| Dystrophin: the protein product of the Duchenne muscular dystrophy locus EP Hoffman, RH Brown Jr, LM Kunkel Cell 51 (6), 919-928, 1987 | 5679 | 1987 |
| Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals M Koenig, EP Hoffman, CJ Bertelson, AP Monaco, C Feener, LM Kunkel Cell 50 (3), 509-517, 1987 | 3097 | 1987 |
| Conversion of mdx myofibres from dystrophin-negative to-positive by injection of normal myoblasts TA Partridge, JE Morgan, GR Coulton, EP Hoffman, LM Kunkel Nature 337 (6203), 176-179, 1989 | 1111 | 1989 |
| Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy EP Hoffman, KH Fischbeck, RH Brown, M Johnson, R Medori, JD Loire, ... New England Journal of Medicine 318 (21), 1363-1368, 1988 | 1081 | 1988 |
| Multiple-laboratory comparison of microarray platforms RA Irizarry, D Warren, F Spencer, IF Kim, S Biswal, BC Frank, ... Nature methods 2 (5), 345-350, 2005 | 1074 | 2005 |
| Glucose restriction inhibits skeletal myoblast differentiation by activating SIRT1 through AMPK-mediated regulation of Nampt M Fulco, Y Cen, P Zhao, EP Hoffman, MW McBurney, AA Sauve, ... Developmental cell 14 (5), 661-673, 2008 | 924 | 2008 |
| Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface E Bonilla, CE Samitt, AF Miranda, AP Hays, G Salviati, S DiMauro, ... Cell 54 (4), 447-452, 1988 | 768 | 1988 |
| Sir2 regulates skeletal muscle differentiation as a potential sensor of the redox state M Fulco, RL Schiltz, S Iezzi, MT King, P Zhao, Y Kashiwaya, E Hoffman, ... Molecular cell 12 (1), 51-62, 2003 | 745 | 2003 |
| Variability in muscle size and strength gain after unilateral resistance training MJ Hubal, H Gordish-Dressman, PD Thompson, TB Price, EP Hoffman, ... Medicine & science in sports & exercise 37 (6), 964-972, 2005 | 685 | 2005 |
| Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiology YW Chen, P Zhao, R Borup, EP Hoffman The Journal of cell biology 151 (6), 1321-1336, 2000 | 583 | 2000 |
| Molecular cloning, structure, and chromosomal localization of the human inducible nitric oxide synthase gene. NA Chartrain, DA Geller, PP Koty, NF Sitrin, AK Nussler, EP Hoffman, ... Journal of biological chemistry 269 (9), 6765-6772, 1994 | 571 | 1994 |
| β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex CG Bönnemann, R Modi, S Noguchi, Y Mizuno, M Yoshida, E Gussoni, ... Nature genetics 11 (3), 266-273, 1995 | 553 | 1995 |
| Immunoelectron microscopic localization of dystrophin in myofibres SC Watkins, EP Hoffman, HS Slayter, LM Kunkel Nature 333 (6176), 863-866, 1988 | 541 | 1988 |
| Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies. AH Beggs, EP Hoffman, JR Snyder, K Arahata, L Specht, F Shapiro, ... American journal of human genetics 49 (1), 54, 1991 | 533 | 1991 |
| The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs BJ Cooper, NJ Winand, H Stedman, BA Valentine, EP Hoffman, ... Nature 334 (6178), 154-156, 1988 | 530 | 1988 |
| Genomics, intellectual disability, and autism HC Mefford, ML Batshaw, EP Hoffman New England Journal of Medicine 366 (8), 733-743, 2012 | 497 | 2012 |
| Efficacy of systemic morpholino exon‐skipping in Duchenne dystrophy dogs T Yokota, Q Lu, T Partridge, M Kobayashi, A Nakamura, S Takeda, ... Annals of Neurology: Official Journal of the American Neurological …, 2009 | 486 | 2009 |
| Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study CM McDonald, EK Henricson, RT Abresch, T Duong, NC Joyce, F Hu, ... The Lancet 391 (10119), 451-461, 2018 | 469 | 2018 |
| Dystrophin abnormalities in Duchenne/Becker muscular dystrophy EP Hoffman, LM Kunkel Neuron 2 (1), 1019-1029, 1989 | 468 | 1989 |
| Mutations in the integrin α7 gene cause congenital myopathy YK Hayashi, FL Chou, E Engvall, M Ogawa, C Matsuda, S Hirabayashi, ... Nature genetics 19 (1), 94-97, 1998 | 463 | 1998 |
