| The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses DL Boone, EE Turer, EG Lee, RC Ahmad, MT Wheeler, C Tsui, P Hurley, ... Nature immunology 5 (10), 1052-1060, 2004 | 1393 | 2004 |
| Dilated cardiomyopathy: genetic determinants and mechanisms EM McNally, L Mestroni Circulation research 121 (7), 731-748, 2017 | 910 | 2017 |
| The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma KA Lapidos, R Kakkar, EM McNally Circulation research 94 (8), 1023-1031, 2004 | 710 | 2004 |
| The dystrophin complex: structure, function, and implications for therapy QQ Gao, EM McNally Comprehensive physiology 5 (3), 1223-1239, 2015 | 667 | 2015 |
| Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy S Noguchi, EM McNally, KB Othmane, Y Hagiwara, Y Mizuno, M Yoshida, ... Science 270 (5237), 819-822, 1995 | 666 | 1995 |
| Myosin subfragment-1 is sufficient to move actin filaments in vitro YY Toyoshima, SJ Kron, EM McNally, KR Niebling, C Toyoshima, ... Nature 328 (6130), 536-539, 1987 | 662 | 1987 |
| Genetic mutations and mechanisms in dilated cardiomyopathy EM McNally, JR Golbus, MJ Puckelwartz The Journal of clinical investigation 123 (1), 19-26, 2013 | 586 | 2013 |
| 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 | 561 | 1995 |
| Desmoplakin cardiomyopathy, a fibrotic and inflammatory form of cardiomyopathy distinct from typical dilated or arrhythmogenic right ventricular cardiomyopathy ED Smith, NK Lakdawala, N Papoutsidakis, G Aubert, A Mazzanti, ... Circulation 141 (23), 1872-1884, 2020 | 472 | 2020 |
| Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies GQ Wallace, EM McNally Annual review of physiology 71 (1), 37-57, 2009 | 422 | 2009 |
| Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein TG Thompson, YM Chan, AA Hack, M Brosius, M Rajala, HGW Lidov, ... The Journal of cell biology 148 (1), 115-126, 2000 | 379 | 2000 |
| γ-Sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin AA Hack, CT Ly, F Jiang, CJ Clendenin, KS Sigrist, RL Wollmann, ... The Journal of cell biology 142 (5), 1279-1287, 1998 | 375 | 1998 |
| Nesprin‐1α self‐associates and binds directly to emerin and lamin A in vitro JMK Mislow, JM Holaska, MS Kim, KK Lee, M Segura-Totten, KL Wilson, ... FEBS letters 525 (1-3), 135-140, 2002 | 366 | 2002 |
| Contemporary cardiac issues in Duchenne muscular dystrophy EM McNally, JR Kaltman, DW Benson, CE Canter, LH Cripe, D Duan, ... Circulation 131 (18), 1590-1598, 2015 | 347 | 2015 |
| Episodic coronary artery vasospasm and hypertension develop in the absence of Sur2 KATP channels WA Chutkow, J Pu, MT Wheeler, T Wada, JC Makielski, CF Burant, ... The Journal of clinical investigation 110 (2), 203-208, 2002 | 323 | 2002 |
| Dominant negative myostatin produces hypertrophy without hyperplasia in muscle X Zhu, M Hadhazy, M Wehling, JG Tidball, EM McNally FEBS letters 474 (1), 71-75, 2000 | 299 | 2000 |
| Caveolin-3 in muscular dystrophy EM McNally, E de Sá Moreira, DJ Duggan, CG Bönnemann, MP Lisanti, ... Human molecular genetics 7 (5), 871-877, 1998 | 294 | 1998 |
| LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy KM Flanigan, E Ceco, KM Lamar, Y Kaminoh, DM Dunn, JR Mendell, ... Annals of neurology 73 (4), 481-488, 2013 | 275 | 2013 |
| Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism DP Millay, SA Goonasekera, MA Sargent, M Maillet, BJ Aronow, ... Proceedings of the National Academy of Sciences 106 (45), 19023-19028, 2009 | 274 | 2009 |
| Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains DB Davis, KR Doherty, AJ Delmonte, EM McNally Journal of Biological Chemistry 277 (25), 22883-22888, 2002 | 257 | 2002 |
