SIRCHIA, SILVIA MARIA
SIRCHIA, SILVIA MARIA
Dipartimento di Scienze della Salute
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines
2024 S. Pileggi, E.A. Colombo, S. Ancona, R. Quadri, C. Bernardelli, P. Colapietro, M. Taiana, L. Fontana, M. Miozzo, E. Lesma, S.M. Sirchia
Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review
2024 L. Fontana, S.M. Sirchia, C. Pesenti, G.M. Colpi, M.R. Miozzo
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study
2023 A. Piccinini, P. Bailo, G. Barbara, M. Miozzo, S. Tabano, P. Colapietro, C. Farè, S.M. Sirchia, E. Battaglioli, P. Bertuccio, G. Manenti, L. Micci, C. La Vecchia, A. Kustermann, S. Gaudi
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes
2022 J. Costanza, M. Camanni, M.M. Ferrari, V. De Cosmi, S. Tabano, L. Fontana, T. Radaelli, G. Privitera, D. Alberico, P. Colapietro, S. Motta, S. Sirchia, T. Stampalija, C. Tabasso, P. Roggero, F. Parazzini, F. Mosca, E. Ferrazzi, S. Bosari, M. Miozzo, C. Agostoni
A perspective on diet, epigenetics and complex diseases: where is the field headed next?
2022 F. Coppedè, M. Franzago, E. Giardina, C. Lo Nigro, G. Matullo, C. Moltrasio, B. Nacmias, S. Pileggi, S.M. Sirchia, A. Stoccoro, C. Tiziana Storlazzi, L. Stuppia, R. Tricarico, G. Merla
Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model
2022 C. Bernardelli, E. Chiaramonte, S. Ancona, S.M. Sirchia, A. Cerri, E.A. Lesma
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines
2021 S. Pileggi, M. La Vecchia, E.A. Colombo, L. Fontana, P. Colapietro, D. Rovina, A. Morotti, S.M. Tabano, G. Porta, M. Alcalay, C.C.G. Gervasini, M.R. Miozzo, S.M. Sirchia
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance
2021 L. Fontana, S. Tabano, S. Maitz, P. Colapietro, E. Garzia, A.G. Gerli, S.M. Sirchia, M. Miozzo
Extensive placental methylation profiling in normal pregnancies
2021 O. Rondinone, A. Murgia, J. Costanza, S. Tabano, M. Camanni, L. Corsaro, L. Fontana, P. Colapietro, L. Calzari, S. Motta, C. Santaniello, T. Radaelli, E. Ferrazzi, S. Bosari, D. Gentilini, S.M. Sirchia, M. Miozzo
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome
2020 L. Fontana, M.F. Bedeschi, G.A. Cagnoli, J. Costanza, N. Persico, S. Gangi, M. Porro, P. Ajmone, P. Colapietro, C. Santaniello, M. Crippa, S.M. Sirchia, M. Miozzo, S. Tabano
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients
2020 D. Rovina, M. La Vecchia, A. Cortesi, L. Fontana, M. Pesant, S. Maitz, S. Tabano, B. Bodega, M. Miozzo, S.M. Sirchia
DNA methylation in the diagnosis of monogenic diseases
2020 F. Cerrato, A. Sparago, F. Ariani, F. Brugnoletti, L. Calzari, F. Coppede, A. De Luca, C. Gervasini, E. Giardina, F. Gurrieri, C.L. Nigro, G. Merla, M. Miozzo, S. Russo, E. Sangiorgi, S.M. Sirchia, G.M. Squeo, S. Tabano, E. Tabolacci, I. Torrente, M. Genuardi, G. Neri, A. Riccio
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer
2019 J. Azzollini, C. Pesenti, S. Pizzamiglio, L. Fontana, C. Guarino, B. Peissel, M. Plebani, S. Tabano, S.M. Sirchia, P. Colapietro, R. Villa, B. Paolini, P. Verderio, M. Miozzo, S. Manoukian
Introduzione al genoma umano
2018 A. Marozzi, M. Capasso, L. Ferrari, B. Franco, A. Iolascon, L. Migliore, M.R. Miozzo, A. Pizzuti, B. Porfirio, N. Resta, P.V. Riva, S.M. Sirchia, A. Turco, O. Zuffardi
Thompson & Thompson : Genetica in medicina
2018 S. Sirchia, M. Miozzo, A. Marozzi, P. Riva, P. Finelli
Introduzione
2018 A. Marozzi, M. Capasso, L. Ferrari, B. Franco, A. Iolascon, L. Migliore, M.R. Miozzo, A. Pizzuti, B. Porfirio, N. Resta, P.V. Riva, S.M. Sirchia, A. Turco, O. Zuffardi
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
2018 L. Fontana, M. Bedeschi, S. Maitz, A. Cereda, C. Faré, S. Motta, A. Seresini, P. D'Ursi, A. Orro, V. Pecile, M. Calvello, A. Selicorni, F. Lalatta, D. Milani, S. Sirchia, M. Miozzo, S. Tabano
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins
2018 L. Paganini, L.A. Hadi, M. Chetta, D. Rovina, L. Fontana, P. Colapietro, E. Bonaparte, L. Pezzani, P. Marchisio, S.M. Tabano, J. Costanza, S.M. Sirchia, L. Riboni, D. Milani, M. Miozzo
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome
2018 L. Paganini, C. Pesenti, D. Milani, L. Fontana, S. Motta, S.M. Sirchia, G. Scuvera, P. Marchisio, S. Esposito, C.M. Cinnante, S.M. Tabano, M.R. Miozzo
GDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML
2018 A. Rainero, F. Angaroni, A. Conti, C. Pirrone, G. Micheloni, L. Tararà, G. Millefanti, E. Maserati, R. Valli, O. Spinelli, K. Buklijas, A. Michelato, R. Casalone, C. Barlassina, M. Barcella, S. Sirchia, E. Piscitelli, M. Caccia, G. Porta