Predictive functional, statistical and structural analysis of CSNK2A1 and CSNK2B variants linked to neurodevelopmental diseases.
Research Articles
Dopaminergic gene dosage reveals distinct biological partitions between autism and developmental delay as revealed by complex network analysis and machine learning approaches.
Clinical, neuroimaging and molecular characteristics of PPP2R5D-related neurodevelopmental disorders: An expanded series with functional characterisation and genotype-phenotype analysis.
Parental tuning of language input to autistic and nonspectrum children.
Similar rates of deleterious copy number variants in early-onset psychosis and autism spectrum disorder.
Bias in measurement of autism symptoms by spoken language level and non-verbal mental age in minimally verbal children with neurodevelopmental disorders.
Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functions.
Psychometric validation of a brief self-report measure of misophonia symptoms and functional impairment: The duke-vanderbilt misophonia screening questionnaire.
Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability.
Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.
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