# Henry Houlden

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/henry-houlden/

## Facts

| Field | Value |
| --- | --- |
| Citations | 66,869 |
| Field | Genetic Neurodegenerative Diseases |
| h-index | 121 |
| i10-index | 702 |
| Last Known Institution | Queen Mary University of London |
| OpenAlex ID | https://openalex.org/A5082436384 |
| ORCID iD | https://orcid.org/0000-0002-2866-7777 |
| Works | 1,499 |

## Researcher papers

- [Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease](https://scholariq.org/papers/large-scale-meta-analysis-of-genome-wide-association-data-identifies-six-new/)
- [A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N–terminus of β–amyloid](https://scholariq.org/papers/a-pathogenic-mutation-for-probable-alzheimer-s-disease-in-the-app-gene-at-the-n/)
- [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/)
- [Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions](https://scholariq.org/papers/mutations-in-the-gene-prrt2-cause-paroxysmal-kinesigenic-dyskinesia-with/)
- [Germline selection shapes human mitochondrial DNA diversity](https://scholariq.org/papers/germline-selection-shapes-human-mitochondrial-dna-diversity/)
- [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/)
- [Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes](https://scholariq.org/papers/biallelic-mutations-in-sord-cause-a-common-and-potentially-treatable-hereditary/)
- [Pathogenic VCP Mutations Induce Mitochondrial Uncoupling and Reduced ATP Levels](https://scholariq.org/papers/pathogenic-vcp-mutations-induce-mitochondrial-uncoupling-and-reduced-atp-levels/)

## Researcher topics

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

## Researcher university

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

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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.