MEF2C hypofunction in neuronal and neuroimmune populations produces MEF2C haploinsufficiency syndrome-like behaviors in mice.
Research Articles
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.
De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism.
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.
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