A citation-based method for searching scientific literature

Brent L Fogel, Sonya M Hanson, Esther B E Becker. Mov Disord 2015
Times Cited: 46







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



Times Cited
  Times     Co-cited
Similarity


The mammalian TRPC cation channels.
Guillermo Vazquez, Barbara J Wedel, Omar Aziz, Mohamed Trebak, James W Putney. Biochim Biophys Acta 2004
242
8

Transient receptor potential canonical channels regulate the induction of cerebellar long-term depression.
Hong Goo Chae, Sung Ji Ahn, Yun Hwa Hong, Won Seok Chang, Jun Kim, Sang Jeong Kim. J Neurosci 2012
12
33

Activity-dependent gating of calcium spikes by A-type K+ channels controls climbing fiber signaling in Purkinje cell dendrites.
Yo Otsu, Païkan Marcaggi, Anne Feltz, Philippe Isope, Mihaly Kollo, Zoltan Nusser, Benjamin Mathieu, Masanobu Kano, Mika Tsujita, Kenji Sakimura,[...]. Neuron 2014
36
11

Type 1 metabotropic glutamate receptors (mGlu1) trigger the gating of GluD2 delta glutamate receptors.
Visou Ady, Julie Perroy, Ludovic Tricoire, Claire Piochon, Selma Dadak, Xiaoru Chen, Isabelle Dusart, Laurent Fagni, Bertrand Lambolez, Carole Levenes. EMBO Rep 2014
45
8



A new dominantly inherited pure cerebellar ataxia, SCA 30.
E Storey, M Bahlo, M Fahey, O Sisson, C J Lueck, R J M Gardner. J Neurol Neurosurg Psychiatry 2009
31
12

Retrograde semaphorin signaling regulates synapse elimination in the developing mouse brain.
Naofumi Uesaka, Motokazu Uchigashima, Takayasu Mikuni, Takanobu Nakazawa, Harumi Nakao, Hirokazu Hirai, Atsu Aiba, Masahiko Watanabe, Masanobu Kano. Science 2014
71
8

GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia.
Marie Coutelier, Lydie Burglen, Emeline Mundwiller, Myriam Abada-Bendib, Diana Rodriguez, Sandra Chantot-Bastaraud, Christelle Rougeot, Marie-Anne Cournelle, Mathieu Milh, Annick Toutain,[...]. Neurology 2015
41
9

New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.
Carmen Serrano-Munuera, Marc Corral-Juan, Giovanni Stevanin, Hector San Nicolás, Carles Roig, Jordi Corral, Berta Campos, Laura de Jorge, Carlos Morcillo-Suárez, Arcadi Navarro,[...]. JAMA Neurol 2013
22
18

Clinical features and genetic analysis of a new form of spinocerebellar ataxia.
D Devos, S Schraen-Maschke, I Vuillaume, K Dujardin, P Nazé, C Willoteaux, A Destée, B Sablonnière. Neurology 2001
49
8

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, H Takahashi, R Kondo, A Ishikawa, T Hayashi. Nat Genet 1994
972
8


β-III spectrin is critical for development of purkinje cell dendritic tree and spine morphogenesis.
Yuanzheng Gao, Emma M Perkins, Yvonne L Clarkson, Steven Tobia, Alastair R Lyndon, Mandy Jackson, Jeffrey D Rothstein. J Neurosci 2011
44
9

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
G Imbert, F Saudou, G Yvert, D Devys, Y Trottier, J M Garnier, C Weber, J L Mandel, G Cancel, N Abbas,[...]. Nat Genet 1996
701
8

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.
K Flanigan, K Gardner, K Alderson, B Galster, B Otterud, M F Leppert, C Kaplan, L J Ptácek. Am J Hum Genet 1996
184
8


Phospholipase cbeta4 is specifically involved in climbing fiber synapse elimination in the developing cerebellum.
M Kano, K Hashimoto, M Watanabe, H Kurihara, S Offermanns, H Jiang, Y Wu, K Jun, H S Shin, Y Inoue,[...]. Proc Natl Acad Sci U S A 1998
147
8



Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus.
T E Dudding, K Friend, P W Schofield, S Lee, I A Wilkinson, R I Richards. Neurology 2004
58
8

Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII.
Namik Kaya, Hesham Aldhalaan, Banan Al-Younes, Dilek Colak, Taghreed Shuaib, Fahad Al-Mohaileb, Abdulaziz Al-Sugair, Michael Nester, Suad Al-Yamani, Albandary Al-Bakheet,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
48
8

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.
Claudia Cagnoli, Caterina Mariotti, Franco Taroni, Marco Seri, Alessandro Brussino, Chiara Michielotto, Marina Grisoli, Daniela Di Bella, Nicola Migone, Cinzia Gellera,[...]. Brain 2006
80
8

Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia.
Brent L Fogel, Hane Lee, Joshua L Deignan, Samuel P Strom, Sibel Kantarci, Xizhe Wang, Fabiola Quintero-Rivera, Eric Vilain, Wayne W Grody, Susan Perlman,[...]. JAMA Neurol 2014
150
8


Functional characterization of the P1059L mutation in the inositol 1,4,5-trisphosphate receptor type 1 identified in a Japanese SCA15 family.
Haruka Yamazaki, Hiroaki Nozaki, Osamu Onodera, Takayuki Michikawa, Masatoyo Nishizawa, Katsuhiko Mikoshiba. Biochem Biophys Res Commun 2011
20
20

The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse.
V A Street, M M Bosma, V P Demas, M R Regan, D D Lin, L C Robinson, W S Agnew, B L Tempel. J Neurosci 1997
92
8

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
8

Sporadic infantile-onset spinocerebellar ataxia caused by missense mutations of the inositol 1,4,5-triphosphate receptor type 1 gene.
Masayuki Sasaki, Chihiro Ohba, Mizue Iai, Shinichi Hirabayashi, Hitoshi Osaka, Takuya Hiraide, Hirotomo Saitsu, Naomichi Matsumoto. J Neurol 2015
40
10

Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice.
Yan Jiao, Jian Yan, Yu Zhao, Leah Rae Donahue, Wesley G Beamer, Xinmin Li, Bruce A Roe, Mark S Ledoux, Weikuan Gu. Genetics 2005
89
8


Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein.
Hideyuki Takahashi, Naoko Adachi, Toshihiko Shirafuji, Sally Danno, Takehiko Ueyama, Michele Vendruscolo, Anton N Shuvaev, Takuya Sugimoto, Takahiro Seki, Daizo Hamada,[...]. Hum Mol Genet 2015
11
36

Inositol 1,4,5-trisphosphate receptor type 1 in granule cells, not in Purkinje cells, regulates the dendritic morphology of Purkinje cells through brain-derived neurotrophic factor production.
Chihiro Hisatsune, Yukiko Kuroda, Takumi Akagi, Takashi Torashima, Hirokazu Hirai, Tsutomu Hashikawa, Takafumi Inoue, Katsuhiko Mikoshiba. J Neurosci 2006
45
8

Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function.
S Toru, T Murakoshi, K Ishikawa, H Saegusa, H Fujigasaki, T Uchihara, S Nagayama, M Osanai, H Mizusawa, T Tanabe. J Biol Chem 2000
79
8

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
Kei Watase, Curtis F Barrett, Taisuke Miyazaki, Taro Ishiguro, Kinya Ishikawa, Yuanxin Hu, Toshinori Unno, Yaling Sun, Sayumi Kasai, Masahiko Watanabe,[...]. Proc Natl Acad Sci U S A 2008
103
8

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice.
I A Klement, P J Skinner, M D Kaytor, H Yi, S M Hersch, H B Clark, H Y Zoghbi, H T Orr. Cell 1998
793
8

Ataxia and paroxysmal dyskinesia in mice lacking axonally transported FGF14.
Qing Wang, Mark E Bardgett, Michael Wong, David F Wozniak, Junyang Lou, Benjamin D McNeil, Chen Chen, Anthony Nardi, David C Reid, Kelvin Yamada,[...]. Neuron 2002
127
8

Exercise and genetic rescue of SCA1 via the transcriptional repressor Capicua.
John D Fryer, Peng Yu, Hyojin Kang, Caleigh Mandel-Brehm, Angela N Carter, Juan Crespo-Barreto, Yan Gao, Adriano Flora, Chad Shaw, Harry T Orr,[...]. Science 2011
93
8

RNAi suppresses polyglutamine-induced neurodegeneration in a model of spinocerebellar ataxia.
Haibin Xia, Qinwen Mao, Steven L Eliason, Scott Q Harper, Inês H Martins, Harry T Orr, Henry L Paulson, Linda Yang, Robert M Kotin, Beverly L Davidson. Nat Med 2004
483
8

Ca2+ activity at GABAB receptors constitutively promotes metabotropic glutamate signaling in the absence of GABA.
Toshihide Tabata, Kenji Araishi, Kouichi Hashimoto, Yuki Hashimotodani, Herman van der Putten, Bernhard Bettler, Masanobu Kano. Proc Natl Acad Sci U S A 2004
81
8

Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
L Zu, K P Figueroa, R Grewal, S M Pulst. Am J Hum Genet 1999
92
8

Novel pyrazole compounds for pharmacological discrimination between receptor-operated and store-operated Ca(2+) entry pathways.
H Schleifer, B Doleschal, M Lichtenegger, R Oppenrieder, I Derler, I Frischauf, T N Glasnov, C O Kappe, C Romanin, K Groschner. Br J Pharmacol 2012
108
8

Canonical transient receptor potential 3 channels regulate mitochondrial calcium uptake.
Shengjie Feng, Hongyu Li, Yilin Tai, Junbo Huang, Yujuan Su, Joel Abramowitz, Michael X Zhu, Lutz Birnbaumer, Yizheng Wang. Proc Natl Acad Sci U S A 2013
75
8

Redefining the cerebellar cortex as an assembly of non-uniform Purkinje cell microcircuits.
Nadia L Cerminara, Eric J Lang, Roy V Sillitoe, Richard Apps. Nat Rev Neurosci 2015
115
8

Functional coupling between mGluR1 and Cav3.1 T-type calcium channels contributes to parallel fiber-induced fast calcium signaling within Purkinje cell dendritic spines.
Michael E Hildebrand, Philippe Isope, Taisuke Miyazaki, Toshitaka Nakaya, Esperanza Garcia, Anne Feltz, Toni Schneider, Jürgen Hescheler, Masanobu Kano, Kenji Sakimura,[...]. J Neurosci 2009
64
8


A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
R Koide, S Kobayashi, T Shimohata, T Ikeuchi, M Maruyama, M Saito, M Yamada, H Takahashi, S Tsuji. Hum Mol Genet 1999
276
8

Reduced immunoreactivity to calcium-binding proteins in Purkinje cells precedes onset of ataxia in spinocerebellar ataxia-1 transgenic mice.
P J Vig, S H Subramony, E N Burright, J D Fratkin, D O McDaniel, D Desaiah, Z Qin. Neurology 1998
56
8

Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model.
Warunee Dansithong, Sharan Paul, Karla P Figueroa, Marc D Rinehart, Shaina Wiest, Lance T Pflieger, Daniel R Scoles, Stefan M Pulst. PLoS Genet 2015
40
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.