Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder.
Research Articles
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.
MEF2C hypofunction in neuronal and neuroimmune populations produces MEF2C haploinsufficiency syndrome-like behaviors in mice.
Antigenic targets of patient and maternal autoantibodies in autism spectrum disorder.
Quantitative gait assessment in children with 16p11.2 syndrome.
Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly.
Combinatorial targeting of distributed forebrain networks reverses noise hypersensitivity in a model of autism spectrum disorder.
In vivo functional study of disease-associated rare human variants using Drosophila.
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