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    Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal dementia and GRN mutations: a genome-wide association study von Pottier, Cyril, Zhou, Xiaolai, Perkerson, Ralph B., Baker, Matt, Jenkins, Gregory D., Serie, Daniel J., Ghidoni, Roberta, Benussi, Luisa, Binetti, Giuliano, de Munain, Adolfo López, Zulaica, Miren, Moreno, Fermin, Le Ber, Isabelle, Pasquier, Florence, Hannequin, Didier, Sánchez-Valle, Raquel, Antonell, Anna, Lladó, Albert, Parsons, Tammee M., Finch, NiCole A., Finger, Elizabeth C., Lippa, Carol F., Huey, Edward D., Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Rissman, Robert A., Slawek, Jaroslaw, Sitek, Emilia, Johannsen, Peter, Nielsen, Jørgen E., Ren, Yingxue, van Blitterswijk, Marka, DeJesus-Hernandez, Mariely, Christopher, Elizabeth, Murray, Melissa E., Bieniek, Kevin F., Evers, Bret M., Ferrari, Camilla, Rollinson, Sara, Richardson, Anna, Scarpini, Elio, Fumagalli, Giorgio G., Padovani, Alessandro, Hardy, John, Momeni, Parastoo, Ferrari, Raffaele, Frangipane, Francesca, Maletta, Raffaele, Anfossi, Maria, Gallo, Maura, Petrucelli, Leonard, Suh, EunRan, Lopez, Oscar L., Wong, Tsz H., van Rooij, Jeroen G. J., Seelaar, Harro, Mead, Simon, Caselli, Richard J., Reiman, Eric M., Sabbagh, Marwan Noel, Kjolby, Mads, Nykjaer, Anders, Karydas, Anna M., Boxer, Adam L., Grinberg, Lea T., Grafman, Jordan, Spina, Salvatore, Oblak, Adrian, Mesulam, M-Marsel, Weintraub, Sandra, Geula, Changiz, Hodges, John R., Piguet, Olivier, Brooks, William S., Irwin, David J., Trojanowski, John Q., Lee, Edward B., Josephs, Keith A., Parisi, Joseph E., Ertekin-Taner, Nilüfer, Knopman, David S., Nacmias, Benedetta, Piaceri, Irene, Bagnoli, Silvia, Sorbi, Sandro, Gearing, Marla, Glass, Jonathan, Beach, Thomas G., Black, Sandra E., Masellis, Mario, Rogaeva, Ekaterina, Vonsattel, Jean-Paul, Honig, Lawrence S., Kofler, Julia, Bruni, Amalia C., Snowden, Julie, Mann, David, Pickering-Brown, Stuart

    Veröffentlicht in Lancet neurology

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