A citation-based method for searching scientific literature

Sandra Martins, Jorge Sequeiros. Adv Exp Med Biol 2018
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
62

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
62

Correlation between CAG repeat length and clinical features in Machado-Joseph disease.
P Maciel, C Gaspar, A L DeStefano, I Silveira, P Coutinho, J Radvany, D M Dawson, L Sudarsky, J Guimarães, J E Loureiro. Am J Hum Genet 1995
223
50

Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease.
H Maruyama, S Nakamura, Z Matsuyama, T Sakai, M Doyu, G Sobue, M Seto, M Tsujihata, T Oh-i, T Nishio. Hum Mol Genet 1995
167
37

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
37

Allele-specific RNA silencing of mutant ataxin-3 mediates neuroprotection in a rat model of Machado-Joseph disease.
Sandro Alves, Isabel Nascimento-Ferreira, Gwennaëlle Auregan, Raymonde Hassig, Noëlle Dufour, Emmanuel Brouillet, Maria C Pedroso de Lima, Philippe Hantraye, Luís Pereira de Almeida, Nicole Déglon. PLoS One 2008
113
37

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
37

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
37

Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and Yirrkala.
Sandra Martins, Bing-Wen Soong, Virginia C N Wong, Paola Giunti, Giovanni Stevanin, Laura P W Ranum, Hidenao Sasaki, Olaf Riess, Shoji Tsuji, Paula Coutinho,[...]. Arch Neurol 2012
16
25

Machado-Joseph disease in a Nigerian family: mutational origin and review of the literature.
Shamsideen Abayomi Ogun, Sandra Martins, Philip B Adebayo, Clara O Dawodu, Jorge Sequeiros, Michael F Finkel. Eur J Hum Genet 2015
7
28

Improvement in the molecular diagnosis of Machado-Joseph disease.
P Maciel, M C Costa, A Ferro, M Rousseau, C S Santos, C Gaspar, J Barros, G A Rouleau, P Coutinho, J Sequeiros. Arch Neurol 2001
93
25

A multistep mutation mechanism drives the evolution of the CAG repeat at MJD/SCA3 locus.
Sandra Martins, Francesc Calafell, Virginia C N Wong, Jorge Sequeiros, António Amorim. Eur J Hum Genet 2006
21
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

A Pipeline to Assess Disease-Associated Haplotypes in Repeat Expansion Disorders: The Example of MJD/SCA3 Locus.
Inês P D Costa, Beatriz C Almeida, Jorge Sequeiros, António Amorim, Sandra Martins. Front Genet 2019
6
33


Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family.
K Gwinn-Hardy, A Singleton, P O'Suilleabhain, M Boss, D Nicholl, A Adam, J Hussey, P Critchley, J Hardy, M Farrer. Arch Neurol 2001
96
25

Spinocerebellar ataxia type 3 in Israel: phenotype and genotype of a Jew Yemenite subpopulation.
Roy Zaltzman, Reuven Sharony, Colin Klein, Carlos R Gordon. J Neurol 2016
8
25


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,[...]. Eur J Neurol 2017
12
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
25

Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect.
J J Magaña, Y S Tapia-Guerrero, L Velázquez-Pérez, C M Cerecedo-Zapata, M Maldonado-Rodríguez, J S Jano-Ito, N Leyva-García, R González-Piña, E Martínez-Cruz, O Hernández-Hernández,[...]. Clin Genet 2014
25
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
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
286
25

Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.
Irene Paradisi, Vassiliki Ikonomu, Sergio Arias. J Hum Genet 2016
18
25

Spinocerebellar ataxia type 3: subphenotypes in a cohort of Brazilian patients.
Adriana Moro, Renato P Munhoz, Walter O Arruda, Salmo Raskin, Mariana Moscovich, Hélio A G Teive. Arq Neuropsiquiatr 2014
16
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


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
25


Oligonucleotide therapy mitigates disease in spinocerebellar ataxia type 3 mice.
Hayley S McLoughlin, Lauren R Moore, Ravi Chopra, Robert Komlo, Megan McKenzie, Kate G Blumenstein, Hien Zhao, Holly B Kordasiewicz, Vikram G Shakkottai, Henry L Paulson. Ann Neurol 2018
72
25

Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations.
Dineke S Verbeek, Sytse J Piersma, Eric F A M Hennekam, Elly F Ippel, Peter L Pearson, Richard J Sinke. Eur J Hum Genet 2004
9
25

Hereditary ataxia and spastic paraplegia in Portugal: a population-based prevalence study.
Paula Coutinho, Luis Ruano, José L Loureiro, Vitor T Cruz, José Barros, Assunção Tuna, Clara Barbot, João Guimarães, Isabel Alonso, Isabel Silveira,[...]. JAMA Neurol 2013
70
25

Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population.
J J Magaña, R Gómez, M Maldonado-Rodríguez, L Velázquez-Pérez, Y S Tapia-Guerrero, H Cortés, N Leyva-García, O Hernández-Hernández, B Cisneros. Cerebellum 2013
20
25

Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument.
H Jacobi, M Rakowicz, R Rola, R Fancellu, C Mariotti, P Charles, A Dürr, M Küper, D Timmann, C Linnemann,[...]. Cerebellum 2013
66
25

Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study.
Alhassane Diallo, Heike Jacobi, Arron Cook, Robyn Labrum, Alexandra Durr, Alexis Brice, Perrine Charles, Cecilia Marelli, Caterina Mariotti, Lorenzo Nanetti,[...]. Lancet Neurol 2018
42
25


Polyglutamine spinocerebellar ataxias - from genes to potential treatments.
Henry L Paulson, Vikram G Shakkottai, H Brent Clark, Harry T Orr. Nat Rev Neurosci 2017
144
25

Spinocerebellar ataxia.
Thomas Klockgether, Caterina Mariotti, Henry L Paulson. Nat Rev Dis Primers 2019
164
25

Allele-specific silencing of mutant huntingtin and ataxin-3 genes by targeting expanded CAG repeats in mRNAs.
Jiaxin Hu, Masayuki Matsui, Keith T Gagnon, Jacob C Schwartz, Sylvie Gabillet, Khalil Arar, Jun Wu, Ilya Bezprozvanny, David R Corey. Nat Biotechnol 2009
179
25

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
A Dürr, G Stevanin, G Cancel, C Duyckaerts, N Abbas, O Didierjean, H Chneiweiss, A Benomar, O Lyon-Caen, J Julien,[...]. Ann Neurol 1996
344
25

Machado-Joseph disease gene products carrying different carboxyl termini.
J Goto, M Watanabe, Y Ichikawa, S B Yee, N Ihara, K Endo, S Igarashi, Y Takiyama, C Gaspar, P Maciel,[...]. Neurosci Res 1997
61
25

Ataxin-3 protein and RNA toxicity in spinocerebellar ataxia type 3: current insights and emerging therapeutic strategies.
Melvin M Evers, Lodewijk J A Toonen, Willeke M C van Roon-Mom. Mol Neurobiol 2014
50
25

Silencing mutant ATXN3 expression resolves molecular phenotypes in SCA3 transgenic mice.
Edgardo Rodríguez-Lebrón, Maria do Carmo Costa, Katiuska Luna-Cancalon, Therese M Peron, Svetlana Fischer, Ryan L Boudreau, Beverly L Davidson, Henry L Paulson. Mol Ther 2013
78
25

Pathogenesis of SCA3 and implications for other polyglutamine diseases.
Hayley S McLoughlin, Lauren R Moore, Henry L Paulson. Neurobiol Dis 2020
44
25

Silencing ataxin-3 mitigates degeneration in a rat model of Machado-Joseph disease: no role for wild-type ataxin-3?
Sandro Alves, Isabel Nascimento-Ferreira, Noëlle Dufour, Raymonde Hassig, Gwennaëlle Auregan, Clévio Nóbrega, Emmanuel Brouillet, Philippe Hantraye, Maria C Pedroso de Lima, Nicole Déglon,[...]. Hum Mol Genet 2010
76
25

Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins?
Tianjiao Li, Sandra Martins, Yun Peng, Puzhi Wang, Xiaocan Hou, Zhao Chen, Chunrong Wang, Zhaoli Tang, Rong Qiu, Chao Chen,[...]. Front Genet 2019
7
28

Toward RNAi therapy for the polyglutamine disease Machado-Joseph disease.
Maria do Carmo Costa, Katiuska Luna-Cancalon, Svetlana Fischer, Naila S Ashraf, Michelle Ouyang, Rahil M Dharia, Lucas Martin-Fishman, Yemen Yang, Vikram G Shakkottai, Beverly L Davidson,[...]. Mol Ther 2013
72
25

Physiological and pathophysiological characteristics of ataxin-3 isoforms.
Daniel Weishäupl, Juliane Schneider, Barbara Peixoto Pinheiro, Corinna Ruess, Sandra Maria Dold, Felix von Zweydorf, Christian Johannes Gloeckner, Jana Schmidt, Olaf Riess, Thorsten Schmidt. J Biol Chem 2019
19
25

Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
562
25

Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays.
Stephanie Suzanne de Oliveira Scott, José Luiz Pedroso, Orlando Graziani Povoas Barsottini, Marcondes Cavalcante França-Junior, Pedro Braga-Neto. J Neurol Sci 2020
3
66


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.