A citation-based method for searching scientific literature

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, Rune R Frants, Robert W Baloh, Michel D Ferrari, Joanna C Jen, Arn M J M van den Maagdenberg. Arch Neurol 2009
Times Cited: 80







List of co-cited articles
1235 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
J C Jen, J Wan, T P Palos, B D Howard, R W Baloh. Neurology 2005
219
81

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
31

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
319
28

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
197
27

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
26

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
25

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
34
50


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
25
64

Glutamate uptake.
N C Danbolt. Prog Neurobiol 2001
18

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
59
23

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
17

Structure of a glutamate transporter homologue from Pyrococcus horikoshii.
Dinesh Yernool, Olga Boudker, Yan Jin, Eric Gouaux. Nature 2004
585
17

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
942
17

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
40
35

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
83
16

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
J L Steckley, G C Ebers, M Z Cader, R S McLachlan. Neurology 2001
47
25

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
574
15

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
34
35

Localization of neuronal and glial glutamate transporters.
J D Rothstein, L Martin, A I Levey, M Dykes-Hoberg, L Jin, D Wu, N Nash, R W Kuncl. Neuron 1994
15

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
173
13



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
52
21

A quantitative assessment of glutamate uptake into hippocampal synaptic terminals and astrocytes: new insights into a neuronal role for excitatory amino acid transporter 2 (EAAT2).
D N Furness, Y Dehnes, A Q Akhtar, D J Rossi, M Hamann, N J Grutle, V Gundersen, S Holmseth, K P Lehre, K Ullensvang,[...]. Neuroscience 2008
168
12

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
12

Flux coupling in a neuronal glutamate transporter.
N Zerangue, M P Kavanaugh. Nature 1996
630
12

Ion fluxes associated with excitatory amino acid transport.
J I Wadiche, S G Amara, M P Kavanaugh. Neuron 1995
433
12

Activation of a presynaptic glutamate transporter regulates synaptic transmission through electrical signaling.
Margaret Lin Veruki, Svein Harald Mørkve, Espen Hartveit. Nat Neurosci 2006
125
12

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
12

A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.
Karine Choquet, Roberta La Piana, Bernard Brais. Neurogenetics 2015
23
43

Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A.
P Imbrici, L H Eunson, T D Graves, K P Bhatia, N H Wadia, D M Kullmann, M G Hanna. Neurology 2005
35
25

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
C Jodice, E Mantuano, L Veneziano, F Trettel, G Sabbadini, L Calandriello, A Francia, M Spadaro, F Pierelli, F Salvi,[...]. Hum Mol Genet 1997
212
11

Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine.
M Strupp, R Kalla, M Dichgans, T Freilinger, S Glasauer, T Brandt. Neurology 2004
142
11

Hereditary paroxysmal ataxia: response to acetazolamide.
R C Griggs, R T Moxley, R A Lafrance, J McQuillen. Neurology 1978
158
11

Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria.
Charles G Bailey, Renae M Ryan, Annora D Thoeng, Cynthia Ng, Kara King, Jessica M Vanslambrouck, Christiane Auray-Blais, Robert J Vandenberg, Stefan Bröer, John E J Rasko. J Clin Invest 2011
71
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
714
11

Assessment of glutamate transporter GLAST (EAAT1)-deficient mice for phenotypes relevant to the negative and executive/cognitive symptoms of schizophrenia.
Rose-Marie Karlsson, Kohichi Tanaka, Lisa M Saksida, Timothy J Bussey, Markus Heilig, Andrew Holmes. Neuropsychopharmacology 2009
120
11

GABA and Glutamate Transporters in Brain.
Yun Zhou, Niels Christian Danbolt. Front Endocrinol (Lausanne) 2013
188
11

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
25
36

A novel mutation in SLC1A3 causes episodic ataxia.
Kazuhiro Iwama, Aya Iwata, Masaaki Shiina, Satomi Mitsuhashi, Satoko Miyatake, Atsushi Takata, Noriko Miyake, Kazuhiro Ogata, Shuichi Ito, Takeshi Mizuguchi,[...]. J Hum Genet 2018
17
52

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
359
10

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
525
10

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
628
10

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.
L H Eunson, R Rea, S M Zuberi, S Youroukos, C P Panayiotopoulos, R Liguori, P Avoni, R C McWilliam, J B Stephenson, M G Hanna,[...]. Ann Neurol 2000
169
10

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
107
10

Brain glutamate transporter proteins form homomultimers.
O Haugeto, K Ullensvang, L M Levy, F A Chaudhry, T Honoré, M Nielsen, K P Lehre, N C Danbolt. J Biol Chem 1996
391
10


Kinetics of a human glutamate transporter.
J I Wadiche, J L Arriza, S G Amara, M P Kavanaugh. Neuron 1995
327
10


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.