SURFiN Mentors
Hyperactivity and male-specific sleep deficits in the 16p11.2 deletion mouse model of autism.
Sex-biasing influence of autism-associated Ube3a gene overdosage at connectomic, behavioral and transcriptomic levels.
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.
Human microglia states are conserved across experimental models and regulate neural stem cell responses in chimeric organoids.
Targeted long-read sequencing identifies missing disease-causing variation.
Comprehensive behavioral phenotyping of a 16p11.2 del mouse model for neurodevelopmental disorders.
Selective inhibition of glycogen synthase kinase 3α corrects pathophysiology in a mouse model of fragile X syndrome.
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