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Hier finden Sie wissenschaftliche Publikationen aus den Fraunhofer-Instituten.
2020Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; St Pourcain, Beate; 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, Milente; 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
Zeitschriftenaufsatz
2019Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; Pourcain, Beate; Brandler, William; Honbolygó, Ferenc; Tóth, Dénes; Csépe, Valéria; Huguet, Guillaume; Morris, Andrew P.; Hulslander, Jaqueline; 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
Zeitschriftenaufsatz
2018Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis
Kirsten, Holger; Rosendahl, Jonas; Seltsam, Katharina; Zimmer, Constantin; Beer, Sebastian; Masson, Emmanuelle; Chen, Jian-Min; Ruffert, Claudia; Lichtner, Peter K.; Laumen, Helmut; Weiss, Frank Ulrich; Kovacs, Peter; Hegyi, Eszter; Algül, Hana; Bühler, Florence; Bruno, Marco J.; Bugert, Peter; Burkhardt, R.; Cavestro, Giulia Martina; Cichoż-Lach, Halina; Farré, Antoni; Frank, Josef; Gambaro, Giovanni; Gimpfl, Sebastian; Grallert, Harald; Griesmann, Heidi; Grützmann, Robert; Hellerbrand, Claus; Hegyi, Péter P.; Hollenbach, Marcus; Iordache, Sevastitia; Jurkowska, Graźyna E.; Keim, Volker; Kiefer, Falk; Krug, Sebastian; Landt, Olfert; Leo, Milena Di; Lerch, Markus M.; Lévy, Philippe L.; Loeffler, Markus; Löhr, Matthias; Ludwig, Maren; Macek, Milan; Malats, Núria; Małecka-Panas, Ewa I.A.; Malerba, Giovanni; Mann, Karl H.; Mayerle, Julia V.; Mohr, Sonja; Te Morsche, René H.M.; Motyka, Marie; Mueller, Sebastian; Müller, Thomas F.; Nöthen, Markus M.; Pedrazzoli, Sergio; Pereira, Stephen P.; Pete
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