Amélie Bonnefond - Concepedia

Author

Amélie Bonnefond

Centre National de la Recherche Scientifique ORCID

Also Known As

A Bonnefond, A. Bonnefond, AMELIE BONNEFOND, Amelie BONNEFOND, Amelie Bonnefond, Amélie Bonnefond, Amélie Bonnefond (179465), Andrew R. Wood, Bonnefond A, Bonnefond Amelie

354

Publications

16.9K

Citations

H-Index

111

Concepts

All Affiliations

Centre National de la Recherche Scientifique Institut Pasteur de Lille Inserm Université de Lille Imperial College London

About

Amélie Bonnefond is an author at Centre National de la Recherche Scientifique specializing in medicine, metabolic syndrome, and diabetes.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	38	3.8K
2	Public Health	10	10	500
3	Health Sciences	7	7	1.1K
4	Natural Sciences	2	2	232
5	Engineering	1	1	16

Amélie Bonnefond

105

Publications

7.8K

Citations

H-Index

Page 1

	Year	Citations
Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human Atsuhiko Ichimura, Akira Hirasawa, Odile Poulain‐Godefroy, Nature ObesityMetabolic SyndromeEnergy HomeostasisPhysiologyDiabetes	2012	654
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk Nabila Bouatia‐Naji, Amélie Bonnefond, Christine Cavalcanti-Proença, Nature Genetics Metabolic SyndromePlasma Glucose LevelsDiabetes EpidemiologyMetabolic DisorderDiabetes Risk	2008	607
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits Joshua C. Randall, Thomas W. Winkler, Zoltán Kutalik, PLoS Genetics	2013	451
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study Amand F. Schmidt, Daniel I. Swerdlow, Michael V. Holmes, The Lancet Diabetes & Endocrinology	2016	380
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes Amélie Bonnefond, Nathalie Clément, Katherine A. Fawcett, Nature Genetics Metabolic SyndromeSleepRare Mtnr1b VariantsMedicineDiabetes	2012	361
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron Hélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano, Nature Genetics Ion TransportHypertonicityUrologyHypertensionMolecular Physiology	2012	330
Low copy number of the salivary amylase gene predisposes to obesity Mario Falchi, Julia S. El-Sayed Moustafa, Petros Takousis, Nature Genetics ObesityMetabolic SyndromeBiologyEnergy HomeostasisAppetite Control	2014	258
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis Pierre‐Antoine Juge, Raphaël Borie, Caroline Kannengiesser, European Respiratory Journal	2017	225
Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene Amélie Bonnefond, Julien Philippe, Emmanuelle Durand, PLoS ONE	2012	203
Insulin Gene Mutations Resulting in Early-Onset Diabetes: Marked Differences in Clinical Presentation, Metabolic Status, and Pathogenic Effect Through Endoplasmic Reticulum Retention Gargi Meur, Albane Simon, Nasret Harun, Diabetes	2009	150

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