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European Journal of Human Genetics : EJHG|June 4, 2015
High acceptance of an early dyslexia screening test involving genetic analyses in GermanyArndt Wilcke, Bent Müller, Gesa Schaadt, et al.Scientific Reports|June 18, 2016
Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohortBent Müller, Arndt Wilcke, Ivonne Czepezauer, et al.Genetics and Molecular Biology|February 24, 2018
Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1Bent Müller, Johannes Boltze, Ivonne Czepezauer, et al.Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|August 19, 2015
Working-memory endophenotype and dyslexia-associated genetic variant predict dyslexia phenotypeClaudia Männel, Lars Meyer, Arndt Wilcke, et al.Human Genetics|February 4, 2016
Improved prediction of complex diseases by common genetic markers: state of the art and further perspectivesBent Müller, Arndt Wilcke, Anne-Laure Boulesteix, et al.Scientific Reports|August 28, 2019
Combining ZooMS and zooarchaeology to study Late Pleistocene hominin behaviour at Fumane (Italy)Virginie Sinet-Mathiot, Geoff M Smith, Matteo Romandini, et al.Brain : a Journal of Neurology|June 26, 2016
NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before schoolMichael A Skeide, Indra Kraft, Bent Müller, et al.Neuroimage|June 17, 2015
Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in childrenMichael A Skeide, Holger Kirsten, Indra Kraft, et al.Brain and Behavior|December 5, 2017
ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMRBent Müller, Gesa Schaadt, Johannes Boltze, et al.Scientific Reports|May 10, 2020
Non-destructive ZooMS identification reveals strategic bone tool raw material selection by NeandertalsNaomi L Martisius, Frido Welker, Tamara Dogandžić, et al.Pageof 2