Corrado Romano

Messina, Italy

Last Updated: 09/26/2026

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Found 115 publications

Effectiveness of STK Spray® for semen stain localization on solid surfaces: A specificity and sensitivity study.

Effectiveness of STK Spray® for semen stain localization on solid surfaces: A specificity and sensitivity study.

Journal: Science & justice : journal of the Forensic Science Society

Published: March 04, 2026

Dysregulation of miRNAs in Sicilian Patients with Autism Spectrum Disorder.

Dysregulation of miRNAs in Sicilian Patients with Autism Spectrum Disorder.

Journal: Biomedicines

Published: November 27, 2025

GIT1 loss of function causes a recognizable syndromic neurodevelopmental disorder.

GIT1 loss of function causes a recognizable syndromic neurodevelopmental disorder.

Journal: Brain : a journal of neurology

Published: November 26, 2025

De novo mutation in the ARHGAP32 gene endorses the implication of GTPase-activating proteins (RhoGAP family) in idiopathic autism spectrum disorder.

De novo mutation in the ARHGAP32 gene endorses the implication of GTPase-activating proteins (RhoGAP family) in idiopathic autism spectrum disorder.

Journal: Frontiers in psychiatry

Published: November 25, 2025

Focus on Clinical and Genetic Aspects of PKAN Through the Description of New Patients.

Focus on Clinical and Genetic Aspects of PKAN Through the Description of New Patients.

Journal: Genes

Published: July 24, 2025

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 23, 2025

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 23, 2025

Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances.

Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances.

Journal: Clinical epigenetics

Published: May 27, 2025

Expansion of the Genotypic and Phenotypic Spectrum of TCTN3-Related Joubert Syndrome.

Expansion of the Genotypic and Phenotypic Spectrum of TCTN3-Related Joubert Syndrome.

Journal: Genes

Published: May 22, 2025

Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases.

Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases.

Journal: Genetics in medicine open

Published: May 05, 2025

Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis.

Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis.

Journal: International journal of molecular sciences

Published: October 30, 2024

The 9 bp Deletion between the Mitochondrial COII and Lysine tRNA Genes in a Caucasian Population with Cognitive Disorders: An Observational Study.

The 9 bp Deletion between the Mitochondrial COII and Lysine tRNA Genes in a Caucasian Population with Cognitive Disorders: An Observational Study.

Journal: International journal of molecular sciences

Published: September 11, 2024

Showing 1-12 of 115

Last Updated: 09/26/2026