19972020

Research output per year

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

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Research Output

Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations

Accogli, A., Severino, M., Riva, A., Madia, F., Balagura, G., Iacomino, M., Carlini, B., Baldassari, S., Giacomini, T., Croci, C., Pisciotta, L., Messana, T., Boni, A., Russo, A., Bilo, L., Tonziello, R., Coppola, A., Filla, A., Mecarelli, O., Casalone, R. & 19 others, Pisani, F., Falsaperla, R., Marino, S., Parisi, P., Ferretti, A., Elia, M., Luchetti, A., Milani, D., Vanadia, F., Silvestri, L., Rebessi, E., Parente, E., Vatti, G., Mancardi, M. M., Nobili, L., Capra, V., Salpietro, V., Striano, P. & Zara, F., Aug 2020, In : Seizure. 80, p. 145-152 8 p.

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

  • 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., 2019, In : Human Genetics. 138, 3, p. 257-269 13 p.

    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., 2019, In : Human Genetics. 138, 3, p. 257-269 13 p.

    Research output: Contribution to journalArticle

    Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy

    Pellino, G., Chiavarino, F., Fiumana, E., Boni, A., Russo, A. & Faggioli, R., Oct 2019, In : Epilepsy and Behavior. 99, 106465.

    Research output: Contribution to journalArticle