A citation-based method for searching scientific literature

Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil.
T C Gheno, G V Furtado, J A M Saute, K C Donis, A M V Fontanari, V E Emmel, J L Pedroso, O Barsottini, C Godeiro-Junior, H van der Linden, E Ternes Pereira, V P Cintra, W Marques, R M de Castilhos, I Alonso, J Sequeiros, M Cornejo-Olivas, P Mazzetti, V B Leotti, L B Jardim, M L Saraiva-Pereira. Eur J Neurol 2017
Times Cited: 12






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



Times Cited
  Times     Co-cited
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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
72
7
58

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
5
41

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
29
5
41

Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.
Giovana B Bampi, Rafael Bisso-Machado, Tábita Hünemeier, Tailise C Gheno, Gabriel V Furtado, Diego Veliz-Otani, Mario Cornejo-Olivas, Pillar Mazzeti, Maria Cátira Bortolini, Laura B Jardim,[...]. Neuromolecular Med 2017
10
5
50

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
4
33

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
33
4
33

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
12
4
33

Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.
Irene Paradisi, Vassiliki Ikonomu, Sergio Arias. J Hum Genet 2016
18
4
33

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
59
3
25

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
3
25

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
71
3
25

Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.
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
18
3
25

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
48
3
25

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
88
3
25

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
14
3
25

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
29
3
25

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
74
3
25

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
3
25

Evolutionary genomic dynamics of Peruvians before, during, and after the Inca Empire.
Daniel N Harris, Wei Song, Amol C Shetty, Kelly S Levano, Omar Cáceres, Carlos Padilla, Víctor Borda, David Tarazona, Omar Trujillo, Cesar Sanchez,[...]. Proc Natl Acad Sci U S A 2018
61
3
25

The progression rate of spinocerebellar ataxia type 2 changes with stage of disease.
Thais Lampert Monte, Estela da Rosa Reckziegel, Marina Coutinho Augustin, Lucas D Locks-Coelho, Amanda Senna P Santos, Gabriel Vasata Furtado, Eduardo Preusser de Mattos, José Luiz Pedroso, Orlando Póvoas Barsottini, Fernando Regla Vargas,[...]. Orphanet J Rare Dis 2018
9
3
33

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
286
3
25

Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.
Tetsuo Ashizawa, Karla P Figueroa, Susan L Perlman, Christopher M Gomez, George R Wilmot, Jeremy D Schmahmann, Sarah H Ying, Theresa A Zesiewicz, Henry L Paulson, Vikram G Shakkottai,[...]. Orphanet J Rare Dis 2013
76
3
25

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
65
2
16

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
2
16

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
2
16

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
2
16

Spinocerebellar ataxia type 10: from Amerindians to Latin Americans.
Hélio A G Teive, Tetsuo Ashizawa. Curr Neurol Neurosci Rep 2013
6
2
33

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
101
2
16

Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.
Junling Wang, Lu Shen, Lifang Lei, Qian Xu, Jie Zhou, Yutao Liu, Wenjuan Guan, Qian Pan, Kun Xia, Beisha Tang,[...]. Zhong Nan Da Xue Xue Bao Yi Xue Ban 2011
33
2
16

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
13
2
16

Heterogeneity in genetic admixture across different regions of Argentina.
Sergio Avena, Marc Via, Elad Ziv, Eliseo J Pérez-Stable, Christopher R Gignoux, Cristina Dejean, Scott Huntsman, Gabriela Torres-Mejía, Julie Dutil, Jaime L Matta,[...]. PLoS One 2012
91
2
16

A simple salting out procedure for extracting DNA from human nucleated cells.
S A Miller, D D Dykes, H F Polesky. Nucleic Acids Res 1988
15860
2
16

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.
T Matsuura, L P W Ranum, V Volpini, M Pandolfo, H Sasaki, K Tashiro, K Watase, H Y Zoghbi, T Ashizawa. Neurology 2002
34
2
16

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
2
20

Movement disorders in spinocerebellar ataxias in a cohort of Brazilian patients.
Adriana Moro, Renato P Munhoz, Mariana Moscovich, Walter O Arruda, Salmo Raskin, Hélio A G Teive. Eur Neurol 2014
14
2
16

A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.
S E Holmes, E O'Hearn, A Rosenblatt, C Callahan, H S Hwang, R G Ingersoll-Ashworth, A Fleisher, G Stevanin, A Brice, N T Potter,[...]. Nat Genet 2001
196
2
16

The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.
Chris Kay, Indira Tirado-Hurtado, Mario Cornejo-Olivas, Jennifer A Collins, Galen Wright, Miguel Inca-Martinez, Diego Veliz-Otani, Maria E Ketelaar, Ramy A Slama, Colin J Ross,[...]. Eur J Hum Genet 2017
9
2
22

Neurogenetics in Peru: clinical, scientific and ethical perspectives.
Mario Cornejo-Olivas, Keren Espinoza-Huertas, Mario R Velit-Salazar, Diego Veliz-Otani, Indira Tirado-Hurtado, Miguel Inca-Martinez, Gustavo Silva-Paredes, Karina Milla-Neyra, Victoria Marca, Olimpio Ortega,[...]. J Community Genet 2015
5
2
40

Huntington disease and Huntington disease-like in a case series from Brazil.
R M Castilhos, A F D Souza, G V Furtado, T C Gheno, A L Silva, F R Vargas, M-A F D Lima, O Barsottini, J L Pedroso, C Godeiro,[...]. Clin Genet 2014
22
2
16

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
32
2
16

Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.
Mario Cornejo-Olivas, Luis Torres, Mario R Velit-Salazar, Miguel Inca-Martinez, Pilar Mazzetti, Carlos Cosentino, Federico Micheli, Claudia Perandones, Elena Dieguez, Victor Raggio,[...]. NPJ Parkinsons Dis 2017
13
2
16

Tracing the genomic ancestry of Peruvians reveals a major legacy of pre-Columbian ancestors.
Jose R Sandoval, Alberto Salazar-Granara, Oscar Acosta, Wilder Castillo-Herrera, Ricardo Fujita, Sergio D J Pena, Fabricio R Santos. J Hum Genet 2013
40
2
16

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10.
Tohru Matsuura, Ping Fang, Xi Lin, Mehrdad Khajavi, Kuniko Tsuji, Astrid Rasmussen, Raji P Grewal, Madhureeta Achari, Maria E Alonso, Stefan M Pulst,[...]. Am J Hum Genet 2004
45
2
16

Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast.
Nicole Cherng, Alexander A Shishkin, Lucas I Schlager, Ryan H Tuck, Laura Sloan, Robert Matera, Partha S Sarkar, Tetsuo Ashizawa, Catherine H Freudenreich, Sergei M Mirkin. Proc Natl Acad Sci U S A 2011
37
2
16

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
62
2
16

Unstable spinocerebellar ataxia type 10 (ATTCT*(AGAAT) repeats are associated with aberrant replication at the ATX10 locus and replication origin-dependent expansion at an ectopic site in human cells.
Guoqi Liu, John J Bissler, Richard R Sinden, Michael Leffak. Mol Cell Biol 2007
39
2
16

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
2
16

Origins and Spread of Machado-Joseph Disease Ancestral Mutations Events.
Sandra Martins, Jorge Sequeiros. Adv Exp Med Biol 2018
8
2
25

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
61
2
16

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
48
2
16


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.

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