A citation-based method for searching scientific literature

Susan E Tomlinson, S Veronica Tan, David Burke, Robyn W Labrum, Andrea Haworth, Vaneesha S Gibbons, Mary G Sweeney, Robert C Griggs, Dimitri M Kullmann, Hugh Bostock, Michael G Hanna. Brain 2016
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


Nerve excitability studies characterize Kv1.1 fast potassium channel dysfunction in patients with episodic ataxia type 1.
Susan E Tomlinson, S Veronica Tan, Dimitri M Kullmann, Robert C Griggs, David Burke, Michael G Hanna, Hugh Bostock. Brain 2010
70
62

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
J Jen, J Wan, M Graves, H Yu, A F Mock, C J Coulin, G Kim, Q Yue, D M Papazian, R W Baloh. Neurology 2001
101
50


The voltage dependence of I(h) in human myelinated axons.
James Howells, Louise Trevillion, Hugh Bostock, David Burke. J Physiol 2012
101
50

Excitability and the safety margin in human axons during hyperthermia.
James Howells, Dirk Czesnik, Louise Trevillion, David Burke. J Physiol 2013
23
37

Axonal ion channels from bench to bedside: a translational neuroscience perspective.
Arun V Krishnan, Cindy S-Y Lin, Susanna B Park, Matthew C Kiernan. Prog Neurobiol 2009
127
37

Acute tetrodotoxin-induced neurotoxicity after ingestion of puffer fish.
Matthew C Kiernan, Geoffrey K Isbister, Cindy S-Y Lin, David Burke, Hugh Bostock. Ann Neurol 2005
130
37



Primary episodic ataxias: diagnosis, pathogenesis and treatment.
J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
200
37

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia.
J Jen, Q Yue, S F Nelson, H Yu, M Litt, J Nutt, R W Baloh. Neurology 1999
95
37

Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1.
Susan Elizabeth Tomlinson, Sanjeev Rajakulendran, Stella Veronica Tan, Tracey Dawn Graves, Doris-Eva Bamiou, Robyn W Labrum, David Burke, Carolyn M Sue, Paola Giunti, Stephanie Schorge,[...]. J Neurol Neurosurg Psychiatry 2013
31
37


Outwardly rectifying deflections in threshold electrotonus due to K+ conductances.
Louise Trevillion, James Howells, David Burke. J Physiol 2007
18
25

Assessment of axonal excitability properties in two branches of the human facial nerve.
Timothy J Eviston, Arun V Krishnan. J Neurosci Methods 2016
4
50


Mutation in the Na+ channel subunit SCN1B produces paradoxical changes in peripheral nerve excitability.
Matthew C Kiernan, Arun V Krishnan, Cindy S-Y Lin, David Burke, Samuel F Berkovic. Brain 2005
50
25


Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivo.
Susan E Tomlinson, Michael G Hanna, Dimitri M Kullmann, S Veronica Tan, David Burke. Clin Neurophysiol 2009
27
25


Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
25

Excitability of human axons.
D Burke, M C Kiernan, H Bostock. Clin Neurophysiol 2001
316
25

Motor axon excitability during Wallerian degeneration.
Mihai Moldovan, Susana Alvarez, Christian Krarup. Brain 2009
58
25

Action potentials and membrane currents in the human node of Ranvier.
J R Schwarz, G Reid, H Bostock. Pflugers Arch 1995
172
25

In vivo assessment of HCN channel current (I(h)) in human motor axons.
Susan Tomlinson, David Burke, Mike Hanna, Martin Koltzenburg, Hugh Bostock. Muscle Nerve 2010
40
25

Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia.
M Kinali, H Jungbluth, L H Eunson, C A Sewry, A Y Manzur, E Mercuri, M G Hanna, F Muntoni. Neuromuscul Disord 2004
42
25

Muscle cramp in Machado-Joseph disease: altered motor axonal excitability properties and mexiletine treatment.
Kazuaki Kanai, Satoshi Kuwabara, Kimihito Arai, Jia-Ying Sung, Kazue Ogawara, Takamichi Hattori. Brain 2003
80
25

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.
L H Eunson, R Rea, S M Zuberi, S Youroukos, C P Panayiotopoulos, R Liguori, P Avoni, R C McWilliam, J B Stephenson, M G Hanna,[...]. Ann Neurol 2000
169
25

Evolution of peripheral nerve function in humans: novel insights from motor nerve excitability.
Michelle A Farrar, Susanna B Park, Cindy S-Y Lin, Matthew C Kiernan. J Physiol 2013
19
25

Oxaliplatin-induced neurotoxicity: changes in axonal excitability precede development of neuropathy.
Susanna B Park, Cindy S-Y Lin, Arun V Krishnan, David Goldstein, Michael L Friedlander, Matthew C Kiernan. Brain 2009
152
25

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.
S M Zuberi, L H Eunson, A Spauschus, R De Silva, J Tolmie, N W Wood, R C McWilliam, J B Stephenson, D M Kullmann, M G Hanna. Brain 1999
254
25

Nerve excitability properties in Charcot-Marie-Tooth disease type 1A.
Hiroyuki Nodera, Hugh Bostock, Satoshi Kuwabara, Takashi Sakamoto, Kotaro Asanuma, Sung Jia-Ying, Kazue Ogawara, Naoki Hattori, Masaaki Hirayama, Gen Sobue,[...]. Brain 2004
68
25


Association between glycemic variability and peripheral nerve dysfunction in type 1 diabetes.
Natalie C G Kwai, Ria Arnold, Ann M Poynten, Arun V Krishnan. Muscle Nerve 2016
20
25

Threshold tracking techniques in the study of human peripheral nerve.
H Bostock, K Cikurel, D Burke. Muscle Nerve 1998
394
25


Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
581
25

In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission.
Susan E Tomlinson, Hugh Bostock, Bronwyn Grinton, Michael G Hanna, Dimitri M Kullmann, Matthew C Kiernan, Ingrid E Scheffer, Samuel F Berkovic, David Burke. Brain 2012
15
25

KCNQ channels mediate IKs, a slow K+ current regulating excitability in the rat node of Ranvier.
J R Schwarz, G Glassmeier, E C Cooper, T-C Kao, H Nodera, D Tabuena, R Kaji, H Bostock. J Physiol 2006
166
25

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
179
25

Next-generation sequencing identifies novel CACNA1A gene mutations in episodic ataxia type 2.
Neven Maksemous, Bishakha Roy, Robert A Smith, Lyn R Griffiths. Mol Genet Genomic Med 2016
21
25

Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation.
Tracey D Graves, Yoon-Hee Cha, Angelika F Hahn, Richard Barohn, Mohammed K Salajegheh, Robert C Griggs, Brian N Bundy, Joanna C Jen, Robert W Baloh, Michael G Hanna. Brain 2014
55
25

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
C Denier, A Ducros, K Vahedi, A Joutel, P Thierry, A Ritz, G Castelnovo, T Deonna, P GĂ©rard, J L Devoize,[...]. Neurology 1999
146
25

Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature.
Orazio Brunetti, Paola Imbrici, Fabio Massimo Botti, Vito Enrico Pettorossi, Maria Cristina D'Adamo, Mario Valentino, Christian Zammit, Marina Mora, Sara Gibertini, Giuseppe Di Giovanni,[...]. Neurobiol Dis 2012
26
25

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
J L Steckley, G C Ebers, M Z Cader, R S McLachlan. Neurology 2001
48
25

A mouse model of episodic ataxia type-1.
Paco S Herson, Michael Virk, Nathan R Rustay, Chris T Bond, John C Crabbe, John P Adelman, James Maylie. Nat Neurosci 2003
100
25

Mutations underlying Episodic Ataxia type-1 antagonize Kv1.1 RNA editing.
Elizabeth A Ferrick-Kiddie, Joshua J C Rosenthal, Gregory D Ayers, Ronald B Emeson. Sci Rep 2017
12
25

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
M Z Cader, J L Steckley, D A Dyment, R S McLachlan, G C Ebers. Neurology 2005
35
25

A new episodic ataxia syndrome with linkage to chromosome 19q13.
Kevin A Kerber, Joanna C Jen, Hane Lee, Stanley F Nelson, Robert W Baloh. Arch Neurol 2007
35
25

A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias.
M Strupp, R Kalla, J Claassen, C Adrion, U Mansmann, T Klopstock, T Freilinger, H Neugebauer, R Spiegel, M Dichgans,[...]. Neurology 2011
112
25


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.