# Peter M. Andersen

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/peter-m-andersen/

## Facts

| Field | Value |
| --- | --- |
| Citations | 29,666 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 93 |
| i10-index | 260 |
| Last Known Institution | Umeå University |
| OpenAlex ID | https://openalex.org/A5101406818 |
| ORCID iD | https://orcid.org/0000-0003-0094-5429 |
| Works | 404 |

## Researcher papers

- [EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force](https://scholariq.org/papers/efns-guidelines-on-the-clinical-management-of-amyotrophic-lateral-sclerosis-mals/)
- [VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death](https://scholariq.org/papers/vegf-is-a-modifier-of-amyotrophic-lateral-sclerosis-in-mice-and-humans-and/)
- [Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia](https://scholariq.org/papers/haploinsufficiency-of-tbk1-causes-familial-als-and-fronto-temporal-dementia/)
- [Phase 1–2 Trial of Antisense Oligonucleotide Tofersen for <i>SOD1</i> ALS](https://scholariq.org/papers/phase-1-2-trial-of-antisense-oligonucleotide-tofersen-for-i-sod1-i-als/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)
- [The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder](https://scholariq.org/papers/the-c9orf72-expansion-mutation-is-a-common-cause-of-als-ftd-in-europe-and-has-a/)
- [Hot-spot KIF5A mutations cause familial ALS](https://scholariq.org/papers/hot-spot-kif5a-mutations-cause-familial-als/)
- [Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome](https://scholariq.org/papers/transethnic-genome-wide-association-study-provides-insights-in-the-genetic/)

## Researcher topics

- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)

## Researcher university

- [Umeå University](https://scholariq.org/institutions/umea-university/)

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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.