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Entries: 1-10  
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The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language
Authors: Anthoni, H.; Sucheston, L. E.; Lewis, B. A.; Tapia-Paez, I.; Fan, X. T.; Zucchelli, M.; Taipale, M.; Stein, C. M.; Hokkanen, M. E.; Castren, E.; Pennington, B. F.; Smith, S. D.; Olson, R. K.; Tomblin, J. B.; Schulte-Körne, G.; Nöthen, M.; Schumacher, J.; Müller-Myhsok, B.; Hoffmann, P.; Gilger, J. W.; Hynd, G. W.; Nopola-Hemmi, J.; Leppanen, P. H. T.; Lyytinen, H.; Schoumans, J.; Nordenskjöld, M.; Spencer, J.; Stanic, D.; Boon, W. C.; Simpson, E.; Mäkelä, S.; Gustafsson, J. A.; Peyrard-Janvid, M.; Iyengar, S.; Kere, J.
Date of Publication (YYYY-MM-DD): 2012-07
Title of Journal: Behavior Genetics
Volume: 42
Issue / Number: 4
Start Page: 509
End Page: 527
Document Type: Article
ID: 610861.0
Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling
Authors: Becker, J.; Czamara, D.; Hoffmann, P.; Landerl, K.; Blomert, L.; Brandeis, D.; Vaessen, A.; Maurer, U.; Moll, K.; Ludwig, K. U.; Müller-Myhsok, B.; Nöthen, M. M.; Schulte-Körne, G.; Schumacher, J.
Date of Publication (YYYY-MM-DD): 2012-07
Title of Journal: Translational Psychiatry
Volume: 2
Sequence Number of Article: e136
Document Type: Article
ID: 614738.0
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
Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia
Authors: Czamara, D.; Bruder, J.; Becker, J.; Bartling, J.; Hoffmann, P.; Ludwig, K. U.; Müller-Myhsok, B.; Schulte-Körne, G.
Date of Publication (YYYY-MM-DD): 2011-01
Title of Journal: Behavior Genetics
Volume: 41
Issue / Number: 1
Start Page: 110
End Page: 119
Document Type: Article
ID: 562709.0
Brain gene interactions in dyslexia
Authors: Schulte-Körne, G.; Bruder, J.; Neuhoff, N.; Roeske, D.; Hoffmann, P.; Ludwig, K.; Nöthen, M. M.; Müller-Myhsok, B.
Date of Publication (YYYY-MM-DD): 2010-09
Title of Journal: International Journal of Psychophysiology
Volume: 77
Issue / Number: 3
Start Page: 229
End Page: 230
Document Type: Article
ID: 521005.0
Supporting evidence for LRRTM1 imprinting effects in schizophrenia
Authors: Ludwig, K. U.; Mattheisen, M.; Mühleisen, T. W.; Roeske, D.; Schmäl, C.; Breuer, R.; Schulte-Körne, G.; Müller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P.; Rietschel, M.; Cichon, S.
Date of Publication (YYYY-MM-DD): 2009-08
Title of Journal: Molecular Psychiatry
Volume: 14
Issue / Number: 8
Start Page: 743
End Page: 745
Document Type: Article
ID: 433942.0
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
Entries: 1-10  
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