A citation-based method for searching scientific literature

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, Peter Heutink. Am J Hum Genet 2003
Times Cited: 172







List of co-cited articles
1130 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
105
53

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
120
47

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
72
55

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
117
40

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
144
38

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
75
46

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
61
57

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
79
40

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
80
37

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
261
27

FGF14 regulates presynaptic Ca2+ channels and synaptic transmission.
Haidun Yan, Juan L Pablo, Geoffrey S Pitt. Cell Rep 2013
47
57

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
231
25


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
194
24

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
63
38

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
154
23

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
81

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
978
22

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
96
22

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
68
30


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
107
20


Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
Henry Houlden, Janel Johnson, Christopher Gardner-Thorpe, Tammaryn Lashley, Dena Hernandez, Paul Worth, Andrew B Singleton, David A Hilton, Janice Holton, Tamas Revesz,[...]. Nat Genet 2007
106
19

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
Dong-Hui Chen, Zoran Brkanac, Christophe L M J Verlinde, Xiao-Jian Tan, Laura Bylenok, David Nochlin, Mark Matsushita, Hillary Lipe, John Wolff, Magali Fernandez,[...]. Am J Hum Genet 2003
156
19

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.
S E Holmes, E E O'Hearn, M G McInnis, D A Gorelick-Feldman, J J Kleiderlein, C Callahan, N G Kwak, R G Ingersoll-Ashworth, M Sherr, A J Sumner,[...]. Nat Genet 1999
270
19

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
Joyce van de Leemput, Jayanth Chandran, Melanie A Knight, Lynne A Holtzclaw, Sonja Scholz, Mark R Cookson, Henry Houlden, Katrina Gwinn-Hardy, Hon-Chung Fung, Xian Lin,[...]. PLoS Genet 2007
180
19

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
28
67

Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.
Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, Massimo Plumari, Giorgio Battaglia, Annalisa Pastore, Adele Finardi, Claudia Cagnoli, Filippo Tempia, Marina Frontali,[...]. Nat Genet 2010
198
18

Fibroblast growth factor homologous factor 13 regulates Na+ channels and conduction velocity in murine hearts.
Chuan Wang, Jessica A Hennessey, Robert D Kirkton, Chaojian Wang, Victoria Graham, Ram S Puranam, Paul B Rosenberg, Nenad Bursac, Geoffrey S Pitt. Circ Res 2011
62
29

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
58
31

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
M D Koob, M L Moseley, L J Schut, K A Benzow, T D Bird, J W Day, L P Ranum. Nat Genet 1999
367
17

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
T Matsuura, T Yamagata, D L Burgess, A Rasmussen, R P Grewal, K Watase, M Khajavi, A E McCall, C F Davis, L Zu,[...]. Nat Genet 2000
297
17


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
59
27

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
44

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.
K Nakamura, S Y Jeong, T Uchihara, M Anno, K Nagashima, T Nagashima, S Ikeda, S Tsuji, I Kanazawa. Hum Mol Genet 2001
382
15

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.
Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa, M Inoue, S Katayama, H Kawakami, S Nakamura, M Nishimura, I Akiguchi. Nat Genet 1994
15

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
15

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.
Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, Shuichi Asakawa, Taro Ishiguro, Taiji Tsunemi, Makoto Takahashi, Tohru Matsuura, Kevin M Flanigan, Sawa Iwasaki,[...]. Am J Hum Genet 2009
162
15

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
53
28

FGF14 modulates resurgent sodium current in mouse cerebellar Purkinje neurons.
Haidun Yan, Juan L Pablo, Chaojian Wang, Geoffrey S Pitt. Elife 2014
33
45

Long-term inactivation particle for voltage-gated sodium channels.
Katarzyna Dover, Sergio Solinas, Egidio D'Angelo, Mitchell Goldfarb. J Physiol 2010
48
29

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.
G David, N Abbas, G Stevanin, A Dürr, G Yvert, G Cancel, C Weber, G Imbert, F Saudou, E Antoniou,[...]. Nat Genet 1997
453
14

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
596
14

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
S M Pulst, A Nechiporuk, T Nechiporuk, S Gispert, X N Chen, I Lopes-Cendes, S Pearlman, S Starkman, G Orozco-Diaz, A Lunkes,[...]. Nat Genet 1996
686
14

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
Jun Ling Wang, Xu Yang, Kun Xia, Zheng Mao Hu, Ling Weng, Xin Jin, Hong Jiang, Peng Zhang, Lu Shen, Ji Feng Guo,[...]. Brain 2010
176
14

Bioluminescence methodology for the detection of protein-protein interactions within the voltage-gated sodium channel macromolecular complex.
Alexander Shavkunov, Neli Panova, Anesh Prasai, Ron Veselenak, Nigel Bourne, Svetla Stoilova-McPhie, Fernanda Laezza. Assay Drug Dev Technol 2012
31
45

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
63

Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16.
A Iwaki, Y Kawano, S Miura, H Shibata, D Matsuse, W Li, H Furuya, Y Ohyagi, T Taniwaki, J Kira,[...]. J Med Genet 2008
84
15


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.