Fraunhofer-Gesellschaft

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Hier finden Sie wissenschaftliche Publikationen aus den Fraunhofer-Instituten.
2017ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR
Müller, Bent; Schaadt, Gesa; Boltze, Johannes; Emmrich, Frank; Skeide, Michael A.; Neef, Nicole; Kraft, Indra; Brauer, Jens; Friederici, Angela D.; Kirsten, Holger; Wilcke, Arndt
Journal Article
2015Childhood asthma is associated with mutations and gene expression differences of ORMDL genes that can interact
Toncheva, A.A.; Potaczek, D.P.; Schedel, M.; Gersting, S.W.; Michel, S.; Krajnov, N.; Gaertner, V.D.; Klingbeil, J.M.; Illig, T.; Franke, A.; Winkler, Carla; Hohlfeld, Jens M.; Vogelberg, C.; Berg, A. von; Bufe, A.; Heinzmann, A.; Laub, O.; Rietschel, E.; Simma, B.; Genuneit, J.; Muntau, A.C.; Kabesch, Michael
Journal Article
2014Genetic risk variants for dyslexia on chromosome 18 in a german cohort
Müller, Bent; Ahnert, Peter; Burkhardt, Jana; Brauer, J.; Czepezauer, Ivonne; Quente, Elfi; Boltze, Johannes; Wilcke, Arndt; Kirsten, Holger
Journal Article
2010Commentary on "Investigations of somatic NKX2-5 mutations in congenital heart disease (CHD)"
Reamon-Buettner, S.M.; Borlak, J.
Journal Article