A citation-based method for searching scientific literature

Stephen C Cannon. Annu Rev Neurosci 2006
Times Cited: 145







List of co-cited articles
833 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Electromyography guides toward subgroups of mutations in muscle channelopathies.
Emmanuel Fournier, Marianne Arzel, Damien Sternberg, Savine Vicart, Pascal Laforet, Bruno Eymard, Jean-Claude Willer, Nacira Tabti, Bertrand Fontaine. Ann Neurol 2004
180
21

Gating pore current in an inherited ion channelopathy.
Stanislav Sokolov, Todd Scheuer, William A Catterall. Nature 2007
200
20

Correlating phenotype and genotype in the periodic paralyses.
T M Miller, M R Dias da Silva, H A Miller, H Kwiecinski, J R Mendell, R Tawil, P McManis, R C Griggs, C Angelini, S Servidei,[...]. Neurology 2004
140
20

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.
E Matthews, D Fialho, S V Tan, S L Venance, S C Cannon, D Sternberg, B Fontaine, A A Amato, R J Barohn, R C Griggs,[...]. Brain 2010
123
20



Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.
K Jurkat-Rott, N Mitrovic, C Hang, A Kouzmekine, P Iaizzo, J Herzog, H Lerche, S Nicole, J Vale-Santos, D Chauveau,[...]. Proc Natl Acad Sci U S A 2000
182
16

Cold extends electromyography distinction between ion channel mutations causing myotonia.
Emmanuel Fournier, Karine Viala, Hélène Gervais, Damien Sternberg, Marianne Arzel-Hézode, Pascal Laforêt, Bruno Eymard, Nacira Tabti, Jean-Claude Willer, Christophe Vial,[...]. Ann Neurol 2006
96
14

The skeletal muscle chloride channel in dominant and recessive human myotonia.
M C Koch, K Steinmeyer, C Lorenz, K Ricker, F Wolf, M Otto, B Zoll, F Lehmann-Horn, K H Grzeschik, T J Jentsch. Science 1992
591
14

Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions.
D Fialho, S Schorge, U Pucovska, N P Davies, R Labrum, A Haworth, E Stanley, R Sud, W Wakeling, M B Davis,[...]. Brain 2007
75
18


Refined exercise testing can aid DNA-based diagnosis in muscle channelopathies.
S Veronica Tan, Emma Matthews, Melissa Barber, James A Burge, Sanjeev Rajakulendran, Doreen Fialho, Richa Sud, Andrea Haworth, Martin Koltzenburg, Michael G Hanna. Ann Neurol 2011
65
21

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
D Sternberg, T Maisonobe, K Jurkat-Rott, S Nicole, E Launay, D Chauveau, N Tabti, F Lehmann-Horn, B Hainque, B Fontaine. Brain 2001
137
13

The primary periodic paralyses: diagnosis, pathogenesis and treatment.
S L Venance, S C Cannon, D Fialho, B Fontaine, M G Hanna, L J Ptacek, M Tristani-Firouzi, R Tawil, R C Griggs. Brain 2006
180
13



Sodium channelopathies of skeletal muscle result from gain or loss of function.
Karin Jurkat-Rott, Boris Holzherr, Michael Fauler, Frank Lehmann-Horn. Pflugers Arch 2010
102
13

Human skeletal muscle sodium channelopathies.
S Vicart, D Sternberg, B Fontaine, G Meola. Neurol Sci 2005
59
20

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.
E Matthews, R Labrum, M G Sweeney, R Sud, A Haworth, P F Chinnery, G Meola, S Schorge, D M Kullmann, M B Davis,[...]. Neurology 2009
112
12

K+-dependent paradoxical membrane depolarization and Na+ overload, major and reversible contributors to weakness by ion channel leaks.
Karin Jurkat-Rott, Marc-André Weber, Michael Fauler, Xiu-Hai Guo, Boris D Holzherr, Agathe Paczulla, Nikolai Nordsborg, Wolfgang Joechle, Frank Lehmann-Horn. Proc Natl Acad Sci U S A 2009
110
12

Phenotypic variability in myotonia congenita.
Eskild Colding-Jørgensen. Muscle Nerve 2005
101
12

A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.
Fenfen Wu, Wentao Mi, Dennis K Burns, Yu Fu, Hillery F Gray, Arie F Struyk, Stephen C Cannon. J Clin Invest 2011
50
24

A calcium channel mutant mouse model of hypokalemic periodic paralysis.
Fenfen Wu, Wentao Mi, Erick O Hernández-Ochoa, Dennis K Burns, Yu Fu, Hillery F Gray, Arie F Struyk, Martin F Schneider, Stephen C Cannon. J Clin Invest 2012
63
19

Non-dystrophic myotonia: prospective study of objective and patient reported outcomes.
Jaya R Trivedi, Brian Bundy, Jeffrey Statland, Mohammad Salajegheh, Dipa Raja Rayan, Shannon L Venance, Yunxia Wang, Doreen Fialho, Emma Matthews, James Cleland,[...]. Brain 2013
53
22

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis.
L J Ptácek, R Tawil, R C Griggs, A G Engel, R B Layzer, H Kwieciński, P G McManis, L Santiago, M Moore, G Fouad. Cell 1994
329
11

Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro.
N Yang, S Ji, M Zhou, L J Ptácek, R L Barchi, R Horn, A L George. Proc Natl Acad Sci U S A 1994
178
11

On the repetitive discharge in myotonic muscle fibres.
R H Adrian, S H Bryant. J Physiol 1974
253
11

A calcium channel mutation causing hypokalemic periodic paralysis.
K Jurkat-Rott, F Lehmann-Horn, A Elbaz, R Heine, R G Gregg, K Hogan, P A Powers, P Lapie, J E Vale-Santos, J Weissenbach. Hum Mol Genet 1994
245
10

A novel sodium channel mutation in a family with hypokalemic periodic paralysis.
D E Bulman, K A Scoggan, M D van Oene, M W Nicolle, A F Hahn, L L Tollar, G C Ebers. Neurology 1999
136
10

The nondystrophic myotonias.
Chad R Heatwole, Richard T Moxley. Neurotherapeutics 2007
51
19

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.
L J Ptacek, J S Trimmer, W S Agnew, J W Roberts, J H Petajan, M Leppert. Am J Hum Genet 1991
134
10

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.
B Fontaine, T S Khurana, E P Hoffman, G A Bruns, J L Haines, J A Trofatter, M P Hanson, J Rich, H McFarlane, D M Yasek. Science 1990
268
10




A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation.
J W West, D E Patton, T Scheuer, Y Wang, A L Goldin, W A Catterall. Proc Natl Acad Sci U S A 1992
617
10

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation.
M Chahine, A L George, M Zhou, S Ji, W Sun, R L Barchi, R Horn. Neuron 1994
290
10



Mexiletine for symptoms and signs of myotonia in nondystrophic myotonia: a randomized controlled trial.
Jeffrey M Statland, Brian N Bundy, Yunxia Wang, Dipa Raja Rayan, Jaya R Trivedi, Valeria A Sansone, Mohammad K Salajegheh, Shannon L Venance, Emma Ciafaloni, Emma Matthews,[...]. JAMA 2012
99
10

Channelopathies of skeletal muscle excitability.
Stephen C Cannon. Compr Physiol 2015
109
10

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.
S Vicart, D Sternberg, E Fournier, F Ochsner, P Laforet, T Kuntzer, B Eymard, B Hainque, B Fontaine. Neurology 2004
58
15

Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
A L George, M A Crackower, J A Abdalla, A J Hudson, G C Ebers. Nat Genet 1993
251
9

Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane parameters.
R Rüdel, F Lehmann-Horn, K Ricker, G Küther. Muscle Nerve 1984
153
9

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.
N M Plaster, R Tawil, M Tristani-Firouzi, S Canún, S Bendahhou, A Tsunoda, M R Donaldson, S T Iannaccone, E Brunt, R Barohn,[...]. Cell 2001
645
9

Treatment for periodic paralysis.
V Sansone, G Meola, T P Links, M Panzeri, M R Rose. Cochrane Database Syst Rev 2008
34
26


Myotonia fluctuans. A third type of muscle sodium channel disease.
K Ricker, R T Moxley, R Heine, F Lehmann-Horn. Arch Neurol 1994
100
9

Voltage-gated ion channels and hereditary disease.
F Lehmann-Horn, K Jurkat-Rott. Physiol Rev 1999
364
9

Redefining the clinical phenotypes of non-dystrophic myotonic syndromes.
J Trip, G Drost, H B Ginjaar, F H M Nieman, A J van der Kooi, M de Visser, B G M van Engelen, C G Faber. J Neurol Neurosurg Psychiatry 2009
61
14


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.