| The dynamics of genome-wide DNA methylation reprogramming in mouse primordial germ cells S Seisenberger, S Andrews, F Krueger, J Arand, J Walter, F Santos, ... Molecular cell 48 (6), 849-862, 2012 | 735 | 2012 |
| Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of … B Menten, N Maas, B Thienpont, K Buysse, J Vandesompele, C Melotte, ... Journal of medical genetics 43 (8), 625-633, 2006 | 440 | 2006 |
| Phenotype molding of stromal cells in the lung tumor microenvironment D Lambrechts, E Wauters, B Boeckx, S Aibar, D Nittner, O Burton, ... Nature medicine 24 (8), 1277-1289, 2018 | 380 | 2018 |
| Tumour hypoxia causes DNA hypermethylation by reducing TET activity B Thienpont, J Steinbacher, H Zhao, F D’Anna, A Kuchnio, A Ploumakis, ... Nature 537 (7618), 63-68, 2016 | 326 | 2016 |
| Inhibition of the glycolytic activator PFKFB3 in endothelium induces tumor vessel normalization, impairs metastasis, and improves chemotherapy AR Cantelmo, LC Conradi, A Brajic, J Goveia, J Kalucka, A Pircher, ... Cancer cell 30 (6), 968-985, 2016 | 269 | 2016 |
| Single-cell chromosomal imbalances detection by array CGH C Le Caignec, C Spits, K Sermon, M De Rycke, B Thienpont, S Debrock, ... Nucleic acids research 34 (9), e68-e68, 2006 | 242 | 2006 |
| A single-cell transcriptome atlas of the aging Drosophila brain K Davie, J Janssens, D Koldere, M De Waegeneer, U Pech, Ł Kreft, ... Cell 174 (4), 982-998. e20, 2018 | 241 | 2018 |
| Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients B Thienpont, L Mertens, T de Ravel, B Eyskens, D Boshoff, N Maas, ... European heart journal 28 (22), 2778-2784, 2007 | 204 | 2007 |
| Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing A Sifrim, MP Hitz, A Wilsdon, J Breckpot, SH Al Turki, B Thienpont, ... Nature genetics 48 (9), 1060-1065, 2016 | 185 | 2016 |
| The role of fatty acid β-oxidation in lymphangiogenesis BW Wong, X Wang, A Zecchin, B Thienpont, I Cornelissen, J Kalucka, ... Nature 542 (7639), 49-54, 2017 | 147 | 2017 |
| Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH) NMC Maas, G Van Buggenhout, F Hannes, B Thienpont, D Sanlaville, ... Journal of medical genetics 45 (2), 71-80, 2008 | 129 | 2008 |
| Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1 KB Meyer, M O’Reilly, K Michailidou, S Carlebur, SL Edwards, JD French, ... The American Journal of Human Genetics 93 (6), 1046-1060, 2013 | 118 | 2013 |
| Rare variants in NR2F2 cause congenital heart defects in humans S Al Turki, AK Manickaraj, CL Mercer, SS Gerety, MP Hitz, S Lindsay, ... The American Journal of Human Genetics 94 (4), 574-585, 2014 | 116 | 2014 |
| Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation M Ghoussaini, SL Edwards, K Michailidou, S Nord, R Cowper-Sal, ... Nature communications 5, 4999, 2014 | 107 | 2014 |
| Single-Cell Transcriptome Atlas of Murine Endothelial Cells J Kalucka, LPMH de Rooij, J Goveia, K Rohlenova, SJ Dumas, E Meta, ... Cell 180 (4), 764-779. e20, 2020 | 93 | 2020 |
| Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects J Breckpot, B Thienpont, H Peeters, T de Ravel, A Singer, M Rayyan, ... The Journal of pediatrics 156 (5), 810-817. e4, 2010 | 87 | 2010 |
| Subtelomeric imbalances in phenotypically normal individuals I Balikova, B Menten, T de Ravel, C Le Caignec, B Thienpont, M Urbina, ... Human mutation 28 (10), 958-967, 2007 | 80 | 2007 |
| HIF-1α promotes glutamine-mediated redox homeostasis and glycogen-dependent bioenergetics to support postimplantation bone cell survival S Stegen, N van Gastel, G Eelen, B Ghesquière, F D’Anna, B Thienpont, ... Cell metabolism 23 (2), 265-279, 2016 | 76 | 2016 |
| Haploinsufficiency of TAB2 causes congenital heart defects in humans B Thienpont, L Zhang, AV Postma, J Breckpot, LC Tranchevent, ... The American Journal of Human Genetics 86 (6), 839-849, 2010 | 71 | 2010 |
| Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects J Breckpot, B Thienpont, Y Arens, LC Tranchevent, JR Vermeesch, ... Cytogenetic and genome research 135 (3-4), 251-259, 2011 | 68 | 2011 |
joris vermeeschVerified email at uzleuven.be
