Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Pottier, C; Zhou, X; Perkerson, RB; Baker, M; Jenkins, GD; Serie, DJ; Ghidoni, R; ... Rademakers, R; + view all Pottier, C; Zhou, X; Perkerson, RB; Baker, M; Jenkins, GD; Serie, DJ; Ghidoni, R; Benussi, L; Binetti, G; López de Munain, A; Zulaica, M; Moreno, F; Le Ber, I; Pasquier, F; Hannequin, D; Sánchez-Valle, R; Antonell, A; Lladó, A; Parsons, TM; Finch, NA; Finger, EC; Lippa, CF; Huey, ED; Neumann, M; Heutink, P; Synofzik, M; Wilke, C; Rissman, RA; Slawek, J; Sitek, E; Johannsen, P; Nielsen, JE; Ren, Y; van Blitterswijk, M; DeJesus-Hernandez, M; Christopher, E; Murray, ME; Bieniek, KF; Evers, BM; Ferrari, C; Rollinson, S; Richardson, A; Scarpini, E; Fumagalli, GG; Padovani, A; Hardy, J; Momeni, P; Ferrari, R; Frangipane, F; Maletta, R; Anfossi, M; Gallo, M; Petrucelli, L; Suh, E; Lopez, OL; Wong, TH; van Rooij, JGJ; Seelaar, H; Mead, S; Caselli, RJ; Reiman, EM; Noel Sabbagh, M; Kjolby, M; Nykjaer, A; Karydas, AM; Boxer, AL; Grinberg, LT; Grafman, J; Spina, S; Oblak, A; Mesulam, M-M; Weintraub, S; Geula, C; Hodges, JR; Piguet, O; Brooks, WS; Irwin, DJ; Trojanowski, JQ; Lee, EB; Josephs, KA; Parisi, JE; Ertekin-Taner, N; Knopman, DS; Nacmias, B; Piaceri, I; Bagnoli, S; Sorbi, S; Gearing, M; Glass, J; Beach, TG; Black, SE; Masellis, M; Rogaeva, E; Vonsattel, J-P; Honig, LS; Kofler, J; Bruni, AC; Snowden, J; Mann, D; Pickering-Brown, S; Diehl-Schmid, J; Winkelmann, J; Galimberti, D; Graff, C; Öijerstedt, L; Troakes, C; Al-Sarraj, S; Cruchaga, C; Cairns, NJ; Rohrer, JD; Halliday, GM; Kwok, JB; van Swieten, JC; White, CL; Ghetti, B; Murell, JR; Mackenzie, IRA; Hsiung, G-YR; Borroni, B; Rossi, G; Tagliavini, F; Wszolek, ZK; Petersen, RC; Bigio, EH; Grossman, M; Van Deerlin, VM; Seeley, WW; Miller, BL; Graff-Radford, NR; Boeve, BF; Dickson, DW; Biernacka, JM; Rademakers, R; - view fewer (2018) Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. The Lancet Neurology 10.1016/S1474-4422(18)30126-1 . (In press).

https://ift.tt/2IJV0xM