A citation-based method for searching scientific literature

Emma Perkins, Daumante Suminaite, Mandy Jackson. J Physiol 2016
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
244
50

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
85
38

Spectrins: a structural platform for stabilization and activation of membrane channels, receptors and transporters.
Beata Machnicka, Aleksander Czogalla, Anita Hryniewicz-Jankowska, Dżamila M Bogusławska, Renata Grochowalska, Elżbieta Heger, Aleksander F Sikorski. Biochim Biophys Acta 2014
98
38

Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development.
Stefano Lise, Yvonne Clarkson, Emma Perkins, Alexandra Kwasniewska, Elham Sadighi Akha, Ricardo Parolin Schnekenberg, Daumante Suminaite, Jilly Hope, Ian Baker, Lorna Gregory,[...]. PLoS Genet 2012
63
27

Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes.
Michael C Stankewich, Babette Gwynn, Thomas Ardito, Lan Ji, Jung Kim, Raymond F Robledo, Samuel E Lux, Luanne L Peters, Jon S Morrow. Proc Natl Acad Sci U S A 2010
55
27

Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.
Yvonne L Clarkson, Trudi Gillespie, Emma M Perkins, Alastair R Lyndon, Mandy Jackson. Hum Mol Genet 2010
37
27


De novo point mutations in patients diagnosed with ataxic cerebral palsy.
Ricardo Parolin Schnekenberg, Emma M Perkins, Jack W Miller, Wayne I L Davies, Maria Cristina D'Adamo, Mauro Pessia, Katherine A Fawcett, David Sims, Elodie Gillard, Karl Hudspith,[...]. Brain 2015
88
27

Case of infantile onset spinocerebellar ataxia type 5.
Francois-Dominique Jacob, Eugenia S Ho, Mayra Martinez-Ojeda, Basil T Darras, Omar S Khwaja. J Child Neurol 2013
27
27


Modulation of the neuronal glutamate transporter EAAT4 by two interacting proteins.
M Jackson, W Song, M Y Liu, L Jin, M Dykes-Hoberg, C I Lin, W J Bowers, H J Federoff, P C Sternweis, J D Rothstein. Nature 2001
190
22

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
45
22

A Japanese SCA5 family with a novel three-nucleotide in-frame deletion mutation in the SPTBN2 gene: a clinical and genetic study.
Ying Wang, Kishin Koh, Michiaki Miwa, Nobuo Yamashiro, Kazumasa Shindo, Yoshihisa Takiyama. J Hum Genet 2014
17
23

Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain.
Esra Yıldız Bölükbaşı, Muhammad Afzal, Sara Mumtaz, Nafees Ahmad, Sajid Malik, Aslıhan Tolun. Am J Med Genet A 2017
11
36

Posterior cerebellar Purkinje cells in an SCA5/SPARCA1 mouse model are especially vulnerable to the synergistic effect of loss of β-III spectrin and GLAST.
Emma M Perkins, Daumante Suminaite, Yvonne L Clarkson, Sin Kwan Lee, Alastair R Lyndon, Jeffrey D Rothstein, David J A Wyllie, Kohichi Tanaka, Mandy Jackson. Hum Mol Genet 2016
11
36

Spinocerebellar ataxia type 5.
Katherine A Dick, Yoshio Ikeda, John W Day, Laura P W Ranum. Handb Clin Neurol 2012
20
22

Cell organization, growth, and neural and cardiac development require αII-spectrin.
Michael C Stankewich, Carol D Cianci, Paul R Stabach, Lan Ji, Anjali Nath, Jon S Morrow. J Cell Sci 2011
47
22

Mutant β-III spectrin causes mGluR1α mislocalization and functional deficits in a mouse model of spinocerebellar ataxia type 5.
Karen R Armbrust, Xinming Wang, Tyisha J Hathorn, Samuel W Cramer, Gang Chen, Tao Zu, Takashi Kangas, Anastasia N Zink, Gülin Öz, Timothy J Ebner,[...]. J Neurosci 2014
41
16

STED nanoscopy reveals the ubiquity of subcortical cytoskeleton periodicity in living neurons.
Elisa D'Este, Dirk Kamin, Fabian Göttfert, Ahmed El-Hady, Stefan W Hell. Cell Rep 2015
155
16

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.
K Bürk, C Zühlke, I R König, A Ziegler, E Schwinger, C Globas, J Dichgans, Y Hellenbroich. Neurology 2004
44
16

Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.
Solaf M Elsayed, Raoul Heller, Michaela Thoenes, Maha S Zaki, Daniel Swan, Ezzat Elsobky, Christine Zühlke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg,[...]. Eur J Hum Genet 2014
27
16

Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration in Drosophila.
Damaris N Lorenzo, Min-gang Li, Sarah E Mische, Karen R Armbrust, Laura P W Ranum, Thomas S Hays. J Cell Biol 2010
61
16

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
154
16


SPTAN1 encephalopathy: distinct phenotypes and genotypes.
Jun Tohyama, Mitsuko Nakashima, Shin Nabatame, Ch'ng Gaik-Siew, Rie Miyata, Zvonka Rener-Primec, Mitsuhiro Kato, Naomichi Matsumoto, Hirotomo Saitsu. J Hum Genet 2015
43
16

β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations.
Yvonne L Clarkson, Emma M Perkins, Callum J Cairncross, Alastair R Lyndon, Paul A Skehel, Mandy Jackson. Hum Mol Genet 2014
18
16

Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice.
Heliane G Serra, Courtney E Byam, Jeffrey D Lande, Susan K Tousey, Huda Y Zoghbi, Harry T Orr. Hum Mol Genet 2004
130
16

Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1.
X Lin, B Antalffy, D Kang, H T Orr, H Y Zoghbi. Nat Neurosci 2000
272
16

Developmental delay in motor skill acquisition in Niemann-Pick C1 mice reveals abnormal cerebellar morphogenesis.
Paola Caporali, Francesco Bruno, Giampiero Palladino, Jessica Dragotto, Laura Petrosini, Franco Mangia, Robert P Erickson, Sonia Canterini, Maria Teresa Fiorenza. Acta Neuropathol Commun 2016
21
16

A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.
Mohammad A Al-Muhaizea, Faten AlMutairi, Rawan Almass, Safinaz AlHarthi, Mazhor S Aldosary, Maysoon Alsagob, Ali AlOdaib, Dilek Colak, Namik Kaya. Cerebellum 2018
10
30

Between SCA5 and SCAR14: delineation of the SPTBN2 p.R480W-associated phenotype.
Sara Nuovo, Alessia Micalizzi, Stefano D'Arrigo, Monia Ginevrino, Tommaso Biagini, Tommaso Mazza, Enza Maria Valente. Eur J Hum Genet 2018
12
25


Characterization of a new beta-spectrin gene which is predominantly expressed in brain.
O Ohara, R Ohara, H Yamakawa, D Nakajima, M Nakayama. Brain Res Mol Brain Res 1998
51
11

A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles.
M C Stankewich, W T Tse, L L Peters, Y Ch'ng, K M John, P R Stabach, P Devarajan, J S Morrow, S E Lux. Proc Natl Acad Sci U S A 1998
114
11

Ankyrin-G and beta2-spectrin collaborate in biogenesis of lateral membrane of human bronchial epithelial cells.
Krishnakumar Kizhatil, Woohyun Yoon, Peter J Mohler, Lydia H Davis, Janis A Hoffman, Vann Bennett. J Biol Chem 2007
102
11

Genetic defects in β-spectrin and tau sensitize C. elegans axons to movement-induced damage via torque-tension coupling.
Michael Krieg, Jan Stühmer, Juan G Cueva, Richard Fetter, Kerri Spilker, Daniel Cremers, Kang Shen, Alexander R Dunn, Miriam B Goodman. Elife 2017
55
11

Prevalent presence of periodic actin-spectrin-based membrane skeleton in a broad range of neuronal cell types and animal species.
Jiang He, Ruobo Zhou, Zhuhao Wu, Monica A Carrasco, Peri T Kurshan, Jonathan E Farley, David J Simon, Guiping Wang, Boran Han, Junjie Hao,[...]. Proc Natl Acad Sci U S A 2016
78
11

A distal axonal cytoskeleton forms an intra-axonal boundary that controls axon initial segment assembly.
Mauricio R Galiano, Smita Jha, Tammy Szu-Yu Ho, Chuansheng Zhang, Yasuhiro Ogawa, Kae-Jiun Chang, Michael C Stankewich, Peter J Mohler, Matthew N Rasband. Cell 2012
163
11

The spectrin repeat: a structural platform for cytoskeletal protein assemblies.
Kristina Djinovic-Carugo, Mathias Gautel, Jari Ylänne, Paul Young. FEBS Lett 2002
215
11

Clinical and MRI findings in spinocerebellar ataxia type 5.
G Stevanin, A Herman, A Brice, A Dürr. Neurology 1999
55
11

A Novel Missense Mutation in the Spectrin Beta Nonerythrocytic 2 Gene Likely Associated with Spinocerebellar Ataxia Type 5.
Li-Zhi Liu, Ming Ren, Mao Li, Yu-Ting Ren, Bo Sun, Xiao-Sun Sun, Si-Yu Chen, Si-Yuan Li, Xu-Sheng Huang. Chin Med J (Engl) 2016
7
28

Spectrin: structure, function and disease.
Rui Zhang, ChenYu Zhang, Qi Zhao, DongHai Li. Sci China Life Sci 2013
43
11




Genome engineering using the CRISPR-Cas9 system.
F Ann Ran, Patrick D Hsu, Jason Wright, Vineeta Agarwala, David A Scott, Feng Zhang. Nat Protoc 2013
11

Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delay.
Hirotomo Saitsu, Jun Tohyama, Tatsuro Kumada, Kiyoshi Egawa, Keisuke Hamada, Ippei Okada, Takeshi Mizuguchi, Hitoshi Osaka, Rie Miyata, Tomonori Furukawa,[...]. Am J Hum Genet 2010
109
11


Decreased calcium flux in Niemann-Pick type C1 patient-specific iPSC-derived neurons due to higher amount of calcium-impermeable AMPA receptors.
Michael Rabenstein, Franziska Peter, Sarah Joost, Michaela Trilck, Arndt Rolfs, Moritz J Frech. Mol Cell Neurosci 2017
20
11

An excitatory amino-acid transporter with properties of a ligand-gated chloride channel.
W A Fairman, R J Vandenberg, J L Arriza, M P Kavanaugh, S G Amara. Nature 1995
945
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.