# Nigel Williams

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/nigel-williams/

## Facts

| Field | Value |
| --- | --- |
| Citations | 42,262 |
| Field | Genetic Associations and Epidemiology |
| h-index | 87 |
| i10-index | 244 |
| Last Known Institution | Cardiff University |
| OpenAlex ID | https://openalex.org/A5073614894 |
| ORCID iD | https://orcid.org/0000-0003-1177-6931 |
| Works | 629 |

## 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/)
- [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/)
- [Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis](https://scholariq.org/papers/rare-chromosomal-deletions-and-duplications-in-attention-deficit-hyperactivity/)
- [Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder](https://scholariq.org/papers/meta-analysis-of-genome-wide-association-studies-of-attention-deficit/)
- [Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3](https://scholariq.org/papers/genome-wide-analysis-of-copy-number-variants-in-attention-deficit-hyperactivity/)
- [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/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

## Researcher university

- [Cardiff University](https://scholariq.org/institutions/cardiff-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.