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1
Understanding comorbidity of learning disorders: task‐dependent estimates of prevalence by Moll, K, Landerl, K, Snowling, M, Schulte-Körne, G
Published 2018Journal article -
2
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. by Pagnamenta, A, Bacchelli, E, de Jonge, M, Mirza, G, Scerri, T, Minopoli, F, Chiocchetti, A, Ludwig, K, Hoffmann, P, Paracchini, S, Lowy, E, Harold, D, Chapman, J, Klauck, S, Poustka, F, Houben, R, Staal, W, Ophoff, R, O'Donovan, M, Williams, J, Nöthen, M, Schulte-Körne, G, Deloukas, P, Ragoussis, J, Bailey, A
Published 2010Journal article -
3
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
Published 2019Journal article