Maria C. Scaduto
Bologna, Italy
Last Updated: 09/26/2026
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Found 11 publications
Further characterization of the BRSK2-associated neurodevelopmental disorder.
Journal: European journal of human genetics : EJHG
Published: January 13, 2026
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.
Journal: Research square
Published: November 14, 2023
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.
Journal: NPJ genomic medicine
Published: October 20, 2023
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder.
Journal: Frontiers in genetics
Published: May 26, 2022
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: April 05, 2022
Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility.
Journal: Frontiers in psychiatry
Published: January 19, 2022
Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years Old.
Journal: Brain sciences
Published: August 20, 2020
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.
Journal: Journal of cellular and molecular medicine
Published: July 24, 2020
Neuropsychiatric phenotype in a child with pseudohypoparathyroidism.
Journal: Journal of pediatric neurosciences
Published: November 19, 2016
Neuropsychological implications of adjunctive levetiracetam in childhood epilepsy.
Journal: Journal of pediatric neurosciences
Published: September 25, 2014
Is cognitive behavioural therapy an effective complement to antidepressants in adolescents? A meta-analysis.
Journal: Acta neuropsychiatrica
Published: December 01, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026