PEVERELLI, SILVIA
PEVERELLI, SILVIA
Universita' degli Studi di MILANO
Characterization of human healthy i3 lower motor neurons exposed to CSF from ALS patients stratified by UNC13A and C9ORF72 genotype
2025 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, F. Verde, N. Ticozzi, V. Silani, A. Ratti
Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patients
2025 V. Pensato, S. Peverelli, C. Tiloca, S. Magri, A. Brusati, M. Pingue, C. Morelli, E. Dalla Bella, A. Manini, P. Tannorella, A. Doretti, J. Mandrioli, F. Terenghi, A. Prelle, N. Riva, F. Verde, R. Eleopra, F. Taroni, G. Lauria Pinter, V. Silani, N. Ticozzi, C. Gellera, A. Ratti
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genes
2025 A. Manini, A. Brusati, M. Grassano, G. Scacciatella, S. Peverelli, J. Spagliardi, V. Pensato, A. Doretti, R. Vasta, U. Manera, A. Canosa, M. Brunetti, D. Gentilini, S. Messina, F. Verde, C. Moglia, C. Morelli, E. Dalla Bella, P.J. Keagle, J.E. Landers, C. Gellera, G. Lauria Pinter, A. Chio, A. Ratti, A. Calvo, V. Silani, N. Ticozzi
Impact of APOE and MAPT genetic profile on the cognitive functions among Amyotrophic Lateral Sclerosis Tunisian patients
2025 I. Sghaier, I. Kacem, A. Ratti, K. Takout, Y. Abida, S. Peverelli, N. Ticozzi, A. Gargouri-Berrachid, V. Silani, R. Gouider
KIF5Ap.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral Sclerosis
2025 A. Manini, R. Vasta, A. Brusati, F. Scheveger, S. Peverelli, A. Maranzano, A. Doretti, F. Gentile, E. Colombo, M. Brunetti, C. Moglia, A. Canosa, U. Manera, M. Grassano, D. Gentilini, S. Messina, F. Verde, C. Morelli, J.E. Landers, B.J. Traynor, A. Chiò, V. Silani, A. Calvo, A. Ratti, N. Ticozzi
Characterization of human healthy i3 lower motor neurons exposed to CSF from ALS patients stratified by UNC13A and C9ORF72 genotype
2025 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, F. Verde, N. Ticozzi, V. Silani, A. Ratti
Analysis of normal C9orf72 repeat length as possible disease modifier in amyotrophic lateral sclerosis
2024 S. Peverelli, A. Brusati, V. Casiraghi, M.N. Sorce, S. Invernizzi, S. Santangelo, C. Morelli, F. Verde, V. Silani, N. Ticozzi, A. Ratti
Characterization of human i3 motor neurons exposed to CSF from ALS patients stratified by C9ORF72 and UNC13A genotype
2024 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, V. Silani, A. Ratti
Characterization of human i3 motor neurons exposed to CSF from ALS patients stratified by C9ORF72 and UNC13A genotype
2024 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, V. Silani, A. Ratti
Characterization of human i3 motor neurons exposed to CSF from ALS patients stratified by C9ORF72 and UNC13A genotype
2024 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, V. Silani, A. Ratti
Defective primary cilia in NEK1 and C9ORF72 iPSC-derived motoneurons and brain organoids
2024 S. Invernizzi, S. Santangelo, V. Casiraghi, S. Peverelli, P. Paola, Q. Angelo, V. Silani, P. Bossolasco, A. Ratti
Defective primary cilia in NEK1 and C9ORF72 iPSC-derived motoneurons and brain organoids
2024 S. Invernizzi, S. Santangelo, V. Casiraghi, S. Peverelli, P. Paola, Q. Angelo, V. Silani, P. Bossolasco, A. Ratti
Distribution of the C9orf72 hexanucleotide repeat expansion in healthy subjects: a multicenter study promoted by the Italian IRCCS network of neuroscience and neurorehabilitation
2024 E. Giardina, P. Mandich, R. Ghidoni, N. Ticozzi, G. Rossi, C. Fenoglio, F.D. Tiziano, F. Esposito, S. Capellari, B. Nacmias, R. Mineri, R. Campopiano, L. Di Pilla, F. Sammarone, S. Zampatti, C. Peconi, F. De Angelis, I. Palmieri, C. Galandra, E. Nicodemo, P. Origone, F. Gotta, C. Ponti, R. Nicsanu, L. Benussi, S. Peverelli, A. Ratti, M. Ricci, G. Di Fede, S. Magri, M. Serpente, S. Lattante, T. Domi, P. Carrera, E. Saltimbanco, S. Bagnoli, A. Ingannato, A. Albanese, F. Tagliavini, R. Lodi, C. Caltagirone, S. Gambardella, E.M. Valente, V. Silani
NEK1 haploinsufficiency worsens DNA damage, but not defective ciliogenesis, in C9ORF72 patient-derived iPSC-motoneurons
2024 S. Santangelo, S. Invernizzi, M.N. Sorce, V. Casiraghi, S. Peverelli, A. Brusati, C. Colombrita, N. Ticozzi, V. Silani, P. Bossolasco, A. Ratti
Optineurin in patients with Amyotrophic Lateral Sclerosis associated to atypical Parkinsonism in Tunisian population
2024 I. Kacem, I. Sghaier, S. Peverelli, Y. Abida, H. Ben Brahim, A. Ratti, A. Nasri, N. Ticozzi, V. Silani, R. Gouider
NEK1 loss-of-function mutation impairs ciliogenesis in iPSC-motoneurons
2023 M. Nice Sorce, S. Invernizzi, C. Lattuada, S. Santangelo, V. Casiraghi, A. Brusati, A. Silva, S. Peverelli, V. Silani, P. Bossolasco, A. Ratti
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study
2023 A. Brusati, S. Peverelli, L. Calzari, C. Tiloca, V. Casiraghi, M.N. Sorce, S. Invernizzi, E. Carbone, R. Cavagnola, F. Verde, V. Silani, N. Ticozzi, A. Ratti, D. Gentilini
Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis
2023 E. Colombo, B. Poletti, A. Maranzano, S. Peverelli, F. Solca, C. Colombrita, S. Torre, C. Tiloca, F. Verde, R. Bonetti, L. Carelli, C. Morelli, A. Ratti, V. Silani, N. Ticozzi
Serum neurofilament light chain levels in Covid-19 patients without major neurological manifestations
2022 F. Verde, I. Milone, I. Bulgarelli, S. Peverelli, C. Colombrita, A. Maranzano, N. Calcagno, N. Ticozzi, G.B. Perego, G. Parati, E. Torresani, A. Ratti, V. Silani
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects
2022 A. Brusati, A. Ratti, V. Pensato, S. Peverelli, D. Gentilini, E. Dalla Bella, M.N. Sorce, M. Meneri, D. Gagliardi, S. Corti, C. Gellera, G. Lauria Pinter, N. Ticozzi, V. Silani