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Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population.
Gialluisi A, Reccia MG, Tirozzi A, Nutile T, Lombardi A, De Sanctis C; International Parkinson's Disease Genomic Consortium (IPDGC); Varanese S, Pietracupa S, Modugno N, Simeone A, Ciullo M, Esposito T. Gialluisi A, et al. Among authors: tirozzi a. Front Neurol. 2020 Jan 10;10:1362. doi: 10.3389/fneur.2019.01362. eCollection 2019. Front Neurol. 2020. PMID: 31998221 Free PMC article.
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix.
Sampaolo S, Napolitano F, Tirozzi A, Reccia MG, Lombardi L, Farina O, Barra A, Cirillo F, Melone MAB, Gianfrancesco F, Iorio GD, Esposito T. Sampaolo S, et al. Among authors: tirozzi a. J Med Genet. 2017 Oct;54(10):710-720. doi: 10.1136/jmedgenet-2017-104555. Epub 2017 Jul 22. J Med Genet. 2017. PMID: 28735299
NMU DNA methylation in blood is associated with metabolic and inflammatory indices: results from the Moli-sani study.
Marotta A, Noro F, Parisi R, Gialluisi A, Tirozzi A, De Curtis A, Costanzo S, Di Castelnuovo A, Cerletti C, Donati MB, de Gaetano G, Iacoviello L, Izzi B, Gianfagna F. Marotta A, et al. Among authors: tirozzi a. Epigenetics. 2021 Dec;16(12):1347-1360. doi: 10.1080/15592294.2020.1864167. Epub 2021 Jan 4. Epigenetics. 2021. PMID: 33393847 Free PMC article.
24 results