A citation-based method for searching scientific literature

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







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



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
453
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
309
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
81
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
101
33

Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan.
Y Ikeda, M Shizuka, M Watanabe, K Okamoto, M Shoji. Neurology 2000
60
33

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
667
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
47
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
36
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
31
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
57
29


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
51
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
65
25

Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.
Yoshio Ikeda, Randy S Daughters, Laura P W Ranum. Cerebellum 2008
59
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
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
329
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
39
33


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
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
355
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
62
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
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
29
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
39
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
286
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
24
41

Sporadic SCA8 mutation resembling corticobasal degeneration.
Yasuhiko Baba, Ryan J Uitti, Matthew J Farrer, Zbigniew K Wszolek. Parkinsonism Relat Disord 2005
20
50


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
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
24
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
607
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
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
984
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
189
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
889
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
177
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
464
14


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
64
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
61
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
180
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
15
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
836
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
19
42

SCA8 in the Spanish population including one homozygous patient.
B Tazón, C Badenas, L Jiménez, E Muñoz, M Milà. Clin Genet 2002
13
61

Cognitive impairment in spinocerebellar ataxia type 8.
Arja Lilja, Päivi Hämäläinen, Elina Kaitaranta, Riitta Rinne. J Neurol Sci 2005
23
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
623
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
195
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
173
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.