A citation-based method for searching scientific literature

T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, A Filla, C Mariotti, M Rakowicz, P Charles, P Ribai, S Szymanski, J Infante, B P C van de Warrenburg, A Dürr, D Timmann, S Boesch, R Fancellu, R Rola, C Depondt, L Schöls, E Zdienicka, J-S Kang, S Döhlinger, B Kremer, D A Stephenson, B Melegh, M Pandolfo, S di Donato, S Tezenas du Montcel, T Klockgether. Neurology 2008
Times Cited: 167







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



Times Cited
  Times     Co-cited
Similarity


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
27
18

Motor cortex activation by transcranial magnetic stimulation in ataxia patients depends on the genetic defect.
Peter Schwenkreis, Martin Tegenthoff, Katja Witscher, Christian Börnke, Horst Przuntek, Jean-Pierre Malin, Ludger Schöls. Brain 2002
62
8

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
C M Gomez, R M Thompson, J T Gammack, S L Perlman, W B Dobyns, C L Truwit, D S Zee, H B Clark, J H Anderson. Ann Neurol 1997
201
5

Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.
K Bürk, M Fetter, M Abele, F Laccone, A Brice, J Dichgans, T Klockgether. J Neurol 1999
105
5

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
27

Spinocerebellar ataxia type 2 (SCA2): identification of early brain degeneration in one monozygous twin in the initial disease stage.
Franziska Hoche, Laszlo Balikó, Wilfred den Dunnen, Katalin Steinecker, Laszlo Bartos, Eniko Sáfrány, Georg Auburger, Thomas Deller, Horst-Werner Korf, Thomas Klockgether,[...]. Cerebellum 2011
23
21

Neocortical atrophy in Machado-Joseph disease: a longitudinal neuroimaging study.
Anelyssa D'Abreu, Marcondes C França, Clarissa L Yasuda, Bruno A G Campos, Iscia Lopes-Cendes, Fernando Cendes. J Neuroimaging 2012
55
9

Cognitive impairments in Machado-Joseph disease.
Yoshinari Kawai, Akinori Takeda, Yuji Abe, Yukihiko Washimi, Fumiaki Tanaka, Gen Sobue. Arch Neurol 2004
57
8

Survival estimates for patients with Machado-Joseph disease (SCA3).
C Kieling, P R Prestes, M L Saraiva-Pereira, L B Jardim. Clin Genet 2007
40
12

Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.
D H Geschwind, S Perlman, K P Figueroa, J Karrim, R W Baloh, S M Pulst. Neurology 1997
133
5

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
35

Machado-Joseph disease/spinocerebellar ataxia type 3.
Henry Paulson. Handb Clin Neurol 2012
78
6

Depressive symptoms in Machado-Joseph disease (SCA3) patients and their relatives.
C R Cecchin, A P Pires, C R Rieder, T L Monte, I Silveira, T Carvalho, M L Saraiva-Pereira, J Sequeiros, L B Jardim. Community Genet 2007
33
15

Central motor conduction time as prodromal biomarker in spinocerebellar ataxia type 2.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Reidenis Torres-Vega, Jacqueline Medrano Montero, Yaimeé Vazquez-Mojena, Georg Auburger, Ulf Ziemann. Mov Disord 2016
14
35

Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6.
Sophie Tezenas du Montcel, Alexandra Durr, Maria Rakowicz, Lorenzo Nanetti, Perrine Charles, Anna Sulek, Caterina Mariotti, Rafal Rola, Ludger Schols, Peter Bauer,[...]. J Med Genet 2014
39
12

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
91
5

Mammalian ataxin-2 modulates translation control at the pre-initiation complex via PI3K/mTOR and is induced by starvation.
Isabel Lastres-Becker, David Nonis, Florian Eich, Michael Klinkenberg, Myriam Gorospe, Peter Kötter, Fabrice A C Klein, Nancy Kedersha, Georg Auburger. Biochim Biophys Acta 2016
47
10

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
25
20

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
34
14

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
35

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
22
22

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
18
27

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
26
19

Serum insulin-like system alterations in patients with spinocerebellar ataxia type 3.
Jonas Alex Morales Saute, Andrew Chaves Feitosa da Silva, Alexandre Pastoris Muller, Gisele Hansel, Alexandre Silva de Mello, Fábio Maeda, Leonardo Vedolin, Maria Luiza Saraiva-Pereira, Diogo Onofre Souza, Javier Arpa,[...]. Mov Disord 2011
19
26

Insulin receptor and lipid metabolism pathology in ataxin-2 knock-out mice.
Isabel Lastres-Becker, Susanne Brodesser, Dieter Lütjohann, Mekhman Azizov, Jana Buchmann, Edith Hintermann, Konrad Sandhoff, Annette Schürmann, Joachim Nowock, Georg Auburger. Hum Mol Genet 2008
80
6

Serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study.
Carlo Wilke, Friedemann Bender, Stefanie N Hayer, Kathrin Brockmann, Ludger Schöls, Jens Kuhle, Matthis Synofzik. J Neurol 2018
33
15

Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Robyn Labrum, Michael H Parkinson, Alexandra Durr, Alexis Brice, Perrine Charles,[...]. J Neurol 2018
14
35

Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia.
Maria R Stefanescu, Moritz Dohnalek, Stefan Maderwald, Markus Thürling, Martina Minnerop, Andreas Beck, Marc Schlamann, Joern Diedrichsen, Mark E Ladd, Dagmar Timmann. Brain 2015
58
8

Hereditary Ataxias in Cuba: A Nationwide Epidemiological and Clinical Study in 1001 Patients.
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,[...]. Cerebellum 2020
9
55

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

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
6

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
100
4

Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
Stefan-M Pulst, Nieves Santos, Dai Wang, Huiying Yang, Duong Huynh, Luis Velazquez, K Pattie Figueroa. Brain 2005
92
4


Riluzole in cerebellar ataxia: a randomized, double-blind, placebo-controlled pilot trial.
G Ristori, S Romano, A Visconti, S Cannoni, M Spadaro, M Frontali, F E Pontieri, N Vanacore, M Salvetti. Neurology 2010
100
4

[Effects of a physical training program on quantitative neurological indices in mild stage type 2 spinocerebelar ataxia patients].
I Pérez-Avila, J A Fernández-Vieitez, E Martínez-Góngora, R Ochoa-Mastrapa, M G Velázquez-Manresa. Rev Neurol 2004
17
23

Double-blind crossover trial of trimethoprim-sulfamethoxazole in spinocerebellar ataxia type 3/Machado-Joseph disease.
T Schulte, R Mattern, K Berger, S Szymanski, P Klotz, P H Kraus, H Przuntek, L Schöls. Arch Neurol 2001
30
13

Gray matter volume deficits in spinocerebellar ataxia: an optimized voxel based morphometric study.
Gaurav Goel, Pramod Kumar Pal, Shivashankar Ravishankar, Ganesan Venkatasubramanian, Peruvumba N Jayakumar, Nithin Krishna, Meera Purushottam, Jitender Saini, Mohammed Faruq, Mitali Mukherji,[...]. Parkinsonism Relat Disord 2011
44
9

Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights.
U Rüb, K Bürk, D Timmann, W den Dunnen, K Seidel, K Farrag, E Brunt, H Heinsen, R Egensperger, A Bornemann,[...]. Neuropathol Appl Neurobiol 2012
35
11

Heart rate variability in type 2 spinocerebellar ataxia.
J Montes-Brown, G Sánchez-Cruz, A M García, M E Báez, L Velázquez-Pérez. Acta Neurol Scand 2010
14
28

Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: confirmation of 14q CAG expansion.
P J Tuite, E A Rogaeva, P H St George-Hyslop, A E Lang. Ann Neurol 1995
79
5

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
155
4

Prevalence and ethnic differences of autosomal-dominant cerebellar ataxia in Singapore.
Y Zhao, E K Tan, H Y Law, C S Yoon, M C Wong, I Ng. Clin Genet 2002
35
11

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
192
4

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
8


Usefulness of the Scale for Assessment and Rating of Ataxia (SARA).
Ichiro Yabe, Masaaki Matsushima, Hiroyuki Soma, Rehana Basri, Hidenao Sasaki. J Neurol Sci 2008
64
6

Widespread neuronal damage and cognitive dysfunction in spinocerebellar ataxia type 3.
Tátila Martins Lopes, Anelyssa D'Abreu, Marcondes Cavalcante França, Clarissa Lin Yasuda, Luiz Eduardo Betting, Adriana Bastos Samara, Gabriela Castellano, Júlio César Somazz, Marcio Luiz Figueredo Balthazar, Iscia Lopes-Cendes,[...]. J Neurol 2013
35
11




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.