Neuhoff, N., J. Bruder, J. Bartling, A. Warnke, H. Remschmidt, B. Müller-Myhsok and G. Schulte-Körne: Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia. In: PLoS ONE 7, 5, Seq. No.: e34909 (2012).
König, I. R., J. Schumacher, P. Hoffmann, A. Kleensang, K. U. Ludwig, T. Grimm, N. Neuhoff, M. Preis, D. Roeske, A. Warnke, P. Propping, H. Remschmidt, M. M. Nöthen, A. Ziegler, B. Müller-Myhsok and G. Schulte-Körne: Mapping for Dyslexia and Related Cognitive Trait Loci Provides Strong Evidence for Further Risk Genes on Chromosome 6p21. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 156B, 1, 36-43 (2011).
Roeske, D., K. U. Ludwig, N. Neuhoff, J. Becker, J. Bartling, J. Bruder, F. F. Brockschmidt, A. Warnke, H. Remschmidt, P. Hoffmann, B. Müller-Myhsok, M. M. Nöthen and G. Schulte-Körne: First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. In: Molecular Psychiatry 16, 1, 97-107 (2011).
Dittmann, R. W., E. Meyer, F. J. Freisleder, H. Remschmidt, C. Mehler-Wex, J. Junghanss, U. Hagenah, M. Schulte-Markwort, F. Poustka, E. Schulz, M. Kluge, A. Mastele, P. M. Wehmeier and M. H. Schmidt: Olanzapine in Male and Female Adolescent Patients With Schizophrenia and Related Disorders Minor Sex Differences in Outcomes. In: Journal of Clinical Psychopharmacology 30, 3, 328-331 (2010).
Ludwig, K. U., D. Roeske, S. Herms, J. Schumacher, A. Warnke, E. Plume, N. Neuhoff, J. Bruder, H. Remschmidt, G. Schulte-Korne, B. Müller-Myhsok, M. M. Nöthen and P. Hoffmann: Variation in GRIN2B Contributes to Weak Performance in Verbal Short-Term Memory in Children With Dyslexia. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 153B, 2, 503-511 (2010).
Dahdouh, F., H. Anthoni, I. Tapia-Paez, M. Peyrard-Janvid, G. Schulte-Körne, A. Warnke, H. Remschmidt, A. Ziegler, J. Kere, B. Müller-Myhsok, M. M. Nöthen, J. Schumacher and M. Zucchelli: Further evidence for DYX1C1 as a susceptibility factor for dyslexia. In: Psychiatric Genetics 19, 2, 59-63 (2009).
Ludwig, K. U., J. Schumacher, G. Schulte-Körne, I. R. König, A. Warnke, E. Plume, H. Anthoni, M. Peyrard-Janvid, H. Meng, A. Ziegler, H. Remschmidt, J. Kere, J. R. Gruen, B. Mueller-Myhsok, M. M. Nöthen and P. Hoffmann: Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. In: Psychiatric Genetics 18, 6, 310-312 (2008).
Ludwig, K. U., D. Roeske, J. Schumacher, G. Schulte-Körne, I. R. König, A. Warnke, E. Plume, A. Ziegler, H. Remschmidt, B. Müller-Myhsok, M. M. Nöthen and P. Hoffmann: Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. In: Journal of Neural Transmission 115, 11, 1587-1589 (2008).
Theisen, F. M., S. Beyenburg, S. Gebhardt, M. Kluge, W. F. Blum, H. Remschmidt, C. E. Elger and J. Hebebrand: A prospective study of body weight and serum leptin levels in patients treated with topiramate. In: Clinical Neuropharmacology 31, 4, 226-230 (2008).
Friedel, S., K. Saar, S. Sauer, A. Dempfle, S. Walitza, T. Renner, M. Romanos, C. Freitag, C. Seitz, H. Palmason, A. Scherag, C. Windemuth-Kieselbach, B. G. Schimmelmann, C. Wewetzer, J. Meyer, A. Warnke, K. P. Lesch, R. Reinhardt, B. Herpertz-Dahlmann, M. Linder, A. Hinney, H. Remschmidt, H. Schäfer, K. Konrad, N. Hübner and J. Hebebrand: Association and linkage of allelic variants of the dopamine transporter gene in ADHD. In: Molecular Psychiatry 12, 10, 923-933 (2007).
doi: 10.1038/sj.mp.4001986
url: http://www.nature.com/mp/journal/v12/n10/pdf/4001986a.pdf
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