A citation-based method for searching scientific literature

Luis Velázquez-Pérez, Jacqueline Medrano-Montero, Roberto Rodríguez-Labrada, Nalia Canales-Ochoa, Jandy Campins Alí, Frank J Carrillo Rodes, Tania Rodríguez Graña, María O Hernández Oliver, Raul Aguilera Rodríguez, Yennis Domínguez Barrios, Reydenis Torres Vega, Lissi Flores Angulo, Noharis Y Cordero Navarro, Aldo A Sigler Villanueva, Osiel Gámez Rodríguez, Ilya Sagaró Zambrano, Nayime Y Navas Napóles, Javier García Zacarías, Orlando R Serrano Barrera, María B Ramírez Bautista, Annelié Estupiñán Rodríguez, Leonardo A Guerra Rondón, Yaimeé Vázquez-Mojena, Yanetza González-Zaldivar, Luis E Almaguer Mederos, Alejandro Leyva-Mérida. Cerebellum 2020
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
168
45

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
73
45

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
941
36

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
214
36

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
263
27

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
878
27

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
709
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
39
27

Spinocerebellar ataxias: prospects and challenges for therapy development.
Tetsuo Ashizawa, Gülin Öz, Henry L Paulson. Nat Rev Neurol 2018
80
18

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
67
18

Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2.
Kathrin Reetz, Roberto Rodríguez-Labrada, Imis Dogan, Shahram Mirzazade, Sandro Romanzetti, Jörg B Schulz, Edilia M Cruz-Rivas, Jose A Alvarez-Cuesta, Raul Aguilera Rodríguez, Yanetza Gonzalez Zaldivar,[...]. Ann Clin Transl Neurol 2018
26
18

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
108
18

The cerebellar cognitive affective/Schmahmann syndrome scale.
Franziska Hoche, Xavier Guell, Mark G Vangel, Janet C Sherman, Jeremy D Schmahmann. Brain 2018
131
18

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
56
18

Neurophysiological studies and non-motor symptoms prior to ataxia in a patient with machado-joseph disease: trying to understand the natural history of brain degeneration.
José Luiz Pedroso, Edson Bor-Seng-Shu, Pedro Braga-Neto, Rodrigo Souza Ribeiro, Márcio Luiz Escorcio Bezerra, Lucila B F do Prado, Ilza Rosa Batista, Helena Alessi, Manoel Jacobsen Teixeira, Gilberto Mastrocola Manzano,[...]. Cerebellum 2014
12
18

Antisense oligonucleotide-mediated ataxin-1 reduction prolongs survival in SCA1 mice and reveals disease-associated transcriptome profiles.
Jillian Friedrich, Holly B Kordasiewicz, Brennon O'Callaghan, Hillary P Handler, Carmen Wagener, Lisa Duvick, Eric E Swayze, Orion Rainwater, Bente Hofstra, Michael Benneyworth,[...]. JCI Insight 2018
46
18

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
8
25

Spinocerebellar ataxias.
Bing-Wen Soong, Patrick J Morrison. Handb Clin Neurol 2018
30
18

The preclinical stage of spinocerebellar ataxias.
Roderick P P W M Maas, Judith van Gaalen, Thomas Klockgether, Bart P C van de Warrenburg. Neurology 2015
56
18

Polyglutamine spinocerebellar ataxias - from genes to potential treatments.
Henry L Paulson, Vikram G Shakkottai, H Brent Clark, Harry T Orr. Nat Rev Neurosci 2017
136
18

Spinocerebellar ataxia.
Thomas Klockgether, Caterina Mariotti, Henry L Paulson. Nat Rev Dis Primers 2019
136
18


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
14
18

Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression.
Alhassane Diallo, Heike Jacobi, Tanja Schmitz-Hübsch, Arron Cook, Robyn Labrum, Alexandra Durr, Alexis Brice, Perrine Charles, Cecilia Marelli, Caterina Mariotti,[...]. Mov Disord Clin Pract 2017
13
18

Body mass index is inversely correlated with the expanded CAG repeat length in SCA3/MJD patients.
Jonas Alex Morales Saute, Andrew Chaves Feitosa da Silva, Gabriele Nunes Souza, Aline Dutra Russo, Karina Carvalho Donis, Leonardo Vedolin, Maria Luiza Saraiva-Pereira, Luis Valmor Cruz Portela, Laura Bannach Jardim. Cerebellum 2012
28
18

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches.
Luis C Velázquez-Pérez, Roberto Rodríguez-Labrada, Juan Fernandez-Ruiz. Front Neurol 2017
40
18

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
603
18

Molecular pathogenesis of spinocerebellar ataxias.
Antoni Matilla Dueñas, Robert Goold, Paola Giunti. Brain 2006
156
18

C-termini of P/Q-type Ca2+ channel alpha1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity.
Holly B Kordasiewicz, Randall M Thompson, H Brent Clark, Christopher M Gomez. Hum Mol Genet 2006
96
18

Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families.
Lizbeth E García-Velázquez, Samuel Canizales-Quinteros, Sandra Romero-Hidalgo, Adriana Ochoa-Morales, Leticia Martínez-Ruano, Carla Márquez-Luna, Víctor Acuña-Alonzo, M Teresa Villarreal-Molina, M Elisa Alonso-Vilatela, Petra Yescas-Gómez. Neurogenetics 2014
9
11

A neurological examination score for the assessment of spinocerebellar ataxia 3 (SCA3).
C Kieling, C R M Rieder, A C F Silva, J A M Saute, C R Cecchin, T L Monte, L B Jardim. Eur J Neurol 2008
44
9

Evidence of a common founder for SCA12 in the Indian population.
S Bahl, K Virdi, U Mittal, M P Sachdeva, A K Kalla, S E Holmes, E O'Hearn, R L Margolis, S Jain, A K Srivastava,[...]. Ann Hum Genet 2005
41
9


Consensus Paper: Revisiting the Symptoms and Signs of Cerebellar Syndrome.
Florian Bodranghien, Amy Bastian, Carlo Casali, Mark Hallett, Elan D Louis, Mario Manto, Peter Mariën, Dennis A Nowak, Jeremy D Schmahmann, Mariano Serrao,[...]. Cerebellum 2016
144
9

Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence.
Karina Carvalho Donis, Jonas Alex Morales Saute, Ana Carolina Krum-Santos, Gabriel Vasata Furtado, Eduardo Preusser Mattos, Maria Luiza Saraiva-Pereira, Vanessa Leotti Torman, Laura Bannach Jardim. Neurogenetics 2016
10
10

Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.
Lidia Sarro, Lorenzo Nanetti, Anna Castaldo, Caterina Mariotti. Expert Rev Neurother 2017
6
16

Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
Yoshio Ikeda, Joline C Dalton, Melinda L Moseley, Kathy L Gardner, Thomas D Bird, Tetsuo Ashizawa, William K Seltzer, Massimo Pandolfo, Aubrey Milunsky, Nicholas T Potter,[...]. Am J Hum Genet 2004
62
9

Machado-Joseph disease in Brazil: from the first descriptions to the emergence as the most common spinocerebellar ataxia.
José Luiz Pedroso, Pedro Braga-Neto, João Radvany, Orlando Graziani Povoas Barsottini. Arq Neuropsiquiatr 2012
14
9

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
K K Sinha, P F Worth, D K Jha, S Sinha, V J Stinton, M B Davis, N W Wood, M G Sweeney, K P Bhatia. J Neurol Neurosurg Psychiatry 2004
50
9

A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease.
Chris Kay, Jennifer A Collins, Nicholas S Caron, Luciana de Andrade Agostinho, Hailey Findlay-Black, Lorenzo Casal, Dulika Sumathipala, Vajira H W Dissanayake, Mario Cornejo-Olivas, Fiona Baine,[...]. Am J Hum Genet 2019
8
12

Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48).
David Genis, Sara Ortega-Cubero, Hector San Nicolás, Jordi Corral, Josep Gardenyes, Laura de Jorge, Eva López, Berta Campos, Elena Lorenzo, Raúl Tonda,[...]. Neurology 2018
43
9

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3.
K Bürk, C Globas, S Bösch, T Klockgether, C Zühlke, I Daum, J Dichgans. J Neurol 2003
131
9

Origins and Spread of Machado-Joseph Disease Ancestral Mutations Events.
Sandra Martins, Jorge Sequeiros. Adv Exp Med Biol 2018
7
14

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
11

A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7.
L Velázquez-Pérez, C M Cerecedo-Zapata, O Hernández-Hernández, E Martínez-Cruz, Y S Tapia-Guerrero, R González-Piña, J Salas-Vargas, R Rodríguez-Labrada, R Gurrola-Betancourth, N Leyva-García,[...]. Neurogenetics 2015
21
9


Survival and severity in dominant cerebellar ataxias.
Marie-Lorraine Monin, Sophie Tezenas du Montcel, Cecilia Marelli, Cecile Cazeneuve, Perrine Charles, Chantal Tallaksen, Sylvie Forlani, Giovanni Stevanin, Alexis Brice, Alexandra Durr. Ann Clin Transl Neurol 2015
16
9

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
10

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
11
9

Safety and efficacy of valproic acid treatment in SCA3/MJD patients.
Li-Fang Lei, Guo-Ping Yang, Jun-Ling Wang, De-Maw Chuang, Wei-Hong Song, Bei-Sha Tang, Hong Jiang. Parkinsonism Relat Disord 2016
34
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.