DAGA SERGIO | Professor page

Daga, S., Loberti, L., Rollo, G., Adamo, L., Colavecchio, O.L., Brunelli, G., et al. (2024). Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant. EUROPEAN JOURNAL OF HUMAN GENETICS [10.1038/s41431-024-01706-8]. - view more
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]. - view more
Croci, S., Carriero, M.L., Capitani, K., Daga, S., Donati, F., Frullanti, E., et al. (2024). Correction to: High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot. EUROPEAN JOURNAL OF HUMAN GENETICS, 32(1), 134-134 [10.1038/s41431-023-01290-3]. - view more
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]. - view more
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]. - view more