COLAPIETRO, PATRIZIA
COLAPIETRO, PATRIZIA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
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
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
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
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
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
Circulating microRNAs Suggest Networks Associated with Biological Functions in Aggressive Refractory Type 2 Celiac Disease
2022 N. Bianchi, L. Doneda, L. Elli, C. Taccioli, V. Vaira, A. Scricciolo, V. Lombardo, A. Terrazzan, P. Colapietro, L. Terranova, C. Bergamini, M. Vecchi, L. Scaramella, N. Nandi, L. Roncoroni
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
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
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
(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 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
Mismatch repair protein loss is a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability
2019 N. Fusco, G. Lopez, C. Corti, C. Pesenti, P. Colapietro, G. Ercoli, G. Gaudioso, A. Faversani, D. Gambini, L. Despini, C. Blundo, V. Vaira, M. Miozzo, S. Ferrero, S. Bosari
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
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
Mismatch repair protein loss as a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability
2018 N. Fusco, G. Lopez, C. Corti, C. Pesenti, P. Colapietro, G. Ercoli, G. Gaudioso, A. Faversani, D. Gambini, A. Michelotti, L. Despini, C. Blundo, V. Vaira, M. Miozzo, S. Ferrero, S. Bosari
From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients : New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks
2016 G. Negri, P. Magini, D. Milani, P. Colapietro, D. Rusconi, E. Scarano, M.T. Bonati, M. Priolo, M. Crippa, L. Mazzanti, A. Wischmeijer, F. Tamburrino, T. Pippucci, P. Finelli, L. Larizza, C. Gervasini
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi Syndrome patients
2015 S. Spena, D. Milani, D. Rusconi, G. Negri, P. Colapietro, N. Elcioglu, F. Bedeschi, A. Pilotta, L. Spaccini, A. Ficcadenti, C. Magnani, G. Scarano, A. Selicorni, L. Larizza, C. Gervasini
Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome : an update of the CREBBP deletion repertoire
2015 D. Rusconi, G. Negri, P. Colapietro, C. Picinelli, D. Milani, S. Spena, C. Magnani, M.C. Silengo, L. Sorasio, V. Curtisova, M.L. Cavaliere, P. Prontera, G. Stangoni, G.B. Ferrero, E. Biamino, R. Fischetto, M. Piccione, P. Gasparini, L. Salviati, A. Selicorni, P. Finelli, L. Larizza, C. Gervasini
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene
2015 G. Negri, D. Milani, P. Colapietro, F. Forzano, M. Della Monica, D. Rusconi, L. Consonni, L.G. Caffi, P. Finelli, G. Scarano, C. Magnani, A. Selicorni, S. Spena, L. Larizza, C. Gervasini