Spin-dependent limits from the DRIFT-IId directional dark matter detector by Daw, E, Fox, JR, Gauvreau, J, Ghag, C, Harmon, L, Gold, M, Lee, E, Loomba, D, Miller, E, Murphy, A, Paling, S, Landers, J, Pipe, M, Pushkin, K, Robinson, M, Snowden-Ifft, D, Spooner, N, Walker, D

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration. by Simpson, C, Lemmens, R, Miskiewicz, K, Broom, W, Hansen, V, van Vught, P, Landers, J, Sapp, P, Van Den Bosch, L, Knight, J, Neale, B, Turner, M, Veldink, J, Ophoff, R, Tripathi, V, Beleza, A, Shah, M, Proitsi, P, Van Hoecke, A, Carmeliet, P, Horvitz, H, Leigh, P, Shaw, C, van den Berg, L, Sham, 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

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis by Smith, B, Topp, S, Fallini, C, Shibata, H, Chen, H, Troakes, C, King, A, Ticozzi, N, Kenna, K, Sato, A, Soragia-Gkazi, A, Miller, J, Vance, C, Wong, C, de Majo, M, Kuttuah, W, Mitchell, J, Scotter, E, Parkin, N, Sapp, P, Nolan, M, Nestor, P, Simpson, M, Baas, F, de Jong, V, ten Asbroek, A, Redondo, A, Esteban-Perez, J, Tiloca, C, Verde, F, Dugo, S, Leigh, P, Pall, H, Morrison, K, Al-Chalabi, A, Shaw, P, Kirby, J, Turner, M, Talbot, K, Hardiman, O, Glass, J, de Belleroche, J, Maki, M, Moss, S, Miller, C, Gellera, C, Ratti, A, Al-Sarraj, S, Brown, R, Silani, V, Landers, J, Shaw, C

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis by Kenna, P, van Doormaal PTC, P, Dekker, A, Ticozzi, N, Kenna, B, Diekstra, F, van Rheenen, W, van Eijk, K, Jones, A, Keagle, P, Shatunov, A, Sproviero, W, Smith, B, van Es, M, Topp, S, Kenna, A, Miller, J, Fallini, C, Tiloca, C, McLaughlin, R, Vance, C, Troakes, C, Colombrita, C, Mora, G, Calvo, A, Verde, F, Al-Sarraj, S, King, A, Calini, D, de Belleroche, J, Baas, F, van der Kooi, A, de Visser, M, ten Asbroek, A, Sapp, P, McKenna-Yasek, D, Polak, M, Asress, S, Munoz-Blanco, J, SLAGEN Consortium, Lauria, G, Williams, K, Leigh, P, Nicholson, G, Blair, I, Leblond, C, Dion, P, Rouleau, G, Pall, H, Shaw, P, Turner, M, Talbot, K, Taroni, F, Boylan, K, Van Blitterswijk, M, Rademakers, R, Esteban-Perez, J, Garcia-Redondo, A, Van Damme, P, Robberecht, W, Chio, A, Gellera, C, Drepper, C, Sendtner, M, Ratti, A, Glass, J, Mora, J, Basak, A, Hardiman, O, Ludolph, A, Andersen, P, Wesihaupt, J, Brown, R, Al-Chalabi, A, Silani, V, Shaw, C, van den Berg, L, Veldink, J, Landers, J