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    Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von Dekker, Annelot M., Diekstra, Frank P., van der Spek, Rick A. A., Võsa, Urmo, Yang, Jian, Vajda, Alice, Lin, Kuang, Vrabec, Katarina, Koritnik, Blaž, Zidar, Janez, de Visser, Marianne, Leonardis, Lea, Millecamps, Stéphanie, Meininger, Vincent, Mora, Jesus S., Colville, Shuna, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Pittman, Alan, Sidle, Katie, Malaspina, Andrea, Petri, Susanne, Drepper, Carsten, Meyer, Thomas, Ophoff, Roel A., Staats, Kim A., Van Deerlin, Vivianna M., Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Basak, A Nazli, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Smith, Bradley N., Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R., Maurel, Cindy, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A. M., Saker-Delye, Safaa, Tittmann, Lukas, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M., Tzourio, Christophe, Dartigues, Jean-François, Cereda, Cristina, Uitterlinden, Andre G., Estrada, Karol, Hofman, Albert, Curtis, Charles, Comi, Giacomo P., D'Alfonso, Sandra, Fogh, Isabella, Bertolin, Cinzia, Sorarù, Gianni, Tiloca, Cinzia, Ratti, Antonia, Calvo, Andrea, Brunetti, Maura, van Doormaal, Perry T. C., Arcuti, Simona, Capozzo, Rosa, Lunetta, Christian, Riva, Nilo, Filosto, Massimiliano, Muller, Bernard, Tazelaar, Gijs H. P., Zhang, Katharine, McCann, Emily P., Rowe, Dominic B., Grosskreutz, Julian, Ringer, Thomas, Prell, Tino, Stubendorff, Beatrice, Beghi, Ettore, Pupillo, Elisabetta, Blokhuis, Anna M., Tortelli, Rosanna, Powell, John, Ludolph, Albert C., Van Damme, Philip, Franke, Lude, Brown, Robert H., Sproviero, William, Andersen, Peter M., Silani, Vincenzo, Jones, Ashley R., Pasterkamp, R Jeroen, Breen, Gerome, Al-Chalabi, Ammar, Veldink, Jan H., Kenna, Kevin P., Harschnitz, Oliver, Schellevis, Raymond D., Brands, William J.

    Veröffentlicht in Nature genetics

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    Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von van Rheenen, Wouter, Shatunov, Aleksey, Dekker, Annelot M, McLaughlin, Russell L, Diekstra, Frank P, Pulit, Sara L, van der Spek, Rick A.A, Võsa, Urmo, de Jong, Simone, Robinson, Matthew R, Yang, Jian, Fogh, Isabella, van Doormaal, Perry Tc, Tazelaar, Gijs H.P, Koppers, Max, Blokhuis, Anna M, Sproviero, William, Jones, Ashley R, Kenna, Kevin P, van Eijk, Kristel R, Harschnitz, Oliver, Schellevis, Raymond D, Brands, William J, Medic, Jelena, Menelaou, Androniki, Vajda, Alice, Ticozzi, Nicola, Lin, Kuang, Rogelj, Boris, Vrabec, Katarina, Ravnik-Glavač, Metka, Koritnik, Blaž, Zidar, Janez, Leonardis, Lea, Grošelj, Leja Dolenc, Millecamps, Stéphanie, Salachas, François, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Mora, Jesus S, Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Topp, Simon, Petri, Susanne, Abdulla, Susanne, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Ophoff, Roel A, Staats, Kim A, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M, Trojanowski, John Q, Elman, Lauren, McCluskey, Leo, Basak, A. Nazli, Tunca, Ceren, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R, Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A.M, Saker-Delye, Safaa, Dürr, Alexandra, Wood, Nicholas W, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-François, Uitterlinden, Andre G, Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, Blauw, Hylke M, van der Kooi, Anneke J

    Veröffentlicht in Nature Genetics

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