A citation-based method for searching scientific literature

C Biervert, B C Schroeder, C Kubisch, S F Berkovic, P Propping, T J Jentsch, O K Steinlein. Science 1998
Times Cited: 795







List of co-cited articles
1073 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
876
64

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
915
49

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
C Charlier, N A Singh, S G Ryan, T B Lewis, B E Reus, R J Leach, M Leppert. Nat Genet 1998
728
45

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
290
34


Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.
Sarah Weckhuysen, Vanja Ivanovic, Rik Hendrickx, Rudy Van Coster, Helle Hjalgrim, Rikke S Møller, Sabine Grønborg, An-Sofie Schoonjans, Berten Ceulemans, Sinead B Heavin,[...]. Neurology 2013
130
26


Neural KCNQ (Kv7) channels.
David A Brown, Gayle M Passmore. Br J Pharmacol 2009
421
21


KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness.
C Kubisch, B C Schroeder, T Friedrich, B Lütjohann, A El-Amraoui, S Marlin, C Petit, T J Jentsch. Cell 1999
615
20




Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.
Mitsuhiro Kato, Takanori Yamagata, Masaya Kubota, Hiroshi Arai, Sumimasa Yamashita, Taku Nakagawa, Takanari Fujii, Kenji Sugai, Kaoru Imai, Tami Uster,[...]. Epilepsia 2013
132
18


Pathways modulating neural KCNQ/M (Kv7) potassium channels.
Patrick Delmas, David A Brown. Nat Rev Neurosci 2005
469
18

PIP(2) activates KCNQ channels, and its hydrolysis underlies receptor-mediated inhibition of M currents.
Hailin Zhang, Liviu C Craciun, Tooraj Mirshahi, Tibor Rohács, Coeli M B Lopes, Taihao Jin, Diomedes E Logothetis. Neuron 2003
401
18

Molecular determinants of KCNQ (Kv7) K+ channel sensitivity to the anticonvulsant retigabine.
Anne Schenzer, Thomas Friedrich, Michael Pusch, Paul Saftig, Thomas J Jentsch, Joachim Grötzinger, Michael Schwake. J Neurosci 2005
191
18

Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits.
Francesco Miceli, Maria Virginia Soldovieri, Paolo Ambrosino, Vincenzo Barrese, Michele Migliore, Maria Roberta Cilio, Maurizio Taglialatela. Proc Natl Acad Sci U S A 2013
109
17

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.
Francesco Miceli, Maria Virginia Soldovieri, Paolo Ambrosino, Michela De Maria, Michele Migliore, Rosanna Migliore, Maurizio Taglialatela. J Neurosci 2015
89
19

KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients.
John J Millichap, Kristen L Park, Tammy Tsuchida, Bruria Ben-Zeev, Lionel Carmant, Robert Flamini, Nishtha Joshi, Paul M Levisohn, Eric Marsh, Srishti Nangia,[...]. Neurol Genet 2016
99
17

A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon.
Zongming Pan, Tingching Kao, Zsolt Horvath, Julia Lemos, Jai-Yoon Sul, Stephen D Cranstoun, Vann Bennett, Steven S Scherer, Edward C Cooper. J Neurosci 2006
374
16

The KCNQ5 potassium channel mediates a component of the afterhyperpolarization current in mouse hippocampus.
Anastassios V Tzingounis, Matthias Heidenreich, Tatjana Kharkovets, Guillermo Spitzmaul, Henrik S Jensen, Roger A Nicoll, Thomas J Jentsch. Proc Natl Acad Sci U S A 2010
71
22

Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.
Gökce Orhan, Merle Bock, Dorien Schepers, Elena I Ilina, Stephanie Nadine Reichel, Heidi Löffler, Nicole Jezutkovic, Sarah Weckhuysen, Simone Mandelstam, Arvid Suls,[...]. Ann Neurol 2014
124
14

Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels.
A D Wickenden, W Yu, A Zou, T Jegla, P K Wagoner. Mol Pharmacol 2000
240
14

Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine.
M J Main, J E Cryan, J R Dupere, B Cox, J J Clare, S A Burbidge. Mol Pharmacol 2000
225
14

Atomic basis for therapeutic activation of neuronal potassium channels.
Robin Y Kim, Michael C Yau, Jason D Galpin, Guiscard Seebohm, Christopher A Ahern, Stephan A Pless, Harley T Kurata. Nat Commun 2015
48
27

KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents.
B C Schroeder, M Hechenberger, F Weinreich, C Kubisch, T J Jentsch. J Biol Chem 2000
283
13

Regulation of Kv7 (KCNQ) K+ channel open probability by phosphatidylinositol 4,5-bisphosphate.
Yang Li, Nikita Gamper, Donald W Hilgemann, Mark S Shapiro. J Neurosci 2005
188
12

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.
N Neyroud, F Tesson, I Denjoy, M Leibovici, C Donger, J Barhanin, S Fauré, F Gary, P Coumel, C Petit,[...]. Nat Genet 1997
658
12

Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy.
E C Cooper, K D Aldape, A Abosch, N M Barbaro, M S Berger, W S Peacock, Y N Jan, L Y Jan. Proc Natl Acad Sci U S A 2000
159
12


The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7.2 (KCNQ2) channel by binding to its activation gate.
Thomas V Wuttke, Guiscard Seebohm, Sigrid Bail, Snezana Maljevic, Holger Lerche. Mol Pharmacol 2005
194
12

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
Nanda A Singh, Peter Westenskow, Carole Charlier, Chris Pappas, Jonathan Leslie, Jessica Dillon, V Elving Anderson, Michael C Sanguinetti, Mark F Leppert. Brain 2003
199
12


Distribution of M-channel subunits KCNQ2 and KCNQ3 in rat hippocampus.
Felicia Klinger, Georgianna Gould, Stefan Boehm, Mark S Shapiro. Neuroimage 2011
36
33


De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe. Am J Hum Genet 2001
795
11

Direct neurotransmitter activation of voltage-gated potassium channels.
Rían W Manville, Maria Papanikolaou, Geoffrey W Abbott. Nat Commun 2018
39
28

Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity.
C Lerche, C R Scherer, G Seebohm, C Derst, A D Wei, A E Busch, K Steinmeyer. J Biol Chem 2000
210
11

Structural Basis of Human KCNQ1 Modulation and Gating.
Ji Sun, Roderick MacKinnon. Cell 2020
68
16

A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.
R Borgatti, C Zucca, A Cavallini, M Ferrario, C Panzeri, P Castaldo, M V Soldovieri, C Baschirotto, N Bresolin, B Dalla Bernardina,[...]. Neurology 2004
112
10

Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.
Nanda A Singh, James F Otto, E Jill Dahle, Chris Pappas, Jonathan D Leslie, Alex Vilaythong, Jeffrey L Noebels, H Steve White, Karen S Wilcox, Mark F Leppert. J Physiol 2008
83
12

Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.
Hirotomo Saitsu, Mitsuhiro Kato, Ayaka Koide, Tomohide Goto, Takako Fujita, Kiyomi Nishiyama, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Kiyoshi Hayasaka,[...]. Ann Neurol 2012
72
13

Molecular correlates of the M-current in cultured rat hippocampal neurons.
M M Shah, M Mistry, S J Marsh, D A Brown, P Delmas. J Physiol 2002
156
10

Kv7.1 ion channels require a lipid to couple voltage sensing to pore opening.
Mark A Zaydman, Jonathan R Silva, Kelli Delaloye, Yang Li, Hongwu Liang, H Peter Larsson, Jingyi Shi, Jianmin Cui. Proc Natl Acad Sci U S A 2013
118
10


Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.
M C Sanguinetti, M E Curran, A Zou, J Shen, P S Spector, D L Atkinson, M T Keating. Nature 1996
10

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels.
Maria Virginia Soldovieri, Francesco Miceli, Maurizio Taglialatela. Physiology (Bethesda) 2011
98
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.