A citation-based method for searching scientific literature

Anna Lehman, Samrat Thouta, Grazia M S Mancini, Sakkubai Naidu, Marjon van Slegtenhorst, Kirsty McWalter, Richard Person, Jill Mwenifumbo, Ramona Salvarinova, Ilaria Guella, Marna B McKenzie, Anita Datta, Mary B Connolly, Somayeh Mojard Kalkhoran, Damon Poburko, Jan M Friedman, Matthew J Farrer, Michelle Demos, Sonal Desai, Thomas Claydon. Am J Hum Genet 2017
Times Cited: 54







List of co-cited articles
634 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
930
27

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
622
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
24

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
22

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
20

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
287
20

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
18

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
74
18

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
94
16


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
193
14

Modulation of Kv7 channels and excitability in the brain.
Derek L Greene, Naoto Hoshi. Cell Mol Life Sci 2017
78
14


Neural KCNQ (Kv7) channels.
David A Brown, Gayle M Passmore. Br J Pharmacol 2009
438
14

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
731
14

Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.
Krishna R Veeramah, Laurel Johnstone, Tatiana M Karafet, Daniel Wolf, Ryan Sprissler, John Salogiannis, Asa Barth-Maron, Michael E Greenberg, Till Stuhlmann, Stefanie Weinert,[...]. Epilepsia 2013
176
14


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
133
14

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
211
14


Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability.
Giulia Rosti, Elisa Tassano, Simone Bossi, Maria Teresa Divizia, Patrizia Ronchetto, Martina Servetti, Margherita Lerone, Livia Pisciotta, Maria Margherita Mancardi, Edvige Veneselli,[...]. Eur J Med Genet 2019
9
88

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
194
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
51
15

Pathways modulating neural KCNQ/M (Kv7) potassium channels.
Patrick Delmas, David A Brown. Nat Rev Neurosci 2005
480
14

Structural Basis of Human KCNQ1 Modulation and Gating.
Ji Sun, Roderick MacKinnon. Cell 2020
78
14

Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H.
Sarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, John L Carroll, Sabine Grønborg, Yong-Hui Jiang, Nishtha Joshi, Megan Kelly, David A Koolen, Mohamad A Mikati,[...]. Epilepsia 2017
36
19

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
12

De novo KCNB1 mutations in epileptic encephalopathy.
Ali Torkamani, Kevin Bersell, Benjamin S Jorge, Robert L Bjork, Jennifer R Friedman, Cinnamon S Bloss, Julie Cohen, Siddharth Gupta, Sakkubai Naidu, Carlos G Vanoye,[...]. Ann Neurol 2014
85
12

A constitutively open potassium channel formed by KCNQ1 and KCNE3.
B C Schroeder, S Waldegger, S Fehr, M Bleich, R Warth, R Greger, T J Jentsch. Nature 2000
388
12

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
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
662
12


Direct neurotransmitter activation of voltage-gated potassium channels.
Rían W Manville, Maria Papanikolaou, Geoffrey W Abbott. Nat Commun 2018
41
17

Autism and developmental disability caused by KCNQ3 gain-of-function variants.
Tristan T Sands, Francesco Miceli, Gaetan Lesca, Anita E Beck, Lynette G Sadleir, Daniel K Arrington, Bitten Schönewolf-Greulich, Sébastien Moutton, Anna Lauritano, Piera Nappi,[...]. Ann Neurol 2019
25
28

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
411
12

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
122
12

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
11

Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant.
John J Millichap, Francesco Miceli, Michela De Maria, Cynthia Keator, Nishtha Joshi, Baouyen Tran, Maria Virginia Soldovieri, Paolo Ambrosino, Vandana Shashi, Mohamad A Mikati,[...]. Epilepsia 2017
41
14

KCNQ5 K(+) channels control hippocampal synaptic inhibition and fast network oscillations.
Pawel Fidzinski, Tatiana Korotkova, Matthias Heidenreich, Nikolaus Maier, Sebastian Schuetze, Oliver Kobler, Werner Zuschratter, Dietmar Schmitz, Alexey Ponomarenko, Thomas J Jentsch. Nat Commun 2015
30
20

A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly.
Michael Schwake, Thomas J Jentsch, Thomas Friedrich. EMBO Rep 2003
112
11

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current.
J Barhanin, F Lesage, E Guillemare, M Fink, M Lazdunski, G Romey. Nature 1996
11

The C-terminus of Kv7 channels: a multifunctional module.
Yoni Haitin, Bernard Attali. J Physiol 2008
103
11

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
Q Wang, M E Curran, I Splawski, T C Burn, J M Millholland, T J VanRaay, J Shen, K W Timothy, G M Vincent, T de Jager,[...]. Nat Genet 1996
11

A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.
Francesco Miceli, Pasquale Striano, Maria Virginia Soldovieri, Antonina Fontana, Rosaria Nardello, Angela Robbiano, Giulia Bellini, Maurizio Elia, Federico Zara, Maurizio Taglialatela,[...]. Epilepsia 2015
43
13


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
380
11

Gabapentin Is a Potent Activator of KCNQ3 and KCNQ5 Potassium Channels.
Rían W Manville, Geoffrey W Abbott. Mol Pharmacol 2018
32
18


Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion.
Nicholas M Allen, Judith Conroy, Amre Shahwan, Bryan Lynch, Raony G Correa, Sergio D J Pena, Dara McCreary, Tiago R Magalhães, Sean Ennis, Sally A Lynch,[...]. Epilepsia 2016
106
11

Molecular and functional characterization of Kv7 K+ channel in murine gastrointestinal smooth muscles.
Thomas A Jepps, Iain A Greenwood, James D Moffatt, Kenton M Sanders, Susumu Ohya. Am J Physiol Gastrointest Liver Physiol 2009
55
11


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.