A citation-based method for searching scientific literature

Yucai Chen, Jianjun Lu, Hong Pan, Yuehua Zhang, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Xinhua Bao, Zhijian Yao, Keyue Ding, Wilson H Y Lo, Boqin Qiang, Piu Chan, Yan Shen, Xiru Wu. Ann Neurol 2003
Times Cited: 256







List of co-cited articles
1420 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
46

Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy.
Houman Khosravani, Christophe Altier, Brett Simms, Kevin S Hamming, Terrance P Snutch, Janette Mezeyova, John E McRory, Gerald W Zamponi. J Biol Chem 2004
128
30

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
27


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
23



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
20

Mechanisms by which a CACNA1H mutation in epilepsy patients increases seizure susceptibility.
Veit-Simon Eckle, Aleksandr Shcheglovitov, Iuliia Vitko, Deblina Dey, Chan Choo Yap, Bettina Winckler, Edward Perez-Reyes. J Physiol 2014
52
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
19

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
24

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
18

Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online.
Baljinder Singh, Arnaud Monteil, Isabelle Bidaud, Yoshihisa Sugimoto, Toshimitsu Suzuki, Shin-ichiro Hamano, Hirokazu Oguni, Makiko Osawa, Maria E Alonso, Antonio V Delgado-Escueta,[...]. Hum Mutat 2007
54
33

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
18

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
23

New variants in the CACNA1H gene identified in childhood absence epilepsy.
Jianmin Liang, Yuehua Zhang, Juli Wang, Hong Pan, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Yan Shen, Xiru Wu. Neurosci Lett 2006
36
44

T-type calcium channel blockers that attenuate thalamic burst firing and suppress absence seizures.
Elizabeth Tringham, Kim L Powell, Stuart M Cain, Kristy Kuplast, Janette Mezeyova, Manjula Weerapura, Cyrus Eduljee, Xinpo Jiang, Paula Smith, Jerrie-Lynn Morrison,[...]. Sci Transl Med 2012
103
15

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
17

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
15

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
14

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
14

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
213
14

Childhood absence epilepsy: genes, channels, neurons and networks.
Vincenzo Crunelli, Nathalie Leresche. Nat Rev Neurosci 2002
393
14

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
31

Transcriptional upregulation of Cav3.2 mediates epileptogenesis in the pilocarpine model of epilepsy.
Albert J Becker, Julika Pitsch, Dmitry Sochivko, Thoralf Opitz, Matthäus Staniek, Chien-Chang Chen, Kevin P Campbell, Susanne Schoch, Yoel Yaari, Heinz Beck. J Neurosci 2008
143
13

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
915
13


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

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
12


Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism.
Ute I Scholl, Gabriel Stölting, Carol Nelson-Williams, Alfred A Vichot, Murim Choi, Erin Loring, Manju L Prasad, Gerald Goh, Tobias Carling, C Christofer Juhlin,[...]. Elife 2015
155
12

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
11

Selective T-type calcium channel block in thalamic neurons reveals channel redundancy and physiological impact of I(T)window.
Fanny M Dreyfus, Anne Tscherter, Adam C Errington, John J Renger, Hee-Sup Shin, Victor N Uebele, Vincenzo Crunelli, Régis C Lambert, Nathalie Leresche. J Neurosci 2010
134
11

A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.
Snezana Maljevic, Klaus Krampfl, Joana Cobilanschi, Nikola Tilgen, Susanne Beyer, Yvonne G Weber, Friedrich Schlesinger, Daniel Ursu, Werner Melzer, Patrick Cossette,[...]. Ann Neurol 2006
128
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

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
11

Contributions of T-type calcium channel isoforms to neuronal firing.
Stuart M Cain, Terrance P Snutch. Channels (Austin) 2010
107
10

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
16


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
788
10

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
869
10

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
10

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
10

Voltage-gated calcium channels and idiopathic generalized epilepsies.
Houman Khosravani, Gerald W Zamponi. Physiol Rev 2006
125
10

On the cellular and network bases of epileptic seizures.
D A McCormick, D Contreras. Annu Rev Physiol 2001
613
10

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
10

Cortical focus drives widespread corticothalamic networks during spontaneous absence seizures in rats.
Hanneke K M Meeren, Jan Pieter M Pijn, Egidius L J M Van Luijtelaar, Anton M L Coenen, Fernando H Lopes da Silva. J Neurosci 2002
573
10

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Michael Steffens, Costin Leu, Ann-Kathrin Ruppert, Federico Zara, Pasquale Striano, Angela Robbiano, Giuseppe Capovilla, Paolo Tinuper, Antonio Gambardella, Amedeo Bianchi,[...]. Hum Mol Genet 2012
105
10

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Ingo Helbig, Heather C Mefford, Andrew J Sharp, Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak,[...]. Nat Genet 2009
394
10

T-type calcium channels in burst-firing, network synchrony, and epilepsy.
Stuart M Cain, Terrance P Snutch. Biochim Biophys Acta 2013
73
13


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.