Karen Hollanders

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 · 623 citations · Full text

Severe Mental Retardation, Mendelian Disorder, Psychiatry +12

Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of<i>XLMR</i>genes

Guy Froyen, Hilde Van Esch, Marijke Bauters et al. · Human Mutation · 2007 · 175 citations

High Resolution, Genetics, Pathology +18

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

Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

Hilde Van Esch, Karen Hollanders, Liesbeth Badisco et al. · Human Molecular Genetics · 2005 · 114 citations · Full text

Chromatin, Mendelian Disorder, Major Role +15

The Effect of AMA0428, a Novel and Potent ROCK Inhibitor, in a Model of Neovascular Age-Related Macular Degeneration

Karen Hollanders, Tine Van Bergen, Nadège Kindt et al. · Investigative Ophthalmology & Visual Science · 2015 · 48 citations