Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. by Smith, B, Ticozzi, N, Fallini, C, Gkazi, A, Topp, S, Kenna, K, Scotter, E, Kost, J, Keagle, P, Miller, J, Calini, D, Vance, C, Danielson, E, Troakes, C, Tiloca, C, Al-Sarraj, S, Lewis, E, King, A, Colombrita, C, Pensato, V, Castellotti, B, de Belleroche, J, Baas, F, ten Asbroek, A, Sapp, P

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis by Fogh, I, Lin, K, Tiloca, C, Rooney, J, Gellera, C, Diekstra, F, Ratti, A, Shatunov, A, Es, V, Proitsi, P, Jones, A, Sproviero, W, Chiò, A, McLaughlin, R, Sorarù, G, Corrado, L, Stahl, D, Del Bo, R, Cereda, C, Castellotti, B, Glass, J, Newhouse, S, Dobson, R, Smith, B, Topp, S, Van Rheenen, W, Meininger, V, Melki, J, Morrison, K, Shaw, P, Leigh, P, Andersen, P, Comi, G, Ticozzi, N, Mazzini, L, D'Alfonso, S, Traynor, B, Van Damme, P, Robberecht, W, Brown, R, Landers, J, Hardiman, O, Lewis, C, Van Den Berg, L, Shaw, C, Veldink, J, Silani, V, Al-Chalabi, A, Powell, J