| 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 | 8821 | 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 | 3972 | 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 | 2970 | 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 | 1443 | 2011 |
| Functional and Evolutionary Insights from the Genomes of Three Parasitoid Nasonia Species JH Werren, S Richards, CA Desjardins, O Niehuis, J Gadau, ... Science 327 (5963), 343-348, 2010 | 943 | 2010 |
| 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 | 636 | 2007 |
| 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 | 634 | 2012 |
| 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 | 352 | 2006 |
| AnnotSV: an integrated tool for structural variations annotation V Geoffroy, Y Herenger, A Kress, C Stoetzel, A Piton, H Dollfus, J Muller Bioinformatics 34 (20), 3572-3574, 2018 | 348 | 2018 |
| 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 | 303 | 2014 |
| 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 | 300 | 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 | 296 | 2010 |
| 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 | 232 | 2011 |
| 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 | 172 | 2014 |
| 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 | 166 | 2015 |
| 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 | 155 | 2011 |
| 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 Hellé, ... Human genetics 127, 583-593, 2010 | 153 | 2010 |
| 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 | 150 | 2005 |
| 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 | 147 | 2003 |
| Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family O Okutman, J Muller, Y Baert, M Serdarogullari, M Gultomruk, A Piton, ... Human molecular genetics 24 (19), 5581-5588, 2015 | 141 | 2015 |
Olivier POCHCSTB ICube UMR7357Verified email at unistra.fr
