# Lüdger Schöls

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/ludger-schols/

## Facts

| Field | Value |
| --- | --- |
| Citations | 37,450 |
| Field | Genetic Neurodegenerative Diseases |
| h-index | 99 |
| i10-index | 427 |
| Last Known Institution | German Center for Neurodegenerative Diseases |
| OpenAlex ID | https://openalex.org/A5076004371 |
| ORCID iD | https://orcid.org/0000-0001-7774-5025 |
| Works | 1,015 |

## Researcher papers

- [Leitlinien für Diagnostik und Therapie in der Neurologie](https://scholariq.org/papers/leitlinien-fur-diagnostik-und-therapie-in-der-neurologie/)
- [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/)
- [A Pan‐<scp>E</scp>uropean Study of the<i>C9orf72</i>Repeat Associated with<scp>FTLD</scp>: Geographic Prevalence, Genomic Instability, and Intermediate Repeats](https://scholariq.org/papers/a-pan-scp-e-scp-uropean-study-of-the-i-c9orf72-i-repeat-associated-with-scp-ftld/)
- [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/)
- [Variant in the sequence of the LINGO1 gene confers risk of essential tremor](https://scholariq.org/papers/variant-in-the-sequence-of-the-lingo1-gene-confers-risk-of-essential-tremor/)
- [Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients](https://scholariq.org/papers/reliability-and-validity-of-the-international-cooperative-ataxia-rating-scale-a/)
- [Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6](https://scholariq.org/papers/early-symptoms-in-spinocerebellar-ataxia-type-1-2-3-and-6/)

## Researcher topics

- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)

## Researcher university

- [German Center for Neurodegenerative Diseases](https://scholariq.org/institutions/german-center-for-neurodegenerative-diseases/)

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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.