# Garth A. Nicholson

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/garth-a-nicholson/

## Facts

| Field | Value |
| --- | --- |
| Citations | 25,801 |
| Field | Hereditary Neurological Disorders |
| h-index | 79 |
| i10-index | 233 |
| Last Known Institution | The University of Sydney |
| OpenAlex ID | https://openalex.org/A5077466041 |
| ORCID iD | https://orcid.org/0000-0001-9694-066X |
| Works | 401 |

## Researcher papers

- [Controversies and priorities in amyotrophic lateral sclerosis](https://scholariq.org/papers/controversies-and-priorities-in-amyotrophic-lateral-sclerosis/)
- [Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis](https://scholariq.org/papers/cortical-hyperexcitability-may-precede-the-onset-of-familial-amyotrophic-lateral/)
- [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/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)
- [CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia](https://scholariq.org/papers/ccnf-mutations-in-amyotrophic-lateral-sclerosis-and-frontotemporal-dementia/)
- [Compound Heterozygosity for Loss-of-Function Lysyl-tRNA Synthetase Mutations in a Patient with Peripheral Neuropathy](https://scholariq.org/papers/compound-heterozygosity-for-loss-of-function-lysyl-trna-synthetase-mutations-in/)
- [Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy](https://scholariq.org/papers/use-of-whole-exome-sequencing-for-diagnosis-of-limb-girdle-muscular-dystrophy/)

## Researcher topics

- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)

## Researcher university

- [The University of Sydney](https://scholariq.org/institutions/the-university-of-sydney/)

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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.