A citation-based method for searching scientific literature

Iori Ohmori, Mamoru Ouchida, Takafumi Miki, Nobuyoshi Mimaki, Shigeki Kiyonaka, Teiichi Nishiki, Kazuhito Tomizawa, Yasuo Mori, Hideki Matsui. Neurobiol Dis 2008
Times Cited: 36







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



Times Cited
  Times     Co-cited
Similarity


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
36

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
643
27

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
785
25

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
693
25

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
A Escayg, M De Waard, D D Lee, D Bichet, P Wolf, T Mayer, J Johnston, R Baloh, T Sander, M H Meisler. Am J Hum Genet 2000
270
25

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.
Melinda S Martin, Bin Tang, Ligia A Papale, Frank H Yu, William A Catterall, Andrew Escayg. Hum Mol Genet 2007
141
22

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
22

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
499
19

The spectrum of SCN1A-related infantile epileptic encephalopathies.
Louise A Harkin, Jacinta M McMahon, Xenia Iona, Leanne Dibbens, James T Pelekanos, Sameer M Zuberi, Lynette G Sadleir, Eva Andermann, Deepak Gill, Kevin Farrell,[...]. Brain 2007
345
19

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
208
19

Sodium channel mutations in epilepsy and other neurological disorders.
Miriam H Meisler, Jennifer A Kearney. J Clin Invest 2005
333
16

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
773
16

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
Ingrid E Scheffer, Yue-Hua Zhang, Floor E Jansen, Leanne Dibbens. Brain Dev 2009
107
16

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
239
16

Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.
Tara Klassen, Caleb Davis, Alica Goldman, Dan Burgess, Tim Chen, David Wheeler, John McPherson, Traci Bourquin, Lora Lewis, Donna Villasana,[...]. Cell 2011
215
16

CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.
Iori Ohmori, Mamoru Ouchida, Katsuhiro Kobayashi, Yoshimi Jitsumori, Akiko Mori, Hiroyuki Michiue, Teiichi Nishiki, Yoko Ohtsuka, Hideki Matsui. Neurobiol Dis 2013
24
25

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
320
13

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
871
13

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
727
13

Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
Carla Marini, Davide Mei, Teresa Temudo, Anna Rita Ferrari, Daniela Buti, Charlotte Dravet, Ana I Dias, Ana Moreira, Eulalia Calado, Stefano Seri,[...]. Epilepsia 2007
125
13


Mutations in EFHC1 cause juvenile myoclonic epilepsy.
Toshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, Maria E Alonso, Jun Shi, Yuji Hara, Motohiro Nishida, Tomohiro Numata, Marco T Medina, Tamaki Takeuchi,[...]. Nat Genet 2004
224
13

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
C Depienne, O Trouillard, C Saint-Martin, I Gourfinkel-An, D Bouteiller, W Carpentier, B Keren, B Abert, A Gautier, S Baulac,[...]. J Med Genet 2009
225
11

Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy.
Ji-wen Wang, Hirokazu Kurahashi, Atsushi Ishii, Toshio Kojima, Masaharu Ohfu, Takahito Inoue, Atsushi Ogawa, Sawa Yasumoto, Hirokazu Oguni, Shigeo Kure,[...]. Epilepsia 2008
53
11

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
11

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
174
11

Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.
R H Wallace, I E Scheffer, G Parasivam, S Barnett, G B Wallace, G R Sutherland, S F Berkovic, J C Mulley. Neurology 2002
109
11

SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Davide Mei, Kathy Cox, Leanne M Dibbens, Jacinta M McMahon, Xenia Iona, Rochio Sanchez Carpintero, Maurizio Elia,[...]. Epilepsia 2009
115
11


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
11

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures.
R H Wallace, C Marini, S Petrou, L A Harkin, D N Bowser, R G Panchal, D A Williams, G R Sutherland, J C Mulley, I E Scheffer,[...]. Nat Genet 2001
566
11


Beta subunits of voltage-gated calcium channels.
Annette C Dolphin. J Bioenerg Biomembr 2003
280
11

Calcium channel regulation and presynaptic plasticity.
William A Catterall, Alexandra P Few. Neuron 2008
409
11

Auxiliary subunits: essential components of the voltage-gated calcium channel complex.
Jyothi Arikkath, Kevin P Campbell. Curr Opin Neurobiol 2003
363
11

Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation.
Vera M Kalscheuer, Jiong Tao, Andrew Donnelly, Georgina Hollway, Eberhard Schwinger, Sabine Kübart, Corinna Menzel, Maria Hoeltzenbein, Niels Tommerup, Helen Eyre,[...]. Am J Hum Genet 2003
201
11

Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.
Christel Depienne, Delphine Bouteiller, Boris Keren, Emmanuel Cheuret, Karine Poirier, Oriane Trouillard, Baya Benyahia, Chloé Quelin, Wassila Carpentier, Sophie Julia,[...]. PLoS Genet 2009
221
11

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
Leanne M Dibbens, Patrick S Tarpey, Kim Hynes, Marta A Bayly, Ingrid E Scheffer, Raffaella Smith, Jamee Bomar, Edwina Sutton, Lucianne Vandeleur, Cheryl Shoubridge,[...]. Nat Genet 2008
258
11

A long-term follow-up study of Dravet syndrome up to adulthood.
Mari Akiyama, Katsuhiro Kobayashi, Harumi Yoshinaga, Yoko Ohtsuka. Epilepsia 2010
111
11

Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects.
Miriam H Meisler, Janelle E O'Brien, Lisa M Sharkey. J Physiol 2010
138
11

Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene.
Renzo Guerrini, Elena Cellini, Davide Mei, Tiziana Metitieri, Cristina Petrelli, Daniela Pucatti, Carla Marini, Nelia Zamponi. Epilepsia 2010
39
11

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.
Yu Liu, Luis F Lopez-Santiago, Yukun Yuan, Julie M Jones, Helen Zhang, Heather A O'Malley, Gustavo A Patino, Janelle E O'Brien, Raffaella Rusconi, Ajay Gupta,[...]. Ann Neurol 2013
148
11


Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy.
Iori Ohmori, Mamoru Ouchida, Yoko Ohtsuka, Eiji Oka, Kenji Shimizu. Biochem Biophys Res Commun 2002
170
8

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
789
8

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
819
8

Selective blockade of N-type calcium channels by levetiracetam.
E A Lukyanetz, V M Shkryl, P G Kostyuk. Epilepsia 2002
237
8

An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy.
P Striano, A Coppola, M Pezzella, C Ciampa, N Specchio, F Ragona, M M Mancardi, E Gennaro, F Beccaria, G Capovilla,[...]. Neurology 2007
82
8

Severe myoclonic epilepsy in infancy: a systematic review and a meta-analysis of individual patient data.
Behrouz Kassaï, Catherine Chiron, Ségolène Augier, Michel Cucherat, Elisabeth Rey, François Gueyffier, Renzo Guerrini, Julien Vincent, Olivier Dulac, Gérard Pons. Epilepsia 2008
89
8

Masking epilepsy by combining two epilepsy genes.
Edward Glasscock, Jing Qian, Jong W Yoo, Jeffrey L Noebels. Nat Neurosci 2007
92
8


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.