BALDASSARRI MARGHERITA | Elenco docenti

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
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
Farias, T.D.J., Brugiapaglia, S., Croci, S., Magistroni, P., Curcio, C., Zguro, K., et al. (2024). HLA-DPB1*13:01 associates with enhanced, and KIR2DS4*001 with diminished protection from developing severe COVID-19. HLA, 103(1) [10.1111/tan.15251]. - dettaglio
Martelloni, G., Turchi, A., Fallerini, C., Degl'Innocenti, A., Baldassarri, M., Olmi, S., et al. (2024). Host genetics and COVID-19 severity: increasing the accuracy of latest severity scores by Boolean quantum features. FRONTIERS IN GENETICS, 15 [10.3389/fgene.2024.1362469]. - 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