Alexandra Dürr

Centre National de la Recherche Scientifique — France

Neuroscience · Life Sciences

119h-index59.1kcitations858works3.62yr avg
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Research Topics

Genetic Neurodegenerative Diseases(538), Mitochondrial Function and Pathology(324), Neurological disorders and treatments(175), Parkinson's Disease Mechanisms and Treatments(151), Neurological diseases and metabolism(134)

Publications843 total

Sequence Variants in Small CAG Repeat Expansions of the <i>HTT</i> Gene and Disease Onset and Progression in Huntington Disease
Neurology·2025· 1 citedOpen Access
Patient-reported, psychosocial and health economic outcomes in mild to moderate Friedreich's ataxia: baseline results of the PROFA study
The Lancet Regional Health - Europe·2025Open Access
Lessons learned from 30 years of presymptomatic testing in Huntington Disease
Revue Neurologique·2025
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3
Brain·2025Open Access
Should ITSN1 be considered as a Mendelian Parkinson’s disease gene? Description of three novel families
npj Parkinson s Disease·2025Open Access
Analysis of a Modified Version of the Inventory of Non‐Ataxia Signs Over 12 Years in Patients with Friedreich's Ataxia in the <scp>EFACTS</scp> Study
Movement Disorders·2025Open Access
Comparison of tetrabenazine, tiapride and olanzapine in Huntington's disease: a one-year French randomized multicenter study (Neuro-HD)
Parkinsonism & Related Disorders·2025Open Access
357PLong-term vatiquinone treatment slows Friedreich’s ataxia disease progression relative to FACOMS natural history
Neuromuscular Disorders·2025
Parkinson’s disease and multiple system atrophy are gateways to <i>RFC1</i> -related disorders
2025Open Access
Characterizing Medication Timelines in Huntington’s Disease: A Cluster-Based Analysis of Treatment Patterns
SPIRE - Sciences Po Institutional REpository·2025
A founder variant in TBCB is associated with global developmental delay, autism spectrum, and spastic paraparesis
Genetics in Medicine·2025
Spastic Ataxia Composite ( <scp>SPAXCOM</scp> ): A Scale to Evaluate the Progression of Subjects with Spasticity and Ataxia
Movement Disorders·2025· 1 citedOpen Access
Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias
Neurology·2025· 2 citedOpen Access
A Core Pattern of Cerebellar and Brainstem Degeneration and Reduced Cerebrocerebellar Structural Covariance in Spinocerebellar Ataxia Type 3 (SCA3): MRI Volumetrics from ENIGMA-Ataxia
2025Open Access
The Two Faces of Pediatric <scp>SCA2</scp>
European Journal of Neurology·2025· 1 citedOpen Access
SPG11 models reveal lysosomal calcium as a regulator of neural progenitor proliferation
2025Open Access
Fixel‐Based Analysis of Diffusion Imaging as a Quantitative Marker of Disease State in Spinocerebellar Ataxia
Annals of Clinical and Translational Neurology·2025· 1 citedOpen Access
Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series
Journal of Neurology·2025· 2 cited
Cell-specific mechanisms drive connectivity across the time course of Huntington’s disease
Nature Communications·2025· 4 citedOpen Access
Neuropathy in <scp>GAA</scp>‐<scp>FGF14</scp> Late‐Onset Cerebellar Ataxia (<scp>SCA27B</scp>): Prevalence and Characteristics
European Journal of Neurology·2025· 5 citedOpen Access
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Frequent Co-authors

Alexis Brice(32), Giovanni Stévanin(14), Yves Agid(11), Suzanne Lesage(11), Nicholas Wood(9), Marie Vidailhet(9), Lüdger Schöls(8), Ebba Lohmann(8), Paola Giunti(7), Pierre Pollak(7), Sarah J. Tabrizi(7), Mathieu Anheim(7), Jean‐Christophe Corvol(7), Thomas Klockgether(6), Thomas Gasser(6), François Tison(6), G. Bernhard Landwehrmeyer(6), Christine Tranchant(6), Joshua Shulman(6), Perrine Charles(6)