Cognitive impairment across ALS clinical stages in a population-based cohort von Chiò, Adriano, Moglia, Cristina, Canosa, Antonio, Manera, Umberto, Vasta, Rosario, Brunetti, Maura, Barberis, Marco, Corrado, Lucia, DʼAlfonso, Sandra, Bersano, Enrica, Sarnelli, Maria Francesca, Solara, Valentina, Zucchetti, Jean Pierre, Peotta, Laura, Iazzolino, Barbara, Mazzini, Letizia, Mora, Gabriele, Calvo, Andrea

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Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort von Grassano, Maurizio, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Barberis, Marco, Sbaiz, Luca, Canosa, Antonio, Manera, Umberto, Vasta, Rosario, Corrado, Lucia, D'Alfonso, Sandra, Mazzini, Letizia, Scholz, Sonja W., Dalgard, Clifton, Ding, Jinhui, Gibbs, Raphael J., Chia, Ruth, Traynor, Bryan J., Chiò, Adriano

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Author Correction: Next Generation Sequencing of Pooled Samples: Guideline for Variants’ Filtering von Anand, Santosh, Mangano, Eleonora, Barizzone, Nadia, Bordoni, Roberta, Sorosina, Melissa, Clarelli, Ferdinando, Corrado, Lucia, Martinelli Boneschi, Filippo, D’Alfonso, Sandra, De Bellis, Gianluca

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Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus von Kozyrev, Sergey V, Wojcik, Jerome, Barizzone, Nadia, González-Escribano, Maria Francisca, Zaghlool, Ammar, Sturfelt, Gunnar, Pons-Estel, Bernardo A, Svenungsson, Elisabet, Junker, Peter, Sanchez, Elena, Martin, Javier, Jönsen, Andreas, Gutierrez, Carmen, Suarez, Ana, Linga Reddy, M V Prasad, Abelson, Anna-Karin, Gunnarsson, Iva, Laustrup, Helle, Truedsson, Lennart, D'Alfonso, Sandra, Abderrahim, Hadi, Alarcón-Riquelme, Marta E, Witte, Torsten, Danieli, Maria Giovanna

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Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series von Magistrelli, Luca, Croce, Roberta, De Marchi, Fabiola, Basagni, Chiara, Carecchio, Miryam, Nasuelli, Nicola, Cantello, Roberto, Invernizzi, Federica, Garavaglia, Barbara, Comi, Cristoforo, Mazzini, Letizia, D’Alfonso, Sandra, Corrado, Lucia

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Validation of an Algorithm to Detect Multiple Sclerosis Cases in Administrative Health Databases in Piedmont (Italy): An Application to the Estimate of Prevalence by Age and Urbani... von Gnavi, Roberto, Picariello, Roberta, Alboini, Paolo Emilio, Cavalla, Paola, Grasso, Maria Federica, Richiardi, Paola, Bertolotto, Antonio, Barizzone, Nadia, Cantello, Roberto, Leone, Maurizio Angelo, D’Alfonso, Sandra, Golini, Natalia

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A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility von 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

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Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers von Tondo, Giacomo, Mazzini, Letizia, Caminiti, Silvia Paola, Sarnelli, Maria Francesca, Corrado, Lucia, Matheoud, Roberta, D'Alfonso, Sandra, Cantello, Roberto, Sacchetti, Gian Mauro, Perani, Daniela, Comi, Cristoforo, De Marchi, Fabiola

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Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility von 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

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C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect von Ratti, Antonia, Corrado, Lucia, Castellotti, Barbara, Del Bo, Roberto, Fogh, Isabella, Cereda, Cristina, Tiloca, Cinzia, D'Ascenzo, Carla, Bagarotti, Alessandra, Pensato, Viviana, Ranieri, Michela, Gagliardi, Stella, Calini, Daniela, Mazzini, Letizia, Taroni, Franco, Corti, Stefania, Ceroni, Mauro, Oggioni, Gaia D, Lin, Kuang, Powell, John F, Sorarù, Gianni, Ticozzi, Nicola, Comi, Giacomo P, D'Alfonso, Sandra, Gellera, Cinzia, Silani, Vincenzo

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TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations von Pensato, Viviana, Tiloca, Cinzia, Corrado, Lucia, Bertolin, Cinzia, Sardone, Valentina, Del Bo, Roberto, Calini, Daniela, Mandrioli, Jessica, Lauria, Giuseppe, Mazzini, Letizia, Querin, Giorgia, Ceroni, Mauro, Cantello, Roberto, Corti, Stefania, Castellotti, Barbara, Soldà, Giulia, Duga, Stefano, Comi, Giacomo P., Cereda, Cristina, Sorarù, Gianni, D’Alfonso, Sandra, Taroni, Franco, Shaw, Christopher E., Landers, John E., Ticozzi, Nicola, Ratti, Antonia, Gellera, Cinzia, Silani, Vincenzo

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Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene von D'Anzi, Angela, Altieri, Filomena, Perciballi, Elisa, Ferrari, Daniela, Bernardini, Laura, Goldoni, Marina, Mazzini, Letizia, De Marchi, Fabiola, Di Pierro, Alice, D'Alfonso, Sandra, Gelati, Maurizio, Vescovi, Angelo Luigi, Rosati, Jessica

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Next Generation Sequencing of Pooled Samples: Guideline for Variants’ Filtering von Anand, Santosh, Mangano, Eleonora, Barizzone, Nadia, Bordoni, Roberta, Sorosina, Melissa, Clarelli, Ferdinando, Corrado, Lucia, Martinelli Boneschi, Filippo, D’Alfonso, Sandra, De Bellis, Gianluca

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A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus von Orrú, Valeria, Tsai, Sophia J., Rueda, Blanca, Fiorillo, Edoardo, Stanford, Stephanie M., Dasgupta, Jhimli, Hartiala, Jaana, Zhao, Lei, Ortego-Centeno, Norberto, D’Alfonso, Sandra, Arnett, Frank C., Wu, Hui, Gonzalez-Gay, Miguel A., Tsao, Betty P., Pons-Estel, Bernardo, Alarcon-Riquelme, Marta E., He, Yantao, Zhang, Zhong-Yin, Allayee, Hooman, Chen, Xiaojiang S., Martin, Javier, Bottini, Nunzio

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Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population von Clarelli, Ferdinando, Barizzone, Nadia, Mangano, Eleonora, Zuccalà, Miriam, Basagni, Chiara, Anand, Santosh, Sorosina, Melissa, Mascia, Elisabetta, Santoro, Silvia, Guerini, Franca Rosa, Virgilio, Eleonora, Gallo, Antonio, Pizzino, Alessandro, Comi, Cristoforo, Martinelli, Vittorio, Comi, Giancarlo, De Bellis, Gianluca, Leone, Maurizio, Filippi, Massimo, Esposito, Federica, Bordoni, Roberta, Martinelli Boneschi, Filippo, D'Alfonso, Sandra

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Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis von 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, Martinelli Boneschi, Filippo

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Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis von Gemmati, Donato, Zeri, Giulia, Orioli, Elisa, De Gaetano, Francesca E, Salvi, Fabrizio, Bartolomei, Ilaria, D'Alfonso, Sandra, Dall'osso, Claudia, Leone, Maurizio A, Singh, Ajay V, Asselta, Rosanna, Zamboni, Paolo

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Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1) von Anedda, Francesca, Zucchelli, Marco, Schepis, Danika, Hellquist, Anna, Corrado, Lucia, D'Alfonso, Sandra, Achour, Adnane, McInerney, Gerald, Bertorello, Alejandro, Lördal, Mikael, Befrits, Ragnar, Björk, Jan, Bresso, Francesca, Törkvist, Leif, Halfvarson, Jonas, Kere, Juha, D'Amato, Mauro

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Rare Variants in the TREX1 Gene and Susceptibility to Autoimmune Diseases von D'Alfonso, Sandra, Scorza, Raffaella, Marchini, Maurizio, Godi, Michela, Mellone, Simona, Monti, Sara, Barizzone, Nadia, Danieli, Maria Giovanna

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A Census of Tandemly Repeated Polymorphic Loci in Genic Regions Through the Comparative Integration of Human Genome Assemblies von 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

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