Discovery of 42 genome-wide significant loci associated with dyslexia by Doust, C, Fontanillas, P, Eising, E, Gordon, SD, Wang, Z, Alagöz, G, Molz, B, Pourcain, BS, Francks, C, Marioni, RE, Zhao, J, Paracchini, S, Talcott, JB, Monaco, AP, Stein, JF, Gruen, JR, Olson, RK, Willcutt, EG, DeFries, JC, Pennington, BF, Smith, SD, Wright, MJ, Martin, NG, Auton, A, Bates, TC, Fisher, SE, Luciano, M

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