A citation-based method for searching scientific literature

David A Brown, Gayle M Passmore. Br J Pharmacol 2009
Times Cited: 444







List of co-cited articles
1016 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
936
35



Pathways modulating neural KCNQ/M (Kv7) potassium channels.
Patrick Delmas, David A Brown. Nat Rev Neurosci 2005
484
26


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
415
18


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
808
17


Modulation of Kv7 channels and excitability in the brain.
Derek L Greene, Naoto Hoshi. Cell Mol Life Sci 2017
80
20

Functional significance of axonal Kv7 channels in hippocampal pyramidal neurons.
Mala M Shah, Michele Migliore, Ignacio Valencia, Edward C Cooper, David A Brown. Proc Natl Acad Sci U S A 2008
187
16

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
887
15


KCNQ2 is a nodal K+ channel.
Jérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, Steven S Scherer. J Neurosci 2004
309
15

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
304
15

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
384
14



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
292
12

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
195
11

Heteromeric Kv7.2/7.3 channels differentially regulate action potential initiation and conduction in neocortical myelinated axons.
Arne Battefeld, Baouyen T Tran, Jason Gavrilis, Edward C Cooper, Maarten H P Kole. J Neurosci 2014
103
11


Disruption of the epilepsy KCNQ2 gene results in neural hyperexcitability.
H Watanabe, E Nagata, A Kosakai, M Nakamura, M Yokoyama, K Tanaka, H Sasai. J Neurochem 2000
137
11

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
139
11

KCNQ/M currents in sensory neurons: significance for pain therapy.
Gayle M Passmore, Alexander A Selyanko, Mohini Mistry, Mona Al-Qatari, Stephen J Marsh, Elizabeth A Matthews, Anthony H Dickenson, Terry A Brown, Stephen A Burbidge, Martin Main,[...]. J Neurosci 2003
242
11

Control of M-current.
N V Marrion. Annu Rev Physiol 1997
275
11



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
110
10

M-type K+ channels in peripheral nociceptive pathways.
Xiaona Du, Haixia Gao, David Jaffe, Hailin Zhang, Nikita Gamper. Br J Pharmacol 2018
35
28


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
81
11




Regulation of neural KCNQ channels: signalling pathways, structural motifs and functional implications.
Ciria C Hernandez, Oleg Zaika, Gleb P Tolstykh, Mark S Shapiro. J Physiol 2008
123
9

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
136
9

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels.
Maria Virginia Soldovieri, Francesco Miceli, Maurizio Taglialatela. Physiology (Bethesda) 2011
100
9

Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons.
Brian J Wainger, Evangelos Kiskinis, Cassidy Mellin, Ole Wiskow, Steve S W Han, Jackson Sandoe, Numa P Perez, Luis A Williams, Seungkyu Lee, Gabriella Boulting,[...]. Cell Rep 2014
385
9

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
732
9

KCNQ-Encoded Potassium Channels as Therapeutic Targets.
Vincenzo Barrese, Jennifer B Stott, Iain A Greenwood. Annu Rev Pharmacol Toxicol 2018
61
14

KCNQ channel openers reverse depressive symptoms via an active resilience mechanism.
Allyson K Friedman, Barbara Juarez, Stacy M Ku, Hongxing Zhang, Rhodora C Calizo, Jessica J Walsh, Dipesh Chaudhury, Song Zhang, Angel Hawkins, David M Dietz,[...]. Nat Commun 2016
73
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
88
9


Heterozygous loss of epilepsy gene KCNQ2 alters social, repetitive and exploratory behaviors.
Eung Chang Kim, Jaimin Patel, Jiaren Zhang, Heun Soh, Justin S Rhodes, Anastasios V Tzingounis, Hee Jung Chung. Genes Brain Behav 2020
17
47

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
133
8

Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.
Mathieu Milh, Nadia Boutry-Kryza, Julie Sutera-Sardo, Cyril Mignot, Stéphane Auvin, Caroline Lacoste, Nathalie Villeneuve, Agathe Roubertie, Bénédicte Heron, Maryline Carneiro,[...]. Orphanet J Rare Dis 2013
65
12

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
117
8

Structural Basis of Human KCNQ1 Modulation and Gating.
Ji Sun, Roderick MacKinnon. Cell 2020
86
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.