Psychometric validation of the Autism Impact Measure (AIM).
Research Articles
Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.
Single-cell genomics identifies cell type-specific molecular changes in autism.
A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity.
Homozygous non-canonical splice variant in LSM1 in two siblings with multiple congenital anomalies and global developmental delays.
Treatment patterns in children with autism in the United States.
Visual perception, task-induced pupil response trajectories and ASD features in children.
VIP interneurons contribute to avoidance behavior by regulating information flow across hippocampal-prefrontal networks.
Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.
Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug.
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