A citation-based method for searching scientific literature

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
Times Cited: 29







List of co-cited articles
493 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
85
62

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
233
62


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
203
37

Structure of a glutamate transporter homologue from Pyrococcus horikoshii.
Dinesh Yernool, Olga Boudker, Yan Jin, Eric Gouaux. Nature 2004
604
34

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
277
34

Genetic Variants Associated with Episodic Ataxia in Korea.
Kwang-Dong Choi, Ji-Soo Kim, Hyo-Jung Kim, Ileok Jung, Seong-Hae Jeong, Seung-Han Lee, Dong Uk Kim, Sang-Ho Kim, Seo Young Choi, Jin-Hong Shin,[...]. Sci Rep 2017
38
34

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
21
47

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
43
31

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
89
31

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
36
27


Transport mechanism of a bacterial homologue of glutamate transporters.
Nicolas Reyes, Christopher Ginter, Olga Boudker. Nature 2009
308
24

Coupling substrate and ion binding to extracellular gate of a sodium-dependent aspartate transporter.
Olga Boudker, Renae M Ryan, Dinesh Yernool, Keiko Shimamoto, Eric Gouaux. Nature 2007
356
24

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
75
24

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
40
24

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
24

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
29
24

Structure and allosteric inhibition of excitatory amino acid transporter 1.
Juan C Canul-Tec, Reda Assal, Erica Cirri, Pierre Legrand, Sébastien Brier, Julia Chamot-Rooke, Nicolas Reyes. Nature 2017
117
24

Glutamate uptake.
N C Danbolt. Prog Neurobiol 2001
20

Coupled binding mechanism of three sodium ions and aspartate in the glutamate transporter homologue GltTk.
Albert Guskov, Sonja Jensen, Ignacio Faustino, Siewert J Marrink, Dirk Jan Slotboom. Nat Commun 2016
61
20

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
60
20

A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.
Karine Choquet, Roberta La Piana, Bernard Brais. Neurogenetics 2015
25
24

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
55
20


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
36
20

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
324
20

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
21
28

Ion fluxes associated with excitatory amino acid transport.
J I Wadiche, S G Amara, M P Kavanaugh. Neuron 1995
445
20

Allosteric modulation of an excitatory amino acid transporter: the subtype-selective inhibitor UCPH-101 exerts sustained inhibition of EAAT1 through an intramonomeric site in the trimerization domain.
Bjarke Abrahamsen, Nicole Schneider, Mette N Erichsen, Tri H V Huynh, Christoph Fahlke, Lennart Bunch, Anders A Jensen. J Neurosci 2013
35
17

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
183
17

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
115
17

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
J L Steckley, G C Ebers, M Z Cader, R S McLachlan. Neurology 2001
48
17

Episodic Ataxias: Clinical and Genetic Features.
Kwang-Dong Choi, Jae-Hwan Choi. J Mov Disord 2016
43
17

Hereditary myokymia and periodic ataxia.
D H VanDyke, R C Griggs, M J Murphy, M N Goldstein. J Neurol Sci 1975
108
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
585
17

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

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
115
17

Duplications of SLC1A3: Associated with ADHD and autism.
Claudia J M van Amen-Hellebrekers, Sandra Jansen, Rolph Pfundt, Janneke H Schuurs-Hoeijmakers, David A Koolen, Carlo L Marcelis, Nicole de Leeuw, Bert B A de Vries. Eur J Med Genet 2016
14
35

Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.
Mark A Corbett, Susannah T Bellows, Melody Li, Renée Carroll, Silvana Micallef, Gemma L Carvill, Candace T Myers, Katherine B Howell, Snezana Maljevic, Holger Lerche,[...]. Neurology 2016
44
17

Mechanisms of glutamate transport.
Robert J Vandenberg, Renae M Ryan. Physiol Rev 2013
190
17


The glutamate and chloride permeation pathways are colocalized in individual neuronal glutamate transporter subunits.
Gregory P Leary, Emily F Stone, David C Holley, Michael P Kavanaugh. J Neurosci 2007
77
17

Individual subunits of the glutamate transporter EAAC1 homotrimer function independently of each other.
Christof Grewer, Poonam Balani, Christian Weidenfeller, Thorsten Bartusel, Zhen Tao, Thomas Rauen. Biochemistry 2005
119
17

Activation of a presynaptic glutamate transporter regulates synaptic transmission through electrical signaling.
Margaret Lin Veruki, Svein Harald Mørkve, Espen Hartveit. Nat Neurosci 2006
130
17

Glutamate transporter-associated anion channels adjust intracellular chloride concentrations during glial maturation.
Verena Untiet, Peter Kovermann, Niklas J Gerkau, Thomas Gensch, Christine R Rose, Christoph Fahlke. Glia 2017
50
17

FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9.
Julie Piarroux, Florence Riant, Véronique Humbertclaude, Ganaelle Remerand, Jessica Hadjadj, Franck Rejou, Christine Coubes, Lucile Pinson, Pierre Meyer, Agathe Roubertie. Ann Clin Transl Neurol 2020
14
35

Functional consequences of SLC1A3 mutations associated with episodic ataxia 6.
Aparna S Chivukula, Mariia Suslova, Daniel Kortzak, Peter Kovermann, Christoph Fahlke. Hum Mutat 2020
16
31

ASCT2/SLC1A5 controls glutamine uptake and tumour growth in triple-negative basal-like breast cancer.
M van Geldermalsen, Q Wang, R Nagarajah, A D Marshall, A Thoeng, D Gao, W Ritchie, Y Feng, C G Bailey, N Deng,[...]. Oncogene 2016
269
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.