Laura Fontana (L Fontana)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 17

Top Topics

Idiopathic Pulmonary Fibrosis

Gene Expression

Top Venues

International journal of molecular sciences

Diagnostics (Basel, Switzerland)

This page only lists publications with an associated author ORCID identifier.

Publications

Silvana Pileggi, Elisa Adele Colombo, Silvia Ancona, Roberto Quadri, Clara Bernardelli, Patrizia Colapietro, Michela Taiana, Laura Fontana, Monica Miozzo, Elena Lesma, Silvia Maria Sirchia
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines. International journal of molecular sciences 25 (7) (2024)
Silvana Pileggi, Elisa Adele Colombo, Silvia Ancona, Roberto Quadri, Clara Bernardelli, Patrizia Colapietro, Michela Taiana, Laura Fontana, Monica Miozzo, Elena Lesma, Silvia Maria Sirchia
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines. International journal of molecular sciences 25 (7) (2024)
Silvana Pileggi, Elisa Adele Colombo, Silvia Ancona, Roberto Quadri, Clara Bernardelli, Patrizia Colapietro, Michela Taiana, Laura Fontana, Monica Miozzo, Elena Lesma, Silvia Maria Sirchia
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines. International journal of molecular sciences 25 (7) (2024)
Giada Moresco, Maria Francesca Bedeschi, Marco Venturin, Roberta Villa, Jole Costanza, Alessia Mauri, Carlo Santaniello, Odoardo Picciolini, Laura Messina, Fabio Triulzi, Monica Rosa Miozzo, Ornella Rondinone, Laura Fontana
Exploring the Impact of Genetics in a Large Cohort of Moebius Patients by Trio Whole Exome Sequencing. Genes 15 (8) (2024)
Giada Moresco, Maria Francesca Bedeschi, Marco Venturin, Roberta Villa, Jole Costanza, Alessia Mauri, Carlo Santaniello, Odoardo Picciolini, Laura Messina, Fabio Triulzi, Monica Rosa Miozzo, Ornella Rondinone, Laura Fontana
Exploring the Impact of Genetics in a Large Cohort of Moebius Patients by Trio Whole Exome Sequencing. Genes 15 (8) (2024)
Silvana Pileggi, Elisa Adele Colombo, Silvia Ancona, Roberto Quadri, Clara Bernardelli, Patrizia Colapietro, Michela Taiana, Laura Fontana, Monica Miozzo, Elena Lesma, Silvia Maria Sirchia
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines. International journal of molecular sciences 25 (7) (2024)
Claudio Tirelli, Chiara Pesenti, Monica Miozzo, Michele Mondoni, Laura Fontana, Stefano Centanni
The Genetic and Epigenetic Footprint in Idiopathic Pulmonary Fibrosis and Familial Pulmonary Fibrosis: A State-of-the-Art Review. Diagnostics (Basel, Switzerland) 12 (12) (2022)
Claudio Tirelli, Chiara Pesenti, Monica Miozzo, Michele Mondoni, Laura Fontana, Stefano Centanni
The Genetic and Epigenetic Footprint in Idiopathic Pulmonary Fibrosis and Familial Pulmonary Fibrosis: A State-of-the-Art Review. Diagnostics (Basel, Switzerland) 12 (12) (2022)
Vanessa Nicolì, Silvia Maria Tabano, Patrizia Colapietro, Michelangelo Maestri, Roberta Ricciardi, Andrea Stoccoro, Laura Fontana, Melania Guida, Monica Miozzo, Fabio Coppedè, Lucia Migliore
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis. Genes 13 (4) (2022)
Ornella Rondinone, Alessio Murgia, Jole Costanza, Silvia Maria Tabano, Margherita Camanni, Luigi Corsaro, Laura Fontana, Patrizia Colapietro, Luciano Calzari, Silvia Motta, Carlo Santaniello, Tatjana Radaelli, Enrico Ferrazzi, Silvano Bosari, Davide Gentilini, Silvia Maria Sirchia, Monica Miozzo
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22 , 2136. International journal of molecular sciences 23 (10) (2022)
Laura Fontana, Silvia Maria Tabano, Silvia Maitz, Patrizia Colapietro, Emanuele Garzia, Alberto Giovanni Gerli, Silvia Maria Sirchia, Monica Miozzo
Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance. International journal of molecular sciences 22 (7) (2021)
Ornella Rondinone, Alessio Murgia, Jole Costanza, Silvia Maria Tabano, Margherita Camanni, Luigi Corsaro, Laura Fontana, Patrizia Colapietro, Luciano Calzari, Silvia Motta, Carlo Santaniello, Tatjana Radaelli, Enrico Ferrazzi, Silvano Bosari, Davide Gentilini, Silvia Maria Sirchia, Monica Miozzo
Extensive Placental Methylation Profiling in Normal Pregnancies. International journal of molecular sciences 22 (4) (2021)
Silvana Pileggi, Marta La Vecchia, Elisa Adele Colombo, Laura Fontana, Patrizia Colapietro, Davide Rovina, Annamaria Morotti, Silvia Maria Tabano, Giovanni Porta, Myriam Alcalay, Cristina Gervasini, Monica Miozzo, Silvia Maria Sirchia
Cohesin Mutations Induce Chromatin Conformation Perturbation of the H19/IGF2 Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell Lines. Biomolecules 11 (11) (2021)
Laura Fontana, Maria F Bedeschi, Giulia A Cagnoli, Jole Costanza, Nicola Persico, Silvana Gangi, Matteo Porro, Paola F Ajmone, Patrizia Colapietro, Carlo Santaniello, Milena Crippa, Silvia M Sirchia, Monica Rosa Miozzo, Silvia Tabano
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith-Wiedemann syndrome. Molecular genetics & genomic medicine 8 (9) (2020)
Silvia Maria Tabano, Jacopo Azzollini, Chiara Pesenti, Sara Lovati, Jole Costanza, Laura Fontana, Bernard Peissel, Monica Miozzo, Siranoush Manoukian
Analysis of BRCA1 and RAD51C Promoter Methylation in Italian Families at High-Risk of Breast and Ovarian Cancer. Cancers 12 (4) (2020)
Jacopo Azzollini, Chiara Pesenti, Sara Pizzamiglio, Laura Fontana, Carmela Guarino, Bernard Peissel, Maddalena Plebani, Silvia Maria Tabano, Silvia Maria Sirchia, Patrizia Colapietro, Roberta Villa, Biagio Paolini, Paolo Verderio, Monica Miozzo, Siranoush Manoukian
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer. Cancers 11 (1) (2019)
Laura Fontana, M F Bedeschi, S Maitz, A Cereda, C Faré, S Motta, A Seresini, P D'Ursi, Alessandro Orro, V Pecile, M Calvello, A Selicorni, F Lalatta, Donatella Milani, Silvia Maria Sirchia, Monica Rosa Miozzo, Silvia Maria Tabano
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. Epigenetics 13 (9) (2018)