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Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium

Aguirre, Tania, Matthijs, Gert, Robberecht, Wim, Tilkin, Petra, Cassiman, Jean-Jacques
Veröffentlicht in: European Journal of Human Genetics ; volume 7, issue 5, page 599-602 ; ISSN 1018-4813 1476-5438;
1999

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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Gijselinck, Ilse, Van Mossevelde, Sara, van der Zee, Julie, Sieben, Anne, Philtjens, Stéphanie, Heeman, Bavo, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, De Baets, Greet, Bäumer, Veerle, Cuijt, Ivy, Van den Broeck, Marleen, Peeters, Karin, Mattheijssens, Maria, Rousseau, Frederic, Vandenberghe, Rik, De Jonghe, Peter, Cras, Patrick, De Deyn, Peter P., Martin, Jean-Jacques, Cruts, Marc, Van Broeckhoven, Christine, Nuytten, Dirk, Van Langenhove, Tim, Smets, Katrien, Baets, Jonathan, Robberecht, Wim, Van Damme, Philip, De Bleecker, Jan, Santens, Patrick, Dermaut, Bart, Deryck, Olivier, Bergmans, Bruno, Delbeck, Jean, Versijpt, Jan, Michotte, Alex, Willems, Christiana, Ivanoiu, Adrian, Salmon, Eric
Veröffentlicht in: Neurology ; volume 85, issue 24, page 2116-2125 ; ISSN 0028-3878 1526-632X;
2015

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Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

Project Mine Als Sequencing Consortium, Mine Als Sequencing Consortium, Pulit, Sara L., Dekker, Annelot M., Al Khleifat, Ahmad, Brands, William J., Iacoangeli, Alfredo, Kenna, Kevin P., Kavak, Ersen, Kooyman, Maarten, McLaughlin, Russell L., Middelkoop, Bas, Moisse, Matthieu, Schellevis, Raymond D., Shatunov, Aleksey, Sproviero, William, Tazelaar, Gijs H.P., van der Spek, Rick A.A., van Doormaal, Perry T.C., van Eijk, Kristel R., van Vugt, Joke, Basak, A. Nazli, Blair, Ian P., Glass, Jonathan D., Hardiman, Orla, Hide, Winston, Landers, John E., Mora, Jesus S., Morrison, Karen E., Newhouse, Stephen, Robberecht, Wim, Shaw, Christopher E., Shaw, Pamela J., van Damme, Philip, van Es, Michael A., Wray, Naomi R., Al-Chalabi, Ammar, van Den Berg, Leonard H., Veldink, Jan H.
2018

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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

van Rheenen, Wouter, Shatunov, Aleksey, Dekker, Annelot, Mclaughlin, Russell, Diekstra, Frank, Pulit, Sara, van der Spek, Rick, Võsa, Urmo, de Jong, Simone, Robinson, Matthew, Yang, Jian, Fogh, Isabella, van Doormaal, Perry Tc, Tazelaar, Gijs, Koppers, Max, Blokhuis, Anna, Sproviero, William, Jones, Ashley, Kenna, Kevin, van Eijk, Kristel, Harschnitz, Oliver, Schellevis, Raymond, Brands, William, 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, Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen, Shaw, Pamela, Hardy, John, Orrell, Richard, Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Topp, Simon, Petri, Susanne, Abdulla, Susanne, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Ophoff, Roel, Staats, Kim, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, van Deerlin, Vivianna, Trojanowski, John, Elman, Lauren, Mccluskey, Leo, Basak, a Nazli, Tunca, Ceren, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian, Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine, Saker-Delye, Safaa, Dürr, Alexandra, Wood, Nicholas, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-François, Uitterlinden, Andre, Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, Blauw, Hylke, van der Kooi, Anneke, de Visser, Marianne, Goris, An, Weber, Markus, Shaw, Christopher, Smith, Bradley, Pansarasa, Orietta, Cereda, Cristina, del Bo, Roberto, Comi, Giacomo, d'Alfonso, Sandra, Bertolin, Cinzia, Sorarù, Gianni, Mazzini, Letizia, Pensato, Viviana, Gellera, Cinzia, Tiloca, Cinzia, Ratti, Antonia, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Arcuti, Simona, Capozzo, Rosa, Zecca, Chiara, Lunetta, Christian, Penco, Silvana, Riva, Nilo, Padovani, Alessandro, Filosto, Massimiliano, Muller, Bernard, Stuit, Robbert Jan, Blair, Ian, Zhang, Katharine, Mccann, Emily, Fifita, Jennifer, Nicholson, Garth, Rowe, Dominic, Pamphlett, Roger, Kiernan, Matthew, Grosskreutz, Julian, Witte, Otto, Ringer, Thomas, Prell, Tino, Stubendorff, Beatrice, Kurth, Ingo, Hübner, Christian, Leigh, P Nigel, Casale, Federico, Chio, Adriano, Beghi, Ettore, Pupillo, Elisabetta, Tortelli, Rosanna, Logroscino, Giancarlo, Powell, John, Ludolph, Albert, Weishaupt, Jochen, Robberecht, Wim, van Damme, Philip, Franke, Lude, Pers, Tune, Brown, Robert, Glass, Jonathan, Landers, John, Hardiman, Orla, Andersen, Peter, Corcia, Philippe, Vourc'H, Patrick, Silani, Vincenzo, Wray, Naomi, Visscher, Peter, de Bakker, Paul, van Es, Michael, Pasterkamp, R Jeroen, Lewis, Cathryn, Breen, Gerome, Al-Chalabi, Ammar, van den Berg, Leonard, Veldink, Jan
2016