20182019

Research output per year

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Fingerprint Dive into the research topics where Milena Crippa is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression

Bonati, M. T., Castronovo, C., Sironi, A., Zimbalatti, D., Bestetti, I., Crippa, M., Novelli, A., Loddo, S., Dentici, M. L., Taylor, J., Devillard, F., Larizza, L. & Finelli, P., Jun 17 2019, In : Neurogenetics.

Research output: Contribution to journalArticle

  • Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein–Taybi syndrome: the interconnections of epigenetic machinery disorders

    Negri, G., Magini, P., Milani, D., Crippa, M., Biamino, E., Piccione, M., Sotgiu, S., Perrìa, C., Vitiello, G., Frontali, M., Boni, A., Di Fede, E., Gandini, M. C., Colombo, E. A., Bamshad, M. J., Nickerson, D. A., Smith, J. D., Loddo, I., Finelli, P., Seri, M. & 3 others, Pippucci, T., Larizza, L. & Gervasini, C., Mar 4 2019, In : Human Genetics. 138, 3, p. 257-269 13 p.

    Research output: Contribution to journalArticle

  • Open Access
  • Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes

    Crippa, M., Bonati, M. T., Calzari, L., Picinelli, C., Gervasini, C., Sironi, A., Bestetti, I., Guzzetti, S., Bellone, S., Selicorni, A., Mussa, A., Riccio, A., Ferrero, G. B., Russo, S., Larizza, L. & Finelli, P., Oct 15 2019, In : Frontiers in Genetics. 10, 955.

    Research output: Contribution to journalArticle

    Open Access