Mapping 22q11.2 gene dosage effects on brain morphometry.
Research Articles
Predictors of inpatient psychiatric hospitalization for children and adolescents with autism spectrum disorder.
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Indel variant analysis of short-read sequencing data with Scalpel.
Opposing effects on Nav1.2 function underlie differences between SCN2A variants observed in individuals with autism spectrum disorder or infantile seizures.
SMASH, a fragmentation and sequencing method for genomic copy number analysis.
A rapid chemical-genetic screen utilizing impaired movement phenotypes in C. elegans: Input into genetics of neurodevelopmental disorders.
The autism-linked UBE3AT485A mutant E3 ubiquitin ligase activates the Wnt/beta-catenin pathway by inhibiting the proteasome.
Developmental trajectories for young children with 16p11.2 copy number variation.
Hyperactivity and male-specific sleep deficits in the 16p11.2 deletion mouse model of autism.
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