# Alexandra Dürr

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/alexandra-durr/

## Facts

| Field | Value |
| --- | --- |
| Citations | 59,414 |
| Field | Genetic Neurodegenerative Diseases |
| h-index | 119 |
| i10-index | 489 |
| Last Known Institution | Centre National de la Recherche Scientifique |
| OpenAlex ID | https://openalex.org/A5027293126 |
| ORCID iD | https://orcid.org/0000-0002-8921-7104 |
| Works | 855 |

## Researcher papers

Showing 12 of 15.

- [Second consensus statement on the diagnosis of multiple system atrophy](https://scholariq.org/papers/second-consensus-statement-on-the-diagnosis-of-multiple-system-atrophy/)
- [Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease](https://scholariq.org/papers/multicenter-analysis-of-glucocerebrosidase-mutations-in-parkinson-s-disease/)
- [Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis](https://scholariq.org/papers/genome-wide-association-analyses-identify-new-risk-variants-and-the-genetic/)
- [Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease](https://scholariq.org/papers/excessive-burden-of-lysosomal-storage-disorder-gene-variants-in-parkinson-s/)
- [Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy](https://scholariq.org/papers/loss-of-vps13c-function-in-autosomal-recessive-parkinsonism-causes-mitochondrial/)
- [CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion](https://scholariq.org/papers/cag-repeat-expansion-in-huntington-disease-determines-age-at-onset-in-a-fully/)
- [Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease](https://scholariq.org/papers/unbiased-screen-for-interactors-of-leucine-rich-repeat-kinase-2-supports-a/)
- [Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study](https://scholariq.org/papers/long-term-disease-progression-in-spinocerebellar-ataxia-types-1-2-3-and-6-a/)
- [Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients](https://scholariq.org/papers/ataxia-with-oculomotor-apraxia-type-2-clinical-biological-and-genotype-phenotype/)
- [Levodopa-responsive dystonia](https://scholariq.org/papers/levodopa-responsive-dystonia/)
- [Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6](https://scholariq.org/papers/visualization-quantification-and-correlation-of-brain-atrophy-with-clinical/)
- [MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1](https://scholariq.org/papers/msh3-modifies-somatic-instability-and-disease-severity-in-huntington-s-and/)

## Researcher topics

- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)

## Researcher university

- [Centre National de la Recherche Scientifique](https://scholariq.org/institutions/centre-national-de-la-recherche-scientifique/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.