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21
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
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22
Development of orthographic knowledge in German‐speaking children: a 2‐year longitudinal study
In: Journal of research in reading. - Leeds : Wiley-Blackwell 37 (2014) 3, 233-249
OLC Linguistik
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23
Does sensitivity to orthographic regularities influence reading and spelling acquisition? A 1-year prospective study
In: Reading and writing. - New York, NY : Springer Science+Business Media 27 (2014) 7, 1141-1161
OLC Linguistik
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24
What does the brain of children with developmental dyslexia tell us about reading improvement? ERP evidence from an intervention study
In: Frontiers in Human Neuroscience (2014)
BASE
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25
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
BASE
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26
What does the brain of children with developmental dyslexia tell us about reading improvement? ERP evidence from an intervention study
Hasko, Sandra; Groth, Katarina; Bruder, Jennifer. - : Frontiers Media S.A., 2014
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27
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
Becker, Jessica; Czamara, Darina; Scerri, Tom S. - : Nature Publishing Group, 2014
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28
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
BASE
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29
Predictors of developmental dyslexia in European orthographies with varying complexity.
In: ISSN: 0021-9630 ; EISSN: 1469-7610 ; Journal of Child Psychology and Psychiatry ; https://hal.archives-ouvertes.fr/hal-00965034 ; Journal of Child Psychology and Psychiatry, Wiley, 2013, 54 (6), pp.686-94. ⟨10.1111/jcpp.12029⟩ (2013)
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30
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
In: ISSN: 1018-4813 ; EISSN: 1476-5438 ; European Journal of Human Genetics ; https://hal.archives-ouvertes.fr/hal-00964958 ; European Journal of Human Genetics, Nature Publishing Group, 2013, epub ahead of print. ⟨10.1038/ejhg.2013.199⟩ (2013)
BASE
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31
The time course of reading processes in children with and without dyslexia: an ERP study
In: Frontiers in human neuroscience (2013)
BASE
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32
The time course of reading processes in children with and without dyslexia: an ERP study
Hasko, Sandra; Groth, Katarina; Bruder, Jennifer. - : Frontiers Media S.A., 2013
BASE
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33
Spelling disability - neurophysiologic correlates and intervention
In: Reading, writing, mathematics and the developing brain (Dordrecht, 2012), p. 157-176
MPI für Psycholinguistik
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34
Evidence for the late MMN as a neurophysiological endophenotype for dyslexia.
In: PLOS ONE (2012)
BASE
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35
Evidence for the late MMN as a neurophysiological endophenotype for dyslexia. ...
Neuhoff, Nina; Bruder, Jennifer; Bartling, Jürgen; Warnke, Andreas; Remschmidt, Helmut; Müller-Myhsok, Bertram; Schulte-Körne, Gerd. - : Universitätsbibliothek der Ludwig-Maximilians-Universität München, 2012
Abstract: Dyslexia affects 5-10% of school-aged children and is therefore one of the most common learning disorders. Research on auditory event related potentials (AERP), particularly the mismatch negativity (MMN) component, has revealed anomalies in individuals with dyslexia to speech stimuli. Furthermore, candidate genes for this disorder were found through molecular genetic studies. A current challenge for dyslexia research is to understand the interaction between molecular genetics and brain function, and to promote the identification of relevant endophenotypes for dyslexia. The present study examines MMN, a neurophysiological correlate of speech perception, and its potential as an endophenotype for dyslexia in three groups of children. The first group of children was clinically diagnosed with dyslexia, whereas the second group of children was comprised of their siblings who had average reading and spelling skills and were therefore "unaffected" despite having a genetic risk for dyslexia. The third group consisted ...
Keyword: 610
URL: https://epub.ub.uni-muenchen.de/id/eprint/15574
https://dx.doi.org/10.5282/ubm/epub.15574
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36
Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia
Neuhoff, Nina; Bruder, Jennifer; Bartling, Jürgen. - : Public Library of Science, 2012
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37
The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language
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38
Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia
BASE
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39
Support Systems for Poor Readers: Empirical Data From Six EU Member States
In: ISSN: 0022-2194 ; Journal of Learning Disabilities ; https://hal.archives-ouvertes.fr/hal-01440410 ; Journal of Learning Disabilities, SAGE Publications, 2011, 44 (3), pp.228-245. ⟨10.1177/0022219410374235⟩ (2011)
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40
Slow perceptual processing at the core of developmental dyslexia: A parameter-based assessment of visual attention
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