Karen Govaerts

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 · 216 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Nonrecurrent <i>MECP2</i> duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair

Marijke Bauters, Hilde Van Esch, Michael J. Friez et al. · Genome Research · 2008 · 128 citations · Full text

Dna Damage, Genetics, Genomic Mechanism +21

Dosage-Dependent Severity of the Phenotype in Patients with Mental Retardation Due to a Recurrent Copy-Number Gain at Xq28 Mediated by an Unusual Recombination

Joke Vandewalle, Hilde Van Esch, Karen Govaerts et al. · The American Journal of Human Genetics · 2009 · 84 citations · Full text

Recurrent Copy-number Gain, Mendelian Disorder, Genetic Disorder +8

Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

Guy Froyen, Marijke Bauters, Jackie Boyle et al. · Human Genetics · 2007 · 48 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Novel <i>PORCN</i> mutations in focal dermal hypoplasia

Guy Froyen, Karen Govaerts, Hilde Van Esch et al. · Clinical Genetics · 2009 · 23 citations

Mendelian Disorder, Genetic Disorder, Genetics +11