SIRCHIA, SILVIA MARIA
SIRCHIA, SILVIA MARIA
Dipartimento di Scienze della Salute
(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
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 multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes
2016 S. Russo, L. Calzari, A. Mussa, E. Mainini, M. Cassina, S. Di Candia, M. Clementi, S. Guzzetti, S. Tabano, M. Miozzo, S. Sirchia, P. Finelli, P. Prontera, S. Maitz, G. Sorge, A. Calcagno, M. Maghnie, M.T. Divizia, D. Melis, E. Manfredini, G.B. Ferrero, V. Pecile, L. Larizza
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
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
A perspective on diet, epigenetics and complex diseases: where is the field headed next?
2022 F. Coppedè, M. Franzago, E. Giardina, C.L. Nigro, G. Matullo, C. Moltrasio, B. Nacmias, S. Pileggi, S.M. Sirchia, A. Stoccoro, C.T. Storlazzi, L. Stuppia, R. Tricarico, G. Merla
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected
1997 C. De Andreis, G. Simoni, C. Castagna, L. Sacchi, S.M. Sirchia, I.M. Garagiola, T. Persico, P. Serafini, G. Pardi, A.E. Semprini
An epigenetic event may underlies the TSC features in TSC2 ASM cells
2009 E. Lesma, S. Ancona, S.M. Sirchia, V. Grande, E. Chiaramonte, S. Bosari, A.M. Di Giulio, A. Gorio
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute
2011 D. Mari, D. Gentilini, D. Castaldi, D. Remondini, G. Ogliari, R. Ostan, L. Buci, S.M. Sirchia, S. Tabano, F. Cavagnini, D. Monti, C. Franceschi, A.M. Di Blasio, G. Vitale
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva
2005 B. Gentilin, F.R. Grati, P. Invernizzi, C. Selmi, P. Busatto, S.M. Sirchia, F. Rossella, G. Simoni, M. Miozzo
Aneuploid correction and confined placental mosaicism
1996 G. Simoni, S.M. Sirchia, M. Fraccaro
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
Assessment of X chromosome Inactivation pattern in BRCA mutation carriers : evidence for an effect of chemotherapy
2008 M. Miozzo, C. Allemani, F.R. Grati, S.M. Tabano, B. Peissel, P. Antonazzo, V. Pensotti, S.M. Sirchia, P. Radice, S. Manoukian
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi
2015 L. Paganini, N. Carlessi, L. Fontana, R. Silipigni, S. Motta, S. Fiori, S. Guerneri, F. Lalatta, A. Cereda, S. Sirchia, M. Miozzo, S. Tabano
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies
2004 F.R. Grati, S.M. Sirchia, B. Gentilin, F. Rossella, L. Ramoscelli, P. Antonazzo, U. Cavallari , G. Bulfamante, I. Cetin , G. Simoni, M. Miozzo
Blood fetal microchimerism in primary biliary cirrhosis
2000 P. Invernizzi, C. De Andreis, S.M. Sirchia, P.M. Battezzati, M. Zuin, F. Rossella, F. Perego, M. Bignotto, G. Simoni, M. Podda
Characterization of four microsatellites in an Italian population and their application to paternity testing
1996 S.M. Sirchia, I. Garagiola, C. De Andreis, I. Gazzoli, M. Gramegna, G. Colucci
Characterization of human TSC2 cells derived from a TSC/LAM patient chylous effusion
2011 E. Lesma, S. Ancona, V. Grande, S.M. Sirchia, E. Orpianesi, E. Chiaramonte, A.M. Di Giulio, A. Gorio
Characterization of LAM/TSC cells isolated from patient chylous
2010 E. Lesma, S. Ancona, V. Grande, S.M. Sirchia, E. Chiaramonte, S. Bosari, A.M. Di Giulio, A. Gorio
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