# Huw R. Morris

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/huw-r-morris/

## Facts

| Field | Value |
| --- | --- |
| Citations | 35,207 |
| Field | Parkinson's Disease Mechanisms and Treatments |
| h-index | 84 |
| i10-index | 285 |
| Last Known Institution | Queen Mary University of London |
| OpenAlex ID | https://openalex.org/A5082416184 |
| ORCID iD | https://orcid.org/0000-0002-5473-3774 |
| Works | 559 |

## Researcher papers

- [A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD](https://scholariq.org/papers/a-hexanucleotide-repeat-expansion-in-c9orf72-is-the-cause-of-chromosome-9p21/)
- [Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria](https://scholariq.org/papers/clinical-diagnosis-of-progressive-supranuclear-palsy-the-movement-disorder/)
- [Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study](https://scholariq.org/papers/frequency-of-the-c9orf72-hexanucleotide-repeat-expansion-in-patients-with/)
- [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/)
- [Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms](https://scholariq.org/papers/parkinson-s-disease-age-at-onset-genome-wide-association-study-defining/)
- [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/)
- [Genetic and phenotypic characterization of complex hereditary spastic paraplegia](https://scholariq.org/papers/genetic-and-phenotypic-characterization-of-complex-hereditary-spastic-paraplegia/)
- [Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome](https://scholariq.org/papers/diagnosis-across-the-spectrum-of-progressive-supranuclear-palsy-and-corticobasal/)
- [Which ante mortem clinical features predict progressive supranuclear palsy pathology?](https://scholariq.org/papers/which-ante-mortem-clinical-features-predict-progressive-supranuclear-palsy/)
- [Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study](https://scholariq.org/papers/identification-of-genetic-risk-loci-and-causal-insights-associated-with/)

## Researcher topics

- [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/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [Queen Mary University of London](https://scholariq.org/institutions/queen-mary-university-of-london/)

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