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: 41

Alexandra Durr. Lancet Neurol 2010
Times Cited: 395

List of shared articles

Times cited

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

Hereditary ataxias: overview.
Suman Jayadev, Thomas D Bird. Genet Med 2013

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

SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series.
Akhilesh K Sonakar, Uzma Shamim, Mv Padma Srivastava, Mohd Faruq, Achal K Srivastava. Parkinsonism Relat Disord 2021

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

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

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