| Enterotypes of the human gut microbiome M Arumugam, J Raes, E Pelletier, D Le Paslier, T Yamada, DR Mende, ... nature 473 (7346), 174-180, 2011 | 5424 | 2011 |
| The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored D Szklarczyk, A Franceschini, M Kuhn, M Simonovic, A Roth, P Minguez, ... Nucleic acids research 39 (suppl_1), D561-D568, 2010 | 3183 | 2010 |
| STRING 8—a global view on proteins and their functional interactions in 630 organisms LJ Jensen, M Kuhn, M Stark, S Chaffron, C Creevey, J Muller, T Doerks, ... Nucleic acids research 37 (suppl_1), D412-D416, 2009 | 2367 | 2009 |
| The ecoresponsive genome of Daphnia pulex JK Colbourne, ME Pfrender, D Gilbert, WK Thomas, A Tucker, TH Oakley, ... Science 331 (6017), 555-561, 2011 | 1142 | 2011 |
| eggNOG v3. 0: orthologous groups covering 1133 organisms at 41 different taxonomic ranges S Powell, D Szklarczyk, K Trachana, A Roth, M Kuhn, J Muller, R Arnold, ... Nucleic acids research 40 (D1), D284-D289, 2012 | 504 | 2012 |
| eggNOG: automated construction and annotation of orthologous groups of genes LJ Jensen, P Julien, M Kuhn, C von Mering, J Muller, T Doerks, P Bork Nucleic acids research 36 (suppl_1), D250-D254, 2007 | 390 | 2007 |
| BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus C Stoetzel, V Laurier, EE Davis, J Muller, S Rix, JL Badano, CC Leitch, ... Nature genetics 38 (5), 521-524, 2006 | 295 | 2006 |
| Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome C Stoetzel, J Muller, V Laurier, EE Davis, NA Zaghloul, S Vicaire, ... The American Journal of Human Genetics 80 (1), 1-11, 2007 | 261 | 2007 |
| eggNOG v2. 0: extending the evolutionary genealogy of genes with enhanced non-supervised orthologous groups, species and functional annotations J Muller, D Szklarczyk, P Julien, I Letunic, A Roth, M Kuhn, S Powell, ... Nucleic acids research 38 (suppl_1), D190-D195, 2010 | 248 | 2010 |
| Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing C Redin, B Gérard, J Lauer, Y Herenger, J Muller, A Quartier, ... Journal of medical genetics 51 (11), 724-736, 2014 | 205 | 2014 |
| DPY19L2 deletion as a major cause of globozoospermia I Koscinski, E ElInati, C Fossard, C Redin, J Muller, JV de la Calle, ... The American Journal of Human Genetics 88 (3), 344-350, 2011 | 162 | 2011 |
| PipeAlign: A new toolkit for protein family analysis F Plewniak, L Bianchetti, Y Brelivet, A Carles, F Chalmel, O Lecompte, ... Nucleic acids research 31 (13), 3829-3832, 2003 | 139 | 2003 |
| Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18) S Scheidecker, C Etard, NW Pierce, V Geoffroy, E Schaefer, J Muller, ... Journal of medical genetics 51 (2), 132-136, 2014 | 129 | 2014 |
| Orthology prediction methods: a quality assessment using curated protein families K Trachana, TA Larsson, S Powell, WH Chen, T Doerks, J Muller, P Bork Bioessays 33 (10), 769-780, 2011 | 129 | 2011 |
| Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes C Redin, S Le Gras, O Mhamdi, V Geoffroy, C Stoetzel, MC Vincent, ... Journal of medical genetics 49 (8), 502-512, 2012 | 117 | 2012 |
| Sequence and comparative genomic analysis of actin-related proteins J Muller, Y Oma, L Vallar, E Friederich, O Poch, B Winsor Molecular biology of the cell 16 (12), 5736-5748, 2005 | 115 | 2005 |
| Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease J Muller, C Stoetzel, MC Vincent, CC Leitch, V Laurier, JM Danse, S Helle, ... Human genetics 127 (5), 583-593, 2010 | 105 | 2010 |
| Next generation sequencing for molecular diagnosis of neuromuscular diseases N Vasli, J Böhm, S Le Gras, J Muller, C Pizot, B Jost, A Echaniz-Laguna, ... Acta neuropathologica 124 (2), 273-283, 2012 | 95 | 2012 |
| Alström Syndrome: Mutation Spectrum of ALMS1 JD Marshall, J Muller, GB Collin, G Milan, SF Kingsmore, D Dinwiddie, ... Human mutation 36 (7), 660-668, 2015 | 88 | 2015 |
| Mutations in SDCCAG8/NPHP10 cause Bardet-Biedl syndrome and are associated with penetrant renal disease and absent polydactyly E Schaefer, A Zaloszyc, J Lauer, M Durand, F Stutzmann, ... Molecular syndromology 1 (6), 273-281, 2010 | 88 | 2010 |
Olivier POCHVerified email at unistra.fr
