Angelo Gloria

Troina, 94018, Italy

Last Updated: 09/26/2026

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Found 10 publications

A De Novo USP24 Variant as a Candidate Driver in a Neurodevelopmental Disorder: Insights from Trio-Based Whole-Exome Sequencing.

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

Unravelling the role of Neurotrimin (NTM), a member of the IgLON family, in mild intellectual disability and anxiety-like behaviors.

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

Investigating the role of a novel hemizygous FAAH2 variant in neurological and metabolic disorders.

Investigating the role of a novel hemizygous FAAH2 variant in neurological and metabolic disorders.

Journal: Gene

Published: May 07, 2025

Potential Association of the CSMD1 Gene with Moderate Intellectual Disability, Anxiety Disorder, and Obsessive-Compulsive Personality Traits.

Potential Association of the CSMD1 Gene with Moderate Intellectual Disability, Anxiety Disorder, and Obsessive-Compulsive Personality Traits.

Journal: International journal of molecular sciences

Published: March 19, 2025

Exploring the Role of FICD, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic Disorders.

Exploring the Role of FICD, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic Disorders.

Journal: Genes

Published: November 24, 2024

PLEKHG1: New Potential Candidate Gene for Periventricular White Matter Abnormalities.

PLEKHG1: New Potential Candidate Gene for Periventricular White Matter Abnormalities.

Journal: Genes

Published: July 09, 2024

UNC5C: Novel Gene Associated with Psychiatric Disorders Impacts Dysregulation of Axon Guidance Pathways.

UNC5C: Novel Gene Associated with Psychiatric Disorders Impacts Dysregulation of Axon Guidance Pathways.

Journal: Genes

Published: February 05, 2024

Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families.

Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families.

Journal: Medicina (Kaunas, Lithuania)

Published: July 14, 2023

PHF21A Related Disorder: Description of a New Case.

PHF21A Related Disorder: Description of a New Case.

Journal: International journal of molecular sciences

Published: November 02, 2022

Prader-Willi Syndrome with Angelman Syndrome in the Offspring.

Prader-Willi Syndrome with Angelman Syndrome in the Offspring.

Journal: Medicina (Kaunas, Lithuania)

Published: April 10, 2021

Showing 1-10 of 10

Last Updated: 09/26/2026