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Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.
Ludwig KU, Roeske D, Herms S, Schumacher J, Warnke A, Plume E, Neuhoff N, Bruder J, Remschmidt H, Schulte-Körne G, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: bruder j. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):503-511. doi: 10.1002/ajmg.b.31007. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19591125
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
Roeske D, Ludwig KU, Neuhoff N, Becker J, Bartling J, Bruder J, Brockschmidt FF, Warnke A, Remschmidt H, Hoffmann P, Müller-Myhsok B, Nöthen MM, Schulte-Körne G. Roeske D, et al. Among authors: bruder j. Mol Psychiatry. 2011 Jan;16(1):97-107. doi: 10.1038/mp.2009.102. Epub 2009 Sep 29. Mol Psychiatry. 2011. PMID: 19786962
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: bruder j. 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: bruder j. 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.
Specific learning disorder: prevalence and gender differences.
Moll K, Kunze S, Neuhoff N, Bruder J, Schulte-Körne G. Moll K, et al. Among authors: bruder j. PLoS One. 2014 Jul 29;9(7):e103537. doi: 10.1371/journal.pone.0103537. eCollection 2014. PLoS One. 2014. PMID: 25072465 Free PMC article.
181 results