BALDASSARRI MARGHERITA | Professor page

Bruno, L.P., Doddato, G., Baldassarri, M., Rizzo, C.L., Resciniti, S., Bruttini, M., et al. (2023). Expanding the clinical spectrum associated with the PACS1 p.Arg203Trp mutational hot-spot: Two additional Italian patients. AMERICAN JOURNAL OF MEDICAL GENETICS. PART A, 191(1), 284-288 [10.1002/ajmg.a.62984]. - view more
Bergantini, L., Baldassarri, M., D'Alessandro, M., Brunelli, G., Fabbri, G., Zguro, K., et al. (2023). Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder. RESPIRATORY RESEARCH, 24(1), 158 [10.1186/s12931-023-02458-7]. - view more
Daga, S., Ding, J., Deltas, C., Savige, J., Lipska-Ziętkiewicz, B.S., Hoefele, J., et al. (2022). The 2019 and 2021 International Workshops on Alport Syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS, 30(5), 507-516 [10.1038/s41431-022-01075-0]. - view more
Kousathanas, A., Pairo-Castineira, E., Rawlik, K., Stuckey, A., Odhams, C.A., Walker, S., et al. (2022). Whole-genome sequencing reveals host factors underlying critical COVID-19. NATURE, 607(7917), 97-103 [10.1038/s41586-022-04576-6]. - view more
Baldassarri, M., Zguro, K., Tomati, V., Pastorino, C., Fava, F., Croci, S., et al. (2022). Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes. CELLS, 11(24), 4096 [10.3390/cells11244096]. - view more