# Sarah Hunt

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/sarah-hunt/

## Facts

| Field | Value |
| --- | --- |
| Citations | 117,130 |
| Field | Genetic Associations and Epidemiology |
| h-index | 98 |
| i10-index | 171 |
| Last Known Institution | European Bioinformatics Institute |
| OpenAlex ID | https://openalex.org/A5044085246 |
| ORCID iD | https://orcid.org/0000-0002-8350-1235 |
| Works | 245 |

## Researcher papers

Showing 12 of 16.

- [A global reference for human genetic variation](https://scholariq.org/papers/a-global-reference-for-human-genetic-variation/)
- [The International HapMap Project](https://scholariq.org/papers/the-international-hapmap-project/)
- [Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes](https://scholariq.org/papers/large-scale-association-analysis-provides-insights-into-the-genetic-architecture/)
- [Large-scale association analysis identifies new risk loci for coronary artery disease](https://scholariq.org/papers/large-scale-association-analysis-identifies-new-risk-loci-for-coronary-artery/)
- [Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis](https://scholariq.org/papers/analysis-of-immune-related-loci-identifies-48-new-susceptibility-variants-for/)
- [Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants](https://scholariq.org/papers/association-scan-of-14-500-nonsynonymous-snps-in-four-diseases-identifies/)
- [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/)
- [Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease](https://scholariq.org/papers/dense-genotyping-identifies-and-localizes-multiple-common-and-rare-variant/)
- [Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls](https://scholariq.org/papers/genome-wide-association-study-of-cnvs-in-16-000-cases-of-eight-common-diseases/)
- [Variants in MTNR1B influence fasting glucose levels](https://scholariq.org/papers/variants-in-mtnr1b-influence-fasting-glucose-levels/)
- [A global reference for human genetic variation](https://scholariq.org/papers/a-global-reference-for-human-genetic-variation-2/)
- [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/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomics and Phylogenetic Studies](https://scholariq.org/topics/genomics-and-phylogenetic-studies/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Chromosomal and Genetic Variations](https://scholariq.org/topics/chromosomal-and-genetic-variations/)

## Researcher university

- [European Bioinformatics Institute](https://scholariq.org/institutions/european-bioinformatics-institute/)

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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.