A citation-based method for searching scientific literature

Sophie Tezenas du Montcel, Perrine Charles, Cyril Goizet, Cecilia Marelli, Pascale Ribai, Carlo Vincitorio, Mathieu Anheim, Lucie Guyant-Maréchal, Alice Le Bayon, Nadia Vandenberghe, Maya Tchikviladzé, David Devos, Isabelle Le Ber, Karine N'Guyen, Cécile Cazeneuve, Chantal Tallaksen, Alexis Brice, Alexandra Durr. Arch Neurol 2012
Times Cited: 40







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



Times Cited
  Times     Co-cited
Similarity


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
57

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
133
55

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
126
52

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
115
40

Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.
Tetsuo Ashizawa, Karla P Figueroa, Susan L Perlman, Christopher M Gomez, George R Wilmot, Jeremy D Schmahmann, Sarah H Ying, Theresa A Zesiewicz, Henry L Paulson, Vikram G Shakkottai,[...]. Orphanet J Rare Dis 2013
78
40

Responsiveness of different rating instruments in spinocerebellar ataxia patients.
T Schmitz-Hübsch, R Fimmers, M Rakowicz, R Rola, E Zdzienicka, R Fancellu, C Mariotti, C Linnemann, L Schöls, D Timmann,[...]. Neurology 2010
97
35

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
37

Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment.
Sophie Tezenas du Montcel, Perrine Charles, Pascale Ribai, Cyril Goizet, Alice Le Bayon, Pierre Labauge, Lucie Guyant-Maréchal, Sylvie Forlani, Celine Jauffret, Nadia Vandenberghe,[...]. Brain 2008
60
30

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
43
30

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
45
30

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
174
27

SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.
T Schmitz-Hübsch, P Giunti, D A Stephenson, C Globas, L Baliko, F Saccà, C Mariotti, M Rakowicz, S Szymanski, J Infante,[...]. Neurology 2008
88
27

Ataxia rating scales--psychometric profiles, natural history and their application in clinical trials.
Jonas Alex Morales Saute, Karina Carvalho Donis, Carmen Serrano-Munuera, David Genis, Luís Torres Ramirez, Pilar Mazzetti, Luis Velázquez Pérez, Pilar Latorre, Jorge Sequeiros, Antoni Matilla-Dueñas,[...]. Cerebellum 2012
75
27

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
58
27

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology.
P Trouillas, T Takayanagi, M Hallett, R D Currier, S H Subramony, K Wessel, A Bryer, H C Diener, S Massaquoi, C M Gomez,[...]. J Neurol Sci 1997
908
25

Progression of brain atrophy in spinocerebellar ataxia type 2: a longitudinal tensor-based morphometry study.
Mario Mascalchi, Stefano Diciotti, Marco Giannelli, Andrea Ginestroni, Andrea Soricelli, Emanuele Nicolai, Marco Aiello, Carlo Tessa, Lucia Galli, Maria Teresa Dotti,[...]. PLoS One 2014
32
31

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
Kathrin Reetz, Ana S Costa, Shahram Mirzazade, Anna Lehmann, Agnes Juzek, Maria Rakowicz, Romana Boguslawska, Ludger Schöls, Christoph Linnemann, Caterina Mariotti,[...]. Brain 2013
86
22

Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias.
Ellis Chan, Perrine Charles, Pascale Ribai, Cyril Goizet, Cecilia Marelli, Carlo-Maria Vincitorio, Alice Le Bayon, Lucie Guyant-Maréchal, Nadia Vandenberghe, Mathieu Anheim,[...]. Mov Disord 2011
21
42

Progression of ataxia in patients with Machado-Joseph disease.
Marcondes C França, Anelyssa D'Abreu, Anamarli Nucci, Fernando Cendes, Iscia Lopes-Cendes. Mov Disord 2009
30
30

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
22

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
230
20

Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial.
Silvia Romano, Giulia Coarelli, Christian Marcotulli, Luca Leonardi, Francesca Piccolo, Maria Spadaro, Marina Frontali, Michela Ferraldeschi, Maria Chiara Vulpiani, Federica Ponzelli,[...]. Lancet Neurol 2015
108
20

Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument.
H Jacobi, M Rakowicz, R Rola, R Fancellu, C Mariotti, P Charles, A Dürr, M Küper, D Timmann, C Linnemann,[...]. Cerebellum 2013
68
20


Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.
Kathrin Reetz, Imis Dogan, Ana S Costa, Manuel Dafotakis, Kathrin Fedosov, Paola Giunti, Michael H Parkinson, Mary G Sweeney, Caterina Mariotti, Marta Panzeri,[...]. Lancet Neurol 2015
105
17

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, Tanja Schmitz-Hübsch, Maryla Rakowicz, Caterina Mariotti, Ludger Schöls, Dagmar Timmann, Bart van de Warrenburg, Alexandra Dürr,[...]. Neuroimage 2010
115
17

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
59
17

A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.
Kenichi Yasui, Ichiro Yabe, Kunihiro Yoshida, Kazuaki Kanai, Kimihito Arai, Mizuki Ito, Osamu Onodera, Shigeru Koyano, Eiji Isozaki, Setsu Sawai,[...]. Orphanet J Rare Dis 2014
24
29

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
672
15

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
45
15

Brain structural damage in spinocerebellar ataxia type 2. A voxel-based morphometry study.
Riccardo Della Nave, Andrea Ginestroni, Carlo Tessa, Mirco Cosottini, Marco Giannelli, Elena Salvatore, Ferdinando Sartucci, Giuseppe De Michele, Maria Teresa Dotti, Silvia Piacentini,[...]. Mov Disord 2008
37
16

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
57
15

Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients.
Federico D'Agata, Paola Caroppo, Andrea Boghi, Mario Coriasco, Marcella Caglio, Bruno Baudino, Katiuscia Sacco, Franco Cauda, Elisabetta Geda, Mauro Bergui,[...]. Brain Struct Funct 2011
33
18

Parahippocampal gray matter alterations in Spinocerebellar Ataxia Type 2 identified by voxel based morphometry.
Roberto E Mercadillo, Víctor Galvez, Rosalinda Díaz, Carlos Roberto Hernández-Castillo, Aurelio Campos-Romo, Marie-Catherine Boll, Erick H Pasaye, Juan Fernandez-Ruiz. J Neurol Sci 2014
26
23

Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients.
Tanja Schmitz-Hübsch, Sophie Tezenas du Montcel, Laszlo Baliko, Sylvia Boesch, Sara Bonato, Roberto Fancellu, Paola Giunti, Christoph Globas, Jun-Suk Kang, Berry Kremer,[...]. Mov Disord 2006
97
15

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
295
15

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
22
27

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, H Przuntek, J T Epplen, O Riess. Ann Neurol 1997
247
12

Rating disease progression of Friedreich's ataxia by the International Cooperative Ataxia Rating Scale: analysis of a 603-patient database.
Günther Metz, Nicholas Coppard, Jonathon M Cooper, Martin B Delatycki, Alexandra Dürr, Nicholas A Di Prospero, Paola Giunti, David R Lynch, J B Schulz, Christian Rummey,[...]. Brain 2013
35
14

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
12

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
102
12

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
57
12

Spinocerebellar ataxia type 2.
Georg W J Auburger. Handb Clin Neurol 2012
51
12

Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.
L Guerrini, F Lolli, A Ginestroni, G Belli, R Della Nave, C Tessa, S Foresti, M Cosottini, S Piacentini, F Salvi,[...]. Brain 2004
78
12

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
163
12

MRI shows a region-specific pattern of atrophy in spinocerebellar ataxia type 2.
Brian C Jung, Soo I Choi, Annie X Du, Jennifer L Cuzzocreo, Howard S Ying, Bennett A Landman, Susan L Perlman, Robert W Baloh, David S Zee, Arthur W Toga,[...]. Cerebellum 2012
38
13

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
892
12

Executive deficit in spinocerebellar ataxia type 2 is related to expanded CAG repeats: evidence from antisaccadic eye movements.
Roberto Rodríguez-Labrada, Luis Velázquez-Pérez, Raúl Aguilera-Rodríguez, Carola Seifried-Oberschmidt, Arnoy Peña-Acosta, Nalia Canales-Ochoa, Jacqueline Medrano-Montero, Annelié Estupiñan-Rodríguez, Yaimeé Vázquez-Mojena, Yanetza González-Zaldivar,[...]. Brain Cogn 2014
18
27

Cognitive deficits in spinocerebellar ataxia 2.
K Bürk, C Globas, S Bösch, S Gräber, M Abele, A Brice, J Dichgans, I Daum, T Klockgether. Brain 1999
96
12

Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients.
Anja Weyer, Michael Abele, Tanja Schmitz-Hübsch, Beate Schoch, Markus Frings, Dagmar Timmann, Thomas Klockgether. Mov Disord 2007
109
12


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.