Deletions and loss-of-function variants in TP63 associated with orofacial clefting.
European journal of human genetics : EJHG
Authors:
Kriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, Jakob Gebel, Christina Fagerberg, Ellen van Beusekom, Ellen van Binsbergen, Ozan Topaloglu, Marloes Steehouwer, Christian Gilissen, Nina Ishorst, Iris A L M van Rooij, Nel Roeleveld, Kaare Christensen, Joseph Schoenaers, Stefaan Bergé, Jeffrey C Murray, Greet Hens, Koen Devriendt, Kerstin U Ludwig, Elisabeth Mangold, Alexander Hoischen, Huiqing Zhou, Volker Dötsch, Carine E L Carels, Hans van Bokhoven
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Translational psychiatry
Authors:
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U Ludwig, Darina Czamara, Beate St Pourcain, William Brandler, Ferenc Honbolygó, Dénes Tóth, Valéria Csépe, Guillaume Huguet, Andrew P Morris, Jacqueline Hulslander, Erik G Willcutt, John C DeFries, Richard K Olson, Shelley D Smith, Bruce F Pennington, Anniek Vaessen, Urs Maurer, Heikki Lyytinen, Myriam Peyrard-Janvid, Paavo H T Leppänen, Daniel Brandeis, Milene Bonte, John F Stein, Joel B Talcott, Fabien Fauchereau, Arndt Wilcke, Clyde Francks, Thomas Bourgeron, Anthony P Monaco, Franck Ramus, Karin Landerl, Juha Kere, Thomas S Scerri, Silvia Paracchini, Simon E Fisher, Johannes Schumacher, Markus M Nöthen, Bertram Müller-Myhsok, Gerd Schulte-Körne
Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate.
Epigenomics
Authors:
Laurence J Howe, Tom G Richardson, Ryan Arathimos, Lucas Alvizi, Maria R Passos-Bueno, Philip Stanier, Ellen Nohr, Kerstin U Ludwig, Elisabeth Mangold, Michael Knapp, Evie Stergiakouli, Beate St Pourcain, George Davey Smith, Jonathan Sandy, Caroline L Relton, Sarah J Lewis, Gibran Hemani, Gemma C Sharp