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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. Transl Psychiatry. 2013 Feb 19;3(2):e229. doi: 10.1038/tp.2012.148. Transl Psychiatry. 2013. PMID: 23423138 Free PMC article.
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Matsson H, Huss M, Persson H, Einarsdottir E, Tiraboschi E, Nopola-Hemmi J, Schumacher J, Neuhoff N, Warnke A, Lyytinen H, Schulte-Körne G, Nöthen MM, Leppänen PH, Peyrard-Janvid M, Kere J. Matsson H, et al. J Hum Genet. 2015 Jul;60(7):399-401. doi: 10.1038/jhg.2015.37. Epub 2015 Apr 16. J Hum Genet. 2015. PMID: 25877001 Free PMC article.
Supporting evidence for LRRTM1 imprinting effects in schizophrenia.
Ludwig KU, Mattheisen M, Mühleisen TW, Roeske D, Schmäl C, Breuer R, Schulte-Körne G, Müller-Myhsok B, Nöthen MM, Hoffmann P, Rietschel M, Cichon S. Ludwig KU, et al. Mol Psychiatry. 2009 Aug;14(8):743-5. doi: 10.1038/mp.2009.28. Mol Psychiatry. 2009. PMID: 19626025 No abstract available.
Linkage analyses of chromosomal region 18p11-q12 in dyslexia.
Schumacher J, König IR, Plume E, Propping P, Warnke A, Manthey M, Duell M, Kleensang A, Repsilber D, Preis M, Remschmidt H, Ziegler A, Nöthen MM, Schulte-Körne G. Schumacher J, et al. J Neural Transm (Vienna). 2006 Mar;113(3):417-23. doi: 10.1007/s00702-005-0336-y. Epub 2005 Aug 3. J Neural Transm (Vienna). 2006. PMID: 16075186
Interrelationship and familiality of dyslexia related quantitative measures.
Schulte-Körne G, Ziegler A, Deimel W, Schumacher J, Plume E, Bachmann C, Kleensang A, Propping P, Nöthen MM, Warnke A, Remschmidt H, König IR. Schulte-Körne G, et al. Ann Hum Genet. 2007 Mar;71(Pt 2):160-75. doi: 10.1111/j.1469-1809.2006.00312.x. Epub 2006 Oct 13. Ann Hum Genet. 2007. PMID: 17038000
Evidence for linkage of spelling disability to chromosome 15.
Schulte-Körne G, Grimm T, Nöthen MM, Müller-Myhsok B, Cichon S, Vogt IR, Propping P, Remschmidt H. Schulte-Körne G, et al. Am J Hum Genet. 1998 Jul;63(1):279-82. doi: 10.1086/301919. Am J Hum Genet. 1998. PMID: 9634517 Free PMC article. No abstract available.
224 results