A citation-based method for searching scientific literature

Thais Lampert Monte, Fernanda Santos Pereira, Estela da Rosa Reckziegel, Marina Coutinho Augustin, Lucas Dorídio Locks-Coelho, Amanda Senna P Santos, José Luiz Pedroso, Orlando Barsottini, Fernando Regla Vargas, Maria-Luiza Saraiva-Pereira, Laura Bannach Jardim. Parkinsonism Relat Disord 2017
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


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
41

Movement disorders in spinocerebellar ataxias.
Judith van Gaalen, Paola Giunti, Bart P van de Warrenburg. Mov Disord 2011
97
33

Comparison of cerebellar ataxias: A three-year prospective longitudinal assessment.
Yi-chung Lee, Yi-chu Liao, Po-shan Wang, I-Hui Lee, Kon-ping Lin, Bing-wen Soong. Mov Disord 2011
45
25

Extrapyramidal motor signs in degenerative ataxias.
L Schöls, S Peters, S Szymanski, R Krüger, S Lange, C Hardt, O Riess, H Przuntek. Arch Neurol 2000
66
25

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
101
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
153
25

A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies.
Marie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, Juliette Konop, Claire-Sophie Davoine, Christelle Tesson, Rémi Valter, Mathieu Anheim, Anthony Behin, Giovanni Castelnovo,[...]. Brain 2017
62
25

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.
M Rossi, S Perez-Lloret, L Doldan, D Cerquetti, J Balej, P Millar Vernetti, H Hawkes, A Cammarota, M Merello. Eur J Neurol 2014
77
25

Dystonia and ataxia progression in spinocerebellar ataxias.
Pei-Hsin Kuo, Shi-Rui Gan, Jie Wang, Raymond Y Lo, Karla P Figueroa, Darya Tomishon, Stefan M Pulst, Susan Perlman, George Wilmot, Christopher M Gomez,[...]. Parkinsonism Relat Disord 2017
26
25

Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology.
Theresa A Zesiewicz, George Wilmot, Sheng-Han Kuo, Susan Perlman, Patricia E Greenstein, Sarah H Ying, Tetsuo Ashizawa, S H Subramony, Jeremy D Schmahmann, K P Figueroa,[...]. Neurology 2018
56
25

Profile of extrapyramidal manifestations in 85 patients with spinocerebellar ataxia type 1, 2 and 3.
Ketan Jhunjhunwala, M Netravathi, Meera Purushottam, Sanjeev Jain, Pramod Kumar Pal. J Clin Neurosci 2014
18
16

Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.
Vikram G Shakkottai, Amit Batla, Kailash Bhatia, William T Dauer, Christian Dresel, Martin Niethammer, David Eidelberg, Robert S Raike, Yoland Smith, H A Jinnah,[...]. Cerebellum 2017
129
16

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
16

Phenomenology and classification of dystonia: a consensus update.
Alberto Albanese, Kailash Bhatia, Susan B Bressman, Mahlon R Delong, Stanley Fahn, Victor S C Fung, Mark Hallett, Joseph Jankovic, Hyder A Jinnah, Christine Klein,[...]. Mov Disord 2013
16

Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort.
Bart P C van de Warrenburg, Harrie Hendriks, Alexandra Dürr, Martin C A van Zuijlen, Giovanni Stevanin, Agnès Camuzat, Richard J Sinke, Alexis Brice, Berry P H Kremer. Ann Neurol 2005
82
16

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
16

Coenzyme Q10 and spinocerebellar ataxias.
Raymond Y Lo, Karla P Figueroa, Stefan M Pulst, Chi-Ying Lin, Susan Perlman, George Wilmot, Christopher Gomez, Jeremy Schmahmann, Henry Paulson, Vikram G Shakkottai,[...]. Mov Disord 2015
18
16

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
42
16

Movement disorders in hereditary ataxias.
Pedro J Garcia Ruiz, David Mayo, Jaime Hernandez, Susana Cantarero, Carmen Ayuso. J Neurol Sci 2002
25
16

The Initial Symptom and Motor Progression in Spinocerebellar Ataxias.
Lan Luo, Jie Wang, Raymond Y Lo, Karla P Figueroa, Stefan M Pulst, Pei-Hsin Kuo, Susan Perlman, George Wilmot, Christopher M Gomez, Jeremy Schmahmann,[...]. Cerebellum 2017
27
16

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
16

Dystonia in Machado-Joseph disease: Clinical profile, therapy and anatomical basis.
Marcelo B Nunes, Alberto Rolim M Martinez, Thiago Junqueira R Rezende, Joseph H Friedman, Iscia Lopes-Cendes, Anelyssa D'Abreu, Marcondes C França. Parkinsonism Relat Disord 2015
21
16

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
139
16

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
16

Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials.
Roberto Rodríguez-Labrada, Luis Velázquez-Pérez, Georg Auburger, Ulf Ziemann, Nalia Canales-Ochoa, Jacqueline Medrano-Montero, Yaimeé Vázquez-Mojena, Yanetza González-Zaldivar. Mov Disord 2016
27
16

NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2.
Thais L Monte, Estela R Reckziegel, Marina C Augustin, Amanda S P Silva, Lucas D Locks-Coelho, Orlando Barsottini, José L Pedroso, Fernando R Vargas, Maria-Luiza Saraiva-Pereira, Vanessa Bielefeldt Leotti,[...]. Cerebellum 2017
8
25



Longitudinal study of cognitive and psychiatric functions in spinocerebellar ataxia types 1 and 2.
Roberto Fancellu, Dominga Paridi, Chiara Tomasello, Marta Panzeri, Anna Castaldo, Silvia Genitrini, Paola Soliveri, Floriano Girotti. J Neurol 2013
58
16

Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.
Leroy Hubert, Yunfu Lin, Vincent Dion, John H Wilson. Hum Mol Genet 2011
57
16

Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3.
Rui Gao, Yongping Liu, Anabela Silva-Fernandes, Xiang Fang, Adriana Paulucci-Holthauzen, Arpita Chatterjee, Hang L Zhang, Tohru Matsuura, Sanjeev Choudhary, Tetsuo Ashizawa,[...]. PLoS Genet 2015
52
16

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
129
16


Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2.
Hamid Hamzeiy, Doruk Savaş, Ceren Tunca, Nesli Ece Şen, Aslı Gündoğdu Eken, Irmak Şahbaz, Daniela Calini, Cinzia Tiloca, Nicola Ticozzi, Antonia Ratti,[...]. Neurodegener Dis 2018
17
16

Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4.
Jose Bras, Isabel Alonso, Clara Barbot, Maria Manuela Costa, Lee Darwent, Tatiana Orme, Jorge Sequeiros, John Hardy, Paula Coutinho, Rita Guerreiro. Am J Hum Genet 2015
89
16

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
16

ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America.
Fernanda S Pereira, Thais L Monte, Lucas D Locks-Coelho, Amanda S P Silva, Orlando Barsottini, José L Pedroso, Mario Cornejo-Olivas, Pilar Mazzetti, Clecio Godeiro, Fernando R Vargas,[...]. Cerebellum 2015
8
25

Cellular toxicity of expanded RNA repeats: focus on RNA foci.
Marzena Wojciechowska, Wlodzimierz J Krzyzosiak. Hum Mol Genet 2011
160
16


A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
R Koide, S Kobayashi, T Shimohata, T Ikeuchi, M Maruyama, M Saito, M Yamada, H Takahashi, S Tsuji. Hum Mol Genet 1999
290
16

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
Juliane Winkelmann, Ling Lin, Barbara Schormair, Birgitte R Kornum, Juliette Faraco, Giuseppe Plazzi, Atle Melberg, Ferdinando Cornelio, Alexander E Urban, Fabio Pizza,[...]. Hum Mol Genet 2012
154
16

Fan1 deficiency results in DNA interstrand cross-link repair defects, enhanced tissue karyomegaly, and organ dysfunction.
Supawat Thongthip, Marina Bellani, Siobhan Q Gregg, Sunandini Sridhar, Brooke A Conti, Yanglu Chen, Michael M Seidman, Agata Smogorzewska. Genes Dev 2016
31
16

Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.
Marie Coutelier, Monia B Hammer, Giovanni Stevanin, Marie-Lorraine Monin, Claire-Sophie Davoine, Fanny Mochel, Pierre Labauge, Claire Ewenczyk, Jinhui Ding, J Raphael Gibbs,[...]. JAMA Neurol 2018
60
16

Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients.
N G Jaspers, R A Gatti, C Baan, P C Linssen, D Bootsma. Cytogenet Cell Genet 1988
157
16

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, H Takahashi, R Kondo, A Ishikawa, T Hayashi. Nat Genet 1994
987
16


Genetic analysis of age at onset variation in spinocerebellar ataxia type 2.
K P Figueroa, Hilary Coon, Nieves Santos, Luis Velazquez, Luis Almaguer Mederos, Stefan-M Pulst. Neurol Genet 2017
23
16

Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes.
Sandra Martins, Christopher E Pearson, Paula Coutinho, Sylvie Provost, António Amorim, Marie-Pierre Dubé, Jorge Sequeiros, Guy A Rouleau. Hum Genet 2014
27
16


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
895
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.