A citation-based method for searching scientific literature

Jorge Sequeiros, Sandra Martins, Isabel Silveira. Handb Clin Neurol 2012
Times Cited: 45







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



Times Cited
  Times     Co-cited
Similarity


Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
675
28

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
73
28

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
301
24

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
22

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
20

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
20

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.
Anne Kjersti Erichsen, Jeanette Koht, Asbjørg Stray-Pedersen, Michael Abdelnoor, Chantal M E Tallaksen. Brain 2009
129
15

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
15

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
23


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
86
15

Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions.
G N Souza, N Kersting, A C Krum-Santos, A S P Santos, G V Furtado, D Pacheco, T A Gonçalves, J A Saute, L Schuler-Faccini, E P Mattos,[...]. Clin Genet 2016
27
25

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
13

Progression rate of neurological deficits in a 10-year cohort of SCA3 patients.
Laura Bannach Jardim, Lisiane Hauser, Christian Kieling, Jonas Alex Morales Saute, Renan Xavier, Carlos Roberto Mello Rieder, Thais Lampert Monte, Suzi Camey, Vanessa Bielefeld Leotti Torman. Cerebellum 2010
35
17

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
13

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
13

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.
H Jacobi, P Bauer, P Giunti, R Labrum, M G Sweeney, P Charles, A Dürr, C Marelli, C Globas, C Linnemann,[...]. Neurology 2011
127
13

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Sophie Tezenas du Montcel, Alexandra Durr, Peter Bauer, Karla P Figueroa, Yaeko Ichikawa, Alessandro Brussino, Sylvie Forlani, Maria Rakowicz, Ludger Schöls, Caterina Mariotti,[...]. Brain 2014
100
13

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
58
11

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
893
11

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
11

Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
J Infante, O Combarros, V Volpini, J Corral, J Llorca, J Berciano. Acta Neurol Scand 2005
36
13

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
11

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, A Filla, C Mariotti, M Rakowicz, P Charles,[...]. Neurology 2008
175
11

'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization.
María García-Murias, Beatriz Quintáns, Manuel Arias, Ana I Seixas, Pilar Cacheiro, Rosa Tarrío, Julio Pardo, María J Millán, Susana Arias-Rivas, Patricia Blanco-Arias,[...]. Brain 2012
54
11

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
14

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Anna Sulek, Alexandra Durr, Perrine Charles,[...]. Lancet Neurol 2013
116
11

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Robyn Labrum, Michael H Parkinson, Alexandra Durr, Alexis Brice, Perrine Charles,[...]. Lancet Neurol 2015
136
11


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
608
8

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
8

Autosomal recessive cerebellar ataxias.
Francesc Palau, Carmen Espinós. Orphanet J Rare Dis 2006
101
8


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
8

Prevalence of inherited ataxias in the province of Padua, Italy.
M Zortea, M Armani, E Pastorello, G F Nunez, S Lombardi, S Tonello, M T Rigoni, L Zuliani, M L Mostacciuolo, C Gellera,[...]. Neuroepidemiology 2004
27
14

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
12

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
9

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
175
8

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
13

Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegia.
Sophie Tezenas du Montcel, Perrine Charles, Cyril Goizet, Cecilia Marelli, Pascale Ribai, Carlo Vincitorio, Mathieu Anheim, Lucie Guyant-Maréchal, Alice Le Bayon, Nadia Vandenberghe,[...]. Arch Neurol 2012
41
9

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
8

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
14

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
8

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
8

Sporadic ataxias in Japan--a population-based epidemiological study.
Shoji Tsuji, Osamu Onodera, Jun Goto, Masatoyo Nishizawa. Cerebellum 2008
92
8


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
8

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

Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
P Charles, A Camuzat, N Benammar, F Sellal, A Destée, A-M Bonnet, S Lesage, I Le Ber, G Stevanin, A Dürr,[...]. Neurology 2007
94
8

Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2).
Eliana Marisa Ramos, Sandra Martins, Isabel Alonso, Vanessa E Emmel, Maria Luiza Saraiva-Pereira, Laura Bannach Jardim, Paula Coutinho, Jorge Sequeiros, Isabel Silveira. Am J Med Genet B Neuropsychiatr Genet 2010
24
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.