FONTANA, LAURA
FONTANA, LAURA
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 miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls
2019 S. Tabano, A. Caldiroli, A. Terrasi, P. Colapietro, S. Grassi, G.S. Carnevali, L. Fontana, M. Serati, V. Vaira, A.C. Altamura, M. Miozzo, M. Buoli
A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report
2021 G. Moresco, J. Costanza, C. Santaniello, O. Rondinone, F. Grilli, E. Prada, S. Orcesi, I. Coro, A. Pichiecchio, P. Marchisio, M. Miozzo, L. Fontana, D. Milani
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 zebrafish model of Poikiloderma with Neutropenia recapitulates the human syndrome hallmarks and traces back neutropenia to the myeloid progenitor
2015 E.A. Colombo, S. Carra, L. Fontana, E. Bresciani, F. Cotelli, L. Larizza
ANALISI SEMIQUANTITATIVA DELL’ESPRESSIONE DELLE ISOFORME DEL GENE C16orf57 IN UN PANNELLO DI LINEE CELLULARI E TESSUTI ED IN PAZIENTI CON POICHILODERMA CON NEUTROPENIA
2012 L. Fontana, G. Negri, E.A. Colombo, L. Larizza
Analysis of BRCA1 and RAD51C promoter methylation in italian families at high-risk of breast and ovarian cancer
2020 S. Tabano, J. Azzollini, C. Pesenti, S. Lovati, J. Costanza, L. Fontana, B. Peissel, M. Miozzo, S. Manoukian
Angiogenesis in human brain tumors : screening of drug response through a patient-specific cell platform for personalized therapy
2018 L. Guarnaccia, S. Navone, E. Trombetta, C. Cordiglieri, A. Cherubini, F. Crisà, P. Rampini, M. Miozzo, L. Fontana, M. Caroli, M. Locatelli, L. Riboni, R. Campanella, G. Marfia
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
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
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
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
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
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
Decreased serum level of sphingosine-1-phosphate: a novel predictor of clinical severity in COVID-19
2020 G. Marfia, S. Navone, L. Guarnaccia, R. Campanella, M. Mondoni, M. Locatelli, A. Barassi, L. Fontana, F. Palumbo, E. Garzia, G. Ciniglio Appiani, D. Chiumello, M. Miozzo, S. Centanni, L. Riboni
Differential signature of the centrosomal MARK4 isoforms in glioma
2011 I. Magnani, C. Novielli, L. Fontana, S. Tabano, D. Rovina, R.F. Moroni, D. Bauer, S. Mazzoleni, E.A. Colombo, G. Tedeschi, L. Monti, G. Porta, S. Bosari, C. Frassoni, R. Galli, L. Bello, L. Larizza
Epigenetics of functional hypothalamic amenorrhea
2022 L. Fontana, E. Garzia, G. Marfia, V. Galiano, M. Miozzo
Expanding the role of the splicing USB1 gene from Poikiloderma with Neutropenia to acquired myeloid neoplasms
2015 G. Negri, B. Crescenzi, E.A. Colombo, L. Fontana, G. Barba, F. Arcioni, C. Gervasini, C. Mecucci, L. Larizza
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