| An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita E Zanaria, F Muscatelli, B Bardoni, TM Strom, S Guioli, W Guo, E Lalli, ... Nature 372 (6507), 635-641, 1994 | 1013 | 1994 |
| A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules B Franco, S Guioli, A Pragliola, B Incerti, B Bardoni, R Tonlorenzi, ... Nature 353 (6344), 529-536, 1991 | 980 | 1991 |
| Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism F Muscatelli, TM Strom, AP Walker, E Zanaria, D Récan, A Meindl, ... Nature 372 (6507), 672-676, 1994 | 877 | 1994 |
| A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal B Bardoni, E Zanaria, S Guioli, G Floridia, KC Worley, G Tonini, E Ferrante, ... Nature genetics 7 (4), 497-501, 1994 | 806 | 1994 |
| The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif C Schaeffer, B Bardoni, JL Mandel, B Ehresmann, C Ehresmann, H Moine The EMBO journal, 2001 | 552 | 2001 |
| A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P A Schenck, B Bardoni, A Moro, C Bagni, JL Mandel Proceedings of the National Academy of Sciences 98 (15), 8844-8849, 2001 | 422 | 2001 |
| Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology Y Kim, JY Sung, I Ceglia, KW Lee, JH Ahn, JM Halford, AM Kim, SP Kwak, ... Nature 442 (7104), 814-817, 2006 | 381 | 2006 |
| CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein A Schenck, B Bardoni, C Langmann, N Harden, JL Mandel, A Giangrande Neuron 38 (6), 887-898, 2003 | 368 | 2003 |
| Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. A Ballabio, B Bardoni, R Carrozzo, G Andria, D Bick, L Campbell, ... Proceedings of the National Academy of Sciences 86 (24), 10001-10005, 1989 | 320 | 1989 |
| The Hsp90 chaperone controls the biogenesis of L7Ae RNPs through conserved machinery S Boulon, N Marmier-Gourrier, B Pradet-Balade, L Wurth, C Verheggen, ... The Journal of cell biology 180 (3), 579-595, 2008 | 251 | 2008 |
| A novel function for fragile X mental retardation protein in translational activation EG Bechara, MC Didiot, M Melko, L Davidovic, M Bensaid, P Martin, ... PLoS biology 7 (1), e1000016, 2009 | 245 | 2009 |
| Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles EW Khandjian, ME Huot, S Tremblay, L Davidovic, R Mazroui, B Bardoni Proceedings of the National Academy of Sciences 101 (36), 13357-13362, 2004 | 215 | 2004 |
| A transcriptional silencing domain in DAX-1 whose mutation causes adrenal hypoplasia congenita E Lalli, B Bardoni, E Zazopoulos, JM Wurtz, TM Strom, D Moras, ... Molecular Endocrinology 11 (13), 1950-1960, 1997 | 213 | 1997 |
| FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts M Castets, C Schaeffer, E Bechara, A Schenck, EW Khandjian, S Luche, ... Human Molecular Genetics 14 (6), 835-844, 2005 | 200 | 2005 |
| Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes B Bardoni, JL Mandel Current opinion in genetics & development 12 (3), 284-293, 2002 | 185 | 2002 |
| The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules L Davidovic, XH Jaglin, AM Lepagnol-Bestel, S Tremblay, M Simonneau, ... Human molecular genetics 16 (24), 3047-3058, 2007 | 177 | 2007 |
| Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo EJ Mientjes, R Willemsen, LL Kirkpatrick, IM Nieuwenhuizen, ... Human molecular genetics 13 (13), 1291-1302, 2004 | 172 | 2004 |
| A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein B Bardoni, A Schenck, J Louis Mandel Human molecular genetics 8 (13), 2557-2566, 1999 | 171 | 1999 |
| The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction A Ramos, D Hollingworth, S Adinolfi, M Castets, G Kelly, TA Frenkiel, ... Structure 14 (1), 21-31, 2006 | 146 | 2006 |
| A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis B Bardoni, O Zuffardi, S Guioli, A Ballabio, P Simi, P Cavalli, MG Grimoldi, ... Genomics 11 (2), 443-451, 1991 | 143 | 1991 |
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUVerified email at igbmc.fr
