Yoshio Ikeda, Joline C Dalton, Melinda L Moseley, Kathy L Gardner, Thomas D Bird, Tetsuo Ashizawa, William K Seltzer, Massimo Pandolfo, Aubrey Milunsky, Nicholas T Potter, Mikio Shoji, John B Vincent, John W Day, Laura P W Ranum. Am J Hum Genet 2004
Times Cited: 63
Times Cited: 63
Times Cited
Times Co-cited
Similarity
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
M D Koob, M L Moseley, L J Schut, K A Benzow, T D Bird, J W Day, L P Ranum. Nat Genet 1999
66
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
Melinda L Moseley, Tao Zu, Yoshio Ikeda, Wangcai Gao, Anne K Mosemiller, Randy S Daughters, Gang Chen, Marcy R Weatherspoon, H Brent Clark, Timothy J Ebner,[...]. Nat Genet 2006
Melinda L Moseley, Tao Zu, Yoshio Ikeda, Wangcai Gao, Anne K Mosemiller, Randy S Daughters, Gang Chen, Marcy R Weatherspoon, H Brent Clark, Timothy J Ebner,[...]. Nat Genet 2006
39
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia.
P F Worth, H Houlden, P Giunti, M B Davis, N W Wood. Nat Genet 2000
P F Worth, H Houlden, P Giunti, M B Davis, N W Wood. Nat Genet 2000
38
Spinocerebellar ataxia type 8: clinical features in a large family.
J W Day, L J Schut, M L Moseley, A C Durand, L P Ranum. Neurology 2000
J W Day, L J Schut, M L Moseley, A C Durand, L P Ranum. Neurology 2000
33
Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan.
Y Ikeda, M Shizuka, M Watanabe, K Okamoto, M Shoji. Neurology 2000
Y Ikeda, M Shizuka, M Watanabe, K Okamoto, M Shoji. Neurology 2000
33
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
30
SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.
Yuishin Izumi, Hirofumi Maruyama, Masaya Oda, Hiroyuki Morino, Takayuki Okada, Hidefumi Ito, Iwao Sasaki, Hiroyasu Tanaka, Osamu Komure, Fukashi Udaka,[...]. Am J Hum Genet 2003
Yuishin Izumi, Hirofumi Maruyama, Masaya Oda, Hiroyuki Morino, Takayuki Okada, Hidefumi Ito, Iwao Sasaki, Hiroyasu Tanaka, Osamu Komure, Fukashi Udaka,[...]. Am J Hum Genet 2003
38
Do CTG expansions at the SCA8 locus cause ataxia?
Ludger Schöls, Ingrid Bauer, Christine Zühlke, Thorsten Schulte, Christina Kölmel, Katrin Bürk, Helge Topka, Peter Bauer, Horst Przuntek, Olaf Riess. Ann Neurol 2003
Ludger Schöls, Ingrid Bauer, Christine Zühlke, Thorsten Schulte, Christina Kölmel, Katrin Bürk, Helge Topka, Peter Bauer, Horst Przuntek, Olaf Riess. Ann Neurol 2003
47
Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports.
A Zeman, J Stone, M Porteous, E Burns, L Barron, J Warner. J Neurol Neurosurg Psychiatry 2004
A Zeman, J Stone, M Porteous, E Burns, L Barron, J Warner. J Neurol Neurosurg Psychiatry 2004
54
High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles.
I Silveira, I Alonso, L Guimarães, P Mendonça, C Santos, P Maciel, J M Fidalgo De Matos, M Costa, C Barbot, A Tuna,[...]. Am J Hum Genet 2000
I Silveira, I Alonso, L Guimarães, P Mendonça, C Santos, P Maciel, J M Fidalgo De Matos, M Costa, C Barbot, A Tuna,[...]. Am J Hum Genet 2000
29
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance.
M L Moseley, L J Schut, T D Bird, M D Koob, J W Day, L P Ranum. Hum Mol Genet 2000
M L Moseley, L J Schut, T D Bird, M D Koob, J W Day, L P Ranum. Hum Mol Genet 2000
25
Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion.
V Juvonen, M Hietala, M Päivärinta, M Rantamäki, L Hakamies, S Kaakkola, O Vierimaa, M Penttinen, M L Savontaus. Ann Neurol 2000
V Juvonen, M Hietala, M Päivärinta, M Rantamäki, L Hakamies, S Kaakkola, O Vierimaa, M Penttinen, M L Savontaus. Ann Neurol 2000
31
Are (CTG)n expansions at the SCA8 locus rare polymorphisms?
G Stevanin, A Herman, A Dürr, C Jodice, M Frontali, Y Agid, A Brice. Nat Genet 2000
G Stevanin, A Herman, A Dürr, C Jodice, M Frontali, Y Agid, A Brice. Nat Genet 2000
25
Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.
Yoshio Ikeda, Randy S Daughters, Laura P W Ranum. Cerebellum 2008
Yoshio Ikeda, Randy S Daughters, Laura P W Ranum. Cerebellum 2008
27
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
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
22
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
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
20
SCA8 repeat expansions in ataxia: a controversial association.
M J Sobrido, J A Cholfin, S Perlman, S M Pulst, D H Geschwind. Neurology 2001
M J Sobrido, J A Cholfin, S Perlman, S M Pulst, D H Geschwind. Neurology 2001
33
The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1).
J P Nemes, K A Benzow, M L Moseley, L P Ranum, M D Koob. Hum Mol Genet 2000
J P Nemes, K A Benzow, M L Moseley, L P Ranum, M D Koob. Hum Mol Genet 2000
19
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
Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa, M Inoue, S Katayama, H Kawakami, S Nakamura, M Nishimura, I Akiguchi. Nat Genet 1994
19
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
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
17
An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.
J B Vincent, M L Neves-Pereira, A D Paterson, E Yamamoto, S V Parikh, F Macciardi, H M Gurling, S G Potkin, C N Pato, A Macedo,[...]. Am J Hum Genet 2000
J B Vincent, M L Neves-Pereira, A D Paterson, E Yamamoto, S V Parikh, F Macciardi, H M Gurling, S G Potkin, C N Pato, A Macedo,[...]. Am J Hum Genet 2000
17
The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
A E Harding. Brain 1982
A E Harding. Brain 1982
17
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
17
SCA8 repeat expansion coexists with SCA1--not only with SCA6.
Anna Sulek, Dorota Hoffman-Zacharska, Elzbieta Zdzienicka, Jacek Zaremba. Am J Hum Genet 2003
Anna Sulek, Dorota Hoffman-Zacharska, Elzbieta Zdzienicka, Jacek Zaremba. Am J Hum Genet 2003
34
Long repeat tracts at SCA8 in major psychosis.
J B Vincent, Q P Yuan, M Schalling, R Adolfsson, M H Azevedo, A Macedo, A Bauer, C DallaTorre, H M Medeiros, M T Pato,[...]. Am J Med Genet 2000
J B Vincent, Q P Yuan, M Schalling, R Adolfsson, M H Azevedo, A Macedo, A Bauer, C DallaTorre, H M Medeiros, M T Pato,[...]. Am J Med Genet 2000
25
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
R Koide, S Kobayashi, T Shimohata, T Ikeuchi, M Maruyama, M Saito, M Yamada, H Takahashi, S Tsuji. Hum Mol Genet 1999
15
Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCA1-3, 6 and 7 CAG expansions.
Alfredo Brusco, Claudia Cagnoli, Alessandra Franco, Elisa Dragone, Antonella Nardacchione, Enrico Grosso, Paolo Mortara, Roberto Mutani, Nicola Migone, Laura Orsi. J Neurol 2002
Alfredo Brusco, Claudia Cagnoli, Alessandra Franco, Elisa Dragone, Antonella Nardacchione, Enrico Grosso, Paolo Mortara, Roberto Mutani, Nicola Migone, Laura Orsi. J Neurol 2002
41
Sporadic SCA8 mutation resembling corticobasal degeneration.
Yasuhiko Baba, Ryan J Uitti, Matthew J Farrer, Zbigniew K Wszolek. Parkinsonism Relat Disord 2005
Yasuhiko Baba, Ryan J Uitti, Matthew J Farrer, Zbigniew K Wszolek. Parkinsonism Relat Disord 2005
50
Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond.
Alexandra Durr. Lancet Neurol 2010
Alexandra Durr. Lancet Neurol 2010
15
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
15
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy.
E Cellini, B Nacmias, P Forleo, S Piacentini, B M Guarnieri, A Serio, A Calabrò, D Renzi, S Sorbi. Arch Neurol 2001
E Cellini, B Nacmias, P Forleo, S Piacentini, B M Guarnieri, A Serio, A Calabrò, D Renzi, S Sorbi. Arch Neurol 2001
37
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
G David, N Abbas, G Stevanin, A Dürr, G Yvert, G Cancel, C Weber, G Imbert, F Saudou, E Antoniou,[...]. Nat Genet 1997
14
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
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
14
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, H Takahashi, R Kondo, A Ishikawa, T Hayashi. Nat Genet 1994
R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, H Takahashi, R Kondo, A Ishikawa, T Hayashi. Nat Genet 1994
14
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
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
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
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
14
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
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
14
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
K Nakamura, S Y Jeong, T Uchihara, M Anno, K Nagashima, T Nagashima, S Ikeda, S Tsuji, I Kanazawa. Hum Mol Genet 2001
14
The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population.
V Juvonen, M Hietala, V Kairisto, M-L Savontaus. Acta Neurol Scand 2005
V Juvonen, M Hietala, V Kairisto, M-L Savontaus. Acta Neurol Scand 2005
18
Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.
Y R Wu, H Y Lin, C M Chen, K Gwinn-Hardy, L S Ro, Y C Wang, S H Li, J C Hwang, K Fang, H M Hsieh-Li,[...]. Clin Genet 2004
Y R Wu, H Y Lin, C M Chen, K Gwinn-Hardy, L S Ro, Y C Wang, S H Li, J C Hwang, K Fang, H M Hsieh-Li,[...]. Clin Genet 2004
14
Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12.
A K Srivastava, S Choudhry, M S Gopinath, S Roy, M Tripathi, S K Brahmachari, S Jain. Ann Neurol 2001
A K Srivastava, S Choudhry, M S Gopinath, S Roy, M Tripathi, S K Brahmachari, S Jain. Ann Neurol 2001
14
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
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
14
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.
I Topisirovic, N Dragasevic, D Savic, A Ristic, M Keckarevic, D Keckarevic, B Culjkovic, I Petrovic, S Romac, V S Kostic. Clin Genet 2002
I Topisirovic, N Dragasevic, D Savic, A Ristic, M Keckarevic, D Keckarevic, B Culjkovic, I Petrovic, S Romac, V S Kostic. Clin Genet 2002
53
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
12
Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
A K Mosemiller, J C Dalton, J W Day, L P W Ranum. Cytogenet Genome Res 2003
A K Mosemiller, J C Dalton, J W Day, L P W Ranum. Cytogenet Genome Res 2003
42
SCA8 in the Spanish population including one homozygous patient.
B Tazón, C Badenas, L Jiménez, E Muñoz, M Milà. Clin Genet 2002
B Tazón, C Badenas, L Jiménez, E Muñoz, M Milà. Clin Genet 2002
61
Cognitive impairment in spinocerebellar ataxia type 8.
Arja Lilja, Päivi Hämäläinen, Elina Kaitaranta, Riitta Rinne. J Neurol Sci 2005
Arja Lilja, Päivi Hämäläinen, Elina Kaitaranta, Riitta Rinne. J Neurol Sci 2005
34
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
K Sanpei, H Takano, S Igarashi, T Sato, M Oyake, H Sasaki, A Wakisaka, K Tashiro, Y Ishida, T Ikeuchi,[...]. Nat Genet 1996
K Sanpei, H Takano, S Igarashi, T Sato, M Oyake, H Sasaki, A Wakisaka, K Tashiro, Y Ishida, T Ikeuchi,[...]. Nat Genet 1996
12
RNA gain-of-function in spinocerebellar ataxia type 8.
Randy S Daughters, Daniel L Tuttle, Wangcai Gao, Yoshio Ikeda, Melinda L Moseley, Timothy J Ebner, Maurice S Swanson, Laura P W Ranum. PLoS Genet 2009
Randy S Daughters, Daniel L Tuttle, Wangcai Gao, Yoshio Ikeda, Melinda L Moseley, Timothy J Ebner, Maurice S Swanson, Laura P W Ranum. PLoS Genet 2009
12
Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
Hatasu Kobayashi, Koji Abe, Tohru Matsuura, Yoshio Ikeda, Toshiaki Hitomi, Yuji Akechi, Toshiyuki Habu, Wanyang Liu, Hiroko Okuda, Akio Koizumi. Am J Hum Genet 2011
Hatasu Kobayashi, Koji Abe, Tohru Matsuura, Yoshio Ikeda, Toshiaki Hitomi, Yuji Akechi, Toshiyuki Habu, Wanyang Liu, Hiroko Okuda, Akio Koizumi. Am J Hum Genet 2011
12
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.