Genome-wide association study identifies 19p13.3 ( UNC13A ) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis von Giegling, Ina, Lemmens, Robin, Kiemeney, Lambertus A, Ophoff, Roel A, Zwarts, Machiel J, Hofman, Albert, Hendrich, Corinna, Landers, John E, Saris, Christiaan G J, Veldink, Jan H, Melki, Judith, Fumoto, Katsumi, Andersen, Peter M, Birve, Anna, Schreiber, Stefan, de Visser, Marianne, Hardiman, Orla, Uitterlinden, Andre G, Nöthen, Markus M, Meininger, Vincent, Waibel, Stefan, Cichon, Sven, Leigh, P Nigel, Wichmann, H-Erich, Ludolph, Albert C, van Es, Michael A, Vermeulen, Sita H H M, Robberecht, Wim, Meyer, Thomas, Schelhaas, Helenius J, van Vught, Paul W J, Groen, Ewout J N, Rivadeneira, Fernando, Purcell, Shaun, Cronin, Simon, Estrada, Karol, van den Berg, Leonard H, Glass, Jonathan D, Huisman, Mark H B, Slowik, Agnieszka, Wokke, John H J, Pasterkamp, R Jeroen, Brown, Robert H, Shaw, Christopher E, van der Kooi, Anneke J, Tomik, Barbara, van Doormaal, Perry T C, Rujescu, Dan, McLaughlin, Russell L, Dahlberg, Caroline, Al-Chalabi, Ammar, Blauw, Hylke M, Strengman, Eric, Muglia, Pierandrea

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Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis von van Es, Michael A., Schelhaas, Helenius J., van Vught, Paul W. J., Ticozzi, Nicola, Andersen, Peter M., Groen, Ewout J. N., Schulte, Claudia, Blauw, Hylke M., Koppers, Max, Diekstra, Frank P., Fumoto, Katsumi, LeClerc, Ashley Lyn, Keagle, Pamela, Bloem, Bastiaan R., Scheffer, Hans, van Nuenen, Bart F. L., van Blitterswijk, Marka, van Rheenen, Wouter, Wills, Anne-Marie, Lowe, Patrick P., Hu, Guo-fu, Yu, Wenhao, Kishikawa, Hiroko, Wu, David, Folkerth, Rebecca D., Mariani, Claudio, Goldwurm, Stefano, Pezzoli, Gianni, Van Damme, Philip, Lemmens, Robin, Dahlberg, Caroline, Birve, Anna, Fernández-Santiago, Rubén, Waibel, Stefan, Klein, Christine, Weber, Markus, van der Kooi, Anneke J., de Visser, Marianne, Verbaan, Dagmar, van Hilten, Jacobus J., Heutink, Peter, Hennekam, Eric A. M., Cuppen, Edwin, Berg, Daniela, Brown Jr, Robert H., Silani, Vincenzo, Gasser, Thomas, Ludolph, Albert C., Robberecht, Wim, Ophoff, Roel A., Veldink, Jan H., Pasterkamp, R. Jeroen, de Bakker, Paul I. W., Landers, John E., van de Warrenburg, Bart P., van den Berg, Leonard H.

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UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophy von Shorrock, H, van der Hoorn, D, Boyd, P, Hurtado, M, Lamont, D, Wirth, B, Sleigh, JN, Schiavo, G, Wishart, T, Groen, EJN, Gillingwater, TH

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Bakker, MK, Westra, H-J, Deelen, P, Dolzhenko, E, Gawor, K, Tazelaar, GHP, Doherty, M, Al Khleifat, A, Shatunov, A, Smith, BN, Shaw, PJ, Sendtner, M, Fogh, I, Lauria, G, Sproviero, D, D’Alfonso, S, Sorarù, G, Siciliano, G, Padovani, A, Moglia, C, Brunetti, M, Lerner, Y, Zabari, M, Gotkine, M, Millecamps, S, Meininger, V, Rojas-García, R, Dion, PA, Ross, JP, Durr, A, Payan, CAM, Wood, NW, Franke, A, Ripke, S, Whiteman, DC, Gerardi, F, Cotelli, MS, Rinaldi, F, Guaita, MC, Ceroni, M, Ferrarese, C, Delodovici, ML, Vasta, R, Bombaci, A, Casale, F, Fuda, G, Salamone, P, Iazzolino, B, Peotta, L, Palumbo, F, Gallone, S, Sbaiz, L, Mauro, A, De Marchi, F, Gionco, M, Pignatta, P, De Mattei, M, Papurello, DM, Gusmaroli, G, Comi, C, Ruiz, L, Di Vito, N, Meineri, P, Ghiglione, P, Dotta, M, Di Sapio, A, Tiloca, C, Gagliardi, S, Ferlini, A, Mundi, C, Zarrelli, M, Cauchi, RJ, Wiedau-Pazos, M, Lomen-Hoerth, C, van Deerlin, VM, Jörk, A, Graff, C, Fominykh, V, Ataulina, A, Koritnik, B, Zidar, J, Glavač, D, Drory, V, McCombe, PA, Ngo, ST, Pamphlett, R, Williams, KL, Wallace, L, Brown, RH, Andersen, PM, van Es, MA, Fan, D, Garton, FC, Davey Smith, G, Mill, J, Hardiman, O, Wray, NR, Franke, L, van den Berg, LH, Veldink, JH

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von van der Spek, RAA, Bakker, MK, de Klein, N, Westra, H-J, Deelen, P, Dolzhenko, E, Gawor, K, Westeneng, H-J, Tazelaar, GHP, van Eijk, KR, Kooyman, M, Doherty, M, Al Khleifat, A, Shatunov, A, Ticozzi, N, Cooper-Knock, J, Smith, BN, Shaw, PJ, Hardy, J, Sendtner, M, van der Kooi, AJ, Fogh, I, Lauria, G, Sproviero, D, Sorarù, G, Siciliano, G, Padovani, A, Moglia, C, Brunetti, M, Grassano, M, Logroscino, G, Nefussy, B, Nordin, A, Lerner, Y, Zabari, M, Gotkine, M, Millecamps, S, Meininger, V, Mora Pardina, JS, Assialioui, A, Rojas-García, R, Dion, PA, Ross, JP, Freischmidt, A, Bensimon, G, Durr, A, Payan, CAM, Wood, NW, Tittmann, L, Lieb, W, Franke, A, Ripke, S, Whiteman, DC, Hofman, A, PARALS Consortium, SLAP Consortium, Traynor, BJ, Singleton, AB, Mitne Neto, M, Cauchi, RJ, Ophoff, RA, Wiedau-Pazos, M, Grosskreutz, J, Roediger, A, Gaur, N, Jörk, A, Witte, OW, Steinbach, R, Ataulina, A, Rogelj, B, Zidar, J, Glavač, D, Stević, Z, Drory, V, Povedano, M, Henderson, RD, Mathers, S, McCombe, PA, Pamphlett, R, Mather, KA, Henders, AK, Wallace, L, de Carvalho, M, Petri, S, Breen, G, Glass, JD, Shaw, CE, Andersen, PM, Groen, EJN, Pasterkamp, RJ, Fan, D, Garton, FC, McRae, AF, Davey Smith, G, Eberle, MA, Hardiman, O, Kenna, KP, Wray, NR, Runz, H, Veldink, JH

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In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome Biology von Bernabò, P, Tebaldi, T, Groen, EJN, Lane, FM, Perenthaler, E, Mattedi, F, Newbery, HJ, Zhou, H, Zuccotti, P, Potrich, V, Shorrock, HK, Muntoni, F, Quattrone, A, Gillingwater, TH, Viero, G

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Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy von Boyd, PJ, Tu, W-Y, Shorrock, HK, Groen, EJN, Carter, RN, Powis, RA, Thomson, SR, Thomson, D, Graham, LC, Motyl, AAL, Wishart, TM, Highley, JR, Morton, NM, Becker, T, Becker, CG, Heath, PR, Gillingwater, TH

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