| Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018 | 601 | 2018 |
| Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity GA Cox, NM Cole, K Matsumura, SF Phelps, SD Hauschka, KP Campbell, ... Nature 364 (6439), 725-729, 1993 | 377 | 1993 |
| Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice GA Cox, CM Lutz, CL Yang, D Biemesderfer, RT Bronson, A Fu, ... Cell 91 (1), 139-148, 1997 | 323 | 1997 |
| An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model KL Seburn, LA Nangle, GA Cox, P Schimmel, RW Burgess Neuron 51 (6), 715-726, 2006 | 277 | 2006 |
| Postmortem cortex samples identify distinct molecular subtypes of ALS: retrotransposon activation, oxidative stress, and activated glia OH Tam, NV Rozhkov, R Shaw, D Kim, I Hubbard, S Fennessey, N Propp, ... Cell reports 29 (5), 1164-1177. e5, 2019 | 239 | 2019 |
| Forced expression of dystrophin deletion constructs reveals structure-function correlations. JA Rafael, GA Cox, K Corrado, D Jung, KP Campbell, JS Chamberlain The Journal of cell biology 134 (1), 93-102, 1996 | 231 | 1996 |
| New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin GA Cox, SF Phelps, VM Chapman, JS Chamberlain Nature genetics 4 (1), 87-93, 1993 | 231 | 1993 |
| Spontaneous mutations in the mouse Sharpin gene result in multiorgan inflammation, immune system dysregulation and dermatitis RE Seymour, MG Hasham, GA Cox, LD Shultz, H Hogenesch, ... Genes & Immunity 8 (5), 416-421, 2007 | 226 | 2007 |
| Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy GA Cox, Y Sunada, KP Campbell, JS Chamberlain Nature genetics 8 (4), 333-339, 1994 | 226 | 1994 |
| Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency M Ho, CM Post, LR Donahue, HGW Lidov, RT Bronson, H Goolsby, ... Human molecular genetics 13 (18), 1999-2010, 2004 | 225 | 2004 |
| The histone deacetylase HDAC4 connects neural activity to muscle transcriptional reprogramming TJ Cohen, DS Waddell, T Barrientos, Z Lu, G Feng, GA Cox, SC Bodine, ... Journal of Biological Chemistry 282 (46), 33752-33759, 2007 | 221 | 2007 |
| Effect of genetic background on the dystrophic phenotype in mdx mice WD Coley, L Bogdanik, MC Vila, Q Yu, JH Van Der Meulen, ... Human molecular genetics 25 (1), 130-145, 2016 | 206 | 2016 |
| Gait analysis detects early changes in transgenic SOD1 (G93A) mice CM Wooley, RB Sher, A Kale, WN Frankel, GA Cox, KL Seburn Muscle & Nerve: Official Journal of the American Association of …, 2005 | 205 | 2005 |
| The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titin SM Garvey, C Rajan, AP Lerner, WN Frankel, GA Cox Genomics 79 (2), 146-149, 2002 | 177 | 2002 |
| Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking S Hadano, SC Benn, S Kakuta, A Otomo, K Sudo, R Kunita, ... Human molecular genetics 15 (2), 233-250, 2006 | 169 | 2006 |
| Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders W Zhang, L Zhang, B Liang, D Schroeder, Z Zhang, GA Cox, Y Li, DT Lin Nature neuroscience 19 (4), 557-559, 2016 | 165 | 2016 |
| Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele GA Cox, CL Mahaffey, WN Frankel Neuron 21 (6), 1327-1337, 1998 | 156 | 1998 |
| A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis S Mitsuhashi, A Ohkuma, B Talim, M Karahashi, T Koumura, C Aoyama, ... The American Journal of Human Genetics 88 (6), 845-851, 2011 | 146 | 2011 |
| Development-on-chip: in vitro neural tube patterning with a microfluidic device CJ Demers, P Soundararajan, P Chennampally, GA Cox, J Briscoe, ... Development 143 (11), 1884-1892, 2016 | 140 | 2016 |
| The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development GA Cox, CL Mahaffey, A Nystuen, VA Letts, WN Frankel Nature genetics 26 (2), 198-202, 2000 | 138 | 2000 |
