A citation-based method for searching scientific literature

Benjamin S Jorge, Courtney M Campbell, Alison R Miller, Elizabeth D Rutter, Christina A Gurnett, Carlos G Vanoye, Alfred L George, Jennifer A Kearney. Proc Natl Acad Sci U S A 2011
Times Cited: 47







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



Times Cited
  Times     Co-cited
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Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.
Huimin Wu, Jill A Cowing, Michel Michaelides, Susan E Wilkie, Glen Jeffery, Sharon A Jenkins, Viktoria Mester, Alan C Bird, Anthony G Robson, Graham E Holder,[...]. Am J Hum Genet 2006
87
31

Fine mapping of an epilepsy modifier gene on mouse Chromosome 19.
Sarah K Bergren, Elizabeth D Rutter, Jennifer A Kearney. Mamm Genome 2009
25
40


Deletion of the Kv2.1 delayed rectifier potassium channel leads to neuronal and behavioral hyperexcitability.
D J Speca, G Ogata, D Mandikian, H I Bishop, S W Wiler, K Eum, H Jürgen Wenzel, E T Doisy, L Matt, K L Campi,[...]. Genes Brain Behav 2014
62
21

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
117
19

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
19

Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
Bernd Wissinger, Susann Dangel, Herbert Jägle, Lars Hansen, Britta Baumann, Günther Rudolph, Christiane Wolf, Michael Bonin, Katja Koeppen, Thomas Ladewig,[...]. Invest Ophthalmol Vis Sci 2008
64
17


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
255
17

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
Frank H Yu, Massimo Mantegazza, Ruth E Westenbroek, Carol A Robbins, Franck Kalume, Kimberly A Burton, William J Spain, G Stanley McKnight, Todd Scheuer, William A Catterall. Nat Neurosci 2006
676
17

Electrically silent Kv subunits: their molecular and functional characteristics.
Elke Bocksteins, Dirk J Snyders. Physiology (Bethesda) 2012
48
17

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
17

Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a.
Sarah K Bergren, Shu Chen, Andrzej Galecki, Jennifer A Kearney. Mamm Genome 2005
43
16

A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities.
J A Kearney, N W Plummer, M R Smith, J Kapur, T R Cummins, S G Waxman, A L Goldin, M H Meisler. Neuroscience 2001
167
14

Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.
Bernd Wissinger, Simone Schaich, Britta Baumann, Michael Bonin, Herbert Jägle, Christoph Friedburg, Balázs Varsányi, Carel B Hoyng, Hélène Dollfus, John R Heckenlively,[...]. Hum Mutat 2011
39
17

Crystal structure of a mammalian voltage-dependent Shaker family K+ channel.
Stephen B Long, Ernest B Campbell, Roderick Mackinnon. Science 2005
14

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
603
14

"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
Anthony G Robson, Andrew R Webster, Michel Michaelides, Susan M Downes, Jill A Cowing, David M Hunt, Anthony T Moore, Graham E Holder. Retina 2010
46
15

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
14

A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy.
Baljinder Singh, Ikuo Ogiwara, Makoto Kaneda, Natsuko Tokonami, Emi Mazaki, Koichi Baba, Kazumi Matsuda, Yushi Inoue, Kazuhiro Yamakawa. Neurobiol Dis 2006
86
14

K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy.
Maria Cristina D'Adamo, Luigi Catacuzzeno, Giuseppe Di Giovanni, Fabio Franciolini, Mauro Pessia. Front Cell Neurosci 2013
66
14

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
14

Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects.
Miriam H Meisler, Janelle E O'Brien, Lisa M Sharkey. J Physiol 2010
142
12

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
A Escayg, B T MacDonald, M H Meisler, S Baulac, G Huberfeld, I An-Gourfinkel, A Brice, E LeGuern, B Moulard, D Chaigne,[...]. Nat Genet 2000
708
12

Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.
Sureka Thiagalingam, Terri L McGee, Richard G Weleber, Michael A Sandberg, Karmen M Trzupek, Eliot L Berson, Thaddeus P Dryja. Ophthalmic Genet 2007
36
16

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
430
12

Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities.
Melinda S Martin, Karoni Dutt, Ligia A Papale, Céline M Dubé, Stacey B Dutton, Georgius de Haan, Anupama Shankar, Sergio Tufik, Miriam H Meisler, Tallie Z Baram,[...]. J Biol Chem 2010
148
12

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
Nicole A Hawkins, Melinda S Martin, Wayne N Frankel, Jennifer A Kearney, Andrew Escayg. Neurobiol Dis 2011
59
12


High-resolution optical coherence tomography imaging in KCNV2 retinopathy.
Panagiotis I Sergouniotis, Graham E Holder, Anthony G Robson, Michel Michaelides, Andrew R Webster, Anthony T Moore. Br J Ophthalmol 2012
42
14

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
12

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction.
T Sugawara, Y Tsurubuchi, K L Agarwala, M Ito, G Fukuma, E Mazaki-Miyazaki, H Nagafuji, M Noda, K Imoto, K Wada,[...]. Proc Natl Acad Sci U S A 2001
300
12


Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
Wei Du, Jocelyn F Bautista, Huanghe Yang, Ana Diez-Sampedro, Sun-Ah You, Lejin Wang, Prakash Kotagal, Hans O Lüders, Jingyi Shi, Jianmin Cui,[...]. Nat Genet 2005
381
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
114
12

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
12

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata,[...]. J Neurosci 2007
525
12

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
955
12

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
12

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.
Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, Karen L Oliver, Snezana Maljevic, Marta A Bayly, Tarja Joensuu, Laura Canafoglia, Silvana Franceschetti, Roberto Michelucci,[...]. Nat Genet 2015
157
12

Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogram.
Katie E Smith, Susan E Wilkie, Joseph T Tebbs-Warner, Bradley J Jarvis, Linn Gallasch, Martin Stocker, David M Hunt. J Biol Chem 2012
12
50


A novel epileptic encephalopathy mutation in KCNB1 disrupts Kv2.1 ion selectivity, expression, and localization.
Isabelle Thiffault, David J Speca, Daniel C Austin, Melanie M Cobb, Kenneth S Eum, Nicole P Safina, Lauren Grote, Emily G Farrow, Neil Miller, Sarah Soden,[...]. J Gen Physiol 2015
51
12

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
12

Potassium Channels and Human Epileptic Phenotypes: An Updated Overview.
Chiara Villa, Romina Combi. Front Cell Neurosci 2016
66
12

Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.
Thomas N Ferraro, Gregory T Golden, George G Smith, James F Martin, Falk W Lohoff, Tracy A Gieringer, Deborah Zamboni, Candice L Schwebel, Danielle M Press, Stephanie O Kratzer,[...]. Mamm Genome 2004
109
10

New modulatory alpha subunits for mammalian Shab K+ channels.
M Salinas, F Duprat, C Heurteaux, J P Hugnot, M Lazdunski. J Biol Chem 1997
159
10

Kv2.1 and silent Kv subunits underlie the delayed rectifier K+ current in cultured small mouse DRG neurons.
Elke Bocksteins, Adam L Raes, Gerda Van de Vijver, Tine Bruyns, Pierre-Paul Van Bogaert, Dirk J Snyders. Am J Physiol Cell Physiol 2009
45
11

Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram.
Safouane Ben Salah, Satomi Kamei, Audrey Sénéćhal, Séverine Lopez, Christian Bazalgette, Cécile Bazalgette, Claudie Malrieu Eliaou, Xavier Zanlonghi, Christian P Hamel. Am J Ophthalmol 2008
35
14


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.