| Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ... New England Journal of Medicine 359 (16), 1685-1699, 2008 | 736 | 2008 |
| LNCipedia: a database for annotated human lncRNA transcript sequences and structures PJ Volders, K Helsens, X Wang, B Menten, L Martens, K Gevaert, ... Nucleic acids research 41 (D1), D246-D251, 2013 | 482 | 2013 |
| 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 | 442 | 2006 |
| A link between host plant adaptation and pesticide resistance in the polyphagous spider mite Tetranychus urticae W Dermauw, N Wybouw, S Rombauts, B Menten, J Vontas, M Grbić, ... Proceedings of the National Academy of Sciences 110 (2), E113-E122, 2013 | 298 | 2013 |
| Extending the phenotype of recurrent rearrangements of 16p11. 2: deletions in mentally retarded patients without autism and in normal individuals EK Bijlsma, ACJ Gijsbers, JHM Schuurs-Hoeijmakers, A Van Haeringen, ... European journal of medical genetics 52 (2-3), 77-87, 2009 | 272 | 2009 |
| Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome BWM Van Bon, HC Mefford, B Menten, DA Koolen, AJ Sharp, ... Journal of medical genetics 46 (8), 511-523, 2009 | 266 | 2009 |
| Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms WP Kloosterman, M Tavakoli-Yaraki, MJ Van Roosmalen, ... Cell reports 1 (6), 648-655, 2012 | 194 | 2012 |
| Fourteen new cases contribute to the characterization of the 7q11. 23 microduplication syndrome N Van der Aa, L Rooms, G Vandeweyer, J van den Ende, E Reyniers, ... European journal of medical genetics 52 (2-3), 94-100, 2009 | 191 | 2009 |
| Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis JR Vermeesch, C Melotte, G Froyen, S Van Vooren, B Dutta, N Maas, ... Journal of Histochemistry & Cytochemistry 53 (3), 413-422, 2005 | 186 | 2005 |
| The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies C Redin, H Brand, RL Collins, T Kammin, E Mitchell, JC Hodge, ... Nature genetics 49 (1), 36-45, 2017 | 177 | 2017 |
| An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours P Mestdagh, E Fredlund, F Pattyn, A Rihani, T Van Maerken, J Vermeulen, ... Oncogene 29 (24), 3583-3592, 2010 | 146 | 2010 |
| Targeted expression of mutated ALK induces neuroblastoma in transgenic mice LC Heukamp, T Thor, A Schramm, K De Preter, C Kumps, B De Wilde, ... Science translational medicine 4 (141), 141ra91-141ra91, 2012 | 143 | 2012 |
| The H3K27me3 demethylase UTX is a gender-specific tumor suppressor in T-cell acute lymphoblastic leukemia J Van der Meulen, V Sanghvi, K Mavrakis, K Durinck, F Fang, ... Blood 125 (1), 13-21, 2015 | 142 | 2015 |
| Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus G Beunders, E Voorhoeve, C Golzio, LM Pardo, JA Rosenfeld, ... The American Journal of Human Genetics 92 (2), 210-220, 2013 | 124 | 2013 |
| Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience K Buysse, B Delle Chiaie, R Van Coster, B Loeys, A De Paepe, G Mortier, ... European journal of medical genetics 52 (6), 398-403, 2009 | 109 | 2009 |
| Alternative routes to induce naive pluripotency in human embryonic stem cells G Duggal, S Warrier, S Ghimire, D Broekaert, M Van der Jeught, ... Stem cells 33 (9), 2686-2698, 2015 | 108 | 2015 |
| arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays B Menten, F Pattyn, K De Preter, P Robbrecht, E Michels, K Buysse, ... BMC bioinformatics 6 (1), 1-9, 2005 | 106 | 2005 |
| Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening B D'haene, C Attanasio, D Beysen, J Dostie, E Lemire, P Bouchard, ... PLoS Genet 5 (6), e1000522, 2009 | 104 | 2009 |
| Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly DA Braun, J Rao, G Mollet, D Schapiro, MC Daugeron, W Tan, ... Nature genetics 49 (10), 1529, 2017 | 96 | 2017 |
| Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy R Kopajtich, TJ Nicholls, J Rorbach, MD Metodiev, P Freisinger, H Mandel, ... The American Journal of Human Genetics 95 (6), 708-720, 2014 | 93 | 2014 |
Jo Vandesompeleprofessor in functional cancer genomics and applied bioinformaticsVerified email at ugent.be
