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Becker, Jessica, Czamara, Darina, Scerri, Tom S, Ramus, Franck, Csepe, Valeria, Talcott, Joel B, Stein, John, Morris, Andrew, Ludwig, Kerstin U, Hoffmann, Per et al (show 31 more authors) , Honbolygo, Ferenc, Toth, Denes, Fauchereau, Fabien, Bogliotti, Caroline, Iannuzzi, Stephanie, Chaix, Yves, Valdois, Sylviane, Billard, Catherine, George, Florence, Soares-Boucaud, Isabelle, Gerard, Christophe-Loic, van der Mark, Sanne, Schulz, Enrico, Vaessen, Anniek, Maurer, Urs, Lohvansuu, Kaisa, Lyytinen, Heikki, Zucchelli, Marco, Brandeis, Daniel, Blomertw, Leo, Leppanen, Paavo HT, Bruder, Jennifer, Monaco, Anthony P, Mueller-Myhsok, Bertram, Kere, Juha, Landerl, Karin, Noethen, Markus M, Schulte-Koerne, Gerd, Paracchini, Silvia, Peyrard-Janvid, Myriam and Schumacher, Johannes (2014) Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. EUROPEAN JOURNAL OF HUMAN GENETICS, 22 (5). 675 - 680.

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Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Brandler, William et al (show 35 more authors) , Honbolygo, Ferenc, Toth, Denes, Csepe, Valeria, Huguet, Guillaume, Morris, Andrew P, Hulslander, Jacqueline, Willcutt, Erik G, DeFries, John C, Olson, Richard K, Smith, Shelley D, Pennington, Bruce F, Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppanen, Paavo HT, Brandeis, Daniel, Bonte, Milene, Stein, John F, Talcott, Joel B, Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P, Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S, Paracchini, Silvia, Fisher, Simon E, Schumacher, Johannes, Noethen, Markus M, Mueller-Myhsok, Bertram and Schulte-Koerne, Gerd (2019) Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY, 9.