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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.
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.
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 1-gen-2022 Ivashynka, A.; Leone, M. A.; Barizzone, N.; Cucovici, A.; Cantello, R.; Vecchio, D.; Zuccala, M.; Pizzino, A.; Copetti, M.; D'Alfonso, S.; Fontana, A.
Influence of Sex on the Microbiota of the Human Face 1-gen-2022 Robert, Clémence; Cascella, Federica; Mellai, Marta; Barizzone, Nadia; Mignone, Flavio; Massa, Nadia; Nobile, Vincenzo; Bona, Elisa
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 1-gen-2021 Zuccala, M.; Barizzone, N.; Boggio, E.; Gigliotti, L.; Sorosina, M.; Basagni, C.; Bordoni, R.; Clarelli, F.; Anand, S.; Mangano, E.; Vecchio, D.; Corsetti, E.; Martire, S.; Perga, S.; Ferrante, D.; Gajofatto, A.; Ivashynka, A.; Solaro, C.; Cantello, R.; Martinelli, V.; Comi, G.; Filippi, M.; Esposito, F.; Leone, M.; De Bellis, G.; Dianzani, U.; Martinelli-Boneschi, F.; D'Alfonso, S.
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 Urbanization Level 1-gen-2021 Gnavi, R.; Picariello, R.; Alboini, P. E.; Cavalla, P.; Grasso, M. F.; Richiardi, P.; Bertolotto, A.; Barizzone, N.; Cantello, R.; Leone, M. A.; D'Alfonso, S.; Golini, N.
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 1-gen-2021 Cargnin, S.; Barizzone, N.; Basagni, C.; Pisani, C.; Ferrara, E.; Masini, L.; D'Alfonso, S.; Krengli, M.; Terrazzino, S.
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.
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.
Periostin Circulating Levels and Genetic Variants in Patients with Non-Alcoholic Fatty Liver Disease 1-gen-2020 Smirne, Carlo; Mulas, Violante; Barbaglia, Matteo Nazzareno; Ramana Mallela, Venkata; Minisini, Rosalba; Barizzone, Nadia; Burlone, MICHELA Emma; Pirisi, Mario; Grossini, Elena
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 1-gen-2019 Patsopoulos, Na; Baranzini, Se; Santaniello, A; Shoostari, P; Cotsapas, C; Wong, G; Beecham, Ah; James, T; Replogle, J; Vlachos, Is; Mccabe, C; Pers, Th; Brandes, A; White, C; Keenan, B; Cimpean, M; Winn, P; Panteliadis, Ip; Robbins, A; Andlauer, Tfm; Zarzycki, O; Dubois, B; Goris, A; Sondergaard, Hb; Sellebjerg, F; Sorensen, Ps; Ullum, H; Thorner, Lw; Saarela, J; Cournu-Rebeix, I; Damotte, V; Fontaine, B; Guillot-Noel, L; Lathrop, M; Vukusic, S; Berthele, A; Pongratz, V; Pongratz, V; Gasperi, C; Graetz, C; Grummel, V; Hemmer, B; Hoshi, M; Knier, B; Korn, T; Lill, Cm; Luessi, F; Muhlau, M; Zipp, F; Dardiotis, E; Agliardi, C; Amoroso, A; Barizzone, N; Benedetti, Md; Bernardinelli, L; Cavalla, P; Clarelli, F; Comi, G; Cusi, D; Esposito, F; Ferre, L; Galimberti, D; Guaschino, C; Leone, Ma; Martinelli, V; Moiola, L; Salvetti, M; Sorosina, M; Vecchio, D; Zauli, A; Santoro, S; Mancini, N; Zuccala, M; Mescheriakova, J; van Duijn, C; Bos, Sd; Celius, Eg; Spurkland, A; Comabella, M; Montalban, X; Alfredsson, L; Bomfim, Il; Gomez-Cabrero, D; Hillert, J; Jagodic, M; Linden, M; Piehl, F; Jelcic, I; Martin, R; Sospedra, M; Baker, A; Ban, M; Hawkins, C; Hysi, P; Kalra, S; Karpe, F; Khadake, J; Lachance, G; Molyneux, P; Neville, M; Thorpe, J; Bradshaw, E; Caillier, Sj; Calabresi, P; Cree, Bac; Cross, A; Davis, M; de Bakker, Pwi; Delgado, S; Dembele, M; Edwards, K; Fitzgerald, K; Frohlich, Iy; Gourraud, Pa; Haines, Jl; Hakonarson, H; Kimbrough, D; Isobe, N; Konidari, I; Lathi, E; Lee, Mh; Li, T; An, D; Zimmer, A; Madireddy, L; Manrique, Cp; Mitrovic, M; Olah, M; Patrick, E; Pericak-Vance, Ma; Piccio, L; Schaefer, C; Weiner, H; Lage, K; Scott, Rj; Lechner-Scott, J; Leal, R; Moscato, P; Booth, Dr; Stewart, Gj; Vucic, S; Pame, G; Bametto, M; Mason, D; Griffiths, L; Broadley, S; Tajouri, L; Baxter, A; Slee, M; Taylor, Bv; Charlesworth, J; Kilpatrick, Tj; Rubio, J; Jokubaitis, V; Wiley, J; Butzkueven, H; Leslie, S; Motyer, A; Stankovich, J; Carroll, Wm; Kermode, Ag; Edrin, M; Barclay, M; Peyrin-Biroulet, L; Chamaillard, M; Colombe, Jf; Cottone, M; Croft, A; D'Inca, R; Halfvarson, J; Hanigan, K; Henderson, P; Hugot, Jp; Karban, A; Kennedy, Na; Khan, Ma; Lemann, M; Levine, A; Massey, D; Milla, M; Motoey, Gw; Ng, Sme; Oikonomnou, J; Peeters, H; Proctor, Dd; Rahier, Jf; Roberts, R; Rutgeerts, P; Seibold, F; Stronati, L; Taylor, Km; Torkvist, L; Ublick, K; Van Limbergen, J; Van Gossum, A; Vatn, Mh; Zhang, H; Zhang, W; Donnelly, P; Barroso, I; Blackwe, Jm; Bramon, E; Brown, Ma; Casas, Jp; Corvin, A; Deloukas, P; Duncanson, A; Jankowski, J; Markus, Hs; Mathew, Cg; Palmer, Cna; Plomin, R; Rautanen, A; Sawcer, Sj; Trembath, Rc; Viswanathan, Ac; Wood, Nw; Spencer, Cca; Band, G; Bellenguez, C; Freeman, C; Hellenthal, G; Giannoulatou, E; Pirinen, M; Pearson, R; Strange, A; Sul, Z; Vukcevic, Da; Donnelly, P; Langford, C; Hunt, Se; Edkins, S; Gwilliam, R; Blackburn, H; Bumpstead, Sj; Dronov, S; Gillman, M; Gray, E; Hammond, N; Jayakumar, A; Mccann, Ot; Liddle, J; Potter, Sc; Ravindrarajah, R; Ricketts, M; Waller, M; Weston, P; Widaa, S; Whittaker, P; Barroso, I; Deloukas, P; Mathew, Cg; Blackwe, Jm; Brown, Ma; Corvin, A; Spencer, Cca; Compston, A; Hafler, D; Harbo, Hf; Hauser, Sl; Stewart, G; D'Alfonso, S; Hadjigeorgiou, G; Taylor, B; Barcellos, Lf; Booth, D; Hintzen, R; Kockum, I; Martinelli-Boneschi, F; Mccauley, Jl; Oksenberg, Jr; Oturai, A; Sawcer, S; Ivinson, Aj; Olsson, T; De Jager, Pl
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
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
HLA alleles modulate EBV viral load in multiple sclerosis 1-gen-2018 Agostini, S; Mancuso, R; Guerini, Fr; D'Alfonso, S; Agliardi, C; Hernis, A; Zanzottera, M; Barizzone, N; Leone, Ma; Caputo, D; Rovaris, M; Clerici, M
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
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 1-gen-2018 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; Theunissen, 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
Overexpression of the Cytokine BAFF and Autoimmunity Risk 1-gen-2017 Steri, M; Orrù, V; Idda, Ml; Pitzalis, M; Pala, M; Zara, I; Sidore, C; Faà, V; Floris, M; Deiana, M; Asunis, I; Porcu, E; Mulas, A; Piras, Mg; Lobina, M; Lai, S; Marongiu, M; Serra, V; Marongiu, M; Sole, G; Busonero, F; Maschio, A; Cusano, R; Cuccuru, G; Deidda, F; Poddie, F; Farina, G; Dei, M; Virdis, F; Olla, S; Satta, Ma; Pani, M; Delitala, A; Cocco, E; Frau, J; Coghe, G; Lorefice, L; Fenu, G; Ferrigno, P; Ban, M; Barizzone, Nadia; Leone, M; Guerini, Fr; Piga, M; Firinu, D; Kockum, I; Lima Bomfim, I; Olsson, T; Alfredsson, L; Suarez, A; Carreira, Pe; Castillo Palma, Mj; Marcus, Jh; Congia, M; Angius, A; Melis, M; Gonzalez, A; Alarcón Riquelme, Me; da Silva, Bm; Marchini, M; Danieli, Mg; Del Giacco, S; Mathieu, A; Pani, A; Montgomery, Sb; Rosati, G; Hillert, J; Sawcer, S; D'Alfonso, Sandra; Todd, Ja; Novembre, J; Abecasis, Gr; Whalen, Mb; Marrosu, Mg; Meloni, A; Sanna, S; Gorospe, M; Schlessinger, D; Fiorillo, E; Zoledziewska, M; Cucca, F.
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.
Serum neurofilament light chain levels are increased in patients with a clinically isolated syndrome. 1-gen-2016 Disanto, G; Adiutori, R; Dobson, R; Martinelli, V; Dalla Costa, G; Runia, T; Evdoshenko, E; Thouvenot, E; Trojano, M; Norgren, N; Teunissen, C; Kappos, L; Giovannoni, G; Kuhle, J; International Clinically Isolated Syndrome Study, Group; Kuhle, J; Disanto, G; Dobson, R; Adiutori, R; Bianchi, L; Topping, J; Bestwick, Jp; Meier, Uc; Dalla Costa, G; 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, S; Alvarez-Cermeño, Jc; 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, Ad; Carra, A; Salvetti, M; Uccelli, A; Torkildsen, Ø; Myhr, Km; Galimberti, D; Rejdak, K; Lycke, J; Frederiksen, Jl; Drulovic, J; Confavreux, C; Brassat, D; Enzinger, C; Fuchs, S; Bosca, I; Pelletier, J; Picard, C; Colombo, E; Franciotta, D; Derfuss, T; Lindberg, Rl; Yaldizli, Ö; Vécsei, L; Kieseier, Bc; Hartung, Hp; Villoslada, P; Siva, A; Saiz, A; Tumani, H; Havrdová, E; Villar, Lm; 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, Sv; Giovannoni, G.
NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk 1-gen-2016 Antel, Jack; Ban, Maria; Baranzini, Sergio; Barcellos, Lisa; Barizzone, Nadia; Beecham, Ashley; Berge, Tone; Bernardinelli, Luisa; Booth, David; Bos, Steffan; Buck, Dorothea; Butkiewicz, Mariusz; Celius, Elisabeth G.; Comabella, Manuel; Compston, Alastair; Dedham, Katrina; Cotsapas, Chris; D'Alfonso, Sandra; De Jager, Phil; Dubois, Benedicte; Duquette, Pierre; Fontaine, Bertrand; Gasperi, Christiane; Gil, Elia; Goris, An; Gourraud, Pierre Antoine; Graetz, Christiane; Gyllenberg, Alexandra; Hadjigeorgiou, Georgios; Hafler, David; Hribko, Deanna; Haines, Jonathan; Harbo, Hanne; Hauser, Stephen; Warto, Shannon; Hawkins, Clive; Hemmer, Bernhard; Henry, Roland; Hintzen, Rogier; Horakova, Dana; Ivinson, Adrian; Howard, Melissa; Jelcic, Ilijas; Kaskow, Belinda; Kira, Jun Ichi; Kleinova, Pavlina; Kockum, Ingrid; Kucerova, Karolina; Lill, Christina; Luessi, Felix; Malhotra, Sunny; Martin, Roland; Martinelli, Filippo; Matsushita, Takuya; Mccabe, Cristin; Mccauley, Jacob; Mescheriakkova, Julia; Mitrovic, Mitja; Moen, Stine Marit; Montalban, Xavier; Muhlau, Mark; Nakmura, Yuri; Oksenberg, Jorge; Olsson, Tomas; Oturai, Annette; Palotie, Aarno; Patsopoulos, Nikolaos; Pavlicova, Jana; Pericak Vance, Peggy; Piehl, Fredrik; Rebeix, Isabelle; Rioux, John; Saarela, Janna; Sawcer, Stephen; Sellebjerg, Finn; Sondergaard, Helle Bach; Sorensen, Per Soelberg; Sospedra, Mireia; Spurkland, Anne; Stewart, Graeme; Taylor, Bruce; Uitterlinden, Andre; Van Duijn, Cornelia; Zipp, Frauke
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