FONTANA, LAURA
FONTANA, LAURA
Dipartimento di Scienze della Salute
Case report: Chorea and cognitive decline in a young woman: instrumental and genetic assessment of a case originally diagnosed as multiple sclerosis
2023 C. Dato, E. Micaglio, G. Moresco, O. Rondinone, P. Vitali, C. Pappone, L. Fontana, M. Miozzo, L. Bet
Unraveling the genetic causes of Moebius syndrome
2022 G. Moresco, O. Rondinone, J. Costanza, C. Santaniello, L. Fontana, A. Mauri, M. Venturin, O. Picciolini, R. Villa, M. Miozzo, M.F. Bedeschi
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis
2022 V. Nicol(`(i)), S.M. Tabano, P. Colapietro, M. Maestri, R. Ricciardi, A. Stoccoro, L. Fontana, M. Guida, M.R. Miozzo, F. Copped(`(e)), L. Migliore
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology
2022 G. Moresco, O. Rondinone, A. Mauri, J. Costanza, C. Santaniello, P. Colapietro, E. Micaglio, G. Marfia, C. Pesenti, F. Grilli, B. Rinaldi, E. Prada, G. Scuvera, R. Villa, M.F. Bedeschi, M.R. Miozzo, D. Milani, L. Fontana
The Genetic and Epigenetic Footprint in Idiopathic Pulmonary Fibrosis and Familial Pulmonary Fibrosis: A State-of-the-Art Review
2022 C. Tirelli, C. Pesenti, M. Miozzo, M. Mondoni, L. Fontana, S. Centanni
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
Epigenetics of functional hypothalamic amenorrhea
2022 L. Fontana, E. Garzia, G. Marfia, V. Galiano, M. Miozzo
Novel pathogenetic variants in PTHLH and TRPS1 genes causing syndromic brachydactyly
2022 F.M. Elli, D. Mattinzoli, C. Lucca, M. Piu, M.A. Maffini, J. Costanza, L. Fontana, C. Santaniello, C. Forino, D. Milani, M.T. Bonati, A. Secco, R. Gastaldi, C. Alfieri, P. Messa, M. Miozzo, M. Arosio, G. Mantovani
Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study
2022 S. Tabano, L. Tassi, M. Cannone, G. Brescia, G. Gaudioso, M. Ferrara, P. Colapietro, L. Fontana, M. Miozzo, G. Croci, M. Seia, C. Piuma, M. Solbiati, E. Tobaldini, S. Ferrero, N. Montano, G. Costantino, M. Buoli
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
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
Decreased serum level of sphingosine-1-phosphate: a novel predictor of clinical severity in COVID-19
2021 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
Forecasting the burden of COVID-19 hospitalized patients during the SARS-CoV-2 second wave in Lombardy, Italy
2021 A.G. Gerli, M. Miozzo, S. Centanni, L. Fontana, D. Chiumello, G. Sotgiu, C. La Vecchia
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
Hereditary Breast Cancer: BRCA and Other Susceptibility Genes
2020 J.V. Azzollini, L. Fontana, S. Manoukian
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
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
(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
Molecular Insights into the Classification of Luminal Breast Cancers : the Genomic Heterogeneity of Progesterone-Negative Tumors
2019 G. Lopez, J. Costanza, M. Colleoni, L. Fontana, S. Ferrero, M. Miozzo, N. Fusco