# Timothy M. Frayling

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/timothy-m-frayling/

## Facts

| Field | Value |
| --- | --- |
| Citations | 113,336 |
| Field | Genetic Associations and Epidemiology |
| h-index | 143 |
| i10-index | 395 |
| Last Known Institution | University of Geneva |
| OpenAlex ID | https://openalex.org/A5025710476 |
| ORCID iD | https://orcid.org/0000-0001-8362-2603 |
| Works | 669 |

## Researcher papers

Showing 12 of 13.

- [A Common Variant in the <i>FTO</i> Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity](https://scholariq.org/papers/a-common-variant-in-the-i-fto-i-gene-is-associated-with-body-mass-index-and/)
- [Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression](https://scholariq.org/papers/large-scale-cis-and-trans-eqtl-analyses-identify-thousands-of-genetic-loci-and/)
- [Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps](https://scholariq.org/papers/fine-mapping-type-2-diabetes-loci-to-single-variant-resolution-using-high/)
- [Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes](https://scholariq.org/papers/meta-analysis-of-genome-wide-association-data-and-large-scale-replication/)
- [Systematic identification of trans eQTLs as putative drivers of known disease associations](https://scholariq.org/papers/systematic-identification-of-trans-eqtls-as-putative-drivers-of-known-disease/)
- [Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility](https://scholariq.org/papers/genome-wide-trans-ancestry-meta-analysis-provides-insight-into-the-genetic/)
- [Large-Scale Association Studies of Variants in Genes Encoding the Pancreatic β-Cell KATP Channel Subunits Kir6.2 (<i>KCNJ11</i>) and SUR1 (<i>ABCC8</i>) Confirm That the <i>KCNJ11</i> E23K Variant Is Associated With Type 2 Diabetes](https://scholariq.org/papers/large-scale-association-studies-of-variants-in-genes-encoding-the-pancreatic/)
- [Exome-wide association study of plasma lipids in &gt;300,000 individuals](https://scholariq.org/papers/exome-wide-association-study-of-plasma-lipids-in-and-gt-300-000-individuals/)
- [Estimating sleep parameters using an accelerometer without sleep diary](https://scholariq.org/papers/estimating-sleep-parameters-using-an-accelerometer-without-sleep-diary/)
- [Genetic insights into biological mechanisms governing human ovarian ageing](https://scholariq.org/papers/genetic-insights-into-biological-mechanisms-governing-human-ovarian-ageing/)
- [Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study](https://scholariq.org/papers/association-of-vitamin-d-status-with-arterial-blood-pressure-and-hypertension/)
- [Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes](https://scholariq.org/papers/genetic-evidence-that-raised-sex-hormone-binding-globulin-shbg-levels-reduce-the/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Pancreatic function and diabetes](https://scholariq.org/topics/pancreatic-function-and-diabetes/)
- [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/)
- [Diabetes and associated disorders](https://scholariq.org/topics/diabetes-and-associated-disorders/)

## Researcher university

- [University of Geneva](https://scholariq.org/institutions/university-of-geneva/)

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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.