Feasibility of conducting autism biomarker research in the clinical setting.
Research Articles
Compromising the phosphodependent regulation of the GABAAR β3 subunit reproduces the core phenotypes of autism spectrum disorders.
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.
Psychotic symptoms in 16p11.2 copy-number variant carriers.
Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder.
Elevated polygenic burden for autism spectrum disorder is associated with the broad autism phenotype in mothers of individuals with autism spectrum disorder.
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling.
Spatial preferences account for inter-animal variability during the continual learning of a dynamic cognitive task.
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