| EMT as the ultimate survival mechanism of cancer cells N Tiwari, A Gheldof, M Tatari, G Christofori Seminars in cancer biology 22 (3), 194-207, 2012 | 591 | 2012 |
| Cadherins and epithelial-to-mesenchymal transition A Gheldof, G Berx Progress in molecular biology and translational science 116, 317-336, 2013 | 411 | 2013 |
| Identification of a ZEB2-MITF-ZEB1 transcriptional network that controls melanogenesis and melanoma progression G Denecker, N Vandamme, Ö Akay, D Koludrovic, J Taminau, K Lemeire, ... Cell Death & Differentiation 21 (8), 1250-1261, 2014 | 222 | 2014 |
| Evolutionary functional analysis and molecular regulation of the ZEB transcription factors A Gheldof, P Hulpiau, F Van Roy, B De Craene, G Berx Cellular and Molecular Life Sciences 69, 2527-2541, 2012 | 176 | 2012 |
| Differential impact of TGF-β and EGF on fibroblast differentiation and invasion reciprocally promotes colon cancer cell invasion H Denys, L Derycke, A Hendrix, W Westbroek, A Gheldof, K Narine, ... Cancer letters 266 (2), 263-274, 2008 | 109 | 2008 |
| Are AZF b deletions always incompatible with sperm production? K Stouffs, V Vloeberghs, A Gheldof, H Tournaye, S Seneca Andrology 5 (4), 691-694, 2017 | 41 | 2017 |
| Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts L Vandervore, K Stouffs, I Tanyalçin, T Vanderhasselt, F Roelens, ... Journal of medical genetics 54 (6), 432-440, 2017 | 40 | 2017 |
| Sertoli cell-only syndrome: behind the genetic scenes K Stouffs, A Gheldof, H Tournaye, D Vandermaelen, M Bonduelle, ... BioMed Research International 2016, 2016 | 35 | 2016 |
| Clinical implementation of gene panel testing for lysosomal storage diseases A Gheldof, S Seneca, K Stouffs, W Lissens, A Jansen, H Laeremans, ... Molecular genetics & genomic medicine 7 (2), e00527, 2019 | 25 | 2019 |
| Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics L Vandervore, R Schot, E Kasteleijn, R Oegema, K Stouffs, A Gheldof, ... Brain, 2019 | 25 | 2019 |
| Cadherins and epithelial-to-mesenchymal transition. Prog Mol Biol Transl Sci. 2013; 116: 317–336. doi: 10.1016 A Gheldof, G Berx B978-0-12-394311-8.00014-5.[PubMed][Cross Ref], 2013 | 25* | 2013 |
| Genetic diagnosis of subfertility: the impact of meiosis and maternal effects A Gheldof, DJG Mackay, Y Cheong, W Verpoest Journal of Medical Genetics 56 (5), 271-282, 2019 | 16 | 2019 |
| Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations K Stouffs, S Moortgat, T Vanderhasselt, L Vandervore, A Dica, M Mathot, ... European journal of medical genetics 61 (12), 733-737, 2018 | 15 | 2018 |
| Expanding the clinical spectrum of biallelic ZNF335 variants K Stouffs, AB Stergachis, T Vanderhasselt, A Dica, S Janssens, ... Clinical genetics 94 (2), 246-251, 2018 | 15 | 2018 |
| Cadherins and epithelial-to-mesenchymal transition. Prog Mol Biol Transl Sci. 2013; 116: 317–36. doi: 10.1016 A Gheldof, G Berx B978-0-12-394311-8.00014-5, 0 | 14 | |
| Rare genetic variants potentially involved in ovarian hyperstimulation syndrome K Stouffs, S Daelemans, S Santos-Ribeiro, S Seneca, A Gheldof, ... Journal of Assisted Reproduction and Genetics 36, 491-497, 2019 | 13 | 2019 |
| A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development A Van Der Kelen, Ö Okutman, E Javey, M Serdarogullari, C Janssens, ... Human Reproduction Update 29 (2), 218-232, 2023 | 9 | 2023 |
| Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis A Sassi, J Désir, V Janssens, M Marangoni, D Daneels, A Gheldof, ... F&S Reports 1 (3), 193-201, 2020 | 9 | 2020 |
| Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing S Franck, E Couvreu De Deckersberg, JL Bubenik, C Markouli, L Barbé, ... Biology open 11 (1), bio058978, 2022 | 8 | 2022 |
| MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem … S Franck, L Barbé, S Ardui, Y De Vlaeminck, J Allemeersch, D Dziedzicka, ... Human Molecular Genetics 29 (21), 3566-3577, 2020 | 7 | 2020 |
