Alport syndrome: impact of digenic inheritance in patients management
Fallerini, C., Baldassarri, M., Trevisson, E., Morbidoni, V., La Manna, A., Lazzarin, R., Pasini, A., Barbano, G., Pinciaroli, A.R., Garosi, G., Frullanti, E., Pinto, A.M., Mencarelli, M.A., Mari, F., Renieri, A., Ariani, F.
Published in Clinical genetics (01.07.2017)
Published in Clinical genetics (01.07.2017)
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Journal Article
Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases
Fallerini, C., Dosa, L., Tita, R., Del Prete, D., Feriozzi, S., Gai, G., Clementi, M., La Manna, A., Miglietti, N., Mancini, R., Mandrile, G., Ghiggeri, G.M., Piaggio, G., Brancati, F., Diano, L., Frate, E., Pinciaroli, A.R., Giani, M., Castorina, P., Bresin, E., Giachino, D., De Marchi, M., Mari, F., Bruttini, M., Renieri, A., Ariani, F.
Published in Clinical genetics (01.09.2014)
Published in Clinical genetics (01.09.2014)
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Journal Article
Non-collagen genes role in digenic Alport syndrome
Daga, S, Fallerini, C, Furini, S, Pecoraro, C, Scolari, F, Ariani, F, Bruttini, M, Mencarelli, M A, Mari, F, Renieri, A, Pinto, A M
Published in BMC nephrology (26.02.2019)
Published in BMC nephrology (26.02.2019)
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The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males
Croci, Susanna, Venneri, Mary Anna, Mantovani, Stefania, Fallerini, Chiara, Benetti, Elisa, Picchiotti, Nicola, Campolo, Federica, Imperatore, Francesco, Palmieri, Maria, Daga, Sergio, Gabbi, Chiara, Montagnani, Francesca, Beligni, Giada, Farias, Ticiana D J, Carriero, Miriam Lucia, Di Sarno, Laura, Alaverdian, Diana, Aslaksen, Sigrid, Cubellis, Maria Vittoria, Spiga, Ottavia, Baldassarri, Margherita, Fava, Francesca, Norman, Paul J, Frullanti, Elisa, Isidori, Andrea M, Amoroso, Antonio, Mari, Francesca, Furini, Simone, Mondelli, Mario U, Gen-Covid Multicenter Study, Chiariello, Mario, Renieri, Alessandra, Meloni, Ilaria
Published in Autophagy (03.07.2022)
Published in Autophagy (03.07.2022)
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Journal Article
Gain and loss of function CFTR alleles modulate COVID-19 clinical outcome
Baldassarri, M, Fallerini, C, Fava, F, Zguro, K, Pedemonte, N, Tomati, V, Pastorino, C, Bruttini, M, Picchiotti, N, Furini, S, Gabbi, C, Renieri, A
Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2023)
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Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2023)
Conference Proceeding
A genome-wide association study for survival from a multi-center European study identified variants associated with the risk of death due to COVID-19
Minnai, F, Biscarini, F, Esposito, M, Dragani, TA, Bujanda, L, Rahmouni, S, Alarcon-Riquelme, ME, Buti, M, Zeberg, H, Asselta, R, Gomez, MR, Fernandez-Cadenas, I, Fallerini, C, Zguro, K, Baldassarri, M, Giacomazzi, V, Altemura, C, Furini, S, Renieri, A, Colombo, F
Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2024)
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Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2024)
Conference Proceeding
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes
Baldassarri, Margherita, Zguro, Kristina, Tomati, Valeria, Pastorino, Cristina, Fava, Francesca, Croci, Susanna, Bruttini, Mirella, Picchiotti, Nicola, Furini, Simone, Pedemonte, Nicoletta, Gabbi, Chiara, Renieri, Alessandra, Fallerini, Chiara
Published in Cells (Basel, Switzerland) (16.12.2022)
Published in Cells (Basel, Switzerland) (16.12.2022)
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