| Genes and molecular pathways underpinning ciliopathies JF Reiter, MR Leroux Nature reviews Molecular cell biology 18 (9), 533-547, 2017 | 1272 | 2017 |
| Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene JB Li, JM Gerdes, CJ Haycraft, Y Fan, TM Teslovich, H May-Simera, H Li, ... Cell 117 (4), 541-552, 2004 | 865 | 2004 |
| Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome SJ Ansley, JL Badano, OE Blacque, J Hill, BE Hoskins, CC Leitch, ... Nature 425 (6958), 628-633, 2003 | 827 | 2003 |
| The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4 JA Sayer, EA Otto, JF O'Toole, G Nurnberg, MA Kennedy, C Becker, ... Nature genetics 38 (6), 674-681, 2006 | 729 | 2006 |
| Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates AJ Ross, H May-Simera, ER Eichers, M Kai, J Hill, DJ Jagger, CC Leitch, ... Nature genetics 37 (10), 1135-1140, 2005 | 673 | 2005 |
| The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization JF Reiter, OE Blacque, MR Leroux EMBO reports 13 (7), 608-618, 2012 | 534 | 2012 |
| MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis CL Williams, C Li, K Kida, PN Inglis, S Mohan, L Semenec, NJ Bialas, ... Journal of Cell Biology 192 (6), 1023-1041, 2011 | 508 | 2011 |
| The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression JC Kim, JL Badano, S Sibold, MA Esmail, J Hill, BE Hoskins, CC Leitch, ... Nature genetics 36 (5), 462-470, 2004 | 458 | 2004 |
| Functional coordination of intraflagellar transport motors G Ou, O E. Blacque, JJ Snow, MR Leroux, JM Scholey Nature 436 (7050), 583-587, 2005 | 450 | 2005 |
| Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport OE Blacque, MJ Reardon, C Li, J McCarthy, MR Mahjoub, SJ Ansley, ... Genes & development 18 (13), 1630-1642, 2004 | 449 | 2004 |
| Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome Y Fan, MA Esmail, SJ Ansley, OE Blacque, K Boroevich, AJ Ross, ... Nature genetics 36 (9), 989-993, 2004 | 387 | 2004 |
| Structure of the molecular chaperone prefoldin: unique interaction of multiple coiled coil tentacles with unfolded proteins R Siegert, MR Leroux, C Scheufler, FU Hartl, I Moarefi Cell 103 (4), 621-632, 2000 | 370 | 2000 |
| Functional genomics of the cilium, a sensory organelle OE Blacque, EA Perens, KA Boroevich, PN Inglis, C Li, A Warner, ... Current Biology 15 (10), 935-941, 2005 | 324 | 2005 |
| Structure-function studies on small heat shock protein oligomeric assembly and interaction with unfolded polypeptides MR Leroux, R Melki, B Gordon, G Batelier, EPM Candido Journal of Biological Chemistry 272 (39), 24646-24656, 1997 | 302 | 1997 |
| Piecing together a ciliome PN Inglis, KA Boroevich, MR Leroux TRENDS in Genetics 22 (9), 491-500, 2006 | 269 | 2006 |
| The sensory cilia of Caenorhabditis elegans. PN Inglis, G Ou, MR Leroux, JM Scholey WormBook, 1, 2007 | 264 | 2007 |
| Compartmentation of protein folding in vivo: sequestration of non‐native polypeptide by the chaperonin–GimC system K Siegers, T Waldmann, MR Leroux, K Grein, A Shevchenko, E Schiebel, ... The EMBO journal, 1999 | 264 | 1999 |
| Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet–Biedl patients with two mutations at a second BBS locus JL Badano, JC Kim, BE Hoskins, RA Lewis, SJ Ansley, DJ Cutler, ... Human molecular genetics 12 (14), 1651-1659, 2003 | 240 | 2003 |
| Analysis of xbx genes in C. elegans E Efimenko, K Bubb, HY Mak, T Holzman, MR Leroux, G Ruvkun, ... Oxford University Press for The Company of Biologists Limited 132 (8), 1923-1934, 2005 | 238 | 2005 |
| Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans J Halbritter, AA Bizet, M Schmidts, JD Porath, DA Braun, HY Gee, ... The American Journal of Human Genetics 93 (5), 915-925, 2013 | 236 | 2013 |
