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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


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