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Page 1
Extensive Placental Methylation Profiling in Normal Pregnancies.
Int J Mol Sci. 2021 Feb 21;22(4):2136. doi: 10.3390/ijms22042136.
Int J Mol Sci. 2021.
PMID: 33669975
Free PMC article.
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22, 2136.
Rondinone O, Murgia A, Costanza J, Tabano S, Camanni M, Corsaro L, Fontana L, Colapietro P, Calzari L, Motta S, Santaniello C, Radaelli T, Ferrazzi E, Bosari S, Gentilini D, Sirchia SM, Miozzo M.
Rondinone O, et al. Among authors: corsaro l.
Int J Mol Sci. 2022 May 10;23(10):5298. doi: 10.3390/ijms23105298.
Int J Mol Sci. 2022.
PMID: 35628670
Free PMC article.
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Epigenome Wide Association and Stochastic Epigenetic Mutation Analysis on Cord Blood of Preterm Birth.
Spada E, Calzari L, Corsaro L, Fazia T, Mencarelli M, Di Blasio AM, Bernardinelli L, Zangheri G, Vignali M, Gentilini D.
Spada E, et al. Among authors: corsaro l.
Int J Mol Sci. 2020 Jul 17;21(14):5044. doi: 10.3390/ijms21145044.
Int J Mol Sci. 2020.
PMID: 32708910
Free PMC article.
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Notch, SUMOylation, and ESR-Mediated Signalling Are the Main Molecular Pathways Showing Significantly Different Epimutation Scores between Expressing or Not Oestrogen Receptor Breast Cancer in Three Public EWAS Datasets.
Corsaro L, Gambino VS.
Corsaro L, et al.
Cancers (Basel). 2023 Aug 15;15(16):4109. doi: 10.3390/cancers15164109.
Cancers (Basel). 2023.
PMID: 37627137
Free PMC article.
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Genome-Wide DNA Methylation Analysis of a Cohort of 41 Patients Affected by Oculo-Auriculo-Vertebral Spectrum (OAVS).
Guida V, Calzari L, Fadda MT, Piceci-Sparascio F, Digilio MC, Bernardini L, Brancati F, Mattina T, Melis D, Forzano F, Briuglia S, Mazza T, Bianca S, Valente EM, Salehi LB, Prontera P, Pagnoni M, Tenconi R, Dallapiccola B, Iannetti G, Corsaro L, De Luca A, Gentilini D.
Guida V, et al. Among authors: corsaro l.
Int J Mol Sci. 2021 Jan 26;22(3):1190. doi: 10.3390/ijms22031190.
Int J Mol Sci. 2021.
PMID: 33530447
Free PMC article.
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Characterization of a New Variant in ARHGAP31 Probably Involved in Adams-Oliver Syndrome in a Family with a Variable Phenotypic Spectrum.
Santaniello C, Faversani A, Corsaro L, Melloni G, Motta S, Mandorino E, Sacco D, Stioui S, Ferrara F, Barteselli D, De Vita D, Manuelli D, Costantino L.
Santaniello C, et al. Among authors: corsaro l.
Genes (Basel). 2024 Apr 24;15(5):536. doi: 10.3390/genes15050536.
Genes (Basel). 2024.
PMID: 38790165
Free PMC article.
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