| Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ... autophagy 17 (1), 1-382, 2021 | 10709 | 2021 |
| Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31 P Mburu, M Mustapha, A Varela, D Weil, A El-Amraoui, RH Holme, ... Nature genetics 34 (4), 421-428, 2003 | 371 | 2003 |
| Excretion of ammonium by a nifL mutant of Azotobacter vinelandii fixing nitrogen A Bali, G Blanco, S Hill, C Kennedy Applied and Environmental Microbiology 58 (5), 1711-1718, 1992 | 168 | 1992 |
| The kyphoscoliosis (ky) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific protein G Blanco, GR Coulton, A Biggin, C Grainge, J Moss, M Barrett, A Berquin, ... Human molecular genetics 10 (1), 9-16, 2001 | 119 | 2001 |
| Sequence and molecular analysis of the nifL gene of Azotobacter vinelandii G Blanco, M Drummond, P Woodley, C Kennedy Molecular microbiology 9 (4), 869-879, 1993 | 110 | 1993 |
| The product of the nitrogen fixation regulatory gene nfrX of Azotobacter vinelandii is functionally and structurally homologous to the uridylyltransferase encoded by glnD in … A Contreras, M Drummond, A Bali, G Blanco, E Garcia, G Bush, ... Journal of bacteriology 173 (24), 7741-7749, 1991 | 67 | 1991 |
| Filamin C interacts with the muscular dystrophy KY protein and is abnormally distributed in mouse KY deficient muscle fibres J Beatham, R Romero, SKM Townsend, T Hacker, PFM van der Ven, ... Human molecular genetics 13 (22), 2863-2874, 2004 | 64 | 2004 |
| Mapping of the human and murine X11-like genes (APBA2 and apba2), the murine Fe65 gene (Apbb1), and the human Fe65-like gene (APBB2): genes encoding phosphotyrosine-binding … G Blanco, NG Irving, SDM Brown, CCJ Miller, DM McLoughlin Mammalian genome 9 (6), 473-475, 1998 | 55 | 1998 |
| Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1 J Baker, G Riley, MR Romero, AR Haynes, H Hilton, M Simon, J Hancock, ... Experimental cell research 316 (11), 1856-1870, 2010 | 43 | 2010 |
| Identification of an operon involved in the assimilatory nitrate‐reducing system of Azotobacter vineiandii F Ramos, G Blanco, JC Gutiérrez, F Luque, M Tortolero Molecular microbiology 8 (6), 1145-1153, 1993 | 42 | 1993 |
| Disrupted autophagy undermines skeletal muscle adaptation and integrity EJ Jokl, G Blanco Mammalian Genome 27, 525-537, 2016 | 40 | 2016 |
| The CLE53–SUNN genetic pathway negatively regulates arbuscular mycorrhiza root colonization in Medicago truncatula M Karlo, C Boschiero, KG Landerslev, GS Blanco, J Wen, KS Mysore, ... Journal of Experimental Botany 71 (16), 4972-4984, 2020 | 38 | 2020 |
| Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion N Vasli, E Harris, J Karamchandani, E Bareke, J Majewski, NB Romero, ... Brain 140 (1), 37-48, 2017 | 38 | 2017 |
| Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region T Joensuu, G Blanco, L Pakarinen, P Sistonen, H Kääriäinen, S Brown, ... Genomics 38 (3), 255-263, 1996 | 38 | 1996 |
| Axonal and neuromuscular synaptic phenotypes in WldS, SOD1G93A and ostes mutant mice identified by fiber-optic confocal microendoscopy F Wong, L Fan, S Wells, R Hartley, FE Mackenzie, O Oyebode, R Brown, ... Molecular and Cellular Neuroscience 42 (4), 296-307, 2009 | 35 | 2009 |
| Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis S Corrochano, R Männikkö, PI Joyce, P McGoldrick, J Wettstein, G Lassi, ... Brain 137 (12), 3171-3185, 2014 | 30 | 2014 |
| Candidate testis‐determining gene, Maestro (Mro), encodes a novel HEAT repeat protein L Smith, N Van Hateren, J Willan, R Romero, G Blanco, P Siggers, ... Developmental dynamics: an official publication of the American Association …, 2003 | 30 | 2003 |
| Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse FE Mackenzie, R Romero, D Williams, T Gillingwater, H Hilton, J Dick, ... Human molecular genetics 18 (19), 3553-3566, 2009 | 28 | 2009 |
| Reaching and grasping phenotypes in the mouse (Mus musculus): a characterization of inbred strains and mutant lines V Tucci, F Achilli, G Blanco, HV Lad, S Wells, S Godinho, PM Nolan Neuroscience 147 (3), 573-582, 2007 | 25 | 2007 |
| IGFN1_v1 is required for myoblast fusion and differentiation X Li, J Baker, T Cracknell, AR Haynes, G Blanco PLoS One 12 (6), e0180217, 2017 | 23 | 2017 |
Richard RibchesterEmeritus Professor of Cellular Neuroscience, Edinburgh UniversityVerified email at ed.ac.uk
