| PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences M Lescot, P Déhais, G Thijs, K Marchal, Y Moreau, Y Van de Peer, ... Nucleic acids research 30 (1), 325-327, 2002 | 4577 | 2002 |
| BioMart and Bioconductor: a powerful link between biological databases and microarray data analysis S Durinck, Y Moreau, A Kasprzyk, S Davis, B De Moor, A Brazma, ... Bioinformatics 21 (16), 3439-3440, 2005 | 1850 | 2005 |
| DECIPHER: database of chromosomal imbalance and phenotype in humans using ensembl resources HV Firth, SM Richards, AP Bevan, S Clayton, M Corpas, D Rajan, ... The American Journal of Human Genetics 84 (4), 524-533, 2009 | 1703 | 2009 |
| Gene prioritization through genomic data fusion S Aerts, D Lambrechts, S Maity, P Van Loo, B Coessens, F De Smet, ... Nature biotechnology 24 (5), 537-544, 2006 | 1078 | 2006 |
| A human phenome-interactome network of protein complexes implicated in genetic disorders K Lage, EO Karlberg, ZM Størling, PI Olason, AG Pedersen, O Rigina, ... Nature biotechnology 25 (3), 309-316, 2007 | 1047 | 2007 |
| Chromosome instability is common in human cleavage-stage embryos E Vanneste, T Voet, C Le Caignec, M Ampe, P Konings, C Melotte, ... Nature medicine 15 (5), 577, 2009 | 891 | 2009 |
| A higher-order background model improves the detection of promoter regulatory elements by Gibbs sampling G Thijs, M Lescot, K Marchal, S Rombauts, B De Moor, P Rouze, ... Bioinformatics 17 (12), 1113-1122, 2001 | 548 | 2001 |
| A Gibbs sampling method to detect over-represented motifs in the upstream regions of co-expressed genes G Thijs, K Marchal, M Lescot, S Rombauts, B De Moor, P Rouzé, ... Proceedings of the fifth annual international conference on Computational …, 2001 | 500 | 2001 |
| Computational tools for prioritizing candidate genes: boosting disease gene discovery Y Moreau, LC Tranchevent Nature Reviews Genetics 13 (8), 523-536, 2012 | 495 | 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 | 457 | 2006 |
| Predicting the prognosis of breast cancer by integrating clinical and microarray data with Bayesian networks O Gevaert, FD Smet, D Timmerman, Y Moreau, BD Moor Bioinformatics 22 (14), e184-e190, 2006 | 438 | 2006 |
| Versatile gene-specific sequence tags for Arabidopsis functional genomics: transcript profiling and reverse genetics applications P Hilson, J Allemeersch, T Altmann, S Aubourg, A Avon, J Beynon, ... Genome research 14 (10b), 2176-2189, 2004 | 380 | 2004 |
| An expanded evaluation of protein function prediction methods shows an improvement in accuracy Y Jiang, TR Oron, WT Clark, AR Bankapur, D D’Andrea, R Lepore, ... Genome biology 17 (1), 1-19, 2016 | 366 | 2016 |
| Biclustering microarray data by Gibbs sampling Q Sheng, Y Moreau, B De Moor Bioinformatics 19 (suppl_2), ii196-ii205, 2003 | 306 | 2003 |
| From hype to reality: data science enabling personalized medicine H Fröhlich, R Balling, N Beerenwinkel, O Kohlbacher, S Kumar, ... BMC medicine 16 (1), 1-15, 2018 | 289 | 2018 |
| Adaptive quality-based clustering of gene expression profiles F De Smet, J Mathys, K Marchal, G Thijs, B De Moor, Y Moreau Bioinformatics 18 (5), 735-746, 2002 | 277 | 2002 |
| Optimized data fusion for kernel k-means clustering S Yu, L Tranchevent, X Liu, W Glanzel, JAK Suykens, B De Moor, ... IEEE Transactions on Pattern Analysis and Machine Intelligence 34 (5), 1031-1039, 2011 | 273 | 2011 |
| E ndeavour update: a web resource for gene prioritization in multiple species LC Tranchevent, R Barriot, S Yu, S Van Vooren, P Van Loo, B Coessens, ... Nucleic acids research 36 (suppl_2), W377-W384, 2008 | 272 | 2008 |
| 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 | 259 | 2006 |
| Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome JKJ Van Houdt, BA Nowakowska, SB Sousa, BDC Van Schaik, ... Nature genetics 44 (4), 445-449, 2012 | 255 | 2012 |
