Oligogenic effects of 16p11.2 copy number variation on craniofacial development.
Clinical and genetic characterization of individuals with predicted deleterious PHIP variants.
Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.
Characterization of medication use in a multicenter sample of pediatric inpatients with autism spectrum disorder.
Impaired perceptual learning in a mouse model of fragile X syndrome is mediated by parvalbumin neuron dysfunction and is reversible.
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R-baclofen reverses cognitive deficits and improves social interactions in two lines of 16p11.2 deletion mice.
Dominant-negative SMARCA4 mutants alter the accessibility landscape of tissue-unrestricted enhancers.
MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.
CHD8 mutation leads to autistic-like behaviors and impaired striatal circuits.
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