A citation-based method for searching scientific literature

Khalaf Bushara, Matthew Bower, Jilin Liu, Karen N McFarland, Ivette Landrian, Diane Hutter, Hélio A G Teive, Astrid Rasmussen, Connie J Mulligan, Tetsuo Ashizawa. PLoS One 2013
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


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
357
75

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.
A Rasmussen, T Matsuura, L Ruano, P Yescas, A Ochoa, T Ashizawa, E Alonso. Ann Neurol 2001
89
70

Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).
Teresa Almeida, Isabel Alonso, Sandra Martins, Eliana Marisa Ramos, Luísa Azevedo, Kinji Ohno, António Amorim, Maria Luiza Saraiva-Pereira, Laura Bannach Jardim, Tohru Matsuura,[...]. PLoS One 2009
35
70

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
65

Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.
Karen N McFarland, Jilin Liu, Ivette Landrian, Desmond Zeng, Salmo Raskin, Mariana Moscovich, Emilia M Gatto, Adriana Ochoa, Hélio A G Teive, Astrid Rasmussen,[...]. Neurogenetics 2014
34
55

Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease.
Luca Leonardi, Christian Marcotulli, Karen N McFarland, Alessandra Tessa, Roberto DiFabio, Filippo M Santorelli, Francesco Pierelli, Tetsuo Ashizawa, Carlo Casali. J Neurol 2014
15
73

Ethnic origin and extrapyramidal signs in an Argentinean spinocerebellar ataxia type 10 family.
E M Gatto, R Gao, M C White, M C Uribe Roca, J L Etcheverry, G Persi, J J Poderoso, T Ashizawa. Neurology 2007
30
50

Spinocerebellar ataxia type 10 in Chinese Han.
Kang Wang, Karen N McFarland, Jilin Liu, Desmond Zeng, Ivette Landrian, Guangbin Xia, Ying Hao, Miao Jin, Connie J Mulligan, Weihong Gu,[...]. Neurol Genet 2015
16
62

First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China.
Hiroyuki Naito, Tetsuya Takahashi, Masaki Kamada, Hiroyuki Morino, Hiroyo Yoshino, Nobutaka Hattori, Hirofumi Maruyama, Hideshi Kawakami, Masayasu Matsumoto. PLoS One 2017
14
71

Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.
T Matsuura, M Achari, M Khajavi, L L Bachinski, H Y Zoghbi, T Ashizawa. Ann Neurol 1999
66
40

Purkinje cell loss is the major brain pathology of spinocerebellar ataxia type 10.
Guangbin Xia, Karen N McFarland, Kang Wang, Partha S Sarkar, Anthony T Yachnis, Tetsuo Ashizawa. J Neurol Neurosurg Psychiatry 2013
18
44

Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10.
I Alonso, L B Jardim, O Artigalas, M L Saraiva-Pereira, T Matsuura, T Ashizawa, J Sequeiros, I Silveira. Neurology 2006
30
40

Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.
Karen N McFarland, Jilin Liu, Ivette Landrian, Rui Gao, Partha S Sarkar, Salmo Raskin, Mariana Moscovich, Emilia M Gatto, Hélio A G Teive, Adriana Ochoa,[...]. Eur J Hum Genet 2013
26
35

Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.
J F Baizabal-Carvallo, G Xia, P Botros, J Laguna, T Ashizawa, J Jankovic. Acta Neurol Scand 2015
8
87

Spinocerebellar ataxia type 10 - A review.
Hélio A G Teive, Renato P Munhoz, Walter O Arruda, Salmo Raskin, Lineu César Werneck, Tetsuo Ashizawa. Parkinsonism Relat Disord 2011
60
30

The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease.
Richard H Roxburgh, Corrie O Smith, Jung G Lim, David F Bachman, Erica Byrd, Thomas D Bird. J Neurol Sci 2013
13
46

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
30

Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
Raphael Machado de Castilhos, Gabriel Vasata Furtado, Tailise Conte Gheno, Paola Schaeffer, Aline Russo, Orlando Barsottini, José Luiz Pedroso, Diego Z Salarini, Fernando Regla Vargas, Maria Angélica de Faria Domingues de Lima,[...]. Cerebellum 2014
73
30

Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: a toxic RNA gain-of-function model.
Misti White, Guangbin Xia, Rui Gao, Maki Wakamiya, Partha S Sarkar, Karen McFarland, Tetsuo Ashizawa. J Neurosci Res 2012
32
30

Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?
Tohru Matsuura, Ping Fang, Christopher E Pearson, Parul Jayakar, Tetsuo Ashizawa, Benjamin B Roa, David L Nelson. Am J Hum Genet 2006
63
30

Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
L Zu, K P Figueroa, R Grewal, S M Pulst. Am J Hum Genet 1999
94
30

Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay.
Claudia Cagnoli, Chiara Michielotto, Tohru Matsuura, Tetsuo Ashizawa, Russell L Margolis, Susan E Holmes, Cinzia Gellera, Nicola Migone, Alfredo Brusco. J Mol Diagn 2004
40
25

Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.
Hélio A G Teive, Renato P Munhoz, Salmo Raskin, Walter O Arruda, Luciano de Paola, Lineu C Werneck, Tetsuo Ashizawa. Mov Disord 2010
32
25

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
25

The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.
M Wakamiya, T Matsuura, Y Liu, G C Schuster, R Gao, W Xu, P S Sarkar, X Lin, T Ashizawa. Neurology 2006
52
25

The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Luis Ruano, Claudia Melo, M Carolina Silva, Paula Coutinho. Neuroepidemiology 2014
295
25

Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.
Salmo Raskin, Tetsuo Ashizawa, Hélio A G Teive, Walter O Arruda, Ping Fang, Rui Gao, Misti C White, Lineu C Werneck, Benjamin Roa. Arch Neurol 2007
27
25

Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.
Irene Paradisi, Vassiliki Ikonomu, Sergio Arias. J Hum Genet 2016
18
27

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
20

[Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].
Jun-ling Wang, Yun-qin Wu, Li-fang Lei, Lu Shen, Hong Jiang, Ya-fang Zhou, Ji-ping Yi, Jie Zhou, Xin-xiang Yan, Qian Pan,[...]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2010
15
26

A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations.
L B Jardim, I Silveira, M L Pereira, A Ferro, I Alonso, M do Céu Moreira, P Mendonça, F Ferreirinha, J Sequeiros, R Giugliani. J Neurol 2001
63
20

Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10.
Misti C White, Rui Gao, Weidong Xu, Santi M Mandal, Jung G Lim, Tapas K Hazra, Maki Wakamiya, Sharon F Edwards, Salmo Raskin, Hélio A G Teive,[...]. PLoS Genet 2010
82
20

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
20

Epidemiological, clinical, and molecular characterization of Cuban families with spinocerebellar ataxia type 3/Machado-Joseph disease.
Yanetza González-Zaldívar, Yaimeé Vázquez-Mojena, José M Laffita-Mesa, Luis E Almaguer-Mederos, Roberto Rodríguez-Labrada, Gilberto Sánchez-Cruz, Raúl Aguilera-Rodríguez, Tania Cruz-Mariño, Nalia Canales-Ochoa, Patrick MacLeod,[...]. Cerebellum Ataxias 2015
11
36

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
157
20

Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.
C Gaspar, I Lopes-Cendes, S Hayes, J Goto, K Arvidsson, A Dias, I Silveira, P Maciel, P Coutinho, M Lima,[...]. Am J Hum Genet 2001
85
20

Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in Holguin.
Luis Velázquez Pérez, Gilberto Sánchez Cruz, Nieves Santos Falcón, Luis Enrique Almaguer Mederos, Karel Escalona Batallan, Roberto Rodríguez Labrada, Milena Paneque Herrera, José Miguel Laffita Mesa, Julio C Rodríguez Díaz, Raúl Aguilera Rodríguez,[...]. Neurosci Lett 2009
75
20

Mutational screening of 320 Brazilian patients with autosomal dominant spinocerebellar ataxia.
Vívian Pedigone Cintra, Charles Marques Lourenço, Sandra Elisabete Marques, Luana Michelli de Oliveira, Vitor Tumas, Wilson Marques. J Neurol Sci 2014
21
20

Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.
Raji P Grewal, Madhureeta Achari, Tohru Matsuura, Alberto Durazo, Emilio Tayag, Lan Zu, Stefan M Pulst, Tetsuo Ashizawa. Arch Neurol 2002
49
20

Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia.
R P Grewal, E Tayag, K P Figueroa, L Zu, A Durazo, C Nunez, S M Pulst. Neurology 1998
50
20

Spinocerebellar ataxia type 10 in the South of Brazil: the Amerindian-Belgian connection.
Hélio Afonso Ghizoni Teive, Adriana Moro, Mariana Moscovich, Walter Oleskho Arruda, Renato Puppi Munhoz, Salmo Raskin, Gladys Mary Ghizoni Teive, Norberto Dallabrida, Tetsuo Ashizawa. Arq Neuropsiquiatr 2015
10
40

Design of a bioactive small molecule that targets r(AUUCU) repeats in spinocerebellar ataxia 10.
Wang-Yong Yang, Rui Gao, Mark Southern, Partha S Sarkar, Matthew D Disney. Nat Commun 2016
35
20

SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure.
Karen N McFarland, Jilin Liu, Ivette Landrian, Ronald Godiska, Savita Shanker, Fahong Yu, William G Farmerie, Tetsuo Ashizawa. PLoS One 2015
34
20

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
672
15

Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
Elisa Alonso, Leticia Martínez-Ruano, Irene De Biase, Christopher Mader, Adriana Ochoa, Petra Yescas, Roxana Gutiérrez, Misti White, Luís Ruano, Marcela Fragoso-Benítez,[...]. Mov Disord 2007
33
15

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.
J Jonasson, V Juvonen, P Sistonen, J Ignatius, D Johansson, E J Björck, J Wahlström, A Melberg, G Holmgren, L Forsgren,[...]. Eur J Hum Genet 2000
40
15


Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families.
M L Moseley, K A Benzow, L J Schut, T D Bird, C M Gomez, P E Barkhaus, K A Blindauer, M Labuda, M Pandolfo, M D Koob,[...]. Neurology 1998
157
15

Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.
Hélio A G Teive, Renato P Munhoz, Walter O Arruda, Iscia Lopes-Cendes, Salmo Raskin, Lineu C Werneck, Tetsuo Ashizawa. Clinics (Sao Paulo) 2012
49
15

Spinocerebellar ataxia type 10.
Tetsuo Ashizawa. Handb Clin Neurol 2012
12
25


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.