A citation-based method for searching scientific literature

Houman Khosravani, Christophe Altier, Brett Simms, Kevin S Hamming, Terrance P Snutch, Janette Mezeyova, John E McRory, Gerald W Zamponi. J Biol Chem 2004
Times Cited: 128







List of co-cited articles
1688 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Association between genetic variation of CACNA1H and childhood absence epilepsy.
Yucai Chen, Jianjun Lu, Hong Pan, Yuehua Zhang, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Xinhua Bao, Zhijian Yao,[...]. Ann Neurol 2003
256
66

Effects of Cav3.2 channel mutations linked to idiopathic generalized epilepsy.
Houman Khosravani, Christopher Bladen, David B Parker, Terrance P Snutch, John E McRory, Gerald W Zamponi. Ann Neurol 2005
79
65

Functional characterization and neuronal modeling of the effects of childhood absence epilepsy variants of CACNA1H, a T-type calcium channel.
Iuliia Vitko, Yucai Chen, Juan M Arias, Yen Shen, Xi-Ru Wu, Edward Perez-Reyes. J Neurosci 2005
129
51


Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
Sarah E Heron, Houman Khosravani, Diego Varela, Chris Bladen, Tristiana C Williams, Michelle R Newman, Ingrid E Scheffer, Samuel F Berkovic, John C Mulley, Gerald W Zamponi. Ann Neurol 2007
127
40


The I-II loop controls plasma membrane expression and gating of Ca(v)3.2 T-type Ca2+ channels: a paradigm for childhood absence epilepsy mutations.
Iuliia Vitko, Isabelle Bidaud, Juan Manuel Arias, Alexandre Mezghrani, Philippe Lory, Edward Perez-Reyes. J Neurosci 2007
84
38

Differential distribution of three members of a gene family encoding low voltage-activated (T-type) calcium channels.
E M Talley, L L Cribbs, J H Lee, A Daud, E Perez-Reyes, D A Bayliss. J Neurosci 1999
576
31

Functional analysis of Ca3.2 T-type calcium channel mutations linked to childhood absence epilepsy.
Jean B Peloquin, Houman Khosravani, Wendy Barr, Chris Bladen, Rhian Evans, Janette Mezeyova, David Parker, Terrance P Snutch, John E McRory, Gerald W Zamponi. Epilepsia 2006
44
68

A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy.
Kim L Powell, Stuart M Cain, Caroline Ng, Shreerang Sirdesai, Laurence S David, Mervyn Kyi, Esperanza Garcia, John R Tyson, Christopher A Reid, Melanie Bahlo,[...]. J Neurosci 2009
121
30

Selective increase in T-type calcium conductance of reticular thalamic neurons in a rat model of absence epilepsy.
E Tsakiridou, L Bertollini, M de Curtis, G Avanzini, H C Pape. J Neurosci 1995
281
29

Voltage-gated calcium channels and idiopathic generalized epilepsies.
Houman Khosravani, Gerald W Zamponi. Physiol Rev 2006
125
25

Low-voltage-activated calcium channel subunit expression in a genetic model of absence epilepsy in the rat.
E M Talley, G Solórzano, A Depaulis, E Perez-Reyes, D A Bayliss. Brain Res Mol Brain Res 2000
98
23

Role of the alpha1G T-type calcium channel in spontaneous absence seizures in mutant mice.
Inseon Song, Daesoo Kim, Soonwook Choi, Minjeong Sun, Yeongin Kim, Hee-Sup Shin. J Neurosci 2004
100
22

Genetic variation of CACNA1H in idiopathic generalized epilepsy.
Sarah E Heron, Hilary A Phillips, John C Mulley, Aziz Mazarib, Miriam Y Neufeld, Samuel F Berkovic, Ingrid E Scheffer. Ann Neurol 2004
77
27

Cloning and expression of a novel member of the low voltage-activated T-type calcium channel family.
J H Lee, A N Daud, L L Cribbs, A E Lacerda, A Pereverzev, U Klöckner, T Schneider, E Perez-Reyes. J Neurosci 1999
365
21


CACNA1H mutations in autism spectrum disorders.
Igor Splawski, Dana S Yoo, Stephanie C Stotz, Allison Cherry, David E Clapham, Mark T Keating. J Biol Chem 2006
134
19

International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels.
William A Catterall, Edward Perez-Reyes, Terrance P Snutch, Joerg Striessnig. Pharmacol Rev 2005
829
19

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
567
17

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
415
17

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
A Jouvenceau, L H Eunson, A Spauschus, V Ramesh, S M Zuberi, D M Kullmann, M G Hanna. Lancet 2001
259
17

Cloning and characterization of alpha1H from human heart, a member of the T-type Ca2+ channel gene family.
L L Cribbs, J H Lee, J Yang, J Satin, Y Zhang, A Daud, J Barclay, M P Williamson, M Fox, M Rees,[...]. Circ Res 1998
461
17

Childhood absence epilepsy: genes, channels, neurons and networks.
Vincenzo Crunelli, Nathalie Leresche. Nat Rev Neurosci 2002
393
17


Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
147
16

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
15

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
15



Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels.
Chien-Chang Chen, Kathryn G Lamping, Daniel W Nuno, Rita Barresi, Sally J Prouty, Julie L Lavoie, Leanne L Cribbs, Sarah K England, Curt D Sigmund, Robert M Weiss,[...]. Science 2003
264
14

Molecular characterization of a neuronal low-voltage-activated T-type calcium channel.
E Perez-Reyes, L L Cribbs, A Daud, A E Lacerda, J Barclay, M P Williamson, M Fox, M Rees, J H Lee. Nature 1998
584
14



Absence epilepsy in tottering mutant mice is associated with calcium channel defects.
C F Fletcher, C M Lutz, T N O'Sullivan, J D Shaughnessy, R Hawkes, W N Frankel, N G Copeland, N A Jenkins. Cell 1996
582
14

Correlation of T-channel coding gene expression, IT, and the low threshold Ca2+ spike in the thalamus of a rat model of absence epilepsy.
Tilman Broicher, Tatyana Kanyshkova, Patrick Meuth, Hans-Christian Pape, Thomas Budde. Mol Cell Neurosci 2008
62
22

Role of voltage-gated calcium channels in epilepsy.
Gerald W Zamponi, Philippe Lory, Edward Perez-Reyes. Pflugers Arch 2010
111
14

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
267
13

Plasma membrane expression of T-type calcium channel alpha(1) subunits is modulated by high voltage-activated auxiliary subunits.
Stefan J Dubel, Christophe Altier, Séverine Chaumont, Philippe Lory, Emmanuel Bourinet, Joël Nargeot. J Biol Chem 2004
90
14

The 'window' T-type calcium current in brain dynamics of different behavioural states.
Vincenzo Crunelli, Tibor I Tóth, David W Cope, Kate Blethyn, Stuart W Hughes. J Physiol 2005
119
13



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
774
12

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
772
12

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
12


Specific contribution of human T-type calcium channel isotypes (alpha(1G), alpha(1H) and alpha(1I)) to neuronal excitability.
Jean Chemin, Arnaud Monteil, Edward Perez-Reyes, Emmanuel Bourinet, Joël Nargeot, Philippe Lory. J Physiol 2002
165
12

Block of cloned human T-type calcium channels by succinimide antiepileptic drugs.
J C Gomora, A N Daud, M Weiergräber, E Perez-Reyes. Mol Pharmacol 2001
132
12


Silencing of the Cav3.2 T-type calcium channel gene in sensory neurons demonstrates its major role in nociception.
Emmanuel Bourinet, Abdelkrim Alloui, Arnaud Monteil, Christian Barrère, Brigitte Couette, Olivier Poirot, Anne Pages, John McRory, Terrance P Snutch, Alain Eschalier,[...]. EMBO J 2005
303
12


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.