Publications of Indra Kraft

Kuhl, U.; Neef, N.; Kraft, I.; Schaadt, G.; Dörr, L.; Brauer, J.; Czepezauer, I.; Müller, B.; Wilcke, A.; Kirsten, H. et al.; Emmrich, F.; Boltze, J.; Friederici, A. D.; Skeide, M. A.: The emergence of dyslexia in the developing brain. NeuroImage 211, 116633 (2020)

Müller, B.; Boltze, J.; Czepezauer, I.; Hesse, V.; LEGASCREEN Consortium; Friederici, A. D.; Emmrich, F.; Brauer, J.; Wilcke, A.; Neef, N. et al.; Boltze, J.; Skeide, M. A.; Kirsten, H.; Schaadt, G.; Müller, B.; Kraft, I.; Czepezauer, I.; Dörr, L.; Wilcke, A.; Kirsten, H.: Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1. Genetics and Molecular Biology 41 (1), pp. 41 - 49 (2018)

Müller, B.; Schaadt, G.; Boltze, J.; Emmrich, F.; LEGASCREEN Consortium; Skeide, M. A.; Neef, N.; Kraft, I.; Brauer, J.; Friederici, A. D. et al.; Kirsten, H.; Wilcke, A.: ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR. Brain and Behavior 7 (11), e00851 (2017)

Neef, N.; Müller, B.; Liebig, J.; Schaadt, G.; Grigutsch, M.; Gunter, T. C.; Wilcke, A.; Kirsten, H.; Skeide, M. A.; Kraft, I. et al.; Kraus, N.; Frank, E.; Brauer, J.; Boltze, J.; Friederici, A. D.: Dyslexia risk gene relates to representation of sound in the auditory brainstem. Developmental Cognitive Neuroscience 24, pp. 63 - 71 (2017)

Kraft, I.; Schreiber, J.; Cafiero, R.; Metere, R.; Schaadt, G.; Brauer, J.; Neef, N.; Müller, B.; Kirsten, H.; Wilcke, A. et al.; Boltze, J.; Friederici, A. D.; Skeide, M. A.: Predicting early signs of dyslexia at a preliterate age by combining behavioral assessment with structural MRI. NeuroImage 143, pp. 378 - 386 (2016)

Skeide, M. A.; Kraft, I.; Müller, B.; Schaadt, G.; Neef, N.; Brauer, J.; Wilcke, A.; Kirsten, H.; Boltze, J.; Friederici, A. D.: NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school. Brain 139 (10), pp. 2792 - 2803 (2016)

Müller, B.; Wilcke, A.; Czepezauer, I.; Ahnert, P.; Boltze, J.; Kirsten, H.; the LEGASCREEN Consortium: Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort. Scientific Reports 6, 27901 (2016)

Kraft, I.; Cafiero, R.; Schaadt, G.; Brauer, J.; Neef, N.; Müller, B.; Kirsten, H.; Wilcke, A.; Boltze, J.; Friederici, A. D. et al.; Skeide, M. A.: Cortical differences in preliterate children at familiar risk of dyslexia are similar to those observed in dyslexic readers. Brain 138 (9), e378 (2015)

Skeide, M. A.; Kirsten, H.; Kraft, I.; Schaadt, G.; Müller, B.; Neef, N.; Brauer, J.; Wilcke, A.; Emmrich, F.; Boltze, J. et al.; Friederici, A. D.: Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in children. NeuroImage 118, pp. 414 - 421 (2015)

Krönke, M.; Kraft, I.; Regenbrecht, F.; Obrig, H.: Lexical learning in mild aphasia: Gesture benefit depends on patholinguistic profile and lesion pattern. Cortex 49 (10), pp. 2637 - 2649 (2013)

Skeide, M. A.; Kirsten, H.; Kraft, I.; Schaadt, G.; Müller, B.; Wilcke, A.; Brauer, J.; Boltze, J.; Friederici, A. D.: Genome-wide supported dyslexia risk variant rs11100040 alters neural connectivity profiles affecting phonological awareness in children. In Frontiers in Human Neuroscience. XII International Conference on Cognitive Neuroscience (ICON-XII), Brisbane, Queensland, Australia, July 27, 2014 - July 31, 2014. Frontiers Research Foundation, Lausanne, Switzerland (2015)

Kraft, I.; Schreiber, J.; Cafiero, R.; Brauer, J.; Friederici, A. D.; Skeide, M. A.: Vorschulkinder mit familiärem Risiko für Entwicklungsdyslexie zeigen neuroanatomische Auffälligkeiten. 12. Tagung der Österreichischen Gesellschaft für Psychologie, Innsbruck, Austria (2016)

Skeide, M. A.; Kraft, I.; Müller, B.; Schaadt, G.; Neef, N.; Brauer, J.; Wilcke, A.; Kirsten, H.; Boltze, J.; Friederici, A. D.: NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school. 50. Kongress der Deutschen Gesellschaft für Psychologie, Leipzig, Germany (2016)

Kraft, I.; Schreiber, J.; Cafiero, R.; Brauer, J.; Friederici, A. D.; Skeide, M. A.: Structural brain differences in pre-reading children are associated with familial risk for dyslexia. 21st Annual Meeting of the Organization for Human Brain Mapping (OHBM), Honolulu, HI, USA (2015)

Kraft, I.; Skeide, M. A.; Cafiero, R.; Brauer, J.; Friederici, A. D.: Reduced cortical thickness in pre-reading children at risk for dyslexia. 4th IMPRS NeuroCom Summer School, London, United Kingdom (2014)

Skeide, M. A.; Kirsten, H.; Kraft, I.; Schaadt, G.; Müller, B.; Brauer, J.; Wilcke, A.; Emmrich, F.; Boltze, J.; Friederici, A. D.: Dyslexia risk variant rs11100040 alters brain connectivity profiles affecting phonological awareness. 12th International Conference on Cognitive Neuroscience (ICON), Brisbane, Australia (2014)

Skeide, M. A.; Kirsten, H.; Kraft, I.; Schaadt, G.; Müller, B.; Brauer, J.; Wilcke, A.; Boltze , J.; Friederici, A. D.: Dyslexia risk variant rs11100040 alters brain connectivity profiles affecting phonological awareness. 20th Annual Meeting of the Organization for Human Brain Mapping (OHBM), Hamburg, Germany (2014)

Kraft, I.; Skeide, M. A.; Brauer, J.; Anwander, A.; Friederici, A. D.: Development of white matter in children with developmental dyslexia. 43rd Annual Meeting of the Society for Neuroscience, San Diego, CA, USA (2013)

Kraft, I.; Skeide, M. A.; Brauer, J.; Anwander, A.; Friederici, A. D.: Development of white matter in children with developmental dyslexia. 5th Annual Neurobiology of Language Conference, San Diego, CA, USA (2013)

Kraft, I.; Skeide, M. A.; Brauer, J.; Anwander, A.; Schaadt, G.; Friederici, A. D.: Development of white matter microstructure in children with developmental dyslexia. 43rd Annual Meeting of the Society for Neuroscience (SfN 2013), San Diego, CA, USA (2013)