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


A new autosomal dominant pure cerebellar ataxia.
E Storey, R J Gardner, M A Knight, M L Kennerson, R R Tuck, S M Forrest, G A Nicholson. Neurology 2001
49
13

Selective and direct inhibition of TRPC3 channels underlies biological activities of a pyrazole compound.
Shigeki Kiyonaka, Kenta Kato, Motohiro Nishida, Kazuhiro Mio, Takuro Numaga, Yuichi Sawaguchi, Takashi Yoshida, Minoru Wakamori, Emiko Mori, Tomohiro Numata,[...]. Proc Natl Acad Sci U S A 2009
258
13

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
646
13

The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Luis Ruano, Claudia Melo, M Carolina Silva, Paula Coutinho. Neuroepidemiology 2014
239
13

Cerebellar Transcriptome Profiles of ATXN1 Transgenic Mice Reveal SCA1 Disease Progression and Protection Pathways.
Melissa Ingram, Emily A L Wozniak, Lisa Duvick, Rendong Yang, Paul Bergmann, Robert Carson, Brennon O'Callaghan, Huda Y Zoghbi, Christine Henzler, Harry T Orr. Neuron 2016
50
13

A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.
Ana I Seixas, Joana R Loureiro, Cristina Costa, Andrés Ordóñez-Ugalde, Hugo Marcelino, Cláudia L Oliveira, José L Loureiro, Ashutosh Dhingra, Eva Brandão, Vitor T Cruz,[...]. Am J Hum Genet 2017
46
13

Toward understanding Machado-Joseph disease.
Maria do Carmo Costa, Henry L Paulson. Prog Neurobiol 2012
151
13

Potassium channel dysfunction underlies Purkinje neuron spiking abnormalities in spinocerebellar ataxia type 2.
James M Dell'Orco, Stefan M Pulst, Vikram G Shakkottai. Hum Mol Genet 2017
27
22

Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia.
Jessica L Zambonin, Allison Bellomo, Hilla Ben-Pazi, David B Everman, Lee M Frazer, Michael T Geraghty, Amy D Harper, Julie R Jones, Benjamin Kamien, Kristin Kernohan,[...]. Orphanet J Rare Dis 2017
23
26

Candidate screening of the TRPC3 gene in cerebellar ataxia.
Esther B E Becker, Brent L Fogel, Sanjeev Rajakulendran, Anna Dulneva, Michael G Hanna, Susan L Perlman, Daniel H Geschwind, Kay E Davies. Cerebellum 2011
16
31

Emerging pathogenic pathways in the spinocerebellar ataxias.
Kerri M Carlson, J Michael Andresen, Harry T Orr. Curr Opin Genet Dev 2009
55
10

Mutant gammaPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells.
Takahiro Seki, Takayuki Shimahara, Kazuhiro Yamamoto, Nana Abe, Taku Amano, Naoko Adachi, Hideyuki Takahashi, Kaori Kashiwagi, Naoaki Saito, Norio Sakai. Neurobiol Dis 2009
43
11

SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776.
Lisa Duvick, Justin Barnes, Blake Ebner, Smita Agrawal, Michael Andresen, Janghoo Lim, Glenn J Giesler, Huda Y Zoghbi, Harry T Orr. Neuron 2010
103
10

Distinct roles of Galpha(q) and Galpha11 for Purkinje cell signaling and motor behavior.
J Hartmann, R Blum, Y Kovalchuk, H Adelsberger, R Kuner, G M Durand, M Miyata, M Kano, S Offermanns, A Konnerth. J Neurosci 2004
61
10

STIM1 controls neuronal Ca²⁺ signaling, mGluR1-dependent synaptic transmission, and cerebellar motor behavior.
Jana Hartmann, Rosa M Karl, Ryan P D Alexander, Helmuth Adelsberger, Monika S Brill, Charlotta Rühlmann, Anna Ansel, Kenji Sakimura, Yoshihiro Baba, Tomohiro Kurosaki,[...]. Neuron 2014
107
10

Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol.
T Hofmann, A G Obukhov, M Schaefer, C Harteneck, T Gudermann, G Schultz. Nature 1999
10

Properties of heterologously expressed hTRP3 channels in bovine pulmonary artery endothelial cells.
M Kamouchi, S Philipp, V Flockerzi, U Wissenbach, A Mamin, L Raeymaekers, J Eggermont, G Droogmans, B Nilius. J Physiol 1999
151
10

PKC-dependent coupling of calcium permeation through transient receptor potential canonical 3 (TRPC3) to calcineurin signaling in HL-1 myocytes.
Michael Poteser, Hannes Schleifer, Michaela Lichtenegger, Michaela Schernthaner, Thomas Stockner, C Oliver Kappe, Toma N Glasnov, Christoph Romanin, Klaus Groschner. Proc Natl Acad Sci U S A 2011
57
10


Calcium dynamics and electrophysiological properties of cerebellar Purkinje cells in SCA1 transgenic mice.
T Inoue, X Lin, K A Kohlmeier, H T Orr, H Y Zoghbi, W N Ross. J Neurophysiol 2001
47
10




Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20.
Melanie A Knight, R J McKinlay Gardner, Melanie Bahlo, Tohru Matsuura, Judith A Dixon, Susan M Forrest, Elsdon Storey. Brain 2004
65
10

Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia.
Joy T Walter, Karina Alviña, Mary D Womack, Carolyn Chevez, Kamran Khodakhah. Nat Neurosci 2006
269
10


Spinocerebellar ataxia type 6 protein aggregates cause deficits in motor learning and cerebellar plasticity.
Melanie D Mark, Martin Krause, Henk-Jan Boele, Wolfgang Kruse, Stefan Pollok, Thomas Kuner, Deniz Dalkara, Sebastiaan Koekkoek, Chris I De Zeeuw, Stefan Herlitze. J Neurosci 2015
36
13

FGF14 regulates presynaptic Ca2+ channels and synaptic transmission.
Haidun Yan, Juan L Pablo, Geoffrey S Pitt. Cell Rep 2013
50
10

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
10

CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.
Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, Peter N Robinson. PLoS Genet 2009
88
10

FGF14 regulates the intrinsic excitability of cerebellar Purkinje neurons.
Vikram G Shakkottai, Maolei Xiao, Lin Xu, Michael Wong, Jeanne M Nerbonne, David M Ornitz, Kelvin A Yamada. Neurobiol Dis 2009
76
10

trp, a novel mammalian gene family essential for agonist-activated capacitative Ca2+ entry.
X Zhu, M Jiang, M Peyton, G Boulay, R Hurst, E Stefani, L Birnbaumer. Cell 1996
568
10

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.
K Hara, A Shiga, H Nozaki, J Mitsui, Y Takahashi, H Ishiguro, H Yomono, H Kurisaki, J Goto, T Ikeuchi,[...]. Neurology 2008
89
10

Carbonic anhydrase-related protein is a novel binding protein for inositol 1,4,5-trisphosphate receptor type 1.
Junji Hirota, Hideaki Ando, Kozo Hamada, Katsuhiko Mikoshiba. Biochem J 2003
112
10

Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
Guo-Yun Yu, Michael J Howell, Matthew J Roller, Ting-Dong Xie, Christopher M Gomez. Ann Neurol 2005
46
10

Cellular and circuit mechanisms underlying spinocerebellar ataxias.
Pratap Meera, Stefan M Pulst, Thomas S Otis. J Physiol 2016
30
16

Increased protein kinase C gamma activity induces Purkinje cell pathology in a mouse model of spinocerebellar ataxia 14.
Jingmin Ji, Melanie L Hassler, Etsuko Shimobayashi, Nagendher Paka, Raphael Streit, Josef P Kapfhammer. Neurobiol Dis 2014
25
20

Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKC gamma mutant mice.
C Chen, M Kano, A Abeliovich, L Chen, S Bao, J J Kim, K Hashimoto, R F Thompson, S Tonegawa. Cell 1995
262
10


ATAXIN-1 interacts with the repressor Capicua in its native complex to cause SCA1 neuropathology.
Yung C Lam, Aaron B Bowman, Paymaan Jafar-Nejad, Janghoo Lim, Ronald Richman, John D Fryer, Eric D Hyun, Lisa A Duvick, Harry T Orr, Juan Botas,[...]. Cell 2006
207
10

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
204
10

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
Esther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, Michiel R Fokkens, Juha M Karjalainen, Cleo J L M Smeets, Jelkje J de Boer-Bergsma, Gerben van der Vries, Dennis Dooijes, Giovana B Bampi,[...]. Brain 2017
48
10

Targeting potassium channels to treat cerebellar ataxia.
David D Bushart, Ravi Chopra, Vikrant Singh, Geoffrey G Murphy, Heike Wulff, Vikram G Shakkottai. Ann Clin Transl Neurol 2018
26
19



Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features.
Matthis Synofzik, Christian Beetz, Claudia Bauer, Michael Bonin, Elena Sanchez-Ferrero, Tanja Schmitz-Hübsch, Ullrich Wüllner, Thomas Nägele, Olaf Riess, Ludger Schöls,[...]. J Med Genet 2011
35
14

Synapse elimination in the developing cerebellum.
Kouichi Hashimoto, Masanobu Kano. Cell Mol Life Sci 2013
84
8

TRPC3 and TRPC6 are essential for angiotensin II-induced cardiac hypertrophy.
Naoya Onohara, Motohiro Nishida, Ryuji Inoue, Hiroyuki Kobayashi, Hideki Sumimoto, Yoji Sato, Yasuo Mori, Taku Nagao, Hitoshi Kurose. EMBO J 2006
287
8

Subunit composition of mammalian transient receptor potential channels in living cells.
Thomas Hofmann, Michael Schaefer, Günter Schultz, Thomas Gudermann. Proc Natl Acad Sci U S A 2002
569
8

mRNA distribution analysis of human TRPC family in CNS and peripheral tissues.
Antonio Riccio, Andrew D Medhurst, Cesar Mattei, Rosemary E Kelsell, Andrew R Calver, Andrew D Randall, Christopher D Benham, Menelas N Pangalos. Brain Res Mol Brain Res 2002
218
8


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.