A citation-based method for searching scientific literature

T Sugawara, Y Tsurubuchi, K L Agarwala, M Ito, G Fukuma, E Mazaki-Miyazaki, H Nagafuji, M Noda, K Imoto, K Wada, A Mitsudome, S Kaneko, M Montal, K Nagata, S Hirose, K Yamakawa. Proc Natl Acad Sci U S A 2001
Times Cited: 297







List of co-cited articles
1249 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies.
I Ogiwara, K Ito, Y Sawaishi, H Osaka, E Mazaki, I Inoue, M Montal, T Hashikawa, T Shike, T Fujiwara,[...]. Neurology 2009
137
34

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline.
Kazusaku Kamiya, Makoto Kaneda, Takashi Sugawara, Emi Mazaki, Nami Okamura, Mauricio Montal, Naomasa Makita, Masaki Tanaka, Katsuyuki Fukushima, Tateki Fujiwara,[...]. J Neurosci 2004
141
33

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
245
33

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
695
33

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
R H Wallace, D W Wang, R Singh, I E Scheffer, A L George, H A Phillips, K Saar, A Reis, E W Johnson, G R Sutherland,[...]. Nat Genet 1998
774
30

Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy.
Yunxiang Liao, Liesbet Deprez, Snezana Maljevic, Julika Pitsch, Lieve Claes, Dimitrina Hristova, Albena Jordanova, Sirpa Ala-Mello, Astrid Bellan-Koch, Dragica Blazevic,[...]. Brain 2010
111
26

SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.
Y Liao, A-K Anttonen, E Liukkonen, E Gaily, S Maljevic, S Schubert, A Bellan-Koch, S Petrou, V E Ahonen, H Lerche,[...]. Neurology 2010
94
26

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
790
23


De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Krishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, Xiaoyang Cheng, Sulayman D Dib-Hajj, Stephen G Waxman, Dinesh Talwar, Santhosh Girirajan, Evan E Eichler, Linda L Restifo,[...]. Am J Hum Genet 2012
255
22

Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy.
Katherine D Holland, Jennifer A Kearney, Tracy A Glauser, Gerri Buck, Mehdi Keddache, John R Blankston, Ian W Glaaser, Robert S Kass, Miriam H Meisler. Neurosci Lett 2008
105
20

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
20

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
19

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
648
19

Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome.
Xiuyu Shi, Sawa Yasumoto, Eiji Nakagawa, Tatsuya Fukasawa, Satoshi Uchiya, Shinichi Hirose. Brain Dev 2009
73
24

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
544
18

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, Silvia Masnada, Guido Rubboli, Elena Gardella, Gaetan Lesca, Dorothée Ville, Mathieu Milh, Laurent Villard,[...]. Brain 2017
204
18

Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizures.
Paolo Scalmani, Raffaella Rusconi, Elena Armatura, Federico Zara, Giuliano Avanzini, Silvana Franceschetti, Massimo Mantegazza. J Neurosci 2006
83
20


GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies.
Leanne M Dibbens, Hua-Jun Feng, Michaella C Richards, Louise A Harkin, Bree L Hodgson, Darren Scott, Misty Jenkins, Steven Petrou, Grant R Sutherland, Ingrid E Scheffer,[...]. Hum Mol Genet 2004
240
17


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
504
17

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert,[...]. Nat Genet 2013
409
17

Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures.
Roy Ben-Shalom, Caroline M Keeshen, Kiara N Berrios, Joon Y An, Stephan J Sanders, Kevin J Bender. Biol Psychiatry 2017
100
17

Distinct contributions of Na(v)1.6 and Na(v)1.2 in action potential initiation and backpropagation.
Wenqin Hu, Cuiping Tian, Tun Li, Mingpo Yang, Han Hou, Yousheng Shu. Nat Neurosci 2009
387
15

Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice.
R Planells-Cases, M Caprini, J Zhang, E M Rockenstein, R R Rivera, C Murre, E Masliah, M Montal. Biophys J 2000
105
15

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome.
Kazuyuki Nakamura, Mitsuhiro Kato, Hitoshi Osaka, Sumimasa Yamashita, Eiji Nakagawa, Kazuhiro Haginoya, Jun Tohyama, Mitsuko Okuda, Takahito Wada, Shuichi Shimakawa,[...]. Neurology 2013
130
15

SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.
Eric Herlenius, Sarah E Heron, Bronwyn E Grinton, Deborah Keay, Ingrid E Scheffer, John C Mulley, Samuel F Berkovic. Epilepsia 2007
77
18

Radicals r'aging.
D C Wallace, S Melov. Nat Genet 1998
415
14

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
672
14

A functional null mutation of SCN1B in a patient with Dravet syndrome.
Gustavo A Patino, Lieve R F Claes, Luis F Lopez-Santiago, Emily A Slat, Raja S R Dondeti, Chunling Chen, Heather A O'Malley, Charles B B Gray, Haruko Miyazaki, Nobuyuki Nukina,[...]. J Neurosci 2009
160
13

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes.
Caroline R Fertleman, Mark D Baker, Keith A Parker, Sarah Moffatt, Frances V Elmslie, Bjarke Abrahamsen, Johan Ostman, Norbert Klugbauer, John N Wood, R Mark Gardiner,[...]. Neuron 2006
487
13


Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia.
N Schwarz, A Hahn, T Bast, S Müller, H Löffler, S Maljevic, E Gaily, I Prehl, S Biskup, T Joensuu,[...]. J Neurol 2016
51
25

Molecular basis of an inherited epilepsy.
Christoph Lossin, Dao W Wang, Thomas H Rhodes, Carlos G Vanoye, Alfred L George. Neuron 2002
260
12

Differential control of clustering of the sodium channels Na(v)1.2 and Na(v)1.6 at developing CNS nodes of Ranvier.
M R Kaplan, M H Cho, E M Ullian, L L Isom, S R Levinson, B A Barres. Neuron 2001
212
12

Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.
Ingrid E Scheffer, Louise A Harkin, Bronwyn E Grinton, Leanne M Dibbens, Samantha J Turner, Marta A Zielinski, Ruwei Xu, Graeme Jackson, Judith Adams, Mary Connellan,[...]. Brain 2007
175
12

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
163
12

An SCN2A mutation in a family with infantile seizures from Madagascar reveals an increased subthreshold Na(+) current.
Stephan Lauxmann, Nadia Boutry-Kryza, Clotilde Rivier, Stephan Mueller, Ulrike B S Hedrich, Snezana Maljevic, Pierre Szepetowski, Holger Lerche, Gaetan Lesca. Epilepsia 2013
29
41

SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
Katherine B Howell, Jacinta M McMahon, Gemma L Carvill, Dimira Tambunan, Mark T Mackay, Victoria Rodriguez-Casero, Richard Webster, Damian Clark, Jeremy L Freeman, Sophie Calvert,[...]. Neurology 2015
127
12

Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus.
Louise A Harkin, David N Bowser, Leanne M Dibbens, Rita Singh, Fiona Phillips, Robyn H Wallace, Michaella C Richards, David A Williams, John C Mulley, Samuel F Berkovic,[...]. Am J Hum Genet 2002
321
11

A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel.
Ruwei Xu, Evan A Thomas, Misty Jenkins, Elena V Gazina, Cindy Chiu, Sarah E Heron, John C Mulley, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou. Mol Cell Neurosci 2007
52
21

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
Nanda A Singh, Chris Pappas, E Jill Dahle, Lieve R F Claes, Timothy H Pruess, Peter De Jonghe, Joel Thompson, Missy Dixon, Christina Gurnett, Andy Peiffer,[...]. PLoS Genet 2009
164
11

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
933
11

Action potential initiation in neocortical inhibitory interneurons.
Tun Li, Cuiping Tian, Paolo Scalmani, Carolina Frassoni, Massimo Mantegazza, Yonghong Wang, Mingpo Yang, Si Wu, Yousheng Shu. PLoS Biol 2014
50
22

Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures.
Massimo Mantegazza, Antonio Gambardella, Raffaella Rusconi, Emanuele Schiavon, Ferdinanda Annesi, Rita Restano Cassulini, Angelo Labate, Sara Carrideo, Rosanna Chifari, Maria Paola Canevini,[...]. Proc Natl Acad Sci U S A 2005
131
10

Compact myelin dictates the differential targeting of two sodium channel isoforms in the same axon.
T Boiko, M N Rasband, S R Levinson, J H Caldwell, G Mandel, J S Trimmer, G Matthews. Neuron 2001
291
10

A novel GABRG2 mutation associated with febrile seizures.
D Audenaert, E Schwartz, K G Claeys, L Claes, L Deprez, A Suls, T Van Dyck, L Lagae, C Van Broeckhoven, R L Macdonald,[...]. Neurology 2006
107
10

An SCN9A channelopathy causes congenital inability to experience pain.
James J Cox, Frank Reimann, Adeline K Nicholas, Gemma Thornton, Emma Roberts, Kelly Springell, Gulshan Karbani, Hussain Jafri, Jovaria Mannan, Yasmin Raashid,[...]. Nature 2006
945
10



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.