| Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy A Mankodi, MP Takahashi, H Jiang, CL Beck, WJ Bowers, RT Moxley, ... Molecular cell 10 (1), 35-44, 2002 | 787 | 2002 |
| A peptide encoded by a transcript annotated as long noncoding RNA enhances SERCA activity in muscle BR Nelson, CA Makarewich, DM Anderson, BR Winders, CD Troupes, ... Science 351 (6270), 271-275, 2016 | 747 | 2016 |
| Loss of the neural integrator of the oculomotor system from brain stem lesions in monkey SC Cannon, DA Robinson Journal of neurophysiology 57 (5), 1383-1409, 1987 | 721 | 1987 |
| The primary periodic paralyses: diagnosis, pathogenesis and treatment SL Venance, SC Cannon, D Fialho, B Fontaine, MG Hanna, LJ Ptacek, ... Brain 129 (1), 8-17, 2006 | 397 | 2006 |
| Leukocyte common antigen-related phosphatase is a functional receptor for chondroitin sulfate proteoglycan axon growth inhibitors D Fisher, B Xing, J Dill, H Li, HH Hoang, Z Zhao, XL Yang, R Bachoo, ... Journal of Neuroscience 31 (40), 14051-14066, 2011 | 354 | 2011 |
| MOD-1 is a serotonin-gated chloride channel that modulates locomotory behaviour in C. elegans R Ranganathan, SC Cannon, HR Horvitz Nature 408 (6811), 470-475, 2000 | 293 | 2000 |
| A proposed neural network for the integrator of the oculomotor system SC Cannon, DA Robinson, S Shamma Biological cybernetics 49 (2), 127-136, 1983 | 263 | 1983 |
| The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment E Matthews, D Fialho, SV Tan, SL Venance, SC Cannon, D Sternberg, ... Brain 133 (1), 9-22, 2010 | 252 | 2010 |
| A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation SC Cannon, RH Brown Jr, DP Corey Neuron 6 (4), 619-626, 1991 | 249 | 1991 |
| Review of the diagnosis and treatment of periodic paralysis JM Statland, B Fontaine, MG Hanna, NE Johnson, JT Kissel, VA Sansone, ... Muscle & nerve 57 (4), 522-530, 2018 | 244 | 2018 |
| Pathomechanisms in channelopathies of skeletal muscle and brain SC Cannon Annu. Rev. Neurosci. 29 (1), 387-415, 2006 | 241 | 2006 |
| Channelopathies of skeletal muscle excitability SC Cannon Comprehensive Physiology 5 (2), 761, 2015 | 230 | 2015 |
| Functional expression of sodium channel mutations identified in families with periodic paralysis SC Cannon, SM Strittmatter Neuron 10 (2), 317-326, 1993 | 229 | 1993 |
| Myasthenic syndrome caused by mutation of the SCN4A sodium channel A Tsujino, C Maertens, K Ohno, XM Shen, T Fukuda, CM Harper, ... Proceedings of the National Academy of Sciences 100 (12), 7377-7382, 2003 | 213 | 2003 |
| Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels SC Cannon, RH Brown, DP Corey Biophysical Journal 65 (1), 270-288, 1993 | 197 | 1993 |
| The mechanical behavior of active human skeletal muscle in small oscillations SC Cannon, GI Zahalak Journal of biomechanics 15 (2), 111-121, 1982 | 195 | 1982 |
| A Na+ channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore AF Struyk, SC Cannon The Journal of general physiology 130 (1), 11, 2007 | 190 | 2007 |
| Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis LJ Hayward, RH Brown, SC Cannon Biophysical journal 72 (3), 1204-1219, 1997 | 175 | 1997 |
| Skeletal muscle-specific T-tubule protein STAC3 mediates voltage-induced Ca2+ release and contractility BR Nelson, F Wu, Y Liu, DM Anderson, J McAnally, W Lin, SC Cannon, ... Proceedings of the National Academy of Sciences 110 (29), 11881-11886, 2013 | 165 | 2013 |
| Defective slow inactivation of sodium channels contributes to familial periodic paralysis LJ Hayward, GM Sandoval, SC Cannon Neurology 52 (7), 1447-1447, 1999 | 156 | 1999 |
