Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome.
White matter microstructure and atypical visual orienting in 7-month-olds at risk for autism.
Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data.
Autism in gifted youth is associated with low processing speed and high verbal ability.
The combination of autism and exceptional cognitive ability is associated with suicidal ideation.
Selective inhibition of glycogen synthase kinase 3α corrects pathophysiology in a mouse model of fragile X syndrome.
Human microglia states are conserved across experimental models and regulate neural stem cell responses in chimeric organoids.
Comprehensive behavioral phenotyping of a 16p11.2 del mouse model for neurodevelopmental disorders.
Targeted long-read sequencing identifies missing disease-causing variation.
Maternal modifiers and parent-of-origin bias of the autism-associated 16p11.2 CNV.
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