CORRADO, Lucia
CORRADO, Lucia
Dipartimento di Scienze della Salute
A case of early-onset Parkinson's disease in a patient with KBG syndrome
2023-01-01 Magistrelli, Luca; Contaldi, Elena; Caushi, Fjorilda; Spano, Alice; Cantello, Roberto; D'Alfonso, Sandra; Corrado, Lucia
A case of late-onset OCD developing PLS and FTD
2018-01-01 Bersano, Enrica; Sarnelli, Maria Francesca; Solara, Valentina; De Marchi, Fabiola; Sacchetti, Gian Mauro; Stecco, Alessandro; Corrado, Lucia; D'Alfonso, Sandra; Cantello, Roberto; Mazzini, Letizia
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia
2018-01-01 De Marchi, F; Tondo, G; Sarnelli, M F; Corrado, L; Solara, V; D'Alfonso, S; Cantello, R; Mazzini, L
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies
2018-01-01 Genovese, Loredana M.; Geraci, Filippo; Corrado, Lucia; Mangano, Eleonora; D'Aurizio, Romina; Bordoni, Roberta; Severgnini, Marco; Manzini, Giovanni; De Bellis, Gianluca; D'Alfonso, Sandra; Pellegrini, Marco
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
2014-01-01 Fogh, I; Ratti, A; Gellera, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, Lucia; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, Fl; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, Am; Signorini, S; Shatunov, A; Jones, A; Shaw, Pj; Morrison, Ke; Farmer, Ae; Van Damme, P; Robberecht, W; Chiò, A; Traynor, Bj; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, Pm; Leigh, Np; Glass, Jd; Overste, D; Diekstra, Fp; Veldink, Jh; van Es, Ma; Shaw, Ce; Weale, Me; Lewis, Cm; Williams, J; Brown, Rh; Landers, Je; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, Gp; D'Alfonso, Sandra; van den Berg, Lh; Taroni, F; Al Chalabi, A; Powell, J; Silani, V; the SLAGEN, Consortium; Collaborators,
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient
2011-01-01 Corrado, Lucia; Caromagno, Y; Falasco, L; Mellone, S; Godi, M; Cova, E; Cereda, C; Testa, L; Mazzini, L; D'Alfonso, Sandra
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b
2016-01-01 Corrado, Lucia; Magri, S; Bagarotti, Alessandra; Carecchio, Miryam; Piscosquito, G; Pareyson, D; Varrasi, C; Vecchio, D; Zonta, Andrea; Cantello, Roberto; Taroni, F; D'Alfonso, Sandra
A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?”
2000-01-01 F., Natacci; Corrado, Lucia; M., Pierri; M., Rossetti; C., Zuccarini; P., Riva; M. MIOZZO AND L., Larizza
A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency
2009-01-01 Godi, M; Mellone, S; Petri, Antonella; Arrigo, T; Bardelli, C; Corrado, Lucia; Bellone, Simonetta; Prodam, Flavia; MOMIGLIANO RICHIARDI, P; Bona, Gianni; Giordano, Mara
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study
2020-01-01 Chiò, Adriano; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; D'Ovidio, Fabrizio; Vasta, Rosario; Grassano, Maurizio; Brunetti, Maura; Barberis, Marco; Corrado, Lucia; D'Alfonso, Sandra; Iazzolino, Barbara; Peotta, Laura; Francesca Sarnelli, Maria; Solara, Valentina; Pierre Zucchetti, Jean; DE MARCHI, Fabiola; Mazzini, Letizia; Mora, Gabriele; Calvo, Andrea
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients
2021-01-01 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 hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis
2013-01-01 Calini, D; Corrado, Lucia; Del Bo, R; Gagliardi, S; Pensato, V; Verde, F; Corti, S; Mazzini, L; Milani, P; Castellotti, B; Bertolin, C; Sorarù, G; Cereda, C; Comi, Gp; D'Alfonso, Sandra; Gellera, C; Ticozzi, N; Landers, Je; Ratti, A; Silani, V; Slagen, Consortium
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
2013-01-01 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
2019-01-01 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
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
2014-01-01 van Doormaal, Perry T. C.; Ticozzi, Nicola; Gellera, Cinzia; Ratti, Antonia; Taroni, Franco; Chiò, Adriano; Calvo, Andrea; Mora, Gabriele; Restagno, Gabriella; Traynor, Bryan J.; Birve, Anna; Lemmens, Robin; van Es, Michael A.; Saris, Christiaan G. J.; Blauw, Hylke M.; van Vught, Paul W. J.; Groen, Ewout J. N.; Corrado, Lucia; Mazzini, Letizia; Del Bo, Roberto; Corti, Stefania; Waibel, Stefan; Meyer, Thomas; Ludolph, Albert C.; Goris, An; van Damme, Philip; Robberecht, Wim; Shatunov, Aleksey; Fogh, Isabella; Andersen, Peter M.; D'Alfonso, Sandra; Hardiman, Orla; Cronin, Simon; Rujescu, Dan; Al-Chalabi, Ammar; Landers, John E.; Silani, Vincenzo; van den Berg, Leonard H.; Veldink, Jan H.
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis
2016-01-01 Fogh, Isabella; Lin, Kuang; Tiloca, Cinzia; Rooney, James; Gellera, Cinzia; Diekstra, Frank P.; Ratti, Antonia; Shatunov, Aleksey; Van Es, Michael A.; Proitsi, Petroula; Jones, Ashley; Sproviero, William; Chiò, Adriano; Mclaughlin, Russell Lewis; Sorarù, Gianni; Corrado, Lucia; Stahl, Daniel; Del Bo, Roberto; Cereda, Cristina; Castellotti, Barbara; Glass, Jonathan D.; Newhouse, Steven; Dobson, Richard; Smith, Bradley N.; Topp, Simon; Van Rheenen, Wouter; Meininger, Vincent; Melki, Judith; Morrison, Karen E.; Shaw, Pamela J.; Leigh, P. Nigel; Andersen, Peter M.; Comi, Giacomo P.; Ticozzi, Nicola; Mazzini, Letizia; D'Alfonso, Sandra; Traynor, Bryan J.; Van Damme, Philip; Robberecht, Wim; Brown, Robert H.; Landers, John E.; Hardiman, Orla; Lewis, Cathryn M.; Van Den Berg, Leonard H.; Shaw, Christopher E.; Veldink, Jan H.; Silani, Vincenzo; Al Chalabi, Ammar; Powell, John
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis
2023-01-01 Chiò, Adriano; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; Grassano, Maurizio; Vasta, Rosario; Palumbo, Francesca; Gallone, Salvatore; Brunetti, Maura; Barberis, Marco; De Marchi, Fabiola; Dalgard, Clifton; Chia, Ruth; Mora, Gabriele; Iazzolino, Barbara; Peotta, Laura; Traynor, Bryan J; Corrado, Lucia; D'Alfonso, Sandra; Mazzini, Letizia; Calvo, Andrea
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects.
2011-01-01 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
2011-01-01 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 the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population
2011-01-01 Corrado, Lucia; Bergamaschi, L; Barizzone, Nadia; Fasano, Me; Guerini, Fr; Salvetti, M; Galimberti, D; Benedetti, Md; Leone, M; D'Alfonso, Sandra
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A case of early-onset Parkinson's disease in a patient with KBG syndrome | 1-gen-2023 | Magistrelli, Luca; Contaldi, Elena; Caushi, Fjorilda; Spano, Alice; Cantello, Roberto; D'Alfonso, Sandra; Corrado, Lucia | |
| A case of late-onset OCD developing PLS and FTD | 1-gen-2018 | Bersano, Enrica; Sarnelli, Maria Francesca; Solara, Valentina; De Marchi, Fabiola; Sacchetti, Gian Mauro; Stecco, Alessandro; Corrado, Lucia; D'Alfonso, Sandra; Cantello, Roberto; Mazzini, Letizia | |
| A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia | 1-gen-2018 | De Marchi, F; Tondo, G; Sarnelli, M F; Corrado, L; Solara, V; D'Alfonso, S; Cantello, R; Mazzini, L | |
| A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies | 1-gen-2018 | Genovese, Loredana M.; Geraci, Filippo; Corrado, Lucia; Mangano, Eleonora; D'Aurizio, Romina; Bordoni, Roberta; Severgnini, Marco; Manzini, Giovanni; De Bellis, Gianluca; D'Alfonso, Sandra; Pellegrini, Marco | |
| A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis | 1-gen-2014 | Fogh, I; Ratti, A; Gellera, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, Lucia; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, Fl; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, Am; Signorini, S; Shatunov, A; Jones, A; Shaw, Pj; Morrison, Ke; Farmer, Ae; Van Damme, P; Robberecht, W; Chiò, A; Traynor, Bj; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, Pm; Leigh, Np; Glass, Jd; Overste, D; Diekstra, Fp; Veldink, Jh; van Es, Ma; Shaw, Ce; Weale, Me; Lewis, Cm; Williams, J; Brown, Rh; Landers, Je; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, Gp; D'Alfonso, Sandra; van den Berg, Lh; Taroni, F; Al Chalabi, A; Powell, J; Silani, V; the SLAGEN, Consortium; Collaborators, | |
| A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient | 1-gen-2011 | Corrado, Lucia; Caromagno, Y; Falasco, L; Mellone, S; Godi, M; Cova, E; Cereda, C; Testa, L; Mazzini, L; D'Alfonso, Sandra | |
| A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b | 1-gen-2016 | Corrado, Lucia; Magri, S; Bagarotti, Alessandra; Carecchio, Miryam; Piscosquito, G; Pareyson, D; Varrasi, C; Vecchio, D; Zonta, Andrea; Cantello, Roberto; Taroni, F; D'Alfonso, Sandra | |
| A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?” | 1-gen-2000 | F., Natacci; Corrado, Lucia; M., Pierri; M., Rossetti; C., Zuccarini; P., Riva; M. MIOZZO AND L., Larizza | |
| A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency | 1-gen-2009 | Godi, M; Mellone, S; Petri, Antonella; Arrigo, T; Bardelli, C; Corrado, Lucia; Bellone, Simonetta; Prodam, Flavia; MOMIGLIANO RICHIARDI, P; Bona, Gianni; Giordano, Mara | |
| ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study | 1-gen-2020 | Chiò, Adriano; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; D'Ovidio, Fabrizio; Vasta, Rosario; Grassano, Maurizio; Brunetti, Maura; Barberis, Marco; Corrado, Lucia; D'Alfonso, Sandra; Iazzolino, Barbara; Peotta, Laura; Francesca Sarnelli, Maria; Solara, Valentina; Pierre Zucchetti, Jean; DE MARCHI, Fabiola; Mazzini, Letizia; Mora, Gabriele; Calvo, Andrea | |
| 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 hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis | 1-gen-2013 | Calini, D; Corrado, Lucia; Del Bo, R; Gagliardi, S; Pensato, V; Verde, F; Corti, S; Mazzini, L; Milani, P; Castellotti, B; Bertolin, C; Sorarù, G; Cereda, C; Comi, Gp; D'Alfonso, Sandra; Gellera, C; Ticozzi, N; Landers, Je; Ratti, A; Silani, V; Slagen, Consortium | |
| 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 | |
| Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study | 1-gen-2014 | van Doormaal, Perry T. C.; Ticozzi, Nicola; Gellera, Cinzia; Ratti, Antonia; Taroni, Franco; Chiò, Adriano; Calvo, Andrea; Mora, Gabriele; Restagno, Gabriella; Traynor, Bryan J.; Birve, Anna; Lemmens, Robin; van Es, Michael A.; Saris, Christiaan G. J.; Blauw, Hylke M.; van Vught, Paul W. J.; Groen, Ewout J. N.; Corrado, Lucia; Mazzini, Letizia; Del Bo, Roberto; Corti, Stefania; Waibel, Stefan; Meyer, Thomas; Ludolph, Albert C.; Goris, An; van Damme, Philip; Robberecht, Wim; Shatunov, Aleksey; Fogh, Isabella; Andersen, Peter M.; D'Alfonso, Sandra; Hardiman, Orla; Cronin, Simon; Rujescu, Dan; Al-Chalabi, Ammar; Landers, John E.; Silani, Vincenzo; van den Berg, Leonard H.; Veldink, Jan H. | |
| Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis | 1-gen-2016 | Fogh, Isabella; Lin, Kuang; Tiloca, Cinzia; Rooney, James; Gellera, Cinzia; Diekstra, Frank P.; Ratti, Antonia; Shatunov, Aleksey; Van Es, Michael A.; Proitsi, Petroula; Jones, Ashley; Sproviero, William; Chiò, Adriano; Mclaughlin, Russell Lewis; Sorarù, Gianni; Corrado, Lucia; Stahl, Daniel; Del Bo, Roberto; Cereda, Cristina; Castellotti, Barbara; Glass, Jonathan D.; Newhouse, Steven; Dobson, Richard; Smith, Bradley N.; Topp, Simon; Van Rheenen, Wouter; Meininger, Vincent; Melki, Judith; Morrison, Karen E.; Shaw, Pamela J.; Leigh, P. Nigel; Andersen, Peter M.; Comi, Giacomo P.; Ticozzi, Nicola; Mazzini, Letizia; D'Alfonso, Sandra; Traynor, Bryan J.; Van Damme, Philip; Robberecht, Wim; Brown, Robert H.; Landers, John E.; Hardiman, Orla; Lewis, Cathryn M.; Van Den Berg, Leonard H.; Shaw, Christopher E.; Veldink, Jan H.; Silani, Vincenzo; Al Chalabi, Ammar; Powell, John | |
| Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis | 1-gen-2023 | Chiò, Adriano; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; Grassano, Maurizio; Vasta, Rosario; Palumbo, Francesca; Gallone, Salvatore; Brunetti, Maura; Barberis, Marco; De Marchi, Fabiola; Dalgard, Clifton; Chia, Ruth; Mora, Gabriele; Iazzolino, Barbara; Peotta, Laura; Traynor, Bryan J; Corrado, Lucia; D'Alfonso, Sandra; Mazzini, Letizia; Calvo, Andrea | |
| 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 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 |