A citation-based method for searching scientific literature

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
Times Cited: 435







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



Times Cited
  Times     Co-cited
Similarity



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
119
26

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
589
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
256
22


Ketogenic diet treatment abolishes seizure periodicity and improves diurnal rhythmicity in epileptic Kcna1-null mice.
Kristina A Fenoglio-Simeone, Julianne C Wilke, Heather L Milligan, Charles N Allen, Jong M Rho, Rama K Maganti. Epilepsia 2009
53
30

Ketogenic diet treatment increases longevity in Kcna1-null mice, a model of sudden unexpected death in epilepsy.
Kristina A Simeone, Stephanie A Matthews, Jong M Rho, Timothy A Simeone. Epilepsia 2016
36
44


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
35

Orexin Receptor Antagonism Improves Sleep and Reduces Seizures in Kcna1-null Mice.
Harrison M Roundtree, Timothy A Simeone, Chaz Johnson, Stephanie A Matthews, Kaeli K Samson, Kristina A Simeone. Sleep 2016
35
40

High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.
Tara L Klassen, Valerie C Bomben, Ankita Patel, Janice Drabek, Tim T Chen, Wenli Gu, Feng Zhang, Kevin Chapman, James R Lupski, Jeffrey L Noebels,[...]. Epilepsia 2014
59
23

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
29
48

Kv1.1 and Kv1.2: similar channels, different seizure models.
Carol A Robbins, Bruce L Tempel. Epilepsia 2012
72
18

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
153
13

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
695
12

Structural consequences of Kcna1 gene deletion and transfer in the mouse hippocampus.
H Jürgen Wenzel, Helene Vacher, Eliana Clark, James S Trimmer, Angela L Lee, Robert M Sapolsky, Bruce L Tempel, Philip A Schwartzkroin. Epilepsia 2007
48
25

Developmental seizure susceptibility of kv1.1 potassium channel knockout mice.
J M Rho, P Szot, B L Tempel, P A Schwartzkroin. Dev Neurosci 1999
70
17

Cardiorespiratory profiling reveals primary breathing dysfunction in Kcna1-null mice: Implications for sudden unexpected death in epilepsy.
Hemangini Dhaibar, Nicole M Gautier, Oleg Y Chernyshev, Paari Dominic, Edward Glasscock. Neurobiol Dis 2019
24
50

Loss of the Kv1.1 potassium channel promotes pathologic sharp waves and high frequency oscillations in in vitro hippocampal slices.
Timothy A Simeone, Kristina A Simeone, Kaeli K Samson, Do Young Kim, Jong M Rho. Neurobiol Dis 2013
46
23

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
101
11

The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1.
Uwe Schulte, Jörg-Oliver Thumfart, Nikolaj Klöcker, Claudia A Sailer, Wolfgang Bildl, Martin Biniossek, Doris Dehn, Thomas Deller, Silke Eble, Karen Abbass,[...]. Neuron 2006
226
10


Action potential broadening in a presynaptic channelopathy.
Rahima Begum, Yamina Bakiri, Kirill E Volynski, Dimitri M Kullmann. Nat Commun 2016
37
27

Respiratory dysfunction progresses with age in Kcna1-null mice, a model of sudden unexpected death in epilepsy.
Kristina A Simeone, Jodi Hallgren, Charles S Bockman, Ankita Aggarwal, Vikash Kansal, Lauren Netzel, Shruthi H Iyer, Stephanie A Matthews, Malavika Deodhar, Peter J Oldenburg,[...]. Epilepsia 2018
23
43

Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy.
Yuko Fukata, Kathryn L Lovero, Tsuyoshi Iwanaga, Atsushi Watanabe, Norihiko Yokoi, Katsuhiko Tabuchi, Ryuichi Shigemoto, Roger A Nicoll, Masaki Fukata. Proc Natl Acad Sci U S A 2010
213
9

Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice.
Elodie Chabrol, Vincent Navarro, Giovanni Provenzano, Ivan Cohen, Céline Dinocourt, Sophie Rivaud-Péchoux, Desdemona Fricker, Michel Baulac, Richard Miles, Eric Leguern,[...]. Brain 2010
88
10

Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission.
Yuko Fukata, Hillel Adesnik, Tsuyoshi Iwanaga, David S Bredt, Roger A Nicoll, Masaki Fukata. Science 2006
263
9

Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotonia.
Sarosh R Irani, Sian Alexander, Patrick Waters, Kleopas A Kleopa, Philippa Pettingill, Luigi Zuliani, Elior Peles, Camilla Buckley, Bethan Lang, Angela Vincent. Brain 2010
844
9

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
172
9

Inactivation properties of voltage-gated K+ channels altered by presence of beta-subunit.
J Rettig, S H Heinemann, F Wunder, C Lorra, D N Parcej, J O Dolly, O Pongs. Nature 1994
732
9

Distinctive role of KV1.1 subunit in the biology and functions of low threshold K(+) channels with implications for neurological disease.
Saak V Ovsepian, Marie LeBerre, Volker Steuber, Valerie B O'Leary, Christian Leibold, J Oliver Dolly. Pharmacol Ther 2016
33
27

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
9

Ketone bodies mediate antiseizure effects through mitochondrial permeability transition.
Do Young Kim, Kristina A Simeone, Timothy A Simeone, Jignesh D Pandya, Julianne C Wilke, Younghee Ahn, James W Geddes, Patrick G Sullivan, Jong M Rho. Ann Neurol 2015
111
9

Sudden unexpected death in epilepsy: assessing the public health burden.
David J Thurman, Dale C Hesdorffer, Jacqueline A French. Epilepsia 2014
235
9


Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability.
Y Eugene Yu, Lei Wen, Jeane Silva, Zhongyou Li, Karen Head, Khalid Sossey-Alaoui, Annie Pao, Lin Mei, John K Cowell. Hum Mol Genet 2010
87
9

Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series.
Meizan Lai, Maartje G M Huijbers, Eric Lancaster, Francesc Graus, Luis Bataller, Rita Balice-Gordon, John K Cowell, Josep Dalmau. Lancet Neurol 2010
656
8

Autoantibodies to epilepsy-related LGI1 in limbic encephalitis neutralize LGI1-ADAM22 interaction and reduce synaptic AMPA receptors.
Toshika Ohkawa, Yuko Fukata, Miwako Yamasaki, Taisuke Miyazaki, Norihiko Yokoi, Hiroshi Takashima, Masahiko Watanabe, Osamu Watanabe, Masaki Fukata. J Neurosci 2013
207
8

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

Two heteromeric Kv1 potassium channels differentially regulate action potential firing.
Paul D Dodson, Matthew C Barker, Ian D Forsythe. J Neurosci 2002
158
8

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
19

Masking epilepsy by combining two epilepsy genes.
Edward Glasscock, Jing Qian, Jong W Yoo, Jeffrey L Noebels. Nat Neurosci 2007
93
8

Potassium channels Kv1.1, Kv1.2 and Kv1.6 influence excitability of rat visceral sensory neurons.
Patricia A Glazebrook, Angelina N Ramirez, John H Schild, Char-Chang Shieh, Thanh Doan, Barbara A Wible, Diana L Kunze. J Physiol 2002
88
9

Genomic biomarkers of SUDEP in brain and heart.
Edward Glasscock. Epilepsy Behav 2014
51
15

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions.
Paola Imbrici, Concetta Altamura, Francesca Gualandi, Giuseppe Felice Mangiatordi, Marcella Neri, Giovanni De Maria, Alessandra Ferlini, Alessandro Padovani, Maria Cristina D'Adamo, Orazio Nicolotti,[...]. Mol Cell Neurosci 2017
16
50

De novo KCNA1 variants in the PVP motif cause infantile epileptic encephalopathy and cognitive impairment similar to recurrent KCNA2 variants.
Amanda Rogers, Paul Golumbek, Elena Cellini, Viola Doccini, Renzo Guerrini, Carina Wallgren-Pettersson, Ann-Charlotte Thuresson, Christina A Gurnett. Am J Med Genet A 2018
20
40

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.
Kelsey Paulhus, Lauren Ammerman, Edward Glasscock. Int J Mol Sci 2020
29
27

Chemical corrector treatment ameliorates increased seizure susceptibility in a mouse model of familial epilepsy.
Norihiko Yokoi, Yuko Fukata, Daisuke Kase, Taisuke Miyazaki, Martine Jaegle, Toshika Ohkawa, Naoki Takahashi, Hiroko Iwanari, Yasuhiro Mochizuki, Takao Hamakubo,[...]. Nat Med 2015
45
15

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
Sergey Kalachikov, Oleg Evgrafov, Barbara Ross, Melodie Winawer, Christie Barker-Cummings, Filippo Martinelli Boneschi, Chang Choi, Pavel Morozov, Kamna Das, Elita Teplitskaya,[...]. Nat Genet 2002
437
7



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.