A citation-based method for searching scientific literature

D-H Chen, P J Cimino, L P W Ranum, H Y Zoghbi, I Yabe, L Schut, R L Margolis, H P Lipe, A Feleke, M Matsushita, J Wolff, C Morgan, D Lau, M Fernandez, H Sasaki, W H Raskind, T D Bird. Neurology 2005
Times Cited: 56







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



Times Cited
  Times     Co-cited
Similarity


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
175
66

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.
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
77
55

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, Naima Bouslam, Michel Gouttard, Caroline Soumphonphakdy, Marie-Laure Welter, Elisabeth Ollagnon-Roman, Arnaud Lemainque, Merle Ruberg,[...]. Arch Neurol 2004
70
53


New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
Stephan Klebe, Alexandra Durr, Alexander Rentschler, Valerie Hahn-Barma, Michael Abele, Naima Bouslam, Ludger Schöls, Pierre Jedynak, Sylvie Forlani, Elodie Denis,[...]. Ann Neurol 2005
62
50

Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death.
Takahiro Seki, Naoko Adachi, Yoshitaka Ono, Hideki Mochizuki, Keiko Hiramoto, Taku Amano, Hiroaki Matsubayashi, Masayasu Matsumoto, Hideshi Kawakami, Naoaki Saito,[...]. J Biol Chem 2005
53
50

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
Ichiro Yabe, Hidenao Sasaki, Dong-Hui Chen, Wendy H Raskind, Thomas D Bird, Isao Yamashita, Shoji Tsuji, Seiji Kikuchi, Kunio Tashiro. Arch Neurol 2003
85
42

Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
Keiko Hiramoto, Hideshi Kawakami, Kimiko Inoue, Takahiro Seki, Hirofumi Maruyama, Hiroyuki Morino, Masayasu Matsumoto, Kaoru Kurisu, Norio Sakai. Mov Disord 2006
27
70

Enzymological analysis of mutant protein kinase Cgamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis.
Naoko Adachi, Takeshi Kobayashi, Hideyuki Takahashi, Takumi Kawasaki, Yasuhito Shirai, Takehiko Ueyama, Toshio Matsuda, Takahiro Seki, Norio Sakai, Naoaki Saito. J Biol Chem 2008
73
33

Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype.
Monique H M Vlak, Richard J Sinke, Gwenda M Rabelink, Berry P H Kremer, Bart P C van de Warrenburg. Mov Disord 2006
37
45

A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter.
I Yamashita, H Sasaki, I Yabe, T Fukazawa, S Nogoshi, K Komeichi, A Takada, K Shiraishi, Y Takiyama, M Nishizawa,[...]. Ann Neurol 2000
83
26

A novel H101Q mutation causes PKCgamma loss in spinocerebellar ataxia type 14.
Isabel Alonso, Cristina Costa, André Gomes, Anabela Ferro, Ana I Seixas, Sérgio Silva, Vitor Tedim Cruz, Paula Coutinho, Jorge Sequeiros, Isabel Silveira. J Hum Genet 2005
28
53

Aggregate formation of mutant protein kinase C gamma found in spinocerebellar ataxia type 14 impairs ubiquitin-proteasome system and induces endoplasmic reticulum stress.
Takahiro Seki, Hideyuki Takahashi, Naoko Adachi, Nana Abe, Takayuki Shimahara, Naoaki Saito, Norio Sakai. Eur J Neurosci 2007
36
41

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
25

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
25

Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.
Dineke S Verbeek, Bart P C van de Warrenburg, F A M Hennekam, Dennis Dooijes, P F Ippel, Corien C Verschuuren-Bemelmans, H P H Kremer, Richard J Sinke. Hum Genet 2005
27
51

PKC gamma mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling.
Dineke S Verbeek, Joachim Goedhart, Laurie Bruinsma, Richard J Sinke, Eric A Reits. J Cell Sci 2008
50
28

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
32

Impaired synapse elimination during cerebellar development in PKC gamma mutant mice.
M Kano, K Hashimoto, C Chen, A Abeliovich, A Aiba, H Kurihara, M Watanabe, Y Inoue, S Tonegawa. Cell 1995
276
23

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Zoran Brkanac, Laura Bylenok, Magali Fernandez, Mark Matsushita, Hillary Lipe, John Wolff, David Nochlin, Wendy H Raskind, Thomas D Bird. Arch Neurol 2002
46
26

Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia.
Andreas Dalski, Beate Mitulla, Katrin Bürk, Christoph Schattenfroh, Eberhard Schwinger, Christine Zühlke. J Neurol 2006
26
46

Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.
Hirohide Asai, Makito Hirano, Keiji Shimada, Takao Kiriyama, Yoshiko Furiya, Masanori Ikeda, Takaaki Iwamoto, Toshio Mori, Kazuto Nishinaka, Noboru Konishi,[...]. Hum Mol Genet 2009
28
39

Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene.
M C Fahey, M A Knight, J H Shaw, R J McK Gardner, D du Sart, P J Lockhart, M B Delatycki, P C Gates, E Storey. J Neurol Neurosurg Psychiatry 2005
18
55

Distribution of protein kinase C-like immunoreactive neurons in rat brain.
N Saito, U Kikkawa, Y Nishizuka, C Tanaka. J Neurosci 1988
247
17

Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene.
Stefan Wieczorek, Larissa Arning, Elke R Gizewski, Ingrid Alheite, Duymal Timmann. Mov Disord 2007
12
75

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
14

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
318
14


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
445
14

Protein aggregation and neurodegenerative disease.
Christopher A Ross, Michelle A Poirier. Nat Med 2004
14

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
14

Spinocerebellar ataxia 14: novel mutation in exon 2 of PRKCG in a German family.
Dagmar Nolte, Melanie Landendinger, Eberhard Schmitt, Ulrich Müller. Mov Disord 2007
16
50

Molecular pathogenesis of spinocerebellar ataxias.
Antoni Matilla Dueñas, Robert Goold, Paola Giunti. Brain 2006
153
14

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
192
14

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
42

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
342
12

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
12

Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14.
Stephan Klebe, Laurence Faivre, Sylvie Forlani, Christel Dussert, Ayman Tourbah, Alexis Brice, Giovanni Stevanin, Alexandra Durr. Arch Neurol 2007
10
70

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
12

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
12


Spinocerebellar ataxia type 14.
Dong-Hui Chen, Wendy H Raskind, Thomas D Bird. Handb Clin Neurol 2012
17
41

Propagation of gammaPKC translocation along the dendrites of Purkinje cell in gammaPKC-GFP transgenic mice.
Norio Sakai, Hiroshi Tsubokawa, Masanori Matsuzaki, Taketoshi Kajimoto, Eri Takahashi, Yi Ren, Shiho Ohmori, Yasuhito Shirai, Hiroaki Matsubayashi, Jingshan Chen,[...]. Genes Cells 2004
16
37


Spinocerebellar ataxias: an update.
Bing-wen Soong, Henry L Paulson. Curr Opin Neurol 2007
91
10


SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.
Claudia Cagnoli, Caterina Mariotti, Franco Taroni, Marco Seri, Alessandro Brussino, Chiara Michielotto, Marina Grisoli, Daniela Di Bella, Nicola Migone, Cinzia Gellera,[...]. Brain 2006
81
10

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
599
10

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
R Koide, S Kobayashi, T Shimohata, T Ikeuchi, M Maruyama, M Saito, M Yamada, H Takahashi, S Tsuji. Hum Mol Genet 1999
276
10

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
G Imbert, F Saudou, G Yvert, D Devys, Y Trottier, J M Garnier, C Weber, J L Mandel, G Cancel, N Abbas,[...]. Nat Genet 1996
701
10


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.