# Nicholas Wood

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/nicholas-wood/

## Facts

| Field | Value |
| --- | --- |
| Citations | 77,504 |
| Field | Earthquake Detection and Analysis |
| h-index | 132 |
| i10-index | 579 |
| Last Known Institution | The University of Sydney |
| OpenAlex ID | https://openalex.org/A5064529704 |
| ORCID iD | https://orcid.org/0000-0002-9500-3348 |
| Works | 11,007 |

## Researcher papers

- [Second consensus statement on the diagnosis of multiple system atrophy](https://scholariq.org/papers/second-consensus-statement-on-the-diagnosis-of-multiple-system-atrophy/)
- [Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies](https://scholariq.org/papers/identification-of-novel-risk-loci-causal-insights-and-heritable-risk-for/)
- [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/)
- [Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study](https://scholariq.org/papers/phenotype-genotype-and-worldwide-genetic-penetrance-of-lrrk2-associated/)
- [A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1](https://scholariq.org/papers/a-genome-wide-association-study-identifies-new-psoriasis-susceptibility-loci-and/)
- [Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis](https://scholariq.org/papers/genome-wide-association-analyses-identify-new-risk-variants-and-the-genetic/)
- [Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology](https://scholariq.org/papers/common-and-rare-variant-association-analyses-in-amyotrophic-lateral-sclerosis/)
- [Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy](https://scholariq.org/papers/loss-of-vps13c-function-in-autosomal-recessive-parkinsonism-causes-mitochondrial/)
- [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/)
- [Genetic and phenotypic characterization of complex hereditary spastic paraplegia](https://scholariq.org/papers/genetic-and-phenotypic-characterization-of-complex-hereditary-spastic-paraplegia/)
- [Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease](https://scholariq.org/papers/transcriptional-repression-of-p53-by-parkin-and-impairment-by-mutations/)

## Researcher topics

- [Earthquake Detection and Analysis](https://scholariq.org/topics/earthquake-detection-and-analysis/)
- [Seismology and Earthquake Studies](https://scholariq.org/topics/seismology-and-earthquake-studies/)
- [Seismic Waves and Analysis](https://scholariq.org/topics/seismic-waves-and-analysis/)
- [Methane Hydrates and Related Phenomena](https://scholariq.org/topics/methane-hydrates-and-related-phenomena/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)

## 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.