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Entries: 1-10  
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Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia
Authors: Neuhoff, N.; Bruder, J.; Bartling, J.; Warnke, A.; Remschmidt, H.; Müller-Myhsok, B.; Schulte-Körne, G.
Date of Publication (YYYY-MM-DD): 2012-05-14
Title of Journal: PLoS ONE
Volume: 7
Issue / Number: 5
Sequence Number of Article: e34909
Document Type: Article
ID: 610899.0
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
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
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
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
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
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
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
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
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
Entries: 1-10  
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