Guy Froyen
Jessa Hospital(BE)Hasselt University(BE)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Cancer Genomics and Diagnostics, Genomics and Rare Diseases, RNA modifications and cancer
Most-Cited Works
- → Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males(2005)624 cited
- → X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2015)302 cited
- → Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia(2007)276 cited
- → Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation(2008)217 cited
- → Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins(2014)194 cited
- → Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage ofXLMRgenes(2007)175 cited