human gait.
Common origins of hippocampal Ivy and nitric oxide synthase expressing neurogliaform cells.
Face processing abilities in relatives of individuals with ASD.
Neurexins physically and functionally interact with GABAA receptors.
The cell-intrinsic requirement of Sox6 for cortical interneuron development.
Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.
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