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Mapping for Dyslexia and Related Cognitive Trait Loci Provides Strong Evidence for Further Risk Genes on Chromosome 6p21 |
Authors: König, I. R.; Schumacher, J.; Hoffmann, P.; Kleensang, A.; Ludwig, K. U.; Grimm, T.; Neuhoff, N.; Preis, M.; Roeske, D.; Warnke, A.; Propping, P.; Remschmidt, H.; Nöthen, M. M.; Ziegler, A.; Müller-Myhsok, B.; Schulte-Körne, G. | Date of Publication (YYYY-MM-DD): 2011-01 | Title of Journal: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics | Volume: 156B | Issue / Number: 1 | Start Page: 36 | End Page: 43 | Document Type: Article | ID: 529176.0 |
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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children |
Authors: Roeske, D.; Ludwig, K. U.; Neuhoff, N.; Becker, J.; Bartling, J.; Bruder, J.; Brockschmidt, F. F.; Warnke, A.; Remschmidt, H.; Hoffmann, P.; Müller-Myhsok, B.; Nöthen, M. M.; Schulte-Körne, G. | Date of Publication (YYYY-MM-DD): 2011-01 | Title of Journal: Molecular Psychiatry | Volume: 16 | Issue / Number: 1 | Start Page: 97 | End Page: 107 | Document Type: Article | ID: 529186.0 |
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Variation in GRIN2B Contributes to Weak Performance in Verbal Short-Term Memory in Children With Dyslexia |
Authors: Ludwig, K. U.; Roeske, D.; Herms, S.; Schumacher, J.; Warnke, A.; Plume, E.; Neuhoff, N.; Bruder, J.; Remschmidt, H.; Schulte-Korne, G.; Müller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P. | Date of Publication (YYYY-MM-DD): 2010-03 | Title of Journal: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics | Volume: 153B | Issue / Number: 2 | Start Page: 503 | End Page: 511 | Document Type: Article | ID: 475342.0 |
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Exploring the genetic link between RLS and ADHD |
Authors: Schimmelmann, B. G.; Friedel, S.; Nguyen, T. T.; Sauer, S.; Ganz Vogel, C. I.; Konrad, K.; Wilhelm, C.; Sinzig, J.; Renner, T. J.; Romanos, M.; Palmason, H.; Dempfle, A.; Walitza, S.; Freitag, C.; Meyer, J.; Linder, M.; Schäfer, H.; Warnke, A.; Lesch, K. P.; Herpertz-Dahlman, B.; Hinney, A.; Hebebrand, J. | Date of Publication (YYYY-MM-DD): 2009-07 | Title of Journal: Journal of Psychiatric Research | Volume: 43 | Issue / Number: 10 | Start Page: 941 | End Page: 945 | Document Type: Article | ID: 457532.0 |
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Further evidence for DYX1C1 as a susceptibility factor for dyslexia |
Authors: Dahdouh, F.; Anthoni, H.; Tapia-Paez, I.; Peyrard-Janvid, M.; Schulte-Körne, G.; Warnke, A.; Remschmidt, H.; Ziegler, A.; Kere, J.; Müller-Myhsok, B.; Nöthen, M. M.; Schumacher, J.; Zucchelli, M. | Date of Publication (YYYY-MM-DD): 2009-04 | Title of Journal: Psychiatric Genetics | Volume: 19 | Issue / Number: 2 | Start Page: 59 | End Page: 63 | Document Type: Article | ID: 429204.0 |
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Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample |
Authors: Ludwig, K. U.; Schumacher, J.; Schulte-Körne, G.; König, I. R.; Warnke, A.; Plume, E.; Anthoni, H.; Peyrard-Janvid, M.; Meng, H.; Ziegler, A.; Remschmidt, H.; Kere, J.; Gruen, J. R.; Mueller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P. | Date of Publication (YYYY-MM-DD): 2008-12 | Title of Journal: Psychiatric Genetics | Volume: 18 | Issue / Number: 6 | Start Page: 310 | End Page: 312 | Document Type: Article | ID: 396556.0 |
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Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample |
Authors: Ludwig, K. U.; Roeske, D.; Schumacher, J.; Schulte-Körne, G.; König, I. R.; Warnke, A.; Plume, E.; Ziegler, A.; Remschmidt, H.; Müller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P. | Date of Publication (YYYY-MM-DD): 2008-11 | Title of Journal: Journal of Neural Transmission | Volume: 115 | Issue / Number: 11 | Start Page: 1587 | End Page: 1589 | Document Type: Article | ID: 395629.0 |
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Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21 |
Authors: Schumacher, J.; König, I. R.; Schröder, T.; Duell, M.; Plume, E.; Propping, P.; Warnke, A.; Libertus, C.; Ziegler, A.; Müller-Myhsok, B.; Schulte-Korne, G.; Nöthen, M. M. | Date of Publication (YYYY-MM-DD): 2008-06 | Title of Journal: Psychiatric Genetics | Volume: 18 | Issue / Number: 3 | Start Page: 137 | End Page: 142 | Document Type: Article | ID: 379932.0 |
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Association and linkage of allelic variants of the dopamine transporter gene in ADHD |
Authors: Friedel, S.; Saar, K.; Sauer, S.; Dempfle, A.; Walitza, S.; Renner, T.; Romanos, M.; Freitag, C.; Seitz, C.; Palmason, H.; Scherag, A.; Windemuth-Kieselbach, C.; Schimmelmann, B. G.; Wewetzer, C.; Meyer, J.; Warnke, A.; Lesch, K. P.; Reinhardt, R.; Herpertz-Dahlmann, B.; Linder, M.; Hinney, A.; Remschmidt, H.; Schäfer, H.; Konrad, K.; Hübner, N.; Hebebrand, J. | Date of Publication (YYYY-MM-DD): 2007-10 | Title of Journal: Molecular Psychiatry | Volume: 12 | Issue / Number: 10 | Start Page: 923 | End Page: 933 | Document Type: Article | ID: 334133.0 |
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