Paving the way toward treatment solutions for CTNNB1 syndrome: A patient organization perspective.
Research Articles
m6A-mRNA reader YTHDF2 identified as a potential risk gene in autism with disproportionate megalencephaly.
Noncoding variants and sulcal patterns in congenital heart disease: Machine learning to predict functional impact.
Impact of interaction between individual genomes and preeclampsia on the severity of autism spectrum disorder symptoms.
A normative model representing autistic individuals amidst autism spectrum phenotypic heterogeneity.
Reports of echolalia and related behaviors in autism from parents, teachers, and clinicians: Evidence from the Simon Simplex Collection.
Comparative profiling of white matter development in the human and mouse brain reveals volumetric deficits and delayed myelination in Angelman syndrome.
Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.
Remote monitoring of social attention in neurogenetic syndromes and idiopathic neurodevelopmental disability.
Children’s social preference for teachers versus peers in autism inclusion classrooms: An objective perspective.
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