# Martin R. Turner

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/martin-r-turner/

## Facts

| Field | Value |
| --- | --- |
| Citations | 28,713 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 84 |
| i10-index | 256 |
| Last Known Institution | University of Oxford |
| OpenAlex ID | https://openalex.org/A5045232979 |
| ORCID iD | https://orcid.org/0000-0003-0267-3180 |
| Works | 524 |

## Researcher papers

- [Amyotrophic lateral sclerosis](https://scholariq.org/papers/amyotrophic-lateral-sclerosis/)
- [Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria](https://scholariq.org/papers/amyotrophic-lateral-sclerosis-frontotemporal-spectrum-disorder-als-ftsd-revised/)
- [Diagnostic Value of Cerebrospinal Fluid Neurofilament Light Protein in Neurology](https://scholariq.org/papers/diagnostic-value-of-cerebrospinal-fluid-neurofilament-light-protein-in-neurology/)
- [A proposal for new diagnostic criteria for ALS](https://scholariq.org/papers/a-proposal-for-new-diagnostic-criteria-for-als/)
- [Controversies and priorities in amyotrophic lateral sclerosis](https://scholariq.org/papers/controversies-and-priorities-in-amyotrophic-lateral-sclerosis/)
- [Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model](https://scholariq.org/papers/prognosis-for-patients-with-amyotrophic-lateral-sclerosis-development-and/)
- [Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS](https://scholariq.org/papers/exome-wide-rare-variant-analysis-identifies-tuba4a-mutations-associated-with/)
- [Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry](https://scholariq.org/papers/cerebrospinal-fluid-and-blood-biomarkers-for-neurodegenerative-dementias-an/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)
- [Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-vesicular-trafficking-protein-annexin-a11-are-associated-with/)
- [Primary lateral sclerosis: consensus diagnostic criteria](https://scholariq.org/papers/primary-lateral-sclerosis-consensus-diagnostic-criteria/)

## 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

- [University of Oxford](https://scholariq.org/institutions/university-of-oxford/)

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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.
