A citation-based method for searching scientific literature

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, Yanetza González Zaldivar, Dany Coello Almarales, Dennis Almaguer Gotay, Humberto Jorge Cedeño. Neurosci Lett 2009
Times Cited: 76







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



Times Cited
  Times     Co-cited
Similarity


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
902
51

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
44

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Julio Cesar García-Rodríguez, Luis Enrique Almaguer-Mederos, Tania Cruz-Mariño, José Miguel Laffita-Mesa. Cerebellum 2011
58
43

Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2.
L Velázquez-Pérez, C Seifried, M Abele, F Wirjatijasa, R Rodríguez-Labrada, N Santos-Falcón, G Sánchez-Cruz, L Almaguer-Mederos, R Tejeda, N Canales-Ochoa,[...]. Clin Neurophysiol 2009
56
39

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
G Imbert, F Saudou, G Yvert, D Devys, Y Trottier, J M Garnier, C Weber, J L Mandel, G Cancel, N Abbas,[...]. Nat Genet 1996
724
27

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
164
26

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS.
Andrew C Elden, Hyung-Jun Kim, Michael P Hart, Alice S Chen-Plotkin, Brian S Johnson, Xiaodong Fang, Maria Armakola, Felix Geser, Robert Greene, Min Min Lu,[...]. Nature 2010
836
23

Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2.
Luis Velázquez-Pérez, Carola Seifried, Nieves Santos-Falcón, Michael Abele, Ulf Ziemann, Luis Enrique Almaguer, Edilberto Martínez-Góngora, Gilberto Sánchez-Cruz, Nalia Canales, Ruth Pérez-González,[...]. Ann Neurol 2004
69
24

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
679
22

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
179
22

Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Nalia Canales-Ochoa, Jacqueline Medrano Montero, Gilberto Sánchez-Cruz, Raúl Aguilera-Rodríguez, Luis E Almaguer-Mederos, José M Laffita-Mesa. Lancet Neurol 2014
59
27


Comprehensive study of early features in spinocerebellar ataxia 2: delineating the prodromal stage of the disease.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Edilia M Cruz-Rivas, Juan Fernández-Ruiz, Israel Vaca-Palomares, Jandy Lilia-Campins, Bulmaro Cisneros, Arnoy Peña-Acosta, Yaimeé Vázquez-Mojena, Rosalinda Diaz,[...]. Cerebellum 2014
40
37

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
K Sanpei, H Takano, S Igarashi, T Sato, M Oyake, H Sasaki, A Wakisaka, K Tashiro, Y Ishida, T Ikeuchi,[...]. Nat Genet 1996
629
18

Subtle rapid eye movement sleep abnormalities in presymptomatic spinocerebellar ataxia type 2 gene carriers.
Roberto Rodríguez-Labrada, Luis Velázquez-Perez, Nalia Canales Ochoa, Lourdes Galicia Polo, Reyes Haro Valencia, Gilberto Sánchez Cruz, Jacqueline Medrano Montero, José M Laffita-Mesa, Luis E Almaguer Mederos, Yanetza González Zaldívar,[...]. Mov Disord 2011
30
46

Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2.
Luis Velázquez Pérez, Gilberto Sánchez Cruz, Nalia Canales Ochoa, Roberto Rodríguez Labrada, Julio Rodríguez Díaz, Luis Almaguer Mederos, José Laffita Mesa. J Neurol Sci 2007
37
35

Progression markers of Spinocerebellar ataxia 2. A twenty years neurophysiological follow up study.
Luis Velázquez-Perez, Roberto Rodríguez-Labrada, Nalia Canales-Ochoa, Gilberto Sanchez-Cruz, Juan Fernandez-Ruiz, Jacqueline Medrano Montero, Raúl Aguilera-Rodríguez, Rosalinda Diaz, Luis E Almaguer-Mederos, Agustín Palomino Truitz. J Neurol Sci 2010
34
38

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
35
37

Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles.
José Miguel Laffita-Mesa, Luis C Velázquez-Pérez, Nieves Santos Falcón, Tania Cruz-Mariño, Yanetza González Zaldívar, Yaimee Vázquez Mojena, Dennis Almaguer-Gotay, Luis Enrique Almaguer Mederos, Roberto Rodríguez Labrada. Eur J Hum Genet 2012
32
40

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.
G Auburger, G O Diaz, R F Capote, S G Sanchez, M P Perez, M E del Cueto, M G Meneses, M Farrall, R Williamson, S Chamberlain. Am J Hum Genet 1990
86
17

Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2).
K Gierga, K Bürk, M Bauer, G Orozco Diaz, G Auburger, C Schultz, M Vuksic, L Schöls, R A I de Vos, H Braak,[...]. Acta Neuropathol 2005
67
17

Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis.
L E Almaguer-Mederos, N S Falcón, Y R Almira, Y G Zaldivar, D C Almarales, E M Góngora, M P Herrera, K E Batallán, R R Armiñán, M V Manresa,[...]. Clin Genet 2010
39
30

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
124
15

Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2).
I Tuin, U Voss, J-S Kang, K Kessler, U Rüb, D Nolte, H Lochmüller, S Tinschert, D Claus, K Krakow,[...]. Neurology 2006
50
22

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
159
14

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.
G Orozco, R Estrada, T L Perry, J Araña, R Fernandez, A Gonzalez-Quevedo, J Galarraga, S Hansen. J Neurol Sci 1989
151
14

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
13

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
103
13

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
13

Spinocerebellar ataxia type 2.
Georg W J Auburger. Handb Clin Neurol 2012
53
18

Efficient Prevention of Neurodegenerative Diseases by Depletion of Starvation Response Factor Ataxin-2.
Georg Auburger, Nesli-Ece Sen, David Meierhofer, Ayşe-Nazlı Başak, Aaron D Gitler. Trends Neurosci 2017
37
27

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches.
Luis C Velázquez-Pérez, Roberto Rodríguez-Labrada, Juan Fernandez-Ruiz. Front Neurol 2017
49
20

Spinocerebellar ataxia 2 (SCA2).
Isabel Lastres-Becker, Udo Rüb, Georg Auburger. Cerebellum 2008
144
11

The natural history of degenerative ataxia: a retrospective study in 466 patients.
T Klockgether, R Lüdtke, B Kramer, M Abele, K Bürk, L Schöls, O Riess, F Laccone, S Boesch, I Lopes-Cendes,[...]. Brain 1998
236
11


CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms.
S Choudhry, M Mukerji, A K Srivastava, S Jain, S K Brahmachari. Hum Mol Genet 2001
94
11

Antisense oligonucleotide therapy for spinocerebellar ataxia type 2.
Daniel R Scoles, Pratap Meera, Matthew D Schneider, Sharan Paul, Warunee Dansithong, Karla P Figueroa, Gene Hung, Frank Rigo, C Frank Bennett, Thomas S Otis,[...]. Nature 2017
181
11

Prodromal spinocerebellar ataxia type 2: Prospects for early interventions and ethical challenges.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, José Miguel Laffita-Mesa. Mov Disord 2017
16
56

Disturbance of rapid eye movement sleep in spinocerebellar ataxia type 2.
Sylvia M Boesch, Birgit Frauscher, Elisabeth Brandauer, Gregor K Wenning, Birgit Högl, Werner Poewe. Mov Disord 2006
34
23

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
613
10

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
G Cancel, A Dürr, O Didierjean, G Imbert, K Bürk, A Lezin, S Belal, A Benomar, M Abada-Bendib, C Vial,[...]. Hum Mol Genet 1997
194
10

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
10

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
158
10

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
10

Motor decline in clinically presymptomatic spinocerebellar ataxia type 2 gene carriers.
Luis Velázquez-Perez, Rosalinda Díaz, Ruth Pérez-González, Nalia Canales, Roberto Rodríguez-Labrada, Jacquelín Medrano, Gilberto Sánchez, Luis Almaguer-Mederos, Cira Torres, Juan Fernandez-Ruiz. PLoS One 2009
18
44

Sleep disorders in spinocerebellar ataxia type 2 patients.
Luis Velázquez-Pérez, Ursula Voss, Roberto Rodríguez-Labrada, Georg Auburger, Nalia Canales Ochoa, Gilberto Sánchez Cruz, Lourdes Galicia Polo, Reyes Haro Valencia, Raúl Aguilera Rodríguez, Jacqueline Medrano Montero,[...]. Neurodegener Dis 2011
38
21

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
241
10

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
316
10


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
9


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.