A citation-based method for searching scientific literature

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, P J Cimino, Thomas D Bird, Wendy H Raskind. Am J Hum Genet 2003
Times Cited: 175



B P C van de Warrenburg, D S Verbeek, S J Piersma, F A M Hennekam, P L Pearson, N V A M Knoers, H P H Kremer, R J Sinke. Neurology 2003
Times Cited: 77




List of shared articles



Times cited

Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder.
Tanja Schmitz-Hübsch, Silke Lux, Peter Bauer, Alexander U Brandt, Elena Schlapakow, Susanne Greschus, Michael Scheel, Hanna Gärtner, Mehmet E Kirlangic, Vincent Gras,[...]. Ann Clin Transl Neurol 2021
0

W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34.
Raghavendra Y Nagaraja, David M Sherry, Jennifer L Fessler, Megan A Stiles, Feng Li, Karanpreet Multani, Albert Orock, Mohiuddin Ahmad, Richard S Brush, Robert E Anderson,[...]. Mol Neurobiol 2021
0


Spinocerebellar ataxia type 14 caused by a nonsense mutation in the PRKCG gene.
Toshihiko Shirafuji, Haruo Shimazaki, Tatsuhiro Miyagi, Takehiko Ueyama, Naoko Adachi, Shigeru Tanaka, Izumi Hide, Naoaki Saito, Norio Sakai. Mol Cell Neurosci 2019
6

Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA).
Francesca Prestori, Francesco Moccia, Egidio D'Angelo. Int J Mol Sci 2019
7

Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia.
Ravi Chopra, Aaron H Wasserman, Stefan M Pulst, Chris I De Zeeuw, Vikram G Shakkottai. Hum Mol Genet 2018
18

Spinocerebellar ataxias.
Bing-Wen Soong, Patrick J Morrison. Handb Clin Neurol 2018
28

Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
Esther A R Nibbeling, Cathérine C S Delnooz, Tom J de Koning, Richard J Sinke, Hyder A Jinnah, Marina A J Tijssen, Dineke S Verbeek. Neurosci Biobehav Rev 2017
26

Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency.
Sarah Doss, Jan Leo Rinnenthal, Tanja Schmitz-Hübsch, Alexander U Brandt, Sebastian Papazoglou, Silke Lux, Stephan Maul, Jens Würfel, Matthias Endres, Thomas Klockgether,[...]. J Neurol 2015
9


Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14.
Christos Ganos, Simone Zittel, Martina Minnerop, Odette Schunke, Christina Heinbokel, Christian Gerloff, Christine Zühlke, Peter Bauer, Thomas Klockgether, Alexander Münchau,[...]. Cerebellum 2014
28


SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.
J Koht, G Stevanin, A Durr, E Mundwiller, A Brice, C M E Tallaksen. Acta Neurol Scand 2012
10

Epidemiology and population genetics of degenerative ataxias.
Jorge Sequeiros, Sandra Martins, Isabel Silveira. Handb Clin Neurol 2012
36

Spinocerebellar ataxia type 14.
Dong-Hui Chen, Wendy H Raskind, Thomas D Bird. Handb Clin Neurol 2012
17

Other spinocerebellar ataxias.
Leslie J Cloud, George Wilmot. Handb Clin Neurol 2012
2

Spinocerebellar degenerations.
Susan L Perlman. Handb Clin Neurol 2011
10

Genetics of the dominant ataxias.
Dineke S Verbeek, Bart P C van de Warrenburg. Semin Neurol 2011
21

Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy.
Kazuhiro Yamamoto, Takahiro Seki, Naoko Adachi, Tetsuya Takahashi, Shigeru Tanaka, Izumi Hide, Naoaki Saito, Norio Sakai. Genes Cells 2010
19


Congo red, an amyloid-inhibiting compound, alleviates various types of cellular dysfunction triggered by mutant protein kinase cγ that causes spinocerebellar ataxia type 14 (SCA14) by inhibiting oligomerization and aggregation.
Takahiro Seki, Hideyuki Takahashi, Kazuhiro Yamamoto, Kota Ogawa, Tomoya Onji, Naoko Adachi, Shigeru Tanaka, Izumi Hide, Naoaki Saito, Norio Sakai. J Pharmacol Sci 2010
9

Expansion of the phenotypic spectrum of SCA14 caused by the Gly128Asp mutation in PRKCG.
Shiroh Miura, Hiroko Nakagawara, Hayato Kaida, Minoru Sugita, Kazuhito Noda, Kyoko Motomura, Yasumasa Ohyagi, Mitsuyoshi Ayabe, Hisamichi Aizawa, Masatoshi Ishibashi,[...]. Clin Neurol Neurosurg 2009
18

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

Loss of Purkinje cells in the PKCgamma H101Y transgenic mouse.
Yunong Zhang, Adam Snider, Lloyd Willard, Dolores J Takemoto, Dingbo Lin. Biochem Biophys Res Commun 2009
14

Phosphorylation and transcriptional activity regulation of retinoid-related orphan receptor alpha 1 by protein kinases C.
Eric Duplus, Christelle Gras, Vanessa Soubeyre, Guilan Vodjdani, Yolande Lemaigre-Dubreuil, Bernard Brugg. J Neurochem 2008
9