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Consanguinity as a Risk Factor for Autism Alshaban, Fouad A.; Aldosari, Mohammad; Ghazal, Iman; Al-Shammari, Hawraa; Elhag, Saba; Thompson, I. Richard; Bruder, Jennifer; Shaath, Hibah; Al-Faraj, Fatema; Tolefat, Mohamed; Nasir, Assal; Fombonne, Eric 分享 收藏
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Reproducibility of Brain Responses: High for Speech Perception, Low for Reading Difficulties Leppanen, Paavo H. T.; Toth, Denes; Honbolygo, Ferenc; Lohvansuu, Kaisa; Hamalainen, Jarmo A.; Demonet, Jean-Francois; Schulte-Koerne, Gerd; Csepe, Valeria; Bartling, Juergen; Bruder, Jennifer; Chaix, Yves; Iannuzzi, Stephanie; Nenert, Rodolphe; Neuhoff, Nina; Streiftau, Silke; Tanskanen, Annika; Tuomainen, Jyrki 分享 收藏
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Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort Becker, Jessica; Czamara, Darina; Scerri, Tom S.; Ramus, Franck; Csepe, Valeria; Talcott, Joel B.; Stein, John; Morris, Andrew; Ludwig, Kerstin U.; Hoffmann, Per; 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 H. T.; Bruder, Jennifer; Monaco, Anthony P.; Mueller-Myhsok, Bertram; Kere, Juha; Landerl, Karin; Noethen, Markus M.; Schulte-Koerne, Gerd; Paracchini, Silvia; Peyrard-Janvid, Myriam; Schumacher, Johannes 分享 收藏
A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults Ludwig, K. U.; Saemann, P.; Alexander, M.; Becker, J.; Bruder, J.; Moll, K.; Spieler, D.; Czisch, M.; Warnke, A.; Docherty, S. J.; Davis, O. S. P.; Plomin, R.; Noethen, M. M.; Landerl, K.; Mueller-Myhsok, B.; Hoffmann, P.; Schumacher, J.; Schulte-Koerne, G.; Czamara, D. 分享 收藏
Predictors of developmental dyslexia in European orthographies with varying complexity Landerl, Karin; Ramus, Franck; Moll, Kristina; Lyytinen, Heikki; Leppanen, Paavo H. T.; Lohvansuu, Kaisa; O'Donovan, Michael; Williams, Julie; Bartling, Juergen; Bruder, Jennifer; Kunze, Sarah; Neuhoff, Nina; Toth, Denes; Honbolygo, Ferenc; Csepe, Valeria; Bogliotti, Caroline; Iannuzzi, Stephanie; Chaix, Yves; Demonet, Jean-Francois; Longeras, Emilie; Valdois, Sylviane; Chabernaud, Camille; Delteil-Pinton, Florence; Billard, Catherine; George, Florence; Ziegler, Johannes C.; Comte-Gervais, Isabelle; Soares-Boucaud, Isabelle; Gerard, Christophe-Loic; Blomert, Leo; Vaessen, Anniek; Gerretsen, Patty; Ekkebus, Michel; Brandeis, Daniel; Maurer, Urs; Schulz, Enrico; van der Mark, Sanne; Mueller-Myhsok, Bertram; Schulte-Koerne, Gerd 分享 收藏
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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children Roeske, D.; Ludwig, K. U.; Neuhoff, N.; Becker, J.; Bartling, J.; Bruder, J.; Brockschmidt, F. F.; Warnke, A.; Remschmidt, H.; Hoffmann, P.; Mueller-Myhsok, B.; Noethen, M. M.; Schulte-Koerne, G. 分享 收藏