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BARIZZONE, NADIA

BARIZZONE, NADIA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 20 di 57 (tempo di esecuzione: 0.034 secondi).
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A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility 1-gen-2022 Sorosina, Melissa; Barizzone, Nadia; Clarelli, Ferdinando; Anand, Santosh; Lupoli, Sara; Salvi, Erika; Mangano, Eleonora; Bordoni, Roberta; Roostaei, Tina; Mascia, Elisabetta; Zuccalà, Miriam; Vecchio, Domizia; Cavalla, Paola; Santoro, Silvia; Ferrè, Laura; Zollo, Alen; Barlassina, Cristina; Cusi, Daniele; Martinelli, Vittorio; Comi, Giancarlo; Leone, Maurizio; Filippi, Massimo; Patsopoulos, Nikolaos A; De Jager, Philip L; De Bellis, Gianluca; Esposito, Federica; D'Alfonso, Sandra; Martinelli Boneschi, Filippo
A Scoping Review on Body Fluid Biomarkers for Prognosis and Disease Activity in Patients with Multiple Sclerosis 1-gen-2022 Barizzone, Nadia; Leone, Maurizio; Pizzino, Alessandro; Kockum, Ingrid; Martinelli-Boneschi, Filippo; D'Alfonso, Sandra
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 1-gen-2008 D'Alfonso, Sandra; Bolognesi, Elisabetta; Guerini, Fr; Barizzone, N; Bocca, Sara; Ferrante, Daniela; Castelli, L; Bergamaschi, Laura; Agliardi, C; Ferrante, P; Naldi, P; Leone, M; Caputo, D; Ballerini, C; Salvetti, M; Galimberti, D; Massacesi, L; Trojano, M; Momigliano Richiardi, P.
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 1-gen-2021 Barizzone, N.; Cagliani, R.; Basagni, C.; Clarelli, F.; Mendozzi, L.; Agliardi, C.; Forni, D.; Tosi, M.; Mascia, E.; Favero, F.; Cora', D.; Corrado, L.; Sorosina, M.; Esposito, F.; Zuccala, M.; Vecchio, D.; Liguori, M.; Comi, C.; Comi, G.; Martinelli, V.; Filippi, M.; Leone, M.; Martinelli-Boneschi, F.; Caputo, D.; Sironi, M.; Guerini, F. R.; D'Alfonso, S.
Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis 1-gen-2015 Giacalone, G.; Clarelli, F.; Osiceanu, A. M.; Guaschino, C.; Brambilla, P.; Sorosina, M.; Liberatore, G.; Zauli, A.; Esposito, F.; Rodegher, M.; Ghezzi, A.; Galimberti, D.; Patti, F.; Barizzone, Nadia; Guerini, F.; Martinelli, V.; Leone, M.; Comi, G.; D'Alfonso, Sandra; Martinelli Boneschi, F.
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 1-gen-2013 International Multiple Sclerosis Genetics, Consortium; Beecham, Ah; Patsopoulos, Na; Xifara, Dk; Davis, Mf; Kemppinen, A; Cotsapas, C; Shah, Ts; Spencer, C; Booth, D; Goris, A; Oturai, A; Saarela, J; Fontaine, B; Hemmer, B; Martin, C; Zipp, F; D'Alfonso, Sandra; Martinelli Boneschi, F; Taylor, B; Harbo, Hf; Kockum, I; Hillert, J; Olsson, T; Ban, M; Oksenberg, Jr; Hintzen, R; Barcellos, Lf; Wellcome Trust Case Control Consortium, 2; International IBD Genetics, Consortium; Agliardi, C; Alfredsson, L; Alizadeh, M; Anderson, C; Andrews, R; Søndergaard, Hb; Baker, A; Band, G; Baranzini, Se; Barizzone, Nadia; Barrett, J; Bellenguez, C; Bergamaschi, L; Bernardinelli, L; Berthele, A; Biberacher, V; Binder, Tm; Blackburn, H; Bomfim, Il; Brambilla, P; Broadley, S; Brochet, B; Brundin, L; Buck, D; Butzkueven, H; Caillier, Sj; Camu, W; Carpentier, W; Cavalla, P; Celius, Eg; Coman, I; Comi, G; Corrado, Lucia; Cosemans, L; Cournu Rebeix, I; Cree, Ba; Cusi, D; Damotte, V; Defer, G; Delgado, Sr; Deloukas, P; di Sapio, A; Dilthey, At; Donnelly, P; Dubois, B; Duddy, M; Edkins, S; Elovaara, I; Esposito, F; Evangelou, N; Fiddes, B; Field, J; Franke, A; Freeman, C; Frohlich, Iy; Galimberti, D; Gieger, C; Gourraud, Pa; Graetz, C; Graham, A; Grummel, V; Guaschino, C; Hadjixenofontos, A; Hakonarson, H; Halfpenny, C; Hall, G; Hall, P; Hamsten, A; Harley, J; Harrower, T; Hawkins, C; Hellenthal, G; Hillier, C; Hobart, J; Hoshi, M; Hunt, Se; Jagodic, M; Jelčić, I; Jochim, A; Kendall, B; Kermode, A; Kilpatrick, T; Koivisto, K; Konidari, I; Korn, T; Kronsbein, H; Langford, C; Larsson, M; Lathrop, M; Lebrun Frenay, C; Lechner Scott, J; Lee, Mh; Leone, Ma; Leppä, V; Liberatore, G; Lie, Ba; Lill, Cm; Lindén, M; Link, J; Luessi, F; Lycke, J; Macciardi, F; Männistö, S; Manrique, Cp; Martin, R; Martinelli, V; Mason, D; Mazibrada, G; Mccabe, C; Mero, Il; Mescheriakova, J; Moutsianas, L; Myhr, Km; Nagels, G; Nicholas, R; Nilsson, P; Piehl, F; Pirinen, M; Price, Se; Quach, H; Reunanen, M; Robberecht, W; Robertson, Np; Rodegher, M; Rog, D; Salvetti, M; Schnetz Boutaud, Nc; Sellebjerg, F; Selter, Rc; Schaefer, C; Shaunak, S; Shen, L; Shields, S; Siffrin, V; Slee, M; Sorensen, Ps; Sorosina, M; Sospedra, M; Spurkland, A; Strange, A; Sundqvist, E; Thijs, V; Thorpe, J; Ticca, A; Tienari, P; van Duijn, C; Visser, Em; Vucic, S; Westerlind, H; Wiley, Js; Wilkins, A; Wilson, Jf; Winkelmann, J; Zajicek, J; Zindler, E; Haines, Jl; Pericak Vance, Ma; Ivinson, Aj; Stewart, G; Hafler, D; Hauser, Sl; Compston, A; Mcvean, G; De Jager, P; Sawcer, Sj; Mccauley, J. L.
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 1-gen-2019 Corrado, Lucia; Maura, Brunetti; DI PIERRO, Alice; Barberis, Marco; Croce, Roberta; Bersano, Enrica; DE MARCHI, Fabiola; Zuccala', Miriam; Barizzone, Nadia; Andrea, Calvo; Cristina, Moglia; Mazzini, Letizia; Adriano, Chiò; D'Alfonso, Sandra
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 1-gen-2013 Leone, Ma; Barizzone, N; Esposito, F; Lucenti, A; Harbo, Hf; Goris, A; Kockum, I; Oturai, Ab; Celius, Eg; Mero, Il; Dubois, B; Olsson, T; Søndergaard, Hb; Cusi, D; Lupoli, S; Andreassen, Bk; International Multiple Sclerosis Genetics, Consortium; Wellcome Trust Case Control Consortium, 2; Myhr, Km; Guerini, Fr; Progemus, Group; Progresso, Group; Comi, G; Martinelli Boneschi, F; D'Alfonso, Sandra
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 1-gen-2011 Bergamaschi, L; Ban, M; Barizzone, Nadia; Leone, M; Ferrante, Daniela; Fasano, Me; Guerini, Fr; Corrado, Lucia; Naldi, P; Dametto, E; Agliardi, C; Salvetti, M; Mechelli, R; Galimberti, D; Scarpini, E; Cavalla, P; Bargiggia, V; Caputo, D; Cordera, S; Monaco, F; Momigliano Richiardi, P; D'Alfonso, Sandra
Association of osteopontin regulatory polymorphisms with systemic sclerosis 1-gen-2011 Barizzone, Nadia; Marchini, M; Cappiello, F; Chiocchetti, Annalisa; Orilieri, E; Ferrante, Daniela; Corrado, Lucia; Mellone, S; Scorza, R; Dianzani, Umberto; D'Alfonso, Sandra
Association of Systemic Lupus Erythematosus Clinical Features with European Population Genetic Substructure 1-gen-2011 Alonso-Perez, E; Suarez-Gestal, M; Calaza, M; Witte, T; Papasteriades, C; Marchini, M; Migliaresi, S; Kovacs, A; Ordi-Ros, J; Bijl, M; Santos, Mj; Ruzickova, S; Pullmann, R; Carreira, P; Skopouli, Fn; D'Alfonso, S; Sebastiani, Gd; Suarez, A; Blanco, Fj; Gomez-Reino, Jj; Gonzalez, A; Liz, M; Schmidt, Re; Kappou-Rigatou, I; Scorza, R; Endereffy, E; Balada, E; Kallenberg, Cg; Vinagre, F; Dostal, C; Pullmann, R Jr; Mavromati, M; Barizzone, N; Gutierrez, C; Rego, I.
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 1-gen-2011 Corrado, Lucia; Bergamaschi, L; Barizzone, Nadia; Fasano, Me; Guerini, Fr; Salvetti, M; Galimberti, D; Benedetti, Md; Leone, M; D'Alfonso, Sandra
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 1-gen-2002 D'Alfonso, Sandra; Giordano, Mara; Mellai, M; Lanceni, M; Barizzone, N; Marchini, M; Scorza, R; Danieli, Mg; Cappelli, M; Rovere, P; Sabbadini, Mg; Momigliano, Patricia
Bias in effect size of systemic lupus erythematosus susceptibility loci across Europe: a case-control study. 1-gen-2012 Alonso-Perez, E; Suarez-Gestal, M; Calaza, M; Sebastiani, Gd; Pullmann, R; Papasteriades, C; Kovacs, A; Skopouli, Fn; Bijl, M; Suarez, A; Marchini, M; Migliaresi, S; Carreira, P; Ordi-Ros, J; Witte, T; Ruzickova, S; Santos, Mj; Barizzone, N; Blanco, Fj; Lauwerys, Br; Gomez-Reino, Jj; Gonzalez, A; the European Consortium of SLE DNA, Collections.
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 1-gen-2022 Mascia, E.; Clarelli, F.; Zauli, A.; Guaschino, C.; Sorosina, M.; Barizzone, N.; Basagni, C.; Santoro, S.; Ferre, L.; Bonfiglio, S.; Biancolini, D.; Pozzato, M.; Guerini, F. R.; Protti, A.; Liguori, M.; Moiola, L.; Vecchio, D.; Bresolin, N.; Comi, G.; Filippi, M.; Esposito, F.; D'Alfonso, S.; Martinelli-Boneschi, F.
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 1-gen-2018 Corrado, Lucia; Tiloca, Cinzia; Locci, Clarissa; Bagarotti, Alessandra; Hamzeiy, Hamid; Colombrita, Claudia; De marchi, Fabiola; Barizzone, Nadia; Cotella, Diego; Ticozzi, Nicola; Mazzini, Letizia; Nazli Basak, Ayse; Ratti, Antonia; Silani, Vincenzo; D’Alfonso, Sandra
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 1-gen-2022 Clarelli, F.; Barizzone, N.; Mangano, E.; Zuccala, M.; Basagni, C.; Anand, S.; Sorosina, M.; Mascia, E.; Santoro, S.; Guerini, F. R.; Virgilio, E.; Gallo, A.; Pizzino, A.; Comi, C.; Martinelli, V.; Comi, G.; De Bellis, G.; Leone, M.; Filippi, M.; Esposito, F.; Bordoni, R.; Martinelli Boneschi, F.; D'Alfonso, S.
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 1-gen-2015 Kuhle, J; Disanto, G; Dobson, R; Adiutori, R; Bianchi, L; Topping, J; Bestwick, J. P; Meier, U. C; Marta, M; Costa, G. Dalla; Runia, T; Evdoshenko, E; Lazareva, N; Thouvenot, E; Iaffaldano, P; Direnzo, V; Khademi, M; Piehl, F; Comabella, M; Sombekke, M; Killestein, J; Hegen, H; Rauch, S; D'Alfonso, Sandra; Alvarez Cermeño, J. C; Kleinová, P; Horáková, D; Roesler, R; Lauda, F; Llufriu, S; Avsar, T; Uygunoglu, U; Altintas, A; Saip, S; Menge, T; Rajda, C; Bergamaschi, R; Moll, N; Khalil, M; Marignier, R; Dujmovic, I; Larsson, H; Malmestrom, C; Scarpini, E; Fenoglio, C; Wergeland, S; Laroni, A; Annibali, V; Romano, S; Martínez, A. D; Carra, A; Salvetti, M; Uccelli, A; Torkildsen, Ø; Myhr, K. M; Galimberti, D; Rejdak, K; Lycke, J; Frederiksen, J. L; Drulovic, J; Confavreux, C; Brassat, D; Enzinger, C; Fuchs, S; Bosca, I; Pelletier, J; Picard, C; Colombo, E; Franciotta, D; Derfuss, T; Lindberg, Rlp; Yaldizli, Ö; Vécsei, L; Kieseier, B. C; Hartung, H. P; Villoslada, P; Siva, A; Saiz, A; Tumani, H; Havrdová, E; Villar, L. M; Leone, M; Barizzone, N; Deisenhammer, F; Teunissen, C; Montalban, X; Tintoré, M; Olsson, T; Trojano, M; Lehmann, S; Castelnovo, G; Lapin, S; Hintzen, R; Kappos, L; Furlan, R; Martinelli, V; Comi, G; Ramagopalan, S. V; Giovannoni, G.
Erratum: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (Cell (2018) 175 6 (1679-1687.e7) PII: S0092-8674(19)30679-8) 1-gen-2019 Mitrovič, Mitja; Patsopoulos, Nikolaos A.; Beecham, Ashley H.; Dankowski, Theresa; Goris, An; Dubois, Bénédicte; D’Hooghe, Marie B.; Lemmens, Robin; Van Damme, Philip; Søndergaard, Helle Bach; Sellebjerg, Finn; Sorensen, Per Soelberg; Ullum, Henrik; Thørner, Lise W.; Werge, Thomas; Saarela, Janna; Cournu-Rebeix, Isabelle; Damotte, Vincent; Fontaine, Bertrand; Guillot-Noel, Lena; Lathrop, Mark; Vukusik, Sandra; Gourraud, Pierre-Antoine; Andlauer, Till F. M.; Pongratz, Viola; Buck, Dorothea; Gasperi, Christiane; Bayas, Antonios; Heesen, Christoph; Kümpfel, Tania; Linker, Ralf; Paul, Friedemann; Stangel, Martin; Tackenberg, Björn; Bergh, Florian Then; Warnke, Clemens; Wiendl, Heinz; Wildemann, Brigitte; Zettl, Uwe; Ziemann, Ulf; Tumani, Hayrettin; Gold, Ralf; Grummel, Verena; Hemmer, Bernhard; Knier, Benjamin; Lill, Christina M.; Luessi, Felix; Dardiotis, Efthimios; Agliardi, Cristina; Barizzone, Nadia; Mascia, Elisabetta; Bernardinelli, Luisa; Comi, Giancarlo; Cusi, Daniele; Esposito, Federica; Ferrè, Laura; Comi, Cristoforo; Galimberti, Daniela; Leone, Maurizio A.; Sorosina, Melissa; Mescheriakova, Julia; Hintzen, Rogier; van Duijn, Cornelia; Teunissen, Charlotte E.; Bos, Steffan D.; Myhr, Kjell-Morten; Celius, Elisabeth G.; Lie, Benedicte A.; Spurkland, Anne; Comabella, Manuel; Montalban, Xavier; Alfredsson, Lars; Stridh, Pernilla; Hillert, Jan; Jagodic, Maja; Piehl, Fredrik; Jelčić, Ilijas; Martin, Roland; Sospedra, Mireia; Ban, Maria; Hawkins, Clive; Hysi, Pirro; Kalra, Seema; Karpe, Fredrik; Khadake, Jyoti; Lachance, Genevieve; Neville, Matthew; Santaniello, Adam; Caillier, Stacy J.; Calabresi, Peter A.; Cree, Bruce A. C.; Cross, Anne; Davis, Mary F.; Haines, Jonathan L.; de Bakker, Paul I. W.; Delgado, Silvia; Dembele, Marieme; Edwards, Keith; Fitzgerald, Kathryn C.; Hakonarson, Hakon; Konidari, Ioanna; Lathi, Ellen; Manrique, Clara P.; Pericak-Vance, Margaret A.; Piccio, Laura; Schaefer, Cathy; Mccabe, Cristin; Weiner, Howard; Goldstein, Jacqueline; Olsson, Tomas; Hadjigeorgiou, Georgios; Taylor, Bruce; Tajouri, Lotti; Charlesworth, Jac; Booth, David R.; Harbo, Hanne F.; Ivinson, Adrian J.; Hauser, Stephen L.; Compston, Alastair; Stewart, Graeme; Zipp, Frauke; Barcellos, Lisa F.; Baranzini, Sergio E.; Martinelli-Boneschi, Filippo; D’Alfonso, Sandra; Ziegler, Andreas; Oturai, Annette; Mccauley, Jacob L.; Sawcer, Stephen J.; Oksenberg, Jorge R.; De Jager, Philip L.; Kockum, Ingrid; Hafler, David A.; Cotsapas, Chris
Erratum: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (Cell (2019) 178(1) (262), (S0092867419306798), (10.1016/j.cell.2019.06.016)) 1-gen-2020 Mitrovic, M.; Patsopoulos, N. A.; Beecham, A. H.; Dankowski, T.; Goris, A.; Dubois, B.; D'Hooghe, M. B.; Lemmens, R.; Van Damme, P.; Sondergaard, H. B.; Sellebjerg, F.; Sorensen, P. S.; Ullum, H.; Thorner, L. W.; Werge, T.; Saarela, J.; Cournu-Rebeix, I.; Damotte, V.; Fontaine, B.; Guillot-Noel, L.; Lathrop, M.; Vukusik, S.; Gourraud, P. -A.; Andlauer, T. F. M.; Pongratz, V.; Buck, D.; Gasperi, C.; Bayas, A.; Heesen, C.; Kumpfel, T.; Linker, R.; Paul, F.; Stangel, M.; Tackenberg, B.; Bergh, F. T.; Warnke, C.; Wiendl, H.; Wildemann, B.; Zettl, U.; Ziemann, U.; Tumani, H.; Gold, R.; Grummel, V.; Hemmer, B.; Knier, B.; Lill, C. M.; Luessi, F.; Dardiotis, E.; Agliardi, C.; Barizzone, N.; Mascia, E.; Bernardinelli, L.; Comi, G.; Cusi, D.; Esposito, F.; Ferre, L.; Comi, C.; Galimberti, D.; Leone, M. A.; Sorosina, M.; Mescheriakova, J.; Hintzen, R.; van Duijn, C.; Teunissen, C. E.; Bos, S. D.; Myhr, K. -M.; Celius, E. G.; Lie, B. A.; Spurkland, A.; Comabella, M.; Montalban, X.; Alfredsson, L.; Stridh, P.; Hillert, J.; Jagodic, M.; Piehl, F.; Jelcic, I.; Martin, R.; Sospedra, M.; Ban, M.; Hawkins, C.; Hysi, P.; Kalra, S.; Karpe, F.; Khadake, J.; Lachance, G.; Neville, M.; Santaniello, A.; Caillier, S. J.; Calabresi, P. A.; Cree, B. A. C.; Cross, A.; Davis, M. F.; Haines, J. L.; de Bakker, P. I. W.; Delgado, S.; Dembele, M.; Edwards, K.; Fitzgerald, K. C.; Hakonarson, H.; Konidari, I.; Lathi, E.; Manrique, C. P.; Pericak-Vance, M. A.; Piccio, L.; Schaefer, C.; Mccabe, C.; Weiner, H.; Goldstein, J.; Olsson, T.; Hadjigeorgiou, G.; Taylor, B.; Tajouri, L.; Charlesworth, J.; Booth, D. R.; Harbo, H. F.; Ivinson, A. J.; Hauser, S. L.; Compston, A.; Stewart, G.; Zipp, F.; Barcellos, L. F.; Baranzini, S. E.; Martinelli-Boneschi, F.; D'Alfonso, S.; Ziegler, A.; Oturai, A.; Mccauley, J. L.; Sawcer, S. J.; Oksenberg, J. R.; De Jager, P. L.; Kockum, I.; Hafler, D. A.; Cotsapas, C.