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Page 1
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. Among authors: remschmidt h. 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.
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Körne G, Nöthen MM, Kere J. Schumacher J, et al. Among authors: remschmidt h. Am J Hum Genet. 2006 Jan;78(1):52-62. doi: 10.1086/498992. Epub 2005 Nov 17. Am J Hum Genet. 2006. PMID: 16385449 Free PMC article.
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. Among authors: remschmidt h. 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
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21.
König IR, Schumacher J, Hoffmann P, Kleensang A, Ludwig KU, Grimm T, Neuhoff N, Preis M, Roeske D, Warnke A, Propping P, Remschmidt H, Nöthen MM, Ziegler A, Müller-Myhsok B, Schulte-Körne G. König IR, et al. Among authors: remschmidt h. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):36-43. doi: 10.1002/ajmg.b.31135. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184582
[Genetics of reading-spelling difficulties].
Schulte-Körne G, Remschmidt H, Hebebrand J. Schulte-Körne G, et al. Among authors: remschmidt h. Z Kinder Jugendpsychiatr. 1993 Dec;21(4):242-52. Z Kinder Jugendpsychiatr. 1993. PMID: 8147127 Review. German. No abstract available.
[Diagnosis of reading and spelling disorder].
Schulte-Körne G, Deimel W, Remschmidt H. Schulte-Körne G, et al. Among authors: remschmidt h. Z Kinder Jugendpsychiatr Psychother. 2001 May;29(2):113-6. doi: 10.1024//1422-4917.29.2.113. Z Kinder Jugendpsychiatr Psychother. 2001. PMID: 11393049 German.
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Ludwig KU, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: remschmidt h. Psychiatr Genet. 2008 Dec;18(6):310-2. doi: 10.1097/YPG.0b013e3283063a78. Psychiatr Genet. 2008. PMID: 19018237 Free PMC article.
426 results