| 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 | 637 | 2005 |
| ACTN3 genotype is associated with increases in muscle strength in response to resistance training in women PM Clarkson, JM Devaney, H Gordish-Dressman, PD Thompson, ... Journal of applied physiology 99 (1), 154-163, 2005 | 437 | 2005 |
| 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 | 410 | 2018 |
| Adipocyte-derived exosomal miRNAs: a novel mechanism for obesity-related disease SC Ferrante, EP Nadler, DK Pillai, MJ Hubal, Z Wang, JM Wang, ... Pediatric research 77 (3), 447-454, 2015 | 293 | 2015 |
| Large-scale serum protein biomarker discovery in Duchenne muscular dystrophy Y Hathout, E Brody, PR Clemens, L Cripe, RK DeLisle, P Furlong, ... Proceedings of the National Academy of Sciences 112 (23), 7153-7158, 2015 | 278 | 2015 |
| Behavioral and locomotor measurements using an open field activity monitoring system for skeletal muscle diseases KS Tatem, JL Quinn, A Phadke, Q Yu, H Gordish-Dressman, K Nagaraju JoVE (Journal of Visualized Experiments), e51785, 2014 | 270 | 2014 |
| ACTN3 and MLCK genotype associations with exertional muscle damage PM Clarkson, EP Hoffman, E Zambraski, H Gordish-Dressman, A Kearns, ... Journal of Applied Physiology 99 (2), 564-569, 2005 | 258 | 2005 |
| SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy E Pegoraro, EP Hoffman, L Piva, BF Gavassini, S Cagnin, M Ermani, ... Neurology 76 (3), 219-226, 2011 | 241 | 2011 |
| GFAP mutations, age at onset, and clinical subtypes in Alexander disease M Prust, J Wang, H Morizono, A Messing, M Brenner, E Gordon, T Hartka, ... Neurology 77 (13), 1287-1294, 2011 | 240 | 2011 |
| Prednisone/prednisolone and deflazacort regimens in the CINRG Duchenne Natural History Study L Bello, H Gordish-Dressman, LP Morgenroth, EK Henricson, T Duong, ... Neurology 85 (12), 1048-1055, 2015 | 197 | 2015 |
| Preclinical drug trials in the mdx mouse: Assessment of reliable and sensitive outcome measures CF Spurney, H Gordish‐Dressman, AD Guerron, A Sali, GS Pandey, ... Muscle & Nerve: Official Journal of the American Association of …, 2009 | 193 | 2009 |
| VBP15, a novel anti‐inflammatory and membrane‐stabilizer, improves muscular dystrophy without side effects CR Heier, JM Damsker, Q Yu, BC Dillingham, T Huynh, ... EMBO molecular medicine 5 (10), 1569-1585, 2013 | 192 | 2013 |
| ACE ID genotype and the muscle strength and size response to unilateral resistance training LS Pescatello, MA Kostek, H Gordish-Dressman, PD Thompson, RL Seip, ... Medicine & Science in Sports & Exercise 38 (6), 1074-1081, 2006 | 159 | 2006 |
| Secretome signature of invasive glioblastoma multiforme CA Formolo, R Williams, H Gordish-Dressman, TJ MacDonald, NH Lee, ... Journal of proteome research 10 (7), 3149-3159, 2011 | 152 | 2011 |
| An interactive power analysis tool for microarray hypothesis testing and generation J Seo, H Gordish-Dressman, EP Hoffman Bioinformatics 22 (7), 808-814, 2006 | 152 | 2006 |
| Clinically relevant and minimally invasive tumor surveillance of pediatric diffuse midline gliomas using patient-derived liquid biopsy E Panditharatna, LB Kilburn, MS Aboian, M Kambhampati, ... Clinical Cancer Research 24 (23), 5850-5859, 2018 | 150 | 2018 |
| DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study L Bello, LP Morgenroth, H Gordish-Dressman, EP Hoffman, ... Neurology 87 (4), 401-409, 2016 | 148 | 2016 |
| Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma/DICER1 syndrome: a unique variant of the two-hit … M Brenneman, A Field, J Yang, G Williams, L Doros, C Rossi, KA Schultz, ... F1000Research 4, 2015 | 143 | 2015 |
| DNA methylation profile associated with rapid decline in kidney function: findings from the CRIC study MR Wing, JM Devaney, MM Joffe, D Xie, HI Feldman, EA Dominic, ... Nephrology Dialysis Transplantation 29 (4), 864-872, 2014 | 135 | 2014 |
| Identification of novel substrates for the serine protease HTRA1 in the human RPE secretome E An, S Sen, SK Park, H Gordish-Dressman, Y Hathout Investigative ophthalmology & visual science 51 (7), 3379-3386, 2010 | 131 | 2010 |
