| High-quality binary protein interaction map of the yeast interactome network H Yu, P Braun, MA Yıldırım, I Lemmens, K Venkatesan, J Sahalie, ... Science 322 (5898), 104-110, 2008 | 1713 | 2008 |
| Assessing computational tools for the discovery of transcription factor binding sites M Tompa, N Li, TL Bailey, GM Church, B De Moor, E Eskin, AV Favorov, ... Nature biotechnology 23 (1), 137-144, 2005 | 1585 | 2005 |
| An empirical framework for binary interactome mapping K Venkatesan, JF Rual, A Vazquez, U Stelzl, I Lemmens, ... Nature methods 6 (1), 83-90, 2009 | 1025 | 2009 |
| Proto-genes and de novo gene birth AR Carvunis, T Rolland, I Wapinski, MA Calderwood, MA Yildirim, ... Nature 487 (7407), 370-374, 2012 | 621 | 2012 |
| Edgetic perturbation models of human inherited disorders Q Zhong, N Simonis, QR Li, B Charloteaux, F Heuze, N Klitgord, S Tam, ... Molecular systems biology 5 (1), 321, 2009 | 408 | 2009 |
| Literature-curated protein interaction datasets ME Cusick, H Yu, A Smolyar, K Venkatesan, AR Carvunis, N Simonis, ... Nature methods 6 (1), 39-46, 2009 | 366 | 2009 |
| Empirically controlled mapping of the Caenorhabditis elegans protein-protein interactome network N Simonis, JF Rual, AR Carvunis, M Tasan, I Lemmens, ... Nature methods 6 (1), 47-54, 2009 | 338 | 2009 |
| A protein domain-based interactome network for C. elegans early embryogenesis M Boxem, Z Maliga, N Klitgord, N Li, I Lemmens, M Mana, ... Cell 134 (3), 534-545, 2008 | 241 | 2008 |
| Confirmation of organized modularity in the yeast interactome N Bertin, N Simonis, D Dupuy, ME Cusick, JDJ Han, HB Fraser, FP Roth, ... PLoS biology 5 (6), e153, 2007 | 132 | 2007 |
| tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans M Igoillo-Esteve, A Genin, N Lambert, J Desir, I Pirson, B Abdulkarim, ... PLoS genetics 9 (10), e1003888, 2013 | 127 | 2013 |
| Viral perturbations of host networks reflect disease etiology N Gulbahce, H Yan, A Dricot, M Padi, D Byrdsong, R Franchi, DS Lee, ... PLoS computational biology 8 (6), e1002531, 2012 | 120 | 2012 |
| FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly N Simonis, I Migeotte, N Lambert, C Perazzolo, DC de Silva, B Dimitrov, ... Journal of medical genetics 50 (9), 585-592, 2013 | 95 | 2013 |
| Host-pathogen interactome mapping for HTLV-1 and-2 retroviruses N Simonis, JF Rual, I Lemmens, M Boxus, T Hirozane-Kishikawa, ... Retrovirology 9, 1-20, 2012 | 75 | 2012 |
| Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus A Drielsma, C Jalas, N Simonis, J Désir, N Simanovsky, I Pirson, ... Journal of medical genetics 49 (11), 708-712, 2012 | 66 | 2012 |
| Protein interactions of the transcription factor Hoxa1 B Lambert, J Vandeputte, S Remacle, I Bergiers, N Simonis, JC Twizere, ... BMC developmental biology 12, 1-17, 2012 | 62 | 2012 |
| MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43) C Depondt, S Donatello, M Rai, FC Wang, M Manto, N Simonis, ... Neurology: Genetics 2 (5), e94, 2016 | 53 | 2016 |
| Transcriptional regulation of protein complexes in yeast N Simonis, J van Helden, GN Cohen, SJ Wodak Genome biology 5, 1-22, 2004 | 53 | 2004 |
| The transcription factor ERG recruits CCR4–NOT to control mRNA decay and mitotic progression X Rambout, C Detiffe, J Bruyr, E Mariavelle, M Cherkaoui, S Brohée, ... Nature Structural & Molecular Biology 23 (7), 663-672, 2016 | 49 | 2016 |
| PP2A regulatory subunit Bα controls endothelial contractility and vessel lumen integrity via regulation of HDAC7 M Martin, I Geudens, J Bruyr, M Potente, A Bleuart, M Lebrun, N Simonis, ... The EMBO journal 32 (18), 2491-2503, 2013 | 49 | 2013 |
| Autosomal recessive cerebellar ataxia of adult onset due to STUB1 Mutations C Depondt, S Donatello, N Simonis, M Rai, R Van Heurck, M Abramowicz, ... Neurology 82 (19), 1749-1750, 2014 | 47 | 2014 |
