# Kathleen Stirrups

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/kathleen-stirrups/

## Facts

| Field | Value |
| --- | --- |
| Citations | 45,231 |
| Field | Genetic Associations and Epidemiology |
| h-index | 70 |
| i10-index | 115 |
| Last Known Institution | University of Cambridge |
| OpenAlex ID | https://openalex.org/A5054422460 |
| ORCID iD | https://orcid.org/0000-0002-6823-3252 |
| Works | 175 |

## Researcher papers

- [Discovery and refinement of loci associated with lipid levels](https://scholariq.org/papers/discovery-and-refinement-of-loci-associated-with-lipid-levels/)
- [A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease](https://scholariq.org/papers/a-comprehensive-1000-genomes-based-genome-wide-association-meta-analysis-of/)
- [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/)
- [Rare and low-frequency coding variants alter human adult height](https://scholariq.org/papers/rare-and-low-frequency-coding-variants-alter-human-adult-height/)
- [Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease](https://scholariq.org/papers/comprehensive-rare-variant-analysis-via-whole-genome-sequencing-to-determine-the/)
- [Germline selection shapes human mitochondrial DNA diversity](https://scholariq.org/papers/germline-selection-shapes-human-mitochondrial-dna-diversity/)
- [Whole-genome sequencing of a sporadic primary immunodeficiency cohort](https://scholariq.org/papers/whole-genome-sequencing-of-a-sporadic-primary-immunodeficiency-cohort/)
- [Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci](https://scholariq.org/papers/meta-analysis-of-genome-wide-association-studies-for-abdominal-aortic-aneurysm/)
- [Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension](https://scholariq.org/papers/phenotypic-characterization-of-i-eif2ak4-i-mutation-carriers-in-a-large-cohort/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [SARS-CoV-2 and COVID-19 Research](https://scholariq.org/topics/sars-cov-2-and-covid-19-research/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Nutrition, Genetics, and Disease](https://scholariq.org/topics/nutrition-genetics-and-disease/)
- [Genetic Mapping and Diversity in Plants and Animals](https://scholariq.org/topics/genetic-mapping-and-diversity-in-plants-and-animals/)

## Researcher university

- [University of Cambridge](https://scholariq.org/institutions/university-of-cambridge/)

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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.