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Author

Alexander Gheldof

Observed names: A Gheldof, A. Gheldof, Gheldof, Alexander
Observed institutions: Vrije Universiteit Brussel, Ghent University Hospital, Vlaams Instituut voor Biotechnologie, Ghent University, Universitair Ziekenhuis Brussel, VIB-UGent Center for Inflammation Research
ORCID: 0000-0002-8320-1961
Observed ORCID: 0000-0002-8320-1961
OpenAlex ID: A5018216972
EMT as the ultimate survival mechanism of cancer cells
2012 · Neha Tiwari, Alexander Gheldof, et al. · Seminars in Cancer Biology · 538
Cadherins and Epithelial-to-Mesenchymal Transition
2013 · Alexander Gheldof, Geert Berx · Progress in molecular biology and translational science · 375
Identification of a ZEB2-MITF-ZEB1 transcriptional network that controls melanogenesis and melanoma progression
2014 · G Denecker, N Vandamme, et al. · Cell Death and Differentiation · 214
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Evolutionary functional analysis and molecular regulation of the ZEB transcription factors
2012 · Alexander Gheldof, Paco Hulpiau, et al. · Cellular and Molecular Life Sciences · 190
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Differential impact of TGF-β and EGF on fibroblast differentiation and invasion reciprocally promotes colon cancer cell invasion
2008 · Hannelore Denys, Lara Derycke, et al. · Cancer Letters · 90
Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts
2017 · Laura Vandervore, Katrien Stouffs, et al. · Journal of Medical Genetics · 49
A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development
2022 · Annelore Van Der Kelen, Özlem Okutman, et al. · Human Reproduction Update · 46
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Sertoli Cell-Only Syndrome: Behind the Genetic Scenes
2016 · Katrien Stouffs, Alexander Gheldof, et al. · BioMed Research International · 44
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Are AZF b deletions always incompatible with sperm production?
2017 · K. Stouffs, V. Vloeberghs, et al. · Andrology · 41
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Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics
2019 · Laura V Vandervore, Rachel Schot, et al. · Brain · 38
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Clinical implementation of gene panel testing for lysosomal storage diseases
2018 · Alexander Gheldof, Sara Seneca, et al. · Molecular Genetics & Genomic Medicine · 36
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Genetic diagnosis of subfertility: the impact of meiosis and maternal effects
2019 · Alexander Gheldof, Deborah J G Mackay, et al. · Journal of Medical Genetics · 19
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Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients
2024 · Nathalie Smeets, Alexander Gheldof, et al. · Pediatric Neurology · 17
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Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis
2020 · Asma Sassi, Julie Désir, et al. · F&S Reports · 16
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Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder
2022 · Nuno Maia, Sven Potelle, et al. · The American Journal of Human Genetics · 15
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Rare genetic variants potentially involved in ovarian hyperstimulation syndrome
2018 · Katrien Stouffs, Sari Daelemans, et al. · Journal of Assisted Reproduction and Genetics · 15
Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations
2018 · Katrien Stouffs, Stéphanie Moortgat, et al. · European Journal of Medical Genetics · 15
Expanding the clinical spectrum of biallelic ZNF335 variants
2018 · K. Stouffs, A.B. Stergachis, et al. · Clinical Genetics · 15
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Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm
2021 · C. Markouli, E. Couvreu De Deckersberg, et al. · Scientific Reports · 13
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The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres
2022 · Luca Persani, Martine Cools, et al. · Endocrine Connections · 12
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Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing
2022 · Silvie Franck, Edouard Couvreu De Deckersberg, et al. · Biology Open · 11
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MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells
2020 · Silvie Franck, Lise Barbé, et al. · Human Molecular Genetics · 11
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I-PV: a CIRCOS module for interactive protein sequence visualization
2015 · Ibrahim Tanyalcin, Carla Al Assaf, et al. · Bioinformatics · 7
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Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants
2025 · Annelore Van Der Kelen, Sophie Uyttebroeck, et al. · Journal of Assisted Reproduction and Genetics · 6
Development and validation of a high-throughput screening pipeline of compound libraries to target EMT
2025 · Sven Jonckheere, Joachim Taminau, et al. · Cell Death and Differentiation · 5
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Works count: 63
Citation count: 1,865
H-index: 15
I10-index: 22
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