Gérald Bussy

Epigenetic Modification of the <i>FMR1</i> Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

Sébastien Jacquemont, Aurore Curie, Vincent des Portes et al. · Science Translational Medicine · 2011 · 610 citations

The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males

David Germanaud, Massimiliano Rossi, Gérald Bussy et al. · Clinical Genetics · 2010 · 48 citations

Elderly Patients, Genetics, Genetic Epidemiology +18

Clinical and neurocognitive characterization of a family with a novel <i>MED12</i> gene frameshift mutation

Gaëtan Lesca, Marie‐Pierre Moizard, Gérald Bussy et al. · American Journal of Medical Genetics Part A · 2013 · 40 citations · Full text

Childhood apraxia of speech without intellectual deficit in a patient with cri du chat syndrome

Stéphanie Marignier, Gaëtan Lesca, Jessica Marguin et al. · European Journal of Medical Genetics · 2012 · 40 citations

Implicit procedural learning in fragile X and Down syndrome

Gérald Bussy, E. Charrin, Aurore Curie et al. · Journal of Intellectual Disability Research · 2011 · 31 citations