A citation-based method for searching scientific literature

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, M L McHarg, D Gagnon, T O Rosales, A Peiffer, V E Anderson, M Leppert. Nat Genet 1998
Times Cited: 871







List of co-cited articles
1196 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Deletion of KCNQ2/3 potassium channels from PV+ interneurons leads to homeostatic potentiation of excitatory transmission.
Heun Soh, Suhyeorn Park, Kali Ryan, Kristen Springer, Atul Maheshwari, Anastasios V Tzingounis. Elife 2018
19
31

A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy.
Anna Lauritano, Sebastien Moutton, Elena Longobardi, Frédéric Tran Mau-Them, Giusy Laudati, Piera Nappi, Maria Virginia Soldovieri, Paolo Ambrosino, Mauro Cataldi, Thibaud Jouan,[...]. Epilepsia Open 2019
16
37


KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.
T Kharkovets, J P Hardelin, S Safieddine, M Schweizer, A El-Amraoui, C Petit, T J Jentsch. Proc Natl Acad Sci U S A 2000
293
6

D-23129: a new anticonvulsant with a broad spectrum activity in animal models of epileptic seizures.
A Rostock, C Tober, C Rundfeldt, R Bartsch, J Engel, E E Polymeropoulos, B Kutscher, W Löscher, D Hönack, H S White,[...]. Epilepsy Res 1996
196
6

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Dalia Kasperaviciute, Claudia B Catarino, Mar Matarin, Costin Leu, Jan Novy, Anna Tostevin, Bárbara Leal, Ellen V S Hessel, Kerstin Hallmann, Michael S Hildebrand,[...]. Brain 2013
98
5

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag,[...]. Brain 2010
315
5


Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear.
Paolo Aridon, Carla Marini, Chiara Di Resta, Elisa Brilli, Maurizio De Fusco, Fausta Politi, Elena Parrini, Irene Manfredi, Tiziana Pisano, Dario Pruna,[...]. Am J Hum Genet 2006
146
5

A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy.
Atsushi Ishii, Jing-Qiong Kang, Cara C Schornak, Ciria C Hernandez, Wangzhen Shen, Joseph C Watkins, Robert L Macdonald, Shinichi Hirose. J Med Genet 2017
32
15

Calmodulin mediates Ca2+-dependent modulation of M-type K+ channels.
Nikita Gamper, Mark S Shapiro. J Gen Physiol 2003
173
5

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
153
5

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
240
5

A pore residue of the KCNQ3 potassium M-channel subunit controls surface expression.
Juan Camilo Gómez-Posada, Ainhoa Etxeberría, Meritxell Roura-Ferrer, Pilar Areso, Marianela Masin, Ruth D Murrell-Lagnado, Alvaro Villarroel. J Neurosci 2010
34
14

A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly.
Michael Schwake, Thomas J Jentsch, Thomas Friedrich. EMBO Rep 2003
112
5

KCNQ channels regulate age-related memory impairment.
Sonia Cavaliere, Bilal R Malik, James J L Hodge. PLoS One 2013
21
23


Structural basis of a Kv7.1 potassium channel gating module: studies of the intracellular c-terminal domain in complex with calmodulin.
Dana Sachyani, Meidan Dvir, Roi Strulovich, Giancarlo Tria, William Tobelaim, Asher Peretz, Olaf Pongs, Dmitri Svergun, Bernard Attali, Joel A Hirsch. Structure 2014
56
8

Activation of peripheral KCNQ channels attenuates inflammatory pain.
Hiroki Hayashi, Masashi Iwata, Noboru Tsuchimori, Tatsumi Matsumoto. Mol Pain 2014
30
16

Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors.
A A Selyanko, J K Hadley, I C Wood, F C Abogadie, T J Jentsch, D A Brown. J Physiol 2000
134
5

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
61
8




IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
J Tyson, L Tranebjaerg, S Bellman, C Wren, J F Taylor, J Bathen, B Aslaksen, S J Sørland, O Lund, S Malcolm,[...]. Hum Mol Genet 1997
235
5

Quinidine in the treatment of KCNT1-positive epilepsies.
Mohamad A Mikati, Yong-Hui Jiang, Michael Carboni, Vandana Shashi, Slave Petrovski, Rebecca Spillmann, Carol J Milligan, Melody Li, Annette Grefe, Allyn McConkie,[...]. Ann Neurol 2015
102
5

GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy.
Johannes R Lemke, Rik Hendrickx, Kirsten Geider, Bodo Laube, Michael Schwake, Robert J Harvey, Victoria M James, Alex Pepler, Isabelle Steiner, Konstanze Hörtnagel,[...]. Ann Neurol 2014
129
5

Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.
Cas Simons, Lachlan D Rash, Joanna Crawford, Linlin Ma, Ben Cristofori-Armstrong, David Miller, Kelin Ru, Gregory J Baillie, Yasemin Alanay, Adeline Jacquinet,[...]. Nat Genet 2015
81
6

GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Dong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, Eric D Marsh, Lifeng Tian, Elizabeth M McCormick, Gabrielle J Kosobucki, Wenjuan Chen, Anthony J Schulien, Rosetta Chiavacci,[...]. Am J Hum Genet 2016
97
5

De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
Caroline Nava, Carine Dalle, Agnès Rastetter, Pasquale Striano, Carolien G F de Kovel, Rima Nabbout, Claude Cancès, Dorothée Ville, Eva H Brilstra, Giuseppe Gobbi,[...]. Nat Genet 2014
119
5

Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment.
Scott C Baraban, Matthew T Dinday, Gabriela A Hortopan. Nat Commun 2013
208
5

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
173
5

KCNQ4 channel activation by BMS-204352 and retigabine.
R L Schrøder, T Jespersen, P Christophersen, D Strøbaek, B S Jensen, S P Olesen. Neuropharmacology 2001
96
5


Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Yong-hui Jiang, Ryan K C Yuen, Xin Jin, Mingbang Wang, Nong Chen, Xueli Wu, Jia Ju, Junpu Mei, Yujian Shi, Mingze He,[...]. Am J Hum Genet 2013
279
5

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
Sabine Endele, Georg Rosenberger, Kirsten Geider, Bernt Popp, Ceyhun Tamer, Irina Stefanova, Mathieu Milh, Fanny Kortüm, Angela Fritsch, Friederike K Pientka,[...]. Nat Genet 2010
304
5

Somatodendritic Kv7/KCNQ/M channels control interspike interval in hippocampal interneurons.
J Josh Lawrence, Fernanda Saraga, Joseph F Churchill, Jeffrey M Statland, Katherine E Travis, Frances K Skinner, Chris J McBain. J Neurosci 2006
102
5

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, Natalia Lozovaya, Audrey Labalme, Nadia Boutry-Kryza, Manal Salmi, Timur Tsintsadze, Laura Addis, Jacques Motte,[...]. Nat Genet 2013
249
5

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
Johannes R Lemke, Dennis Lal, Eva M Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin Finsterwalder,[...]. Nat Genet 2013
242
5

Mutations in DEPDC5 cause familial focal epilepsy with variable foci.
Leanne M Dibbens, Boukje de Vries, Simona Donatello, Sarah E Heron, Bree L Hodgson, Satyan Chintawar, Douglas E Crompton, James N Hughes, Susannah T Bellows, Karl Martin Klein,[...]. Nat Genet 2013
188
5

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
5


De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy.
Hirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi, Keisuke Hamada, Hitoshi Osaka, Jun Tohyama, Katsuhisa Uruno, Satoko Kumada, Kiyomi Nishiyama, Akira Nishimura,[...]. Nat Genet 2008
350
5

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
56
8

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
26
19

Blue-gray mucocutaneous discoloration: a new adverse effect of ezogabine.
Tali Garin Shkolnik, Hana Feuerman, Elena Didkovsky, Ilana Kaplan, Reuven Bergman, Lev Pavlovsky, Emmilia Hodak. JAMA Dermatol 2014
44
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
587
5

Abnormal γ-aminobutyric acid neurotransmission in a Kcnq2 model of early onset epilepsy.
Taku Uchida, Christoph Lossin, Yukiko Ihara, Masanobu Deshimaru, Yuchio Yanagawa, Susumu Koyama, Shinichi Hirose. Epilepsia 2017
9
55

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
5

Defining and searching for structural motifs using DeepView/Swiss-PdbViewer.
Maria U Johansson, Vincent Zoete, Olivier Michielin, Nicolas Guex. BMC Bioinformatics 2012
141
5


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.