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Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 1-gen-2016 Anand, S; Mangano, E; Barizzone, Nadia; Bordoni, R; Sorosina, M; Clarelli, F; Corrado, Lucia; Martinelli Boneschi, F; D'Alfonso, Sandra; De Bellis, G.
The burden of multiple sclerosis variants in continental Italians and Sardinians 1-gen-2015 Barizzone, Nadia; Zara, I; Sorosina, M; Lupoli, S; Porcu, E; Pitzalis, M; Zoledziewska, M; Esposito, Fa; Leone, M; Mulas, A; Cocco, E; Ferrigno, P; Guerini, Fr; Brambilla, P; Farina, G; Murru, R; Deidda, F; Sanna, S; Loi, A; Barlassina, C; Vecchio, D; Zauli, A; Clarelli, F; Braga, D; Poddie, F; Cantello, Roberto; Martinelli, V; Comi, G; Frau, J; Lorefice, L; Pugliatti, M; Rosati, G; Melis, M; Marrosu, Mg; Cusi, D; Cucca, F; Martinelli Boneschi, F; Sanna, S; D'Alfonso, Sandra
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.
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis 1-gen-2015 Goris, An; Pauwels, Ine; Gustavsen, Marte W.; Van Son, Brechtje; Hilven, Kelly; Bos, Steffan D.; Celius, Elisabeth Gulowsen; Berg Hansen, Pal; Aarseth, Jan; Myhr, Kjell Morten; D'Alfonso, Sandra; Barizzone, Nadia; Leone, Maurizio A.; Boneschi, Filippo Martinelli; Sorosina, Melissa; Liberatore, Giuseppe; Kockum, Ingrid; Olsson, Tomas; Hillert, Jan; Alfredsson, Lars; Bedri, Sahl Khalid; Hemmer, Bernhard; Buck, Dorothea; Berthele, Achim; Knier, Benjamin; Biberacher, Viola; Van Pesch, Vincent; Sindi, Christian; Oturai, Annette Bang; Søndergaard, Helle Bach; Sellebjerg, Finn; Jensen, Poul Erik H.; Comabella, Manuel; Montalban, Xavier; Pérez Boza, Jennifer; Malhotra, Sunny; Lechner Scott, Jeannette; Broadley, Simon; Slee, Mark; Taylor, Bruce; Kermode, Allan G.; Gourraud, Pierre Antoine; Sawcer, Stephen J.; Andreassen, Bettina Kullle; Dubois, Bénédicte; Harbo, Hanne F.
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.
Inverse correlation of genetic risk score with age at onset in bout-onset and progressiveonset multiple sclerosis 1-gen-2015 Sorosina, Melissa; Esposito, Federica; Guaschino, Clara; Clarelli, Ferdinando; Barizzone, Nadia; Osiceanu, Ana Maria; Brambilla, Paola; Mascia, Elisabetta; Cavalla, Paola; Gallo, Paolo; Martinelli, Vittorio; Leone, Maurizio; Comi, Giancarlo; D'Alfonso, Sandra; Boneschi, Filippo Martinelli
Multiple sclerosis progression is not associated with birth timing in Italy 1-gen-2014 Lucenti, Ausiliatrice; Galimberti, Stefania; Barizzone, Nadia; Naldi, Paola; Comi, Giancarlo; Martinelli Boneschi, Filippo; D'Alfonso, Sandra; Leone, Maurizio A.
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.
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls. 1-gen-2013 International Multiple Sclerosis Genetics, Consortium:; Baranzini, Se; Khankhanian, P; Patsopoulos, Na; Li, M; Stankovich, J; Cotsapas, C; Søndergaard, Hb; Ban, M; Barizzone, Nadia; Bergamaschi, L; Booth, D; Buck, D; Cavalla, P; Celius, Eg; Comabella, M; Comi, G; Compston, A; Cournu Rebeix, I; D'Alfonso, Sandra; Damotte, V; Din, L; Dubois, B; Elovaara, I; Esposito, F; Fontaine, B; Franke, A; Goris, A; Gourraud, Pa; Graetz, C; Guerini, Fr; Guillot Noel, L; Hafler, D; Hakonarson, H; Hall, P; Hamsten, A; Harbo, Hf; Hemmer, B; Hillert, J; Kemppinen, A; Kockum, I; Koivisto, K; Larsson, M; Lathrop, M; Leone, M; Lill, Cm; Macciardi, F; Martin, R; Martinelli, V; Martinelli Boneschi, F; Mccauley, Jl; Myhr, Km; Naldi, P; Olsson, T; Oturai, A; Pericak Vance, Ma; Perla, F; Reunanen, M; Saarela, J; Saker Delye, S; Salvetti, M; Sellebjerg, F; Sørensen, Ps; Spurkland, A; Stewart, G; Taylor, B; Tienari, P; Winkelmann, J; Zipp, F; Ivinson, Aj; Haines, Jl; Sawcer, S; Dejager, P; Hauser, Sl; Oksenberg, J. R.
Rare variants in the TREX1 gene and susceptibility to autoimmune diseases. 1-gen-2013 Barizzone, Nadia; S., Monti; S., Mellone; M., Godi; M., Marchini; R., Scorza; M. G., Danieli; D'Alfonso, Sandra
Genetic burden of common variants in progressive and bout-onset multiple sclerosis. 1-gen-2013 M., Sorosina; P., Brambilla; F., Clarelli; Barizzone, Nadia; S., Lupoli; C., Guaschino; A. M., Osiceanu; L., Moiola; A., Ghezzi; G., Coniglio; F., Patti; G., Mancardi; P., Manunta; N., Glorioso; F. R., Guerini; R., Bergamaschi; F., Perla; P. R. O., P. R. O.; V., Martinelli; D., Cusi; M., Leone; G., Comi; D'Alfonso, Sandra; F., Martinelli Boneschi
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
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. 1-gen-2013 Barizzone, Nadia; Pauwels, I; Luciano, B; Franckaert, D; Guerini, Fr; Cosemans, L; Hilven, K; Salviati, A; Dooley, J; Danso Abeam, D; di Sapio, A; Cavalla, P; Decallonne, B; Mathieu, C; Liston, A; Leone, M; Dubois, B; D'Alfonso, Sandra; Goris, A.
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.
The role of eight polymorphisms in three candidate genes in determining the susceptibility, phenotype, and response to anti-TNF therapy in patients with rheumatoid arthritis. 1-gen-2012 Ceccarelli, F; D'Alfonso, Sandra; Perricone, C; Carlomagno, Y; Alessandri, C; Croia, C; Barizzone, N; Montecucco, C; Galeazzi, M; Sebastiani, Gd; Minisola, G; Fiocco, U; Valesini, G.
The impact of osteopontin gene variations on multiple sclerosis development and progression 1-gen-2012 Comi, Cristoforo; Cappellano, G; Chiocchetti, Annalisa; Orilieri, E; Buttini, S; Ghezzi, L; Galimberti, D; Guerini, F; Barizzone, Nadia; Perla, F; Leone, M; D'Alfonso, Sandra; Caputo, D; Scarpini, E; Cantello, Roberto; Dianzani, Umberto
Further evidence of subphenotype association with systemic lupus erythematosus susceptibility loci: a European cases only study. 1-gen-2012 Alonso-Perez, E; Suarez-Gestal, M; Calaza, M; Ordi-Ros, J; Balada, E; Bijl, M; Papasteriades, C; Carreira, P; Skopouli, Fn; Witte, T; Endreffy, E; Marchini, M; Migliaresi, S; Sebastiani, Gd; Santos, Mj; Suarez, A; Blanco, Fj; Barizzone, N; Pullmann, R; Ruzickova, S; Lauwerys, Br; Gomez-Reino, Jj; Gonzalez, A; European Consortium of SLE DNA, Collections.
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 1-gen-2011 Paraboschi, Em; Soldà, G; Gemmati, D; Orioli, E; Zeri, G; Benedetti, Md; Salviati, A; Barizzone, N; Leone, M; Duga, S; Asselta, R.
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
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