Simone Treccarichi
Troina, 94018, Italy
Last Updated: 09/26/2026
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Found 32 publications
RFX3 Pathogenic Variants as a Rare Cause of Infantile Epileptic Spasms Syndrome.
Journal: International journal of molecular sciences
Published: July 06, 2026
Comparison of Sensory-Adapted and Regular Dental Environments During Professional Oral Hygiene in Children with Mild Intellectual Disability and Moderate Dental Anxiety: A Randomized Clinical Trial.
Journal: Medicina (Kaunas, Lithuania)
Published: June 26, 2026
Deciphering the Role of LNX2 as a Potential Contributor to Neurodevelopmental Disorders.
Journal: Genes
Published: June 01, 2026
Beyond STRs: Integrative Forensic Genomics from MPS to Genetic Genealogy and AI-Based Prediction.
Journal: Genes
Published: April 23, 2026
A De Novo USP24 Variant as a Candidate Driver in a Neurodevelopmental Disorder: Insights from Trio-Based Whole-Exome Sequencing.
Journal: International journal of molecular sciences
Published: April 07, 2026
A de novo Loss-of-function Variant in RAPGEF6 Supports its Role in Neuropsychiatric Disorders.
Journal: Journal of molecular neuroscience : MN
Published: March 11, 2026
Unraveling the Genetic and Molecular Architecture of Autism Spectrum Disorder: Implications for Clinical Genetics and Genomic Diagnostics.
Journal: International journal of molecular sciences
Published: March 02, 2026
Virtual Reality Versus Monitor-Based Distraction in Children with Mild Intellectual Disability: A Preliminary Comparative Observational Study.
Journal: Children (Basel, Switzerland)
Published: February 23, 2026
Potential Link Between a Disruptive CAPN6 Variant and Neurodevelopmental Disorders.
Journal: International journal of molecular sciences
Published: December 22, 2025
Dissecting the Genetic Contribution of Tooth Agenesis.
Journal: International journal of molecular sciences
Published: September 18, 2025
NGS Approaches in Clinical Diagnostics: From Workflow to Disease-Specific Applications.
Journal: International journal of molecular sciences
Published: September 05, 2025
Unravelling the role of Neurotrimin (NTM), a member of the IgLON family, in mild intellectual disability and anxiety-like behaviors.
Journal: Gene
Published: July 19, 2025
Last Updated: 09/26/2026