A citation-based method for searching scientific literature

Valerie C Bomben, Isamu Aiba, Jing Qian, Melanie D Mark, Stefan Herlitze, Jeffrey L Noebels. J Neurosci 2016
Times Cited: 31







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



Times Cited
  Times     Co-cited
Similarity


CaV 2.1 ablation in cortical interneurons selectively impairs fast-spiking basket cells and causes generalized seizures.
Elsa Rossignol, Illya Kruglikov, Arn M J M van den Maagdenberg, Bernardo Rudy, Gord Fishell. Ann Neurol 2013
67
35

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.
Lena Damaj, Alexis Lupien-Meilleur, Anne Lortie, Émilie Riou, Luis H Ospina, Louise Gagnon, Catherine Vanasse, Elsa Rossignol. Eur J Hum Genet 2015
91
32

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit.
K Jun, E S Piedras-Rentería, S M Smith, D B Wheeler, S B Lee, T G Lee, H Chin, M E Adams, R H Scheller, R W Tsien,[...]. Proc Natl Acad Sci U S A 1999
353
29


Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations.
Melanie D Mark, Takashi Maejima, Denise Kuckelsberg, Jong W Yoo, Robert A Hyde, Viral Shah, Davina Gutierrez, Rosa L Moreno, Wolfgang Kruse, Jeffrey L Noebels,[...]. J Neurosci 2011
61
19

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
795
19

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
261
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
653
19

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
935
19

Thalamic synchrony and dynamic regulation of global forebrain oscillations.
John R Huguenard, David A McCormick. Trends Neurosci 2007
254
16

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
583
16

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, Tania Djémié, Stephan Müller, Rikke S Møller, Bridget Maher, Laura Hernandez-Hernandez, Matthis Synofzik, Hande S Caglayan,[...]. Nat Genet 2015
144
16



On the cellular and network bases of epileptic seizures.
D A McCormick, D Contreras. Annu Rev Physiol 2001
624
16

Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy.
Tracy A Glauser, Avital Cnaan, Shlomo Shinnar, Deborah G Hirtz, Dennis Dlugos, David Masur, Peggy O Clark, Edmund V Capparelli, Peter C Adamson. N Engl J Med 2010
295
16



Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: initial monotherapy outcomes at 12 months.
Tracy A Glauser, Avital Cnaan, Shlomo Shinnar, Deborah G Hirtz, Dennis Dlugos, David Masur, Peggy O Clark, Peter C Adamson. Epilepsia 2013
135
16

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
149
16

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
16


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
576
16

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
511
12



Cortical-area specific block of genetically determined absence seizures by ethosuximide.
J P A Manning, D A Richards, N Leresche, V Crunelli, N G Bowery. Neuroscience 2004
119
12

Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna. Nat Rev Neurol 2012
88
12


Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
Sanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, Dimitrios Kotzadimitriou, Louise Eunson, Mary B Davis, Rosalyn Davies, Nicholas W Wood, Dimitri M Kullmann, Michael G Hanna,[...]. J Physiol 2010
54
12

Childhood absence epilepsy: genes, channels, neurons and networks.
Vincenzo Crunelli, Nathalie Leresche. Nat Rev Neurosci 2002
397
12

Cellular mechanisms of a synchronized oscillation in the thalamus.
M von Krosigk, T Bal, D A McCormick. Science 1993
586
12

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
12


ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
12

The genetic landscape of the epileptic encephalopathies of infancy and childhood.
Amy McTague, Katherine B Howell, J Helen Cross, Manju A Kurian, Ingrid E Scheffer. Lancet Neurol 2016
258
12

Regulation of Thalamic and Cortical Network Synchrony by Scn8a.
Christopher D Makinson, Brian S Tanaka, Jordan M Sorokin, Jennifer C Wong, Catherine A Christian, Alan L Goldin, Andrew Escayg, John R Huguenard. Neuron 2017
42
12

Deep layer somatosensory cortical neurons initiate spike-and-wave discharges in a genetic model of absence seizures.
Pierre-Olivier Polack, Isabelle Guillemain, Emilie Hu, Colin Deransart, Antoine Depaulis, Stéphane Charpier. J Neurosci 2007
248
12

Cortical drive and thalamic feed-forward inhibition control thalamic output synchrony during absence seizures.
Cian McCafferty, François David, Marcello Venzi, Magor L Lőrincz, Francis Delicata, Zoe Atherton, Gregorio Recchia, Gergely Orban, Régis C Lambert, Giuseppe Di Giovanni,[...]. Nat Neurosci 2018
32
12

Ablation of Ca(V)2.1 voltage-gated Ca²⁺ channels in mouse forebrain generates multiple cognitive impairments.
Robert Theodor Mallmann, Claudio Elgueta, Faten Sleman, Jan Castonguay, Thomas Wilmes, Arn van den Maagdenberg, Norbert Klugbauer. PLoS One 2013
21
19


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
9

Role of voltage-gated calcium channels in epilepsy.
Gerald W Zamponi, Philippe Lory, Edward Perez-Reyes. Pflugers Arch 2010
116
9


The current state of absence epilepsy: can we have your attention?
Jeffrey R Tenney, Tracy A Glauser. Epilepsy Curr 2013
55
9

Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons.
Bernardo Rudy, Gordon Fishell, SooHyun Lee, Jens Hjerling-Leffler. Dev Neurobiol 2011
712
9

Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy.
Inma Cobos, Maria Elisa Calcagnotto, Alex J Vilaythong, Myo T Thwin, Jeffrey L Noebels, Scott C Baraban, John L R Rubenstein. Nat Neurosci 2005
355
9

Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.
Gökce Orhan, Merle Bock, Dorien Schepers, Elena I Ilina, Stephanie Nadine Reichel, Heidi Löffler, Nicole Jezutkovic, Sarah Weckhuysen, Simone Mandelstam, Arvid Suls,[...]. Ann Neurol 2014
124
9

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
173
9

The cell-intrinsic requirement of Sox6 for cortical interneuron development.
Renata Batista-Brito, Elsa Rossignol, Jens Hjerling-Leffler, Myrto Denaxa, Michael Wegner, Véronique Lefebvre, Vassilis Pachnis, Gord Fishell. Neuron 2009
143
9


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.