# Amélie Bonnefond

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/amelie-bonnefond/

## Facts

| Field | Value |
| --- | --- |
| Citations | 17,645 |
| Field | Pancreatic function and diabetes |
| h-index | 61 |
| i10-index | 154 |
| Last Known Institution | Centre National de la Recherche Scientifique |
| OpenAlex ID | https://openalex.org/A5025636710 |
| ORCID iD | https://orcid.org/0000-0001-9976-3005 |
| Works | 361 |

## Researcher papers

- [New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk](https://scholariq.org/papers/new-genetic-loci-implicated-in-fasting-glucose-homeostasis-and-their-impact-on/)
- [The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study](https://scholariq.org/papers/the-influence-of-age-and-sex-on-genetic-associations-with-adult-body-size-and/)
- [Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human](https://scholariq.org/papers/dysfunction-of-lipid-sensor-gpr120-leads-to-obesity-in-both-mouse-and-human/)
- [Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge](https://scholariq.org/papers/genetic-variation-in-gipr-influences-the-glucose-and-insulin-responses-to-an/)
- [A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk](https://scholariq.org/papers/a-variant-near-mtnr1b-is-associated-with-increased-fasting-plasma-glucose-levels/)
- [Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis](https://scholariq.org/papers/impact-of-common-genetic-determinants-of-hemoglobin-a1c-on-type-2-diabetes-risk/)
- [Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes](https://scholariq.org/papers/rare-mtnr1b-variants-impairing-melatonin-receptor-1b-function-contribute-to-type/)
- [KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron](https://scholariq.org/papers/klhl3-mutations-cause-familial-hyperkalemic-hypertension-by-impairing-ion/)
- [New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk](https://scholariq.org/papers/new-loci-for-body-fat-percentage-reveal-link-between-adiposity-and/)
- [Low copy number of the salivary amylase gene predisposes to obesity](https://scholariq.org/papers/low-copy-number-of-the-salivary-amylase-gene-predisposes-to-obesity/)
- [Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis](https://scholariq.org/papers/identification-of-novel-risk-loci-for-restless-legs-syndrome-in-genome-wide/)

## Researcher topics

- [Pancreatic function and diabetes](https://scholariq.org/topics/pancreatic-function-and-diabetes/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Diabetes and associated disorders](https://scholariq.org/topics/diabetes-and-associated-disorders/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Diabetes Treatment and Management](https://scholariq.org/topics/diabetes-treatment-and-management/)

## Researcher university

- [Centre National de la Recherche Scientifique](https://scholariq.org/institutions/centre-national-de-la-recherche-scientifique/)

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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.