Missense variant contribution to USP9X-female syndrome.
Research Articles
Motor impairment increases in children with autism spectrum disorder as a function of social communication, cognitive and functional impairment, repetitive behavior severity, and comorbid diagnoses: A SPARK study report.
Multi-parametric analysis of 57 SYNGAP1 variants reveal impacts on GTPase signaling, localization, and protein stability.
Serotonin differentially modulates the temporal dynamics of the limbic response to facial emotions in male adults with and without autism spectrum disorder (ASD): A randomised placebo-controlled single-dose crossover trial.
Towards robust and replicable sex differences in the intrinsic brain function of autism.
Acute social isolation evokes midbrain craving responses similar to hunger.
Early motor differences in infants at elevated likelihood of autism spectrum disorder and/or attention deficit hyperactivity disorder.
Neuronal correlates of strategic cooperation in monkeys.
Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.
Mutations in spliceosomal genes PPIL1 and PRP17 cause neurodegenerative pontocerebellar hypoplasia with microcephaly.
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