Guy Froyen

Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males

Hilde Van Esch, Marijke Bauters, Jaakko Ignatius et al. · The American Journal of Human Genetics · 2005 · 627 citations · Full text

Life Sciences, Neurology, Neuroscience +14

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hao Hu, Stefan A. Haas, Jamel Chelly et al. · Molecular Psychiatry · 2015 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia

Idoya Lahortiga, Kim De Keersmaecker, Pieter Van Vlierberghe et al. · Nature Genetics · 2007 · 276 citations

Medicine, Genetics, Molecular Genetics +11

Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation

Guy Froyen, Mark Corbett, Joke Vandewalle et al. · The American Journal of Human Genetics · 2008 · 220 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

Shai Carmi, Ken Hui, Ethan Kochav et al. · Nature Communications · 2014 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16