| Poly (ADP-ribose) polymerase-2 (PARP-2) is required for efficient base excision DNA repair in association with PARP-1 and XRCC1 V Schreiber, JC Amé, P Dollé, I Schultz, B Rinaldi, V Fraulob, ... Journal of Biological Chemistry 277 (25), 23028-23036, 2002 | 974 | 2002 |
| WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy M Kannan, E Bayam, C Wagner, B Rinaldi, PF Kretz, P Tilly, M Roos, ... Proceedings of the National Academy of Sciences 114 (44), E9308-E9317, 2017 | 102 | 2017 |
| Amphiphysin (BIN1) negatively regulates dynamin 2 for normal muscle maturation BS Cowling, I Prokic, H Tasfaout, A Rabai, F Humbert, B Rinaldi, AS Nicot, ... The Journal of clinical investigation 127 (12), 4477-4487, 2017 | 100 | 2017 |
| NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation CN Castro, M Rosenzwajg, R Carapito, M Shahrooei, M Konantz, A Khan, ... Journal of Experimental Medicine 217 (12), e20192275, 2020 | 98 | 2020 |
| Phosphatase-dead myotubularin ameliorates X-linked centronuclear myopathy phenotypes in mice L Amoasii, DL Bertazzi, H Tronchère, K Hnia, G Chicanne, B Rinaldi, ... Public Library of Science 8 (10), e1002965, 2012 | 69 | 2012 |
| Structure of ad (TGGGGT) quadruplex crystallized in the presence of Li+ ions C Creze, B Rinaldi, R Haser, P Bouvet, P Gouet Biological Crystallography 63 (6), 682-688, 2007 | 62 | 2007 |
| Pkh1/2-dependent phosphorylation of Vps27 regulates ESCRT-I recruitment to endosomes J Morvan, B Rinaldi, S Friant Molecular Biology of the Cell 23 (20), 4054-4064, 2012 | 45 | 2012 |
| Expression of the neuropathy-associated MTMR2 gene rescues MTM1-associated myopathy MA Raess, BS Cowling, DL Bertazzi, C Kretz, B Rinaldi, JM Xuereb, ... Human molecular genetics 26 (19), 3736-3748, 2017 | 35 | 2017 |
| Study of the Plant COPII Vesicle Coat Subunits by Functional Complementation of Yeast Saccharomyces cerevisiae Mutants JO De Craene, F Courte, B Rinaldi, C Fitterer, MC Herranz, ... PloS one 9 (2), e90072, 2014 | 29 | 2014 |
| Mutations in KARS cause a severe neurological and neurosensory disease with optic neuropathy S Scheidecker, S Bär, C Stoetzel, V Geoffroy, B Lannes, B Rinaldi, ... Human Mutation 40 (10), 1826-1840, 2019 | 28 | 2019 |
| Recessive PYROXD1 mutations cause adult-onset limb-girdle-type muscular dystrophy MT Sainio, S Välipakka, B Rinaldi, H Lapatto, A Paetau, S Ojanen, ... Journal of Neurology 266 (2), 353-360, 2019 | 25 | 2019 |
| Lsb1 is a negative regulator of las17 dependent actin polymerization involved in endocytosis M Spiess, JO de Craene, A Michelot, B Rinaldi, A Huber, DG Drubin, ... PLoS One 8 (4), e61147, 2013 | 19 | 2013 |
| A Homozygous Missense Variant in PPP1R1B/DARPP‐32 Is Associated With Generalized Complex Dystonia A Khan, A Molitor, S Mayeur, G Zhang, B Rinaldi, B Lannes, B Lhermitte, ... Movement Disorders 37 (2), 365-374, 2022 | 15 | 2022 |
| Btn3 regulates the endosomal sorting function of the yeast Ent3 epsin, an adaptor for SNARE proteins J Morvan, JO de Craene, B Rinaldi, V Addis, C Misslin, S Friant Journal of cell science 128 (4), 706-716, 2015 | 15 | 2015 |
| Contributions of the RNA-binding and linker domains and RNA structure to the specificity and affinity of the nucleolin RBD12/NRE interaction LD Finger, C Johansson, B Rinaldi, P Bouvet, J Feigon Biochemistry 43 (22), 6937-6947, 2004 | 15 | 2004 |
| Novel MYH10 heterozygous variants associated to a syndrome combining mainly ptosis and ocular coloboma expand the MYH10 related phenotypes S Scheidecker, S Bär, A Kröll-Hermi, C Delvallée, B Rinaldi, A Korpioja, ... European Journal of Human Genetics, 1-10, 2025 | 3 | 2025 |
| Cex1 is a component of the COPI intracellular trafficking machinery L Enkler, B Rinaldi, JO de Craene, P Hammann, O Nureki, B Senger, ... Biology Open 10 (3), bio058528, 2021 | 2 | 2021 |
| Galectin-3 mediated endocytosis of the orphan G-protein-coupled receptor GPRC5A A Boucheham, JM Franco, S Bär, E MacDonald, S Zuttion, L Blagec, ... Cells 14 (19), 1571, 2025 | 1 | 2025 |
| Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome E Bayam, P Tilly, SC Collins, J Rivera Alvarez, M Kannan, L Tonneau, ... EMBO Molecular Medicine 17 (1), 129-168, 2025 | | 2025 |
| Bi-allelic variants in WDR47 lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans E Bayam, P Tilly, SC Collins, JR Alvarez, M Kannan, L Tonneau, B Rinaldi, ... bioRxiv, 2023.12. 22.572779, 2023 | | 2023 |
