Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort

por Müller, Bent, Wilcke, Arndt, Czepezauer, Ivonne, Ahnert, Peter, Boltze, Johannes, Kirsten, Holger
Publicado 2016

Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1

por Müller, Bent, Boltze, Johannes, Czepezauer, Ivonne, Hesse, Volker, Wilcke, Arndt, Kirsten, Holger
Publicado 2018

Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives

por Müller, Bent, Wilcke, Arndt, Boulesteix, Anne-Laure, Brauer, Jens, Passarge, Eberhard, Boltze, Johannes, Kirsten, Holger
Publicado 2016

Combining ZooMS and zooarchaeology to study Late Pleistocene hominin behaviour at Fumane (Italy)

por Sinet-Mathiot, Virginie, Smith, Geoff M., Romandini, Matteo, Wilcke, Arndt, Peresani, Marco, Hublin, Jean-Jacques, Welker, Frido
Publicado 2019

ATP2C2 and DYX1C1 are putative modulators of dyslexia‐related MMR

por Müller, Bent, Schaadt, Gesa, Boltze, Johannes, Emmrich, Frank, Skeide, Michael A., Neef, Nicole E., Kraft, Indra, Brauer, Jens, Friederici, Angela D., Kirsten, Holger, Wilcke, Arndt
Publicado 2017

Non-destructive ZooMS identification reveals strategic bone tool raw material selection by Neandertals

por Martisius, Naomi L., Welker, Frido, Dogandžić, Tamara, Grote, Mark N., Rendu, William, Sinet-Mathiot, Virginie, Wilcke, Arndt, McPherron, Shannon J. P., Soressi, Marie, Steele, Teresa E.
Publicado 2020

Dyslexia risk gene relates to representation of sound in the auditory brainstem

por Neef, Nicole E., Müller, Bent, Liebig, Johanna, Schaadt, Gesa, Grigutsch, Maren, Gunter, Thomas C., Wilcke, Arndt, Kirsten, Holger, Skeide, Michael A., Kraft, Indra, Kraus, Nina, Emmrich, Frank, Brauer, Jens, Boltze, Johannes, Friederici, Angela D.
Publicado 2017

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

por Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Brandler, William, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd
Publicado 2019

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

por Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, Pourcain, Beate St, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Müller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd
Publicado 2020