Gervasini Cristina Costanza Giovanna

Research Fellow
SSD
MED/03 - MEDICAL GENETICS
Competition sector
06/A1 - MEDICAL GENETICS

Contacts

Workplace

Via Di Rudinì, 8
20142 MILANO (MI)

Office phone number
02503 23028
Additional phone numbers
0250323028
University email address

Education

Research

Publications
  • Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes / M. Crippa, M.T. Bonati, L. Calzari, C. Picinelli, C. Gervasini, A. Sironi, I. Bestetti, S. Guzzetti, S. Bellone, A. Selicorni, A. Mussa, A. Riccio, G.B. Ferrero, S. Russo, L. Larizza, P. Finelli. - In: FRONTIERS IN GENETICS. - ISSN 1664-8021. - 10(2019 Oct 15), pp. 955.1-955.13.
  • Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations / E.A. Colombo, H. Mutlu-Albayrak, Y. Shafeghati, M. Balasar, J. Piard, D. Gentilini, A.M. Di Blasio, C. Gervasini, L. Van Maldergem, L. Larizza. - In: FRONTIERS IN PEDIATRICS. - ISSN 2296-2360. - 7(2019 May), pp. 210.1-210.7.
  • Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein–Taybi syndrome : the interconnections of epigenetic machinery disorders / G. Negri, P. Magini, D. Milani, M. Crippa, E. Biamino, M. Piccione, S. Sotgiu, C. Perrìa, G. Vitiello, M. Frontali, A. Boni, E. Di Fede, M.C. Gandini, E.A. Colombo, M.J. Bamshad, D.A. Nickerson, J.D. Smith, I. Loddo, P. Finelli, M. Seri, T. Pippucci, L. Larizza, C. Gervasini. - In: HUMAN GENETICS. - ISSN 0340-6717. - 138:3(2019 Mar), pp. 257-269.
  • Lithium as a positive modulator of defective WNT pathway in Cornelia de Lange Syndrome models / C. Parodi, P. Grazioli, D. Bottai, E. Di Fede, T. Vaccari, C.C.G. Gervasini, V. Massa. ((Intervento presentato al 4. convegno Congresso DiSS tenutosi a Milano nel 2018.
  • Use of nutritional devices in Cornelia de Lange syndrome: Data from a large Italian cohort / V. Decimi, B. Parma, R. Panceri, C. Fossati, M. Mariani, S. Russo, C.C. Gervasini, M. Cheli, A. Cereda, A. Selicorni. - In: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A. - ISSN 1552-4825. - 176:9(2018 Sep), pp. 1865-1871.