Brief report: Convergence and discrepancy between self- and informant-reported depressive symptoms in young autistic adults
Research Articles
Quantifying neurobehavioral profiles across neurodevelopmental genetic syndromes and idiopathic neurodevelopmental disorders.
Motor phenotypes associated with genetic neurodevelopmental disorders.
Health supervision for children and adolescents with 16p11.2 deletion syndrome.
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder.
Pervasive alterations of intra-axonal volume and network organization in young children with a 16p11.2 deletion.
Validation of a modified version of the gross motor function measure in PPPR5D related neurodevelopmental disorder.
Beyond the diagnosis: Evaluation of quality-of-life measures and family functioning in SLC6A1-related neurodevelopmental disorder.
Improvement of variant reclassification in genetic neurodevelopmental conditions.
Association of behavioural and social-communicative profiles in children with 16p11.2 copy number variants: a multi-site study.
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