Gerd Schulte -Körne
Gerd Schulte -Körne
Professor für Kinder- und Jugendpsychiatrie und-psychotherapie
Потвърден имейл адрес: med.uni-muenchen.de - Начална страница
Developmental dyslexia in different languages: Language-specific or universal?
JC Ziegler, C Perry, A Ma-Wyatt, D Ladner, G Schulte-Körne
Journal of experimental child psychology 86 (3), 169-193, 2003
Predictors of developmental dyslexia in European orthographies with varying complexity
K Landerl, F Ramus, K Moll, H Lyytinen, PHT Leppänen, K Lohvansuu, ...
Journal of Child Psychology and Psychiatry 54 (6), 686-694, 2013
Auditory processing and dyslexia: evidence for a specific speech processing deficit
G Schulte-Körne, W Deimel, J Bartling, H Remschmidt
Neuroreport 9 (2), 337-340, 1998
Cognitive mechanisms underlying reading and spelling development in five European orthographies
K Moll, F Ramus, J Bartling, J Bruder, S Kunze, N Neuhoff, S Streiftau, ...
Learning and instruction 29, 65-77, 2014
Effectiveness of treatment approaches for children and adolescents with reading disabilities: A meta-analysis of randomized controlled trials
K Galuschka, E Ise, K Krick, G Schulte-Körne
PloS one 9 (2), e89900, 2014
Specific learning disorder: Prevalence and gender differences
K Moll, S Kunze, N Neuhoff, J Bruder, G Schulte-Körne
PLoS one 9 (7), e103537, 2014
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
J Schumacher, H Anthoni, F Dahdouh, IR König, AM Hillmer, N Kluck, ...
The American Journal of Human Genetics 78 (1), 52-62, 2006
Genetics of developmental dyslexia
TS Scerri, G Schulte-Körne
European child & adolescent psychiatry 19 (3), 179-197, 2010
Mental health problems in a school setting in children and adolescents
G Schulte-Körne
Deutsches Ärzteblatt International 113 (11), 183, 2016
Genetics of dyslexia: the evolving landscape
J Schumacher, P Hoffmann, C Schmäl, G Schulte-Körne, MM Nöthen
Journal of medical genetics 44 (5), 289-297, 2007
Evidence for linkage of spelling disability to chromosome 15.
G Schulte-Körne, T Grimm, MM Nöthen, B Müller-Myhsok, S Cichon, ...
American journal of human genetics 63 (1), 279, 1998
Speech perception deficit in dyslexic adults as measured by mismatch negativity (MMN)
G Schulte-Körne, W Deimel, J Bartling, H Remschmidt
International Journal of Psychophysiology 40 (1), 77-87, 2001
Was hilft bei der Lese-Rechtschreibstörung? Ergebnisse einer Metaanalyse zur Wirksamkeit deutschsprachiger Förderansätze
E Ise, RR Engel, G Schulte-Körne
Kindheit und Entwicklung 21 (2), 122-136, 2012
Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high‐functioning level
AK Wermter, I Kamp‐Becker, P Hesse, G Schulte‐Körne, K Strauch, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010
Clinical neurophysiology of visual and auditory processing in dyslexia: a review
G Schulte-Körne, J Bruder
Clinical neurophysiology 121 (11), 1794-1809, 2010
Screening for depression in adolescents: validity of the patient health questionnaire in pediatric care
AK Allgaier, K Pietsch, B Frühe, J Sigl‐Glöckner, G Schulte‐Körne
Depression and anxiety 29 (10), 906-913, 2012
Is the Children's Depression Inventory Short version a valid screening tool in pediatric care? A comparison to its full-length version
AK Allgaier, B Frühe, K Pietsch, B Saravo, M Baethmann, ...
Journal of psychosomatic research 73 (5), 369-374, 2012
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia
AT Pagnamenta, E Bacchelli, MV de Jonge, G Mirza, TS Scerri, F Minopoli, ...
Biological psychiatry 68 (4), 320-328, 2010
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
H Anthoni, M Zucchelli, H Matsson, B Müller-Myhsok, I Fransson, ...
Human molecular genetics 16 (6), 667-677, 2007
The role of phonological awareness, speech perception, and auditory temporal processing for dyslexia
G Schulte-Körne, W Deimel, J Bartling, H Remschmidt
European child & adolescent psychiatry 8 (3), S28-S34, 1999
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