A citation-based method for searching scientific literature

Vikram G Shakkottai, Maolei Xiao, Lin Xu, Michael Wong, Jeanne M Nerbonne, David M Ornitz, Kelvin A Yamada. Neurobiol Dis 2009
Times Cited: 77







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



Times Cited
  Times     Co-cited
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A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected].
John C van Swieten, Esther Brusse, Bianca M de Graaf, Elmar Krieger, Raoul van de Graaf, Inge de Koning, Anneke Maat-Kievit, Peter Leegwater, Dennis Dooijes, Ben A Oostra,[...]. Am J Hum Genet 2003
188
50

The FGF14(F145S) mutation disrupts the interaction of FGF14 with voltage-gated Na+ channels and impairs neuronal excitability.
Fernanda Laezza, Benjamin R Gerber, Jun-Yang Lou, Marie A Kozel, Hali Hartman, Ann Marie Craig, David M Ornitz, Jeanne M Nerbonne. J Neurosci 2007
109
48

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
128
48

Fibroblast growth factor homologous factors control neuronal excitability through modulation of voltage-gated sodium channels.
Mitchell Goldfarb, Jon Schoorlemmer, Anthony Williams, Shyam Diwakar, Qing Wang, Xiao Huang, Joanna Giza, Dafna Tchetchik, Kevin Kelley, Ana Vega,[...]. Neuron 2007
154
44

Fibroblast growth factor 14 is an intracellular modulator of voltage-gated sodium channels.
Jun-Yang Lou, Fernanda Laezza, Benjamin R Gerber, Maolei Xiao, Kathryn A Yamada, Hali Hartmann, Ann Marie Craig, Jeanne M Nerbonne, David M Ornitz. J Physiol 2005
125
42

Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.
Esther Brusse, Inge de Koning, Anneke Maat-Kievit, Ben A Oostra, Peter Heutink, John C van Swieten. Mov Disord 2006
75
40

FGF14 N-terminal splice variants differentially modulate Nav1.2 and Nav1.6-encoded sodium channels.
Fernanda Laezza, Angelika Lampert, Marie A Kozel, Benjamin R Gerber, Anthony M Rush, Jeanne M Nerbonne, Stephen G Waxman, Sulayman D Dib-Hajj, David M Ornitz. Mol Cell Neurosci 2009
82
32

Crystal structure of a fibroblast growth factor homologous factor (FHF) defines a conserved surface on FHFs for binding and modulation of voltage-gated sodium channels.
Regina Goetz, Katarzyna Dover, Fernanda Laezza, Nataly Shtraizent, Xiao Huang, Dafna Tchetchik, Anna V Eliseenkova, Chong-Feng Xu, Thomas A Neubert, David M Ornitz,[...]. J Biol Chem 2009
86
28

Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias.
Andreas Dalski, Jassemien Atici, Friedmar R Kreuz, Yorck Hellenbroich, Eberhard Schwinger, Christine Zühlke. Eur J Hum Genet 2005
66
31

Impaired hippocampal synaptic transmission and plasticity in mice lacking fibroblast growth factor 14.
Maolei Xiao, Lin Xu, Fernanda Laezza, Kelvin Yamada, Sheng Feng, David M Ornitz. Mol Cell Neurosci 2007
64
31

FGF14 regulates presynaptic Ca2+ channels and synaptic transmission.
Haidun Yan, Juan L Pablo, Geoffrey S Pitt. Cell Rep 2013
50
38

Impaired spatial learning and defective theta burst induced LTP in mice lacking fibroblast growth factor 14.
David F Wozniak, Maolei Xiao, Lin Xu, Kelvin A Yamada, David M Ornitz. Neurobiol Dis 2007
70
25

Fibroblast growth factor homologous factor 2B: association with Nav1.6 and selective colocalization at nodes of Ranvier of dorsal root axons.
Ellen K Wittmack, Anthony M Rush, Matthew J Craner, Mitchell Goldfarb, Stephen G Waxman, Sulayman D Dib-Hajj. J Neurosci 2004
103
23

Intracellular FGF14 (iFGF14) Is Required for Spontaneous and Evoked Firing in Cerebellar Purkinje Neurons and for Motor Coordination and Balance.
Marie K Bosch, Yarimar Carrasquillo, Joseph L Ransdell, Ajay Kanakamedala, David M Ornitz, Jeanne M Nerbonne. J Neurosci 2015
36
50

Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development.
P M Smallwood, I Munoz-Sanjuan, P Tong, J P Macke, S H Hendry, D J Gilbert, N G Copeland, N A Jenkins, J Nathans. Proc Natl Acad Sci U S A 1996
310
22


SCA27 caused by a chromosome translocation: further delineation of the phenotype.
D Misceo, M Fannemel, T Barøy, R Roberto, B Tvedt, T Jaeger, V Bryn, P Strømme, E Frengen. Neurogenetics 2009
27
62

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.
Michael F Waters, Natali A Minassian, Giovanni Stevanin, Karla P Figueroa, John P A Bannister, Dagmar Nolte, Allan F Mock, Virgilio Gerald H Evidente, Dominic B Fee, Ulrich Müller,[...]. Nat Genet 2006
200
20

Modulation of the cardiac sodium channel Nav1.5 by fibroblast growth factor homologous factor 1B.
Chuan-ju Liu, Sulayman D Dib-Hajj, Muthukrishnan Renganathan, Theodore R Cummins, Stephen G Waxman. J Biol Chem 2003
115
20


Long-term inactivation particle for voltage-gated sodium channels.
Katarzyna Dover, Sergio Solinas, Egidio D'Angelo, Mitchell Goldfarb. J Physiol 2010
49
32

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy.
Franck Kalume, Frank H Yu, Ruth E Westenbroek, Todd Scheuer, William A Catterall. J Neurosci 2007
166
19

Fibroblast growth factor (FGF) homologous factors share structural but not functional homology with FGFs.
Shaun K Olsen, Meirav Garbi, Niccolo Zampieri, Anna V Eliseenkova, David M Ornitz, Mitchell Goldfarb, Moosa Mohammadi. J Biol Chem 2003
164
18

Differential modulation of sodium channel Na(v)1.6 by two members of the fibroblast growth factor homologous factor 2 subfamily.
Anthony M Rush, Ellen K Wittmack, Lynda Tyrrell, Joel A Black, Sulayman D Dib-Hajj, Stephen G Waxman. Eur J Neurosci 2006
56
25

Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2.
Stephen T Hansen, Pratap Meera, Thomas S Otis, Stefan M Pulst. Hum Mol Genet 2013
102
18

Early changes in cerebellar physiology accompany motor dysfunction in the polyglutamine disease spinocerebellar ataxia type 3.
Vikram G Shakkottai, Maria do Carmo Costa, James M Dell'Orco, Ananthakrishnan Sankaranarayanan, Heike Wulff, Henry L Paulson. J Neurosci 2011
124
18

FGF14 localization and organization of the axon initial segment.
Maolei Xiao, Marie K Bosch, Jeanne M Nerbonne, David M Ornitz. Mol Cell Neurosci 2013
37
35

Spectrin mutations cause spinocerebellar ataxia type 5.
Yoshio Ikeda, Katherine A Dick, Marcy R Weatherspoon, Dan Gincel, Karen R Armbrust, Joline C Dalton, Giovanni Stevanin, Alexandra Dürr, Christine Zühlke, Katrin Bürk,[...]. Nat Genet 2006
242
15


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
15

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
15


A new variable phenotype in spinocerebellar ataxia 27 (SCA 27) caused by a deletion in the FGF14 gene.
J A Coebergh, D E Fransen van de Putte, I N Snoeck, C Ruivenkamp, A van Haeringen, L M Smit. Eur J Paediatr Neurol 2014
32
37

The fibroblast growth factor 14·voltage-gated sodium channel complex is a new target of glycogen synthase kinase 3 (GSK3).
Alexander S Shavkunov, Norelle C Wildburger, Miroslav N Nenov, Thomas F James, Tetyana P Buzhdygan, Neli I Panova-Elektronova, Thomas A Green, Ronald L Veselenak, Nigel Bourne, Fernanda Laezza. J Biol Chem 2013
60
20

FGF14 modulates resurgent sodium current in mouse cerebellar Purkinje neurons.
Haidun Yan, Juan L Pablo, Chaojian Wang, Geoffrey S Pitt. Elife 2014
35
34



Aminopyridines correct early dysfunction and delay neurodegeneration in a mouse model of spinocerebellar ataxia type 1.
Raphael Hourez, Laurent Servais, David Orduz, David Gall, Isabelle Millard, Alban de Kerchove d'Exaerde, Guy Cheron, Harry T Orr, Massimo Pandolfo, Serge N Schiffmann. J Neurosci 2011
86
14

Parallel fiber to Purkinje cell synaptic impairment in a mouse model of spinocerebellar ataxia type 27.
Filippo Tempia, Eriola Hoxha, Giulia Negro, Musaad A Alshammari, Tahani K Alshammari, Neli Panova-Elektronova, Fernanda Laezza. Front Cell Neurosci 2015
22
50

Functional evolutionary history of the mouse Fgf gene family.
Nobuyuki Itoh, David M Ornitz. Dev Dyn 2008
267
12



Selective positive modulator of calcium-activated potassium channels exerts beneficial effects in a mouse model of spinocerebellar ataxia type 2.
Adebimpe W Kasumu, Charlotte Hougaard, Frederik Rode, Thomas A Jacobsen, Jean Marc Sabatier, Birgitte L Eriksen, Dorte Strøbæk, Xia Liang, Polina Egorova, Dasha Vorontsova,[...]. Chem Biol 2012
78
12

Mutations in KCND3 cause spinocerebellar ataxia type 22.
Yi-Chung Lee, Alexandra Durr, Karen Majczenko, Yen-Hua Huang, Yu-Chao Liu, Cheng-Chang Lien, Pei-Chien Tsai, Yaeko Ichikawa, Jun Goto, Marie-Lorraine Monin,[...]. Ann Neurol 2012
97
12

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
104
11

Impaired motor function in mice with cell-specific knockout of sodium channel Scn8a (NaV1.6) in cerebellar purkinje neurons and granule cells.
Stephen I Levin, Zayd M Khaliq, Teresa K Aman, Tina M Grieco, Jennifer A Kearney, Indira M Raman, Miriam H Meisler. J Neurophysiol 2006
90
11


Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 2.
Jing Liu, Tie-Shan Tang, Huiping Tu, Omar Nelson, Emily Herndon, Duong P Huynh, Stefan M Pulst, Ilya Bezprozvanny. J Neurosci 2009
182
11

Open-channel block by the cytoplasmic tail of sodium channel beta4 as a mechanism for resurgent sodium current.
Tina M Grieco, Jyoti D Malhotra, Chunling Chen, Lori L Isom, Indira M Raman. Neuron 2005
172
11

Loss of beta-III spectrin leads to Purkinje cell dysfunction recapitulating the behavior and neuropathology of spinocerebellar ataxia type 5 in humans.
Emma M Perkins, Yvonne L Clarkson, Nancy Sabatier, David M Longhurst, Christopher P Millward, Jennifer Jack, Junko Toraiwa, Mitsunori Watanabe, Jeffrey D Rothstein, Alastair R Lyndon,[...]. J Neurosci 2010
83
11


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.