A citation-based method for searching scientific literature

Christoph Globas, Sophie Tezenas du Montcel, Laslo Baliko, Syliva Boesch, Chantal Depondt, Stefano DiDonato, Alexandra Durr, Alessandro Filla, Thomas Klockgether, Caterina Mariotti, Bela Melegh, Maryla Rakowicz, Pascale Ribai, Rafal Rola, Tanja Schmitz-Hubsch, Sandra Szymanski, Dagmar Timmann, Bart P Van de Warrenburg, Peter Bauer, Ludger Schols. Mov Disord 2008
Times Cited: 73



Alexandra Durr. Lancet Neurol 2010
Times Cited: 377




List of shared articles



Times cited

[The presymptomatic stage of neurodegenerative disorders].
C Klein, J Hagenah, B Landwehrmeyer, T Münte, T Klockgether. Nervenarzt 2011
8

Genetics of the dominant ataxias.
Dineke S Verbeek, Bart P C van de Warrenburg. Semin Neurol 2011
21

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
106

Autosomal dominant cerebellar ataxias.
C Marelli, C Cazeneuve, A Brice, G Stevanin, A Dürr. Rev Neurol (Paris) 2011
7

Spinocerebellar Ataxia Tethering PCR: A Rapid Genetic Test for the Diagnosis of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 by PCR and Capillary Electrophoresis.
Claudia Cagnoli, Alessandro Brussino, Cecilia Mancini, Marina Ferrone, Laura Orsi, Paola Salmin, Patrizia Pappi, Elisa Giorgio, Elisa Pozzi, Simona Cavalieri,[...]. J Mol Diagn 2018
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

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

Oculomotor deficits in spinocerebellar ataxia type 3: Potential biomarkers of preclinical detection and disease progression.
Chao Wu, Ding-Bang Chen, Li Feng, Xiang-Xue Zhou, Ji-Wei Zhang, Hua-Jing You, Xiu-Ling Liang, Zhong Pei, Xun-Hua Li. CNS Neurosci Ther 2017
22

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

The influence of initial symptoms on phenotypes in spinocerebellar ataxia type 3.
Hao-Ling Xu, Qiu-Ni Su, Xian-Jin Shang, Arif Sikandar, Min-Ting Lin, Ning Wang, Hong Lin, Shi-Rui Gan. Mol Genet Genomic Med 2019
4

Retinal Nerve Fibre Layer and Macular Thinning in Spinocerebellar Ataxia and Cerebellar Multisystem Atrophy.
John H Pula, Vernon L Towle, Victoria M Staszak, Dingcai Cao, Jacqueline T Bernard, Christopher M Gomez. Neuroophthalmology 2011
40

(CAG)n loci as genetic modifiers of age at onset in patients with spinocerebellar ataxia type 1 from mainland China.
P Wang, Z Chen, Y Peng, L Cao, X Li, C Wang, H Yang, H Peng, Y Shi, X Zhou,[...]. Eur J Neurol 2019
5


The impact of histone post-translational modifications in neurodegenerative diseases.
Samantha N Cobos, Seth A Bennett, Mariana P Torrente. Biochim Biophys Acta Mol Basis Dis 2019
15

Speech in spinocerebellar ataxia.
Ellika Schalling, Lena Hartelius. Brain Lang 2013
12

Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38).
Barbara Borroni, Eleonora Di Gregorio, Laura Orsi, Giovanna Vaula, Chiara Costanzi, Filippo Tempia, Nico Mitro, Donatella Caruso, Marta Manes, Lorenzo Pinessi,[...]. Parkinsonism Relat Disord 2016
13

RNA therapy for polyglutamine neurodegenerative diseases.
Lauren M Watson, Matthew J A Wood. Expert Rev Mol Med 2012
10

Uses of the postural stability test for differential diagnosis of hereditary ataxias.
J Schwabova, F Zahalka, V Komarek, T Maly, P Hrasky, T Gryc, O Cakrt, A Zumrova. J Neurol Sci 2012
6

Polyglutamine spinocerebellar ataxias - from genes to potential treatments.
Henry L Paulson, Vikram G Shakkottai, H Brent Clark, Harry T Orr. Nat Rev Neurosci 2017
131

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
93

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
71

Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Sandro Romanzetti, Florian Harmuth, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Grzegorz Makowicz, Alexandra Durr, Marie-Lorraine Monin,[...]. Lancet Neurol 2020
7