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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. Among authors: nothen mm. Transl Psychiatry. 2013 Feb 19;3(2):e229. doi: 10.1038/tp.2012.148. Transl Psychiatry. 2013. PMID: 23423138 Free PMC article.
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: nothen mm. 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.
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia.
Schulze TG, Schumacher J, Müller DJ, Krauss H, Alfter D, Maroldt A, Ahle G, Maroldt AO, Novo y Fernández A, Weber T, Held T, Propping P, Maier W, Nöthen MM, Rietschel M. Schulze TG, et al. Among authors: nothen mm. Am J Med Genet. 2001 Aug 8;105(6):498-501. doi: 10.1002/ajmg.1472. Am J Med Genet. 2001. PMID: 11496364
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, Flaquer A, Freudenberg-Hua Y, Jamra RA, Metzen C, Heyn U, Schweiger N, Betz RC, Blaumeiser B, Hampe J, Schreiber S, Schulze TG, Hennies HC, Schumacher J, Propping P, Ruzicka T, Cichon S, Wienker TF, Kruse R, Nothen MM. Hillmer AM, et al. Among authors: nothen mm. Am J Hum Genet. 2005 Jul;77(1):140-8. doi: 10.1086/431425. Epub 2005 May 18. Am J Hum Genet. 2005. PMID: 15902657 Free PMC article.
Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression.
Schumacher J, Jamra RA, Becker T, Ohlraun S, Klopp N, Binder EB, Schulze TG, Deschner M, Schmäl C, Höfels S, Zobel A, Illig T, Propping P, Holsboer F, Rietschel M, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: nothen mm. Biol Psychiatry. 2005 Aug 15;58(4):307-14. doi: 10.1016/j.biopsych.2005.04.006. Biol Psychiatry. 2005. PMID: 16005437
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. Among authors: nothen mm. 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
1,061 results