A citation-based method for searching scientific literature

Lily Yeh Jan, Yuh Nung Jan. J Physiol 2012
Times Cited: 130







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



Times Cited
  Times     Co-cited
Similarity


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
16


De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, Tania Djémié, Stephan Müller, Rikke S Møller, Bridget Maher, Laura Hernandez-Hernandez, Matthis Synofzik, Hande S Caglayan,[...]. Nat Genet 2015
148
13

Localization and targeting of voltage-dependent ion channels in mammalian central neurons.
Helene Vacher, Durga P Mohapatra, James S Trimmer. Physiol Rev 2008
322
11


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
11

Seizures and reduced life span in mice lacking the potassium channel subunit Kv1.2, but hypoexcitability and enlarged Kv1 currents in auditory neurons.
Helen M Brew, Joshua X Gittelman, Robert S Silverstein, Timothy D Hanks, Vas P Demas, Linda C Robinson, Carol A Robbins, Jennifer McKee-Johnson, Shing Yan Chiu, Albee Messing,[...]. J Neurophysiol 2007
117
11

Inwardly rectifying potassium channels: their structure, function, and physiological roles.
Hiroshi Hibino, Atsushi Inanobe, Kazuharu Furutani, Shingo Murakami, Ian Findlay, Yoshihisa Kurachi. Physiol Rev 2010
884
10

The action potential in mammalian central neurons.
Bruce P Bean. Nat Rev Neurosci 2007
830
10

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
9

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
9

Molecular diversity of K+ channels.
W A Coetzee, Y Amarillo, J Chiu, A Chow, D Lau, T McCormack, H Moreno, M S Nadal, A Ozaita, D Pountney,[...]. Ann N Y Acad Sci 1999
899
9


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
8

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel.
H S Wang, Z Pan, W Shi, B S Brown, R S Wymore, I S Cohen, J E Dixon, D McKinnon. Science 1998
930
8

Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines.
S Grissmer, A N Nguyen, J Aiyar, D C Hanson, R J Mather, G A Gutman, M J Karmilowicz, D D Auperin, K G Chandy. Mol Pharmacol 1994
694
8

Crystal structure of a mammalian voltage-dependent Shaker family K+ channel.
Stephen B Long, Ernest B Campbell, Roderick Mackinnon. Science 2005
8

Kv1.1 and Kv1.2: similar channels, different seizure models.
Carol A Robbins, Bruce L Tempel. Epilepsia 2012
71
11


A potassium channel mutation in neonatal human epilepsy.
C Biervert, B C Schroeder, C Kubisch, S F Berkovic, P Propping, T J Jentsch, O K Steinlein. Science 1998
805
7


Deletion of the Kv2.1 delayed rectifier potassium channel leads to neuronal and behavioral hyperexcitability.
D J Speca, G Ogata, D Mandikian, H I Bishop, S W Wiler, K Eum, H Jürgen Wenzel, E T Doisy, L Matt, K L Campi,[...]. Genes Brain Behav 2014
62
11


International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels.
George A Gutman, K George Chandy, Stephan Grissmer, Michel Lazdunski, David McKinnon, Luis A Pardo, Gail A Robertson, Bernardo Rudy, Michael C Sanguinetti, Walter Stühmer,[...]. Pharmacol Rev 2005
603
7

A new Kv1.2 channelopathy underlying cerebellar ataxia.
Gang Xie, John Harrison, Steven J Clapcote, Yun Huang, Jin-Yi Zhang, Lu-Yang Wang, John C Roder. J Biol Chem 2010
64
10

Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environment.
Stephen B Long, Xiao Tao, Ernest B Campbell, Roderick MacKinnon. Nature 2007
7

The Kv1.1 null mouse, a model of sudden unexpected death in epilepsy (SUDEP).
Brian M Moore, Chuanchau Jerry Jou, Milos Tatalovic, Elizabeth S Kaufman, David D Kline, Diana L Kunze. Epilepsia 2014
42
16

Structural mechanism of C-type inactivation in K(+) channels.
Luis G Cuello, Vishwanath Jogini, D Marien Cortes, Eduardo Perozo. Nature 2010
337
7

Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP).
Vikas Mishra, Bharat K Karumuri, Nicole M Gautier, Rui Liu, Timothy N Hutson, Stephanie L Vanhoof-Villalba, Ioannis Vlachos, Leonidas Iasemidis, Edward Glasscock. Hum Mol Genet 2017
28
25

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
N A Singh, C Charlier, D Stauffer, B R DuPont, R J Leach, R Melis, G M Ronen, I Bjerre, T Quattlebaum, J V Murphy,[...]. Nat Genet 1998
883
6

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Dominique Audenaert, Tine Deconinck, Lieve R F Claes, Liesbet Deprez, Katrien Smets, Dimitrina Hristova, Iglika Yordanova,[...]. Ann Neurol 2012
298
6

Neural KCNQ (Kv7) channels.
David A Brown, Gayle M Passmore. Br J Pharmacol 2009
438
6

The structure of the potassium channel: molecular basis of K+ conduction and selectivity.
D A Doyle, J Morais Cabral, R A Pfuetzner, A Kuo, J M Gulbis, S L Cohen, B T Chait, R MacKinnon. Science 1998
6


Expression and function of Kv1.1 potassium channels in human atria from patients with atrial fibrillation.
Edward Glasscock, Niels Voigt, Mark D McCauley, Qiang Sun, Na Li, David Y Chiang, Xiao-Bo Zhou, Cristina E Molina, Dierk Thomas, Constanze Schmidt,[...]. Basic Res Cardiol 2015
23
26

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
6

New insights into the pathogenesis and therapeutics of episodic ataxia type 1.
Maria Cristina D'Adamo, Sonia Hasan, Luca Guglielmi, Ilenio Servettini, Marta Cenciarini, Luigi Catacuzzeno, Fabio Franciolini. Front Cell Neurosci 2015
41
14

Voltage sensor of Kv1.2: structural basis of electromechanical coupling.
Stephen B Long, Ernest B Campbell, Roderick Mackinnon. Science 2005
749
6


Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.
Mark A Corbett, Susannah T Bellows, Melody Li, Renée Carroll, Silvana Micallef, Gemma L Carvill, Candace T Myers, Katherine B Howell, Snezana Maljevic, Holger Lerche,[...]. Neurology 2016
44
13


Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Silvia Masnada, Ulrike B S Hedrich, Elena Gardella, Julian Schubert, Charu Kaiwar, Eric W Klee, Brendan C Lanpher, Ralitza H Gavrilova, Matthis Synofzik, Thomas Bast,[...]. Brain 2017
60
10

Signal processing in the axon initial segment.
Maarten H P Kole, Greg J Stuart. Neuron 2012
247
5


K+ channels at the axon initial segment dampen near-threshold excitability of neocortical fast-spiking GABAergic interneurons.
Ethan M Goldberg, Brian D Clark, Edward Zagha, Mark Nahmani, Alev Erisir, Bernardo Rudy. Neuron 2008
169
5

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
13

Twenty years of dendrotoxins.
A L Harvey. Toxicon 2001
179
5

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene.
Maria C D'Adamo, Constanze Gallenmüller, Ilenio Servettini, Elisabeth Hartl, Stephen J Tucker, Larissa Arning, Saskia Biskup, Alessandro Grottesi, Luca Guglielmi, Paola Imbrici,[...]. Front Physiol 2015
29
17


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
10


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.