Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.
Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.
Clinical and genetic characterization of individuals with predicted deleterious PHIP variants.
Neuroinflammatory gene expression alterations in anterior cingulate cortical white and gray matter of males with autism spectrum disorder.
Intrinsic excitation-inhibition imbalance affects medial prefrontal cortex differently in autistic men versus women.
Dissecting the phenotypic heterogeneity in sensory features in autism spectrum disorder: A factor mixture modelling approach.
Alexithymia in autism: Cross-sectional and longitudinal associations with social-communication difficulties, anxiety and depression symptoms.
Modeling flexible behavior in childhood to adulthood shows age-dependent learning mechanisms and less optimal learning in autism in each age group.
Targeted long-read sequencing identifies missing disease-causing variation.
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