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Predictors of developmental dyslexia in European orthographies with varying complexity.
Landerl K, Ramus F, Moll K, Lyytinen H, Leppänen PH, Lohvansuu K, O'Donovan M, Williams J, Bartling J, Bruder J, Kunze S, Neuhoff N, Tóth D, Honbolygó F, Csépe V, Bogliotti C, Iannuzzi S, Chaix Y, Démonet JF, Longeras E, Valdois S, Chabernaud C, Delteil-Pinton F, Billard C, George F, Ziegler JC, Comte-Gervais I, Soares-Boucaud I, Gérard CL, Blomert L, Vaessen A, Gerretsen P, Ekkebus M, Brandeis D, Maurer U, Schulz E, van der Mark S, Müller-Myhsok B, Schulte-Körne G. Landerl K, et al. J Child Psychol Psychiatry. 2013 Jun;54(6):686-94. doi: 10.1111/jcpp.12029. Epub 2012 Dec 10. J Child Psychol Psychiatry. 2013. PMID: 23227813
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
Ludwig KU, Sämann P, Alexander M, Becker J, Bruder J, Moll K, Spieler D, Czisch M, Warnke A, Docherty SJ, Davis OS, Plomin R, Nöthen MM, Landerl K, Müller-Myhsok B, Hoffmann P, Schumacher J, Schulte-Körne G, Czamara D. Ludwig KU, et al. Among authors: landerl k. Transl Psychiatry. 2013 Feb 19;3(2):e229. doi: 10.1038/tp.2012.148. Transl Psychiatry. 2013. PMID: 23423138 Free PMC article.
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
Becker J, Czamara D, Scerri TS, Ramus F, Csépe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygó F, Tóth D, Fauchereau F, Bogliotti C, Iannuzzi S, Chaix Y, Valdois S, Billard C, George F, Soares-Boucaud I, Gérard CL, van der Mark S, Schulz E, Vaessen A, Maurer U, Lohvansuu K, Lyytinen H, Zucchelli M, Brandeis D, Blomert L, Leppänen PH, Bruder J, Monaco AP, Müller-Myhsok B, Kere J, Landerl K, Nöthen MM, Schulte-Körne G, Paracchini S, Peyrard-Janvid M, Schumacher J. Becker J, et al. Among authors: landerl k. Eur J Hum Genet. 2014 May;22(5):675-80. doi: 10.1038/ejhg.2013.199. Epub 2013 Sep 11. Eur J Hum Genet. 2014. PMID: 24022301 Free PMC article.
55 results