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Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort by Becker, J, Czamara, D, Scerri, T, Ramus, F, Csépe, V, Talcott, J, Stein, J, Morris, A, Ludwig, K, Hoffmann, P, Honbolygó, F, Tóth, D, Fauchereau, F, Bogliotti, C, Iannuzzi, S, Chaix, Y, Valdois, S, Billard, C, George, F, Soares-Boucaud, I, Gérard, C, Van Der Mark, S, Schulz, E, Vaessen, A, Maurer, U

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia by Gialluisi, A, Andlauer, TFM, Mirza-Schreiber, N, Moll, K, Becker, J, Hoffmann, P, Ludwig, KU, Czamara, D, St Pourcain, B, Brandler, W, Honbolygó, F, Tóth, D, Csépe, V, Huguet, G, Morris, AP, Hulslander, J, Willcutt, EG, Defries, JC, Olson, RK, Smith, SD, Pennington, BF, Vaessen, A, Maurer, U, Lyytinen, H, Peyrard-Janvid, M, Leppänen, PHT, Brandeis, D, Bonte, M, Stein, JF, Talcott, JB, Fauchereau, F, Wilcke, A, Francks, C, Bourgeron, T, Monaco, AP, Ramus, F, Landerl, K, Kere, J, Scerri, TS, Paracchini, S, Fisher, SE, Schumacher, J, Nöthen, MM, Müller-Myhsok, B, Schulte-Körne, G