A citation-based method for searching scientific literature

Susan E Tomlinson, S Veronica Tan, Dimitri M Kullmann, Robert C Griggs, David Burke, Michael G Hanna, Hugh Bostock. Brain 2010
Times Cited: 73







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



Times Cited
  Times     Co-cited
Similarity



Excitability of human axons.
D Burke, M C Kiernan, H Bostock. Clin Neurophysiol 2001
323
27

Threshold tracking techniques in the study of human peripheral nerve.
H Bostock, K Cikurel, D Burke. Muscle Nerve 1998
399
27

Multiple measures of axonal excitability: a new approach in clinical testing.
M C Kiernan, D Burke, K V Andersen, H Bostock. Muscle Nerve 2000
334
27

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
131
26


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
131
23


The voltage dependence of I(h) in human myelinated axons.
James Howells, Louise Trevillion, Hugh Bostock, David Burke. J Physiol 2012
103
23

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
255
21


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
585
20

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
170
19

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
168
17

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
24



A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction.
Michelle K Demos, Vincenzo Macri, Kevin Farrell, Tanya N Nelson, Kristine Chapman, Eric Accili, Linlea Armstrong. Mov Disord 2009
36
30

Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons.
H Wang, D D Kunkel, T M Martin, P A Schwartzkroin, B L Tempel. Nature 1993
523
15

Action potentials and membrane currents in the human node of Ranvier.
J R Schwarz, G Reid, H Bostock. Pflugers Arch 1995
177
13

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
41
24


Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel.
K Dedek, B Kunath, C Kananura, U Reuner, T J Jentsch, O K Steinlein. Proc Natl Acad Sci U S A 2001
191
13


Deletion of the K(V)1.1 potassium channel causes epilepsy in mice.
S L Smart, V Lopantsev, C L Zhang, C A Robbins, H Wang, S Y Chiu, P A Schwartzkroin, A Messing, B L Tempel. Neuron 1998
431
13


Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1.
Ruth Rea, Alexander Spauschus, Louise H Eunson, Michael G Hanna, Dimitri M Kullmann. J Physiol 2002
49
18



Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea.
Steven J Shook, Hafsa Mamsa, Joanna C Jen, Robert W Baloh, Lan Zhou. Muscle Nerve 2008
25
36

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
12


Localization and targeting of voltage-dependent ion channels in mammalian central neurons.
Helene Vacher, Durga P Mohapatra, James S Trimmer. Physiol Rev 2008
322
12

Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage.
Kazuaki Kanai, Satoshi Kuwabara, Sonoko Misawa, Noriko Tamura, Kazue Ogawara, Miho Nakata, Setsu Sawai, Takamichi Hattori, Hugh Bostock. Brain 2006
188
10

Strength-duration properties of human peripheral nerve.
I Mogyoros, M C Kiernan, D Burke. Brain 1996
254
10

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1.
P Imbrici, F Gualandi, M C D'Adamo, M Taddei Masieri, P Cudia, D De Grandis, R Mannucci, I Nicoletti, S J Tucker, A Ferlini,[...]. Neuroscience 2008
29
27

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
43
18



Episodic ataxia type 1: a neuronal potassium channelopathy.
Sanjeev Rajakulendran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hanna. Neurotherapeutics 2007
64
12


Hereditary myokymia and periodic ataxia.
D H VanDyke, R C Griggs, M J Murphy, M N Goldstein. J Neurol Sci 1975
108
10

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
203
10

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
16
50

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
30

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
14

Evidence for axonal membrane hyperpolarization in multifocal motor neuropathy with conduction block.
Matthew C Kiernan, Jean-Marc Guglielmi, Ryuji Kaji, Nicholas M F Murray, Hugh Bostock. Brain 2002
138
9

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
70
10

Clinical evaluation of excitability measures in sensory nerve.
M C Kiernan, C S Lin, K V Andersen, N M Murray, H Bostock. Muscle Nerve 2001
120
9

Going native: voltage-gated potassium channels controlling neuronal excitability.
Jamie Johnston, Ian D Forsythe, Conny Kopp-Scheinpflug. J Physiol 2010
185
9


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.