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Author

Angelo Gloria

Observed name: A. Gloria
ORCID: 0000-0002-2848-2844
Observed ORCID: 0000-0002-2848-2844
OpenAlex ID: A5030003567
Fragile X mental retardation protein (FMRP) interacting proteins exhibit different expression patterns during development
2015 · C.M. Bonaccorso, M. Spatuzza, et al. · International Journal of Developmental Neuroscience · 56
PAH Gene Mutations in the Sicilian Population: Association with Minihaplotypes and Expression Analysis
2001 · Mario G. Mirisola, Francesco Cali, et al. · Molecular Genetics and Metabolism · 20
UNC5C: Novel Gene Associated with Psychiatric Disorders Impacts Dysregulation of Axon Guidance Pathways
2024 · Simone Treccarichi, Pinella Failla, et al. · Genes · 13
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Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families
2023 · Francesco Calì, Francesco Domenico Di Blasi, et al. · Medicina · 10
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Investigating the role of a novel hemizygous FAAH2 variant in neurological and metabolic disorders
2025 · Mirella Vinci, Donatella Greco, et al. · Gene · 9
PLEKHG1: New Potential Candidate Gene for Periventricular White Matter Abnormalities
2024 · Francesco Calì, Mirella Vinci, et al. · Genes · 7
PHF21A Related Disorder: Description of a New Case
2022 · Ambra Butera, Antonio Gennaro Nicotera, et al. · International Journal of Molecular Sciences · 7
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Prader–Willi Syndrome with Angelman Syndrome in the Offspring
2021 · Donatella Greco, Luigi Vetri, et al. · Medicina · 7
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Potential Association of the CSMD1 Gene with Moderate Intellectual Disability, Anxiety Disorder, and Obsessive–Compulsive Personality Traits
2025 · Antonino Musumeci, Mirella Vinci, et al. · International Journal of Molecular Sciences · 6
Unravelling the role of Neurotrimin (NTM), a member of the IgLON family, in mild intellectual disability and anxiety-like behaviors
2025 · Mirella Vinci, Simone Treccarichi, et al. · Gene · 5
Exploring the Role of FICD, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic Disorders
2024 · Mirella Vinci, Donatella Greco, et al. · Genes · 3
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A De Novo USP24 Variant as a Candidate Driver in a Neurodevelopmental Disorder: Insights from Trio-Based Whole-Exome Sequencing
2026 · Mirella Vinci, Antonino Musumeci, et al. · International Journal of Molecular Sciences · 1
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Identification of novel mutations in L1CAM gene by a DHPLC-based assay
2016 · Mirella Vinci, Michele Falco, et al. · Genes & Genomics · 1
Whole-Exome Sequencing in Patients with Tooth Agenesis and Neurodevelopmental Disorders: A Descriptive Case Series
2026 · Francesco Calì, Antonino Musumeci, et al. · International Journal of Molecular Sciences
Works count: 14
Citation count: 145
H-index: 7
I10-index: 4
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