A citation-based method for searching scientific literature

R Borgatti, C Zucca, A Cavallini, M Ferrario, C Panzeri, P Castaldo, M V Soldovieri, C Baschirotto, N Bresolin, B Dalla Bernardina, M Taglialatela, M T Bassi. Neurology 2004
Times Cited: 112







List of co-cited articles
868 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
61

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
795
57

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
46

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
46


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
42

Benign familial neonatal convulsions: always benign?
O K Steinlein, C Conrad, B Weidner. Epilepsy Res 2007
60
61

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
36

Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel.
K Dedek, B Kunath, C Kananura, U Reuner, T J Jentsch, O K Steinlein. Proc Natl Acad Sci U S A 2001
190
33



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
21

Neonatal seizures with tonic clonic sequences and poor developmental outcome.
Bernhard Schmitt, Gabriele Wohlrab, Thomas Sander, Ortrud K Steinlein, Beatrice Latal Hajnal. Epilepsy Res 2005
27
74

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
20

Seizure characteristics in chromosome 20 benign familial neonatal convulsions.
G M Ronen, T O Rosales, M Connolly, V E Anderson, M Leppert. Neurology 1993
144
19

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions.
H Lerche, C Biervert, A K Alekov, L Schleithoff, M Lindner, W Klinger, F Bretschneider, N Mitrovic, K Jurkat-Rott, H Bode,[...]. Ann Neurol 1999
100
19

A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes.
G Coppola, P Castaldo, E Miraglia del Giudice, G Bellini, F Galasso, M V Soldovieri, L Anzalone, C Sferro, L Annunziato, A Pascotto,[...]. Neurology 2003
44
43

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
19

De novo KCNQ2 mutations in patients with benign neonatal seizures.
L R F Claes, B Ceulemans, D Audenaert, L Deprez, A Jansen, D Hasaerts, S Weckx, K G Claeys, J Del-Favero, C Van Broeckhoven,[...]. Neurology 2004
41
43

Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels.
Pasqualina Castaldo, Emanuele Miraglia del Giudice, Giangennaro Coppola, Antonio Pascotto, Lucio Annunziato, Maurizio Taglialatela. J Neurosci 2002
78
21


Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction.
M C Richards, S E Heron, H E Spendlove, I E Scheffer, B Grinton, S F Berkovic, J C Mulley, A Davy. J Med Genet 2004
52
32

Sodium-channel defects in benign familial neonatal-infantile seizures.
Sarah E Heron, Kathryn M Crossland, Eva Andermann, Hilary A Phillips, Allison J Hall, Andrew Bleasel, Michael Shevell, Suha Mercho, Marie-Helene Seni, Marie-Christine Guiot,[...]. Lancet 2002
244
17

Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations.
T V Wuttke, K Jurkat-Rott, W Paulus, M Garncarek, F Lehmann-Horn, H Lerche. Neurology 2007
84
19

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.
S E Heron, K Cox, B E Grinton, S M Zuberi, S Kivity, Z Afawi, R Straussberg, S F Berkovic, I E Scheffer, J C Mulley. J Med Genet 2007
50
32

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
22


A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly.
Michael Schwake, Thomas J Jentsch, Thomas Friedrich. EMBO Rep 2003
112
15


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
15

Calmodulin regulates the trafficking of KCNQ2 potassium channels.
Ainhoa Etxeberria, Paloma Aivar, Jose Angel Rodriguez-Alfaro, Alessandro Alaimo, Patricia Villacé, Juan Camilo Gómez-Posada, Pilar Areso, Alvaro Villarroel. FASEB J 2008
81
18

Nervous system KV7 disorders: breakdown of a subthreshold brake.
Snezana Maljevic, Thomas V Wuttke, Holger Lerche. J Physiol 2008
104
15

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
15

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
14


A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions.
S Hirose, F Zenri, H Akiyoshi, G Fukuma, H Iwata, T Inoue, M Yonetani, M Tsutsumi, H Muranaka, T Kurokawa,[...]. Ann Neurol 2000
79
17

KCNQ2 is a nodal K+ channel.
Jérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, Steven S Scherer. J Neurosci 2004
306
14

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
O K Steinlein, J C Mulley, P Propping, R H Wallace, H A Phillips, G R Sutherland, I E Scheffer, S F Berkovic. Nat Genet 1995
823
14

Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions.
Maria Virginia Soldovieri, Pasqualina Castaldo, Luisa Iodice, Francesco Miceli, Vincenzo Barrese, Giulia Bellini, Emanuele Miraglia del Giudice, Antonio Pascotto, Stefano Bonatti, Lucio Annunziato,[...]. J Biol Chem 2006
52
26

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
59
23

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
699
13

Infantile seizures and other epileptic phenotypes in a Chinese family with a missense mutation of KCNQ2.
Xihui Zhou, Aiqun Ma, Xiaohong Liu, Chen Huang, Yanmin Zhang, Ruiming Shi, Shiwei Mao, Tao Geng, Shengbin Li. Eur J Pediatr 2006
30
43

Subthreshold changes of voltage-dependent activation of the K(V)7.2 channel in neonatal epilepsy.
Jessica Hunter, Snezana Maljevic, Anupama Shankar, Anne Siegel, Barbara Weissman, Philip Holt, Larry Olson, Holger Lerche, Andrew Escayg. Neurobiol Dis 2006
23
56

First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene.
S Baulac, G Huberfeld, I Gourfinkel-An, G Mitropoulou, A Beranger, J F Prud'homme, M Baulac, A Brice, R Bruzzone, E LeGuern. Nat Genet 2001
545
13


Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.
Samuel F Berkovic, Sarah E Heron, Lucio Giordano, Carla Marini, Renzo Guerrini, Robert E Kaplan, Antonio Gambardella, Ortrud K Steinlein, Bronwyn E Grinton, Joanne T Dean,[...]. Ann Neurol 2004
175
12

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
Patrick Cossette, Lidong Liu, Katéri Brisebois, Haiheng Dong, Anne Lortie, Michel Vanasse, Jean-Marc Saint-Hilaire, Lionel Carmant, Andrei Verner, Wei-Yang Lu,[...]. Nat Genet 2002
418
12

Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC).
Maria T Bassi, Umberto Balottin, Chris Panzeri, Paolo Piccinelli, Pasqualina Castaldo, Vincenzo Barrese, Maria V Soldovieri, Francesco Miceli, Maria Colombo, Nereo Bresolin,[...]. Neurogenetics 2005
20
60

Pathways modulating neural KCNQ/M (Kv7) potassium channels.
Patrick Delmas, David A Brown. Nat Rev Neurosci 2005
469
12

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.
Maria Virginia Soldovieri, Maria Roberta Cilio, Francesco Miceli, Giulia Bellini, Emanuele Miraglia del Giudice, Pasqualina Castaldo, Ciria C Hernandez, Mark S Shapiro, Antonio Pascotto, Lucio Annunziato,[...]. J Neurosci 2007
33
36


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.