A citation-based method for searching scientific literature

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, Fumitaka Oyama, Peter De Jonghe, Lori L Isom. J Neurosci 2009
Times Cited: 160







List of co-cited articles
1371 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture.
Chunling Chen, Ruth E Westenbroek, Xiaorong Xu, Chris A Edwards, Dorothy R Sorenson, Yuan Chen, Dyke P McEwen, Heather A O'Malley, Vandana Bharucha, Laurence S Meadows,[...]. J Neurosci 2004
182
42

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
42

A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.
Ikuo Ogiwara, Tojo Nakayama, Tetsushi Yamagata, Hideyuki Ohtani, Emi Mazaki, Shigeru Tsuchiya, Yushi Inoue, Kazuhiro Yamakawa. Epilepsia 2012
54
66

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
34

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
31

Na Channel β Subunits: Overachievers of the Ion Channel Family.
William J Brackenbury, Lori L Isom. Front Pharmacol 2011
184
31

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
28

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
26

Primary structure and functional expression of the beta 1 subunit of the rat brain sodium channel.
L L Isom, K S De Jongh, D E Patton, B F Reber, J Offord, H Charbonneau, K Walsh, A L Goldin, W A Catterall. Science 1992
592
26

The sodium channel accessory subunit Navβ1 regulates neuronal excitability through modulation of repolarizing voltage-gated K⁺ channels.
Céline Marionneau, Yarimar Carrasquillo, Aaron J Norris, R Reid Townsend, Lori L Isom, Andrew J Link, Jeanne M Nerbonne. J Neurosci 2012
66
34

Voltage-gated Na+ channel β1B: a secreted cell adhesion molecule involved in human epilepsy.
Gustavo A Patino, William J Brackenbury, Yangyang Bao, Luis F Lopez-Santiago, Heather A O'Malley, Chunling Chen, Jeffrey D Calhoun, Ron G Lafrenière, Patrick Cossette, Guy A Rouleau,[...]. J Neurosci 2011
68
33

Abnormal neuronal patterning occurs during early postnatal brain development of Scn1b-null mice and precedes hyperexcitability.
William J Brackenbury, Yukun Yuan, Heather A O'Malley, Jack M Parent, Lori L Isom. Proc Natl Acad Sci U S A 2013
47
46

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
21

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
21

Sodium channel β subunits: emerging targets in channelopathies.
Heather A O'Malley, Lori L Isom. Annu Rev Physiol 2015
122
21

A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy.
D Audenaert, L Claes, B Ceulemans, A Löfgren, C Van Broeckhoven, P De Jonghe. Neurology 2003
126
20

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
20

Structure and function of the beta 2 subunit of brain sodium channels, a transmembrane glycoprotein with a CAM motif.
L L Isom, D S Ragsdale, K S De Jongh, R E Westenbroek, B F Reber, T Scheuer, W A Catterall. Cell 1995
372
20

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
20


The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
267
20

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
19

Functional reciprocity between Na+ channel Nav1.6 and beta1 subunits in the coordinated regulation of excitability and neurite outgrowth.
William J Brackenbury, Jeffrey D Calhoun, Chunling Chen, Haruko Miyazaki, Nobuyuki Nukina, Fumitaka Oyama, Barbara Ranscht, Lori L Isom. Proc Natl Acad Sci U S A 2010
93
19

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.
Hiroshi Watanabe, Tamara T Koopmann, Solena Le Scouarnec, Tao Yang, Christiana R Ingram, Jean-Jacques Schott, Sophie Demolombe, Vincent Probst, Frédéric Anselme, Denis Escande,[...]. J Clin Invest 2008
303
18


Sodium channel beta4, a new disulfide-linked auxiliary subunit with similarity to beta2.
Frank H Yu, Ruth E Westenbroek, Inmaculada Silos-Santiago, Kimberly A McCormick, Deborah Lawson, Pei Ge, Holly Ferriera, Jeremiah Lilly, Peter S DiStefano, William A Catterall,[...]. J Neurosci 2003
286
17

Molecular determinants of Na+ channel function in the extracellular domain of the beta1 subunit.
K A McCormick, L L Isom, D Ragsdale, D Smith, T Scheuer, W A Catterall. J Biol Chem 1998
125
17

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.
Giulia Barcia, Matthew R Fleming, Aline Deligniere, Valeswara-Rao Gazula, Maile R Brown, Maeva Langouet, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio,[...]. Nat Genet 2012
267
17

Structural requirements for interaction of sodium channel beta 1 subunits with ankyrin.
Jyoti D Malhotra, Matthew C Koopmann, Kristin A Kazen-Gillespie, Nicholas Fettman, Michael Hortsch, Lori L Isom. J Biol Chem 2002
119
17

Sodium channel beta1 subunits promote neurite outgrowth in cerebellar granule neurons.
Tigwa H Davis, Chunling Chen, Lori L Isom. J Biol Chem 2004
75
22

Sodium channel Scn1b null mice exhibit prolonged QT and RR intervals.
Luis F Lopez-Santiago, Laurence S Meadows, Sara J Ernst, Chunling Chen, Jyoti Dhar Malhotra, Dyke P McEwen, Audrey Speelman, Jeffrey L Noebels, Sebastian K G Maier, Anatoli N Lopatin,[...]. J Mol Cell Cardiol 2007
89
19

Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy.
W Ramadan, N Patel, S Anazi, A Y Kentab, F A Bashiri, M H Hamad, L Jad, M A Salih, H Alsaif, M Hashem,[...]. Clin Genet 2017
20
85

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
21

beta 3: an additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kinetics.
K Morgan, E B Stevens, B Shah, P J Cox, A K Dixon, K Lee, R D Pinnock, J Hughes, P J Richardson, K Mizuguchi,[...]. Proc Natl Acad Sci U S A 2000
229
16

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
149
16

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.
Gemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, Corinna Hartmann, Rikke S Møller, Helle Hjalgrim, Joseph Cook, Eileen Geraghty, Brian J O'Roak, Steve Petrou,[...]. Neurology 2014
148
16

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
211
15

Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome.
Christine S Cheah, Frank H Yu, Ruth E Westenbroek, Franck K Kalume, John C Oakley, Gregory B Potter, John L Rubenstein, William A Catterall. Proc Natl Acad Sci U S A 2012
171
15

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
154
15

Crystallographic insights into sodium-channel modulation by the β4 subunit.
John Gilchrist, Samir Das, Filip Van Petegem, Frank Bosmans. Proc Natl Acad Sci U S A 2013
63
23

Functional co-expression of the beta 1 and type IIA alpha subunits of sodium channels in a mammalian cell line.
L L Isom, T Scheuer, A B Brownstein, D S Ragsdale, B J Murphy, W A Catterall. J Biol Chem 1995
188
15

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
147
14

Functional and biochemical analysis of a sodium channel beta1 subunit mutation responsible for generalized epilepsy with febrile seizures plus type 1.
Laurence S Meadows, Jyoti Malhotra, Andrew Loukas, Veena Thyagarajan, Kristin A Kazen-Gillespie, Matthew C Koopman, Steven Kriegler, Lori L Isom, David S Ragsdale. J Neurosci 2002
105
14

Identification of the cysteine residue responsible for disulfide linkage of Na+ channel α and β2 subunits.
Chunling Chen, Jeffrey D Calhoun, Yanqing Zhang, Luis Lopez-Santiago, Ningna Zhou, Tigwa H Davis, James L Salzer, Lori L Isom. J Biol Chem 2012
54
25

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
222
14

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
14

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
14

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
286
14

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
14

Voltage-gated Na+ channel beta1 subunit-mediated neurite outgrowth requires Fyn kinase and contributes to postnatal CNS development in vivo.
William J Brackenbury, Tigwa H Davis, Chunling Chen, Emily A Slat, Matthew J Detrow, Travis L Dickendesher, Barbara Ranscht, Lori L Isom. J Neurosci 2008
83
16


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.