A citation-based method for searching scientific literature

J C Jen, J Wan, T P Palos, B D Howard, R W Baloh. Neurology 2005
Times Cited: 198







List of co-cited articles
1680 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
Boukje de Vries, Hafsa Mamsa, Anine H Stam, Jijun Wan, Stef L M Bakker, Kaate R J Vanmolkot, Joost Haan, Gisela M Terwindt, Elles M J Boon, Bruce D Howard,[...]. Arch Neurol 2009
77
57


Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
22

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
231
21

Motor discoordination and increased susceptibility to cerebellar injury in GLAST mutant mice.
K Watase, K Hashimoto, M Kano, K Yamada, M Watanabe, Y Inoue, S Okuyama, T Sakagawa, S Ogawa, N Kawashima,[...]. Eur J Neurosci 1998
301
20

Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1.
K Tanaka, K Watase, T Manabe, K Yamada, M Watanabe, K Takahashi, H Iwama, T Nishikawa, N Ichihara, T Kikuchi,[...]. Science 1997
19

Glutamate uptake.
N C Danbolt. Prog Neurobiol 2001
18

Primary episodic ataxias: diagnosis, pathogenesis and treatment.
J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
183
18

An excitatory amino-acid transporter with properties of a ligand-gated chloride channel.
W A Fairman, R J Vandenberg, J L Arriza, M P Kavanaugh, S G Amara. Nature 1995
814
18

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
978
17

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
451
16

Late-onset episodic ataxia associated with SLC1A3 mutation.
Kwang-Dong Choi, Joanna C Jen, Seo Young Choi, Jin-Hong Shin, Hyang-Sook Kim, Hyo-Jung Kim, Ji-Soo Kim, Jae-Hwan Choi. J Hum Genet 2017
24
62

Ion fluxes associated with excitatory amino acid transport.
J I Wadiche, S G Amara, M P Kavanaugh. Neuron 1995
401
14

A novel locus for episodic ataxia:UBR4 the likely candidate.
Judith Conroy, Paul McGettigan, Raymond Murphy, David Webb, Sinéad M Murphy, Blathnaid McCoy, Christine Albertyn, Dara McCreary, Cara McDonagh, Orla Walsh,[...]. Eur J Hum Genet 2014
38
36

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
473
13

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
559
13

Activation of a presynaptic glutamate transporter regulates synaptic transmission through electrical signaling.
Margaret Lin Veruki, Svein Harald Mørkve, Espen Hartveit. Nat Neurosci 2006
116
13

Beta-lactam antibiotics offer neuroprotection by increasing glutamate transporter expression.
Jeffrey D Rothstein, Sarjubhai Patel, Melissa R Regan, Christine Haenggeli, Yanhua H Huang, Dwight E Bergles, Lin Jin, Margaret Dykes Hoberg, Svetlana Vidensky, Dorothy S Chung,[...]. Nature 2005
962
13

Structure of a glutamate transporter homologue from Pyrococcus horikoshii.
Dinesh Yernool, Olga Boudker, Yan Jin, Eric Gouaux. Nature 2004
535
13

Genetic and functional studies of a missense variant in a glutamate transporter, SLC1A3, in Tourette syndrome.
Abby Adamczyk, Colin D Gause, Rita Sattler, Svetlana Vidensky, Jeffery D Rothstein, Harvey Singer, Tao Wang. Psychiatr Genet 2011
35
37

A new episodic ataxia syndrome with linkage to chromosome 19q13.
Kevin A Kerber, Joanna C Jen, Hane Lee, Stanley F Nelson, Robert W Baloh. Arch Neurol 2007
30
43

Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate.
J D Rothstein, M Dykes-Hoberg, C A Pardo, L A Bristol, L Jin, R W Kuncl, Y Kanai, M A Hediger, Y Wang, J P Schielke,[...]. Neuron 1996
13

Mechanisms of anion conduction by coupled glutamate transporters.
Jan-Philipp Machtens, Daniel Kortzak, Christine Lansche, Ariane Leinenweber, Petra Kilian, Birgit Begemann, Ulrich Zachariae, David Ewers, Bert L de Groot, Rodolfo Briones,[...]. Cell 2015
79
16

Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation.
Tracey D Graves, Yoon-Hee Cha, Angelika F Hahn, Richard Barohn, Mohammed K Salajegheh, Robert C Griggs, Brian N Bundy, Joanna C Jen, Robert W Baloh, Michael G Hanna. Brain 2014
47
27

Exome sequencing in undiagnosed inherited and sporadic ataxias.
Angela Pyle, Tania Smertenko, David Bargiela, Helen Griffin, Jennifer Duff, Marie Appleton, Konstantinos Douroudis, Gerald Pfeffer, Mauro Santibanez-Koref, Gail Eglon,[...]. Brain 2015
81
16

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
115
13

Disruption of an EAAT-Mediated Chloride Channel in a Drosophila Model of Ataxia.
Neda Parinejad, Emilie Peco, Tiago Ferreira, Stephanie M Stacey, Donald J van Meyel. J Neurosci 2016
24
54

Impaired K+ binding to glial glutamate transporter EAAT1 in migraine.
Peter Kovermann, Margarita Hessel, Daniel Kortzak, Joanna C Jen, Johannes Koch, Christoph Fahlke, Tobias Freilinger. Sci Rep 2017
17
76

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Alice R Gardiner, Kailash P Bhatia, Maria Stamelou, Russell C Dale, Manju A Kurian, Susanne A Schneider, G M Wali, Tim Counihan, Anthony H Schapira, Sian D Spacey,[...]. Neurology 2012
97
12

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Erin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries, F Danilo Tiziano, Bertrand Fontaine, Nicole M Walley, Sinéad Heavin,[...]. Nat Genet 2012
232
12

Flux coupling in a neuronal glutamate transporter.
N Zerangue, M P Kavanaugh. Nature 1996
576
12

Excitatory amino acid transporter 5, a retinal glutamate transporter coupled to a chloride conductance.
J L Arriza, S Eliasof, M P Kavanaugh, S G Amara. Proc Natl Acad Sci U S A 1997
634
12

Conditional deletion of the glutamate transporter GLT-1 reveals that astrocytic GLT-1 protects against fatal epilepsy while neuronal GLT-1 contributes significantly to glutamate uptake into synaptosomes.
Geraldine T Petr, Yan Sun, Natalie M Frederick, Yun Zhou, Sameer C Dhamne, Mustafa Q Hameed, Clive Miranda, Edward A Bedoya, Kathryn D Fischer, Wencke Armsen,[...]. J Neurosci 2015
152
12


A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
M Z Cader, J L Steckley, D A Dyment, R S McLachlan, G C Ebers. Neurology 2005
29
37

Mechanisms of glutamate transport.
Robert J Vandenberg, Renae M Ryan. Physiol Rev 2013
171
11

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
Angelita Tottene, Rossella Conti, Alessandra Fabbro, Dania Vecchia, Maryna Shapovalova, Mirko Santello, Arn M J M van den Maagdenberg, Michel D Ferrari, Daniela Pietrobon. Neuron 2009
204
11

A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.
Karine Choquet, Roberta La Piana, Bernard Brais. Neurogenetics 2015
22
50

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Wan-Jin Chen, Yu Lin, Zhi-Qi Xiong, Wei Wei, Wang Ni, Guo-He Tan, Shun-Ling Guo, Jin He, Ya-Fang Chen, Qi-Jie Zhang,[...]. Nat Genet 2011
275
11

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.
K F Damji, R R Allingham, S C Pollock, K Small, K E Lewis, J M Stajich, L H Yamaoka, J M Vance, M A Pericak-Vance. Arch Neurol 1996
42
26

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
150
10

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
Verneri Anttila, Hreinn Stefansson, Mikko Kallela, Unda Todt, Gisela M Terwindt, M Stella Calafato, Dale R Nyholt, Antigone S Dimas, Tobias Freilinger, Bertram Müller-Myhsok,[...]. Nat Genet 2010
238
10

Transport mechanism of a bacterial homologue of glutamate transporters.
Nicolas Reyes, Christopher Ginter, Olga Boudker. Nature 2009
283
10



PRRT2 mutations cause hemiplegic migraine.
Florence Riant, Emmanuel Roze, Cecile Barbance, Aurélie Méneret, Lucie Guyant-Maréchal, Christian Lucas, Pascal Sabouraud, Agnes Trébuchon, Christel Depienne, Elisabeth Tournier-Lasserve. Neurology 2012
68
14

A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias.
M Strupp, R Kalla, J Claassen, C Adrion, U Mansmann, T Klopstock, T Freilinger, H Neugebauer, R Spiegel, M Dichgans,[...]. Neurology 2011
98
10

Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraine.
Masashi Suzuki, Wim Van Paesschen, Ingeborg Stalmans, Shoko Horita, Hideomi Yamada, Bruno A Bergmans, Eric Legius, Florence Riant, Peter De Jonghe, Yuehong Li,[...]. Proc Natl Acad Sci U S A 2010
92
10

PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, Zaid Afawi, Sameer M Zuberi, James N Hughes, Clair Pridmore, Bree L Hodgson, Xenia Iona, Lynette G Sadleir,[...]. Am J Hum Genet 2012
158
10

The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, Maria Stamelou, Matthew Walker, Dimitri Kullmann,[...]. Brain 2015
71
14


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.