World's Best Scientists 2026 revealed!

D-Index & Metrics

Neuroscience

D-Index
60
Citations
11822
World Ranking
3867
National Ranking
1759

Best Publications

  • Expanded CUG Repeats Trigger Aberrant Splicing of ClC-1 Chloride Channel Pre-mRNA and Hyperexcitability of Skeletal Muscle in Myotonic Dystrophy

    Ami Mankodi;Masanori P. Takahashi;Hong Jiang;Carol L. Beck

  • Loss of the neural integrator of the oculomotor system from brain stem lesions in monkey.

    S. C. Cannon;D. A. Robinson

  • The primary periodic paralyses: diagnosis, pathogenesis and treatment

    S. L. Venance;S. C. Cannon;D. Fialho;B. Fontaine

  • Leukocyte Common Antigen-Related Phosphatase Is a Functional Receptor for Chondroitin Sulfate Proteoglycan Axon Growth Inhibitors

    Daniel Fisher;Bin Xing;John Dill;Hui Li

  • MOD-1 is a serotonin-gated chloride channel that modulates locomotory behaviour in C. elegans

    Rajesh Ranganathan;Stephen C. Cannon;H. Robert Horvitz

  • Review of the Diagnosis and Treatment of Periodic Paralysis.

    Jeffrey M. Statland;Bertrand Fontaine;Michael G. Hanna;Nicholas E. Johnson

  • A proposed neural network for the integrator of the oculomotor system

    Stephen C. Cannon;David A. Robinson;Shihab Shamma

  • A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation.

    Stephen C. Cannon;Robert H. Brown;David P. Corey;David P. Corey

  • An improved neural-network model for the neural integrator of the oculomotor system: More realistic neuron behavior

    Stephen C. Cannon;David A. Robinson

  • The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment

    E. Matthews;D. Fialho;S. V. Tan;S. L. Venance

  • PATHOMECHANISMS IN CHANNELOPATHIES OF SKELETAL MUSCLE AND BRAIN

    Stephen C. Cannon

  • Functional expression of sodium channel mutations identified in families with periodic paralysis

    Stephen C. Cannon;Stephen M. Strittmatter

  • Channelopathies of skeletal muscle excitability

    Stephen C. Cannon

  • Myasthenic syndrome caused by mutation of the SCN4A sodium channel

    Akira Tsujino;Chantal Maertens;Kinji Ohno;Xin-Ming Shen

  • The mechanical behavior of active human skeletal muscle in small oscillations.

    Stephen C. Cannon;George I. Zahalak

  • Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels.

    S.C. Cannon;R.H. Brown;D.P. Corey

  • A Na+ channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore.

    Arie F. Struyk;Stephen C. Cannon

  • Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis

    Lawrence J. Hayward;Robert H. Brown;Stephen C. Cannon

  • Skeletal muscle-specific T-tubule protein STAC3 mediates voltage-induced Ca2+ release and contractility

    Benjamin R. Nelson;Fenfen Wu;Yun Liu;Douglas M. Anderson

  • Defective slow inactivation of sodium channels contributes to familial periodic paralysis

    Lawrence J. Hayward;Gisela M. Sandoval;Stephen C. Cannon

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Recently Published Articles