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
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
Minnai, F., Biscarini, F., Esposito, M., Dragani, T.A., Bujanda, L., Rahmouni, S., et al. (2024). A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death. SCIENTIFIC REPORTS, 14(1) [10.1038/s41598-024-53310-x]. - 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., 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