BALDASSARRI MARGHERITA | Elenco docenti

Pasquinelli, E., Casamassima, G., Brunelli, G., Belakhdar, O., Minetto, S., Grosso, S., et al. (2025). Rare variants modulating phenotype in NF1 carriers. SCIENTIFIC REPORTS, 15(1) [10.1038/s41598-025-09751-z]. - dettaglio
Loberti, L., Adamo, L., Antolini, E., Casamassima, G., Destrèe, A., Brunetti-Pierri, N., et al. (2025). AUTS2-related syndrome: Insights from a large European cohort. GENETICS IN MEDICINE, 27(6) [10.1016/j.gim.2025.101375]. - dettaglio
Esposito, M., Minnai, F., Copetti, M., Miscio, G., Perna, R., Piepoli, A., et al. (2024). Human leukocyte antigen variants associate with BNT162b2 mRNA vaccine response. COMMUNICATIONS MEDICINE, 4(1) [10.1038/s43856-024-00490-2]. - dettaglio
Daga, S., Donati, F., Capitani, K., Croci, S., Tita, R., Giliberti, A., et al. (2024). Correction: New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells. EUROPEAN JOURNAL OF HUMAN GENETICS, 32(1), 131-131 [10.1038/s41431-023-01287-y]. - dettaglio
Daga, S., Ding, J., Deltas, C., Savige, J., Lipska-Ziętkiewicz, B.S., Hoefele, J., et al. (2024). Correction: The 2019 and 2021 International workshops on Alport syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS, 32(1), 130-130 [10.1038/s41431-023-01286-z]. - dettaglio