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Author

Giorgio Fortunato

ORCID: 0000-0002-4279-6145
Observed ORCID: 0000-0002-4279-6145
OpenAlex ID: A5065026426
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson’s Disease in Italian Patients
2023 · Nicole Piera Palomba, Giorgio Fortunato, et al. · Molecular Neurobiology · 28
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Multiomics approach discloses lipids and metabolites profiles associated to Parkinson's disease stages and applied therapies
2024 · Federica Carrillo, Nicole Piera Palomba, et al. · Neurobiology of Disease · 22
Multiomics approach identifies dysregulated lipidomic and proteomic networks in Parkinson’s disease patients mutated in TMEM175
2025 · Federica Carrillo, Marco Ghirimoldi, et al. · npj Parkinson s Disease · 16
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A mutation in the ZNF687 gene that is responsible for the severe form of Paget’s disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model
2023 · Sharon Russo, Federica Scotto di Carlo, et al. · Bone Research · 11
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ANKK1, ANKRD50, GRK5, PACSIN1 and VPS8 are novel candidate genes associated with late onset Parkinson's disease: Definition of a novel predictive protocol based on polygenic model of inheritance
2025 · Federica Carrillo, Nicole Piera Palomba, et al. · Neurobiology of Disease · 6
Preclinical and clinical study on type 3 metabotropic glutamate receptors in Parkinson’s disease
2025 · Luisa Di Menna, Marika Alborghetti, et al. · npj Parkinson s Disease · 5
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Rare variants alter mitochondrial lipid homeostasis and neuronal excitability in PD patient-derived dopaminergic neurons
2026 · Federica Carrillo, Giorgio Fortunato, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Zfp687 knock-in mouse model of Paget’s disease of bone exhibits increased bone marrow adiposity preceding bone remodelling alteration
2022 · Sharon Russo, Federica Scotto di Carlo, et al. · Bone Reports
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Works count: 8
Citation count: 88
H-index: 5
I10-index: 4
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