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



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Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.
Hiroaki Nozaki, Takeshi Ikeuchi, Akio Kawakami, Akio Kimura, Reiji Koide, Miyuki Tsuchiya, Yuusaku Nakmura, Tatsuro Mutoh, Hiroko Yamamoto, Naoki Nakao,[...]. Mov Disord 2007
23
65

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
181
42


16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.
Y Ouyang, K Sakoe, H Shimazaki, M Namekawa, T Ogawa, Y Ando, T Kawakami, J Kaneko, Y Hasegawa, K Yoshizawa,[...]. J Neurol Sci 2006
36
36

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.
Kinya Ishikawa, Shuta Toru, Taiji Tsunemi, Mingshun Li, Kazuhiro Kobayashi, Takanori Yokota, Takeshi Amino, Kiyoshi Owada, Hiroto Fujigasaki, Masaki Sakamoto,[...]. Am J Hum Genet 2005
96
36

Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
Y Onodera, M Aoki, H Mizuno, H Warita, Y Shiga, Y Itoyama. Neurology 2006
20
55

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
675
30

A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.
K Owada, K Ishikawa, S Toru, G Ishida, M Gomyoda, O Tao, Y Noguchi, K Kitamura, I Kondo, E Noguchi,[...]. Neurology 2005
54
30

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, H Przuntek, J T Epplen, O Riess. Ann Neurol 1997
248
27

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.
Takako Ohata, Kunihiro Yoshida, Haruya Sakai, Haruka Hamanoue, Takeshi Mizuguchi, Yusaku Shimizu, Tomomi Okano, Fumio Takada, Kinya Ishikawa, Hidehiro Mizusawa,[...]. J Hum Genet 2006
25
32

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
24


Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
B P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, H Scheffer, E R Brunt, P F Ippel, J A Maat-Kievit, D Dooijes, N C Notermans, D Lindhout,[...]. Neurology 2002
164
24

Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan.
Kunihiro Yoshida, Yusaku Shimizu, Hiroshi Morita, Tomomi Okano, Haruya Sakai, Takako Ohata, Naomichi Matsumoto, Katsuya Nakamura, Ko-ichi Tazawa, Shinji Ohara,[...]. Cerebellum 2009
12
66

Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families.
Yusaku Shimizu, Kunihiro Yoshida, Tomomi Okano, Shinji Ohara, Takao Hashimoto, Yoshimitsu Fukushima, Shu-Ichi Ikeda. J Hum Genet 2004
24
29

Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.
Hirofumi Maruyama, Yuishin Izumi, Hiroyuki Morino, Masaya Oda, Hiromasa Toji, Shigenobu Nakamura, Hideshi Kawakami. Am J Med Genet 2002
73
21

Frequency of spinocerebellar ataxia mutations in the Kinki district of Japan.
R Matsumura, N Futamura, N Ando, S Ueno. Acta Neurol Scand 2003
23
30

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia.
U Nagaoka, M Takashima, K Ishikawa, K Yoshizawa, T Yoshizawa, M Ishikawa, T Yamawaki, S Shoji, H Mizusawa. Neurology 2000
58
18

Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
18

Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.
Takeshi Amino, Kinya Ishikawa, Shuta Toru, Taro Ishiguro, Nozomu Sato, Taiji Tsunemi, Miho Murata, Kazuhiro Kobayashi, Johji Inazawa, Tatsushi Toda,[...]. J Hum Genet 2007
20
30

Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
Won Yong Lee, Dong Kyu Jin, Myung Ryurl Oh, Ji Eun Lee, Seng Mi Song, Eun Ah Lee, Gyeong-Moon Kim, Jin Sang Chung, Kwang Ho Lee. Arch Neurol 2003
62
18


Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
J Vale, P Bugalho, I Silveira, J Sequeiros, J Guimarães, P Coutinho. Eur J Neurol 2010
41
18

Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians.
K Ishikawa, A Dürr, T Klopstock, S Müller, B De Toffol, M Vidailhet, A Vighetto, C Marelli, H-E Wichmann, T Illig,[...]. Neurology 2011
34
18

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.
H Takano, G Cancel, T Ikeuchi, D Lorenzetti, R Mawad, G Stevanin, O Didierjean, A Dürr, M Oyake, T Shimohata,[...]. Am J Hum Genet 1998
158
15

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
Ryuki Hirano, Hiroshi Takashima, Ryuichi Okubo, Keiko Tajima, Yuji Okamoto, Shimon Ishida, Kazuhito Tsuruta, Takayo Arisato, Hitoshi Arata, Masanori Nakagawa,[...]. Neurogenetics 2004
14
35


Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
T Ikeuchi, H Takano, R Koide, Y Horikawa, Y Honma, Y Onishi, S Igarashi, H Tanaka, N Nakao, K Sahashi,[...]. Ann Neurol 1997
110
15

Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.
H A G Teive, B B Roa, S Raskin, P Fang, W O Arruda, Y Correa Neto, R Gao, L C Werneck, T Ashizawa. Neurology 2004
72
15

Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
M A Pujana, J Corral, M Gratacòs, O Combarros, J Berciano, D Genís, I Banchs, X Estivill, V Volpini. Hum Genet 1999
107
15

The hereditary adult-onset ataxias in South Africa.
Alan Bryer, Amanda Krause, Pierre Bill, Virginia Davids, Daphne Bryant, James Butler, Jeannine Heckmann, Rajkumar Ramesar, Jacquie Greenberg. J Neurol Sci 2003
62
15


Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
K K Sinha, P F Worth, D K Jha, S Sinha, V J Stinton, M B Davis, N W Wood, M G Sweeney, K P Bhatia. J Neurol Neurosurg Psychiatry 2004
50
15

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Alfredo Brusco, Cinzia Gellera, Claudia Cagnoli, Alessandro Saluto, Alessia Castucci, Chiara Michielotto, Vincenza Fetoni, Caterina Mariotti, Nicola Migone, Stefano Di Donato,[...]. Arch Neurol 2004
102
15

Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation.
Q Saleem, S Choudhry, M Mukerji, L Bashyam, M V Padma, A Chakravarthy, M C Maheshwari, S Jain, S K Brahmachari. Hum Genet 2000
91
15

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.
Hiroki Takahashi, Kinya Ishikawa, Takeshi Tsutsumi, Hiroto Fujigasaki, Akihiro Kawata, Ryoichi Okiyama, Tsuneo Fujita, Kazuo Yoshizawa, Shigeki Yamaguchi, Hitoshi Tomiyasu,[...]. J Hum Genet 2004
49
12

Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion.
R Matsumura, N Futamura, Y Fujimoto, S Yanagimoto, H Horikawa, A Suzumura, T Takayanagi. Neurology 1997
130
12

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.
Mingshun Li, Kinya Ishikawa, Shuta Toru, Hiroyuki Tomimitsu, Minoru Takashima, Jun Goto, Yoshihisa Takiyama, Hidenao Sasaki, Issei Imoto, Johji Inazawa,[...]. J Hum Genet 2003
23
17

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
C M Gomez, R M Thompson, J T Gammack, S L Perlman, W B Dobyns, C L Truwit, D S Zee, H B Clark, J H Anderson. Ann Neurol 1997
206
12

Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia.
E Storey, D du Sart, J H Shaw, P Lorentzos, L Kelly, R J McKinley Gardner, S M Forrest, I Biros, G A Nicholson. Am J Med Genet 2000
53
12

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
I Silveira, C Miranda, L Guimarães, M-C Moreira, I Alonso, P Mendonça, A Ferro, J Pinto-Basto, J Coelho, F Ferreirinha,[...]. Arch Neurol 2002
129
12

Incidence of genetic subgroups of hereditary spinocerebellar ataxia in Fukushima Prefecture.
Y Kumagai, Y Sugiura, S Shimoji, T Kumagai, S Tochikubo, T Yamamoto. Tohoku J Exp Med 2001
5
80

High prevalence of spinocerebellar ataxia type 1 (SCA1) in an isolated region of Japan.
Y Onodera, M Aoki, T Tsuda, H Kato, T Nagata, T Kameya, K Abe, Y Itoyama. J Neurol Sci 2000
22
18

Asian origin for the worldwide-spread mutational event in Machado-Joseph disease.
Sandra Martins, Francesc Calafell, Claudia Gaspar, Virginia C N Wong, Isabel Silveira, Garth A Nicholson, Ewout R Brunt, Lisbeth Tranebjaerg, Giovanni Stevanin, Mingli Hsieh,[...]. Arch Neurol 2007
47
12



Frequency of spinocerebellar ataxia types 1,2,3,6,7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia.
D K Jin, M R Oh, S M Song, S W Koh, M Lee, G M Kim, W Y Lee, C S Chung, K H Lee, J H Im,[...]. J Neurol 1999
41
12

Evidence of a common founder for SCA12 in the Indian population.
S Bahl, K Virdi, U Mittal, M P Sachdeva, A K Kalla, S E Holmes, E O'Hearn, R L Margolis, S Jain, A K Srivastava,[...]. Ann Hum Genet 2005
43
12


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
454
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.