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Author Details

Amélie Bonnefond
2008
157
43
PMIDPaper TitleJournal TitlePublished Year
36980212Knocking Down in 3D hiPSC-Derived Brown Adipose Progenitors Potentiates Differentiation, Oxidative Metabolism and Browning Process.2023
36435839Women in diabetes research: we can do better.Diabetologia2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37659411High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor.2023
37587118Heimdall, an alternative protein issued from a ncRNA related to kappa light chain variable region of immunoglobulins from astrocytes: a new player in neural proteome.2023
37638789Identification of myokines susceptible to improve glucose homeostasis after bariatric surgery.2023
37978231Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. study.2023
37709961Human GLP1R variants affecting GLP1R cell surface expression are associated with impaired glucose control and increased adiposity.Nat Metab2023
37216637β-Cell-Specific E2f1 Deficiency Impairs Glucose Homeostasis, β-Cell Identity, and Insulin Secretion.2023
37092539Heterozygous pathogenic variants in POMC are not responsible for monogenic obesity: Implication for MC4R agonist use.2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37083980Biallelic Mutations in P4HTM Cause Syndromic Obesity.2023
36894549Monogenic diabetes.2023
36822744Contribution of heterozygous PCSK1 variants to obesity and implications for precision medicine: a case-control study.2023
37015912Astrocytes express aberrant immunoglobulins as putative gatekeeper of astrocytes to neuronal progenitor conversion.2023
36866041Employing non-targeted interactomics approach and subcellular fractionation to increase our understanding of the ghost proteome.2023
36922513A rare human variant that disrupts GPR10 signalling causes weight gain in mice.2023
37039251Control of human pancreatic beta cell kinome by glucagon-like peptide-1 receptor biased agonism.2023
37038246Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.Eur Heart J2023
37502937Multiple genetic variants at the locus affect local super-enhancer activity and influence pancreatic β-cell survival and function.2023
37496675Pharmacological HDAC inhibition impairs pancreatic β-cell function through an epigenome-wide reprogramming.2023
37494602Bidirectional Mendelian Randomization and Multiphenotype GWAS Show Causality and Shared Pathophysiology Between Depression and Type 2 Diabetes.2023
37161092Abdominal obesity is a more important causal risk factor for pancreatic cancer than overall obesity.2023
35053407Glucose Regulates mA Methylation of RNA in Pancreatic Islets.Cells2022
35846981Structural Elements Directing G Proteins and β-Arrestin Interactions with the Human Melatonin Type 2 Receptor Revealed by Natural Variants.ACS Pharmacol Transl Sci2022
35947949The transcription factor E2F1 controls the GLP-1 receptor pathway in pancreatic β cells.Cell Reports2022
35806330Epigenetic and Transcriptomic Programming of HSC Quiescence Signaling in Large for Gestational Age Neonates.International Journal of Molecular Sciences2022
35624321Management of pregnancy in a patient with congenital hyperinsulinism treated with association of diazoxide/calcium channel blocker.Acta Diabetologica2022
35427775Epigenetic changes associated with hyperglycaemia exposure in the longitudinal D.E.S.I.R. cohort.2022
35618782Achievements, prospects and challenges in precision care for monogenic insulin-deficient and insulin-resistant diabetes.Diabetologia2022
36536131The discovery of human agouti-induced obesity and its implication for genetic diagnosis.2022
35227307Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis.Orphanet Journal of Rare Diseases2022
34718610Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia.J Clin Endocrinol Metab2022
35115415Dominant negative mutation in oxalate transporter associated with enteric hyperoxaluria and nephrolithiasis.Journal of Medical Genetics2022
35106505Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study.Cell Rep Med2022
35104326Maternal Glycemic Dysregulation During Pregnancy and Neonatal Blood DNA Methylation: Meta-analyses of Epigenome-Wide Association Studies.Diabetes Care2022
35061034Rare Variant Analysis of Obesity-Associated Genes in Young Adults With Severe Obesity From a Consanguineous Population of Pakistan.2022
34998435The Alzheimer susceptibility gene BIN1 induces isoform-dependent neurotoxicity through early endosome defects.Acta neuropathologica communications2022
34813929Design of a prospective, longitudinal cohort of people living with type 1 diabetes exploring factors associated with the residual cardiovascular risk and other diabetes-related complications: The SFDT1 study.2022
35220425Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.Hum Mol Genet2022
34661078Identification of Key Regions Mediating Human Melatonin Type 1 Receptor Functional Selectivity Revealed by Natural Variants.ACS Pharmacol Transl Sci2021
32189007The Map3k12 (Dlk)/JNK3 signaling pathway is required for pancreatic beta-cell proliferation during postnatal development.Cellular and Molecular Life Sciences2021
34180815[Metabolic syndrome: Towards cell therapy by using CRISPR/Cas9-engineered human adipocytes].Medecine/Sciences2021
34116986Epigenome-Wide Association Study Reveals Methylation Loci Associated With Offspring Gestational Diabetes Mellitus Exposure and Maternal Methylome.Diabetes Care2021
33526906Clustering for a better prediction of type 2 diabetes mellitus.Nature Reviews Endocrinology2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
33242514Monogenic diabetes characteristics in a transnational multicenter study from Mediterranean countries.Diabetes Research and Clinical Practice2021
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
31388097The expression of genes in top obesity-associated loci is enriched in insula and substantia nigra brain regions involved in addiction and reward.International Journal of Obesity2020
32430408Combined RNAseq and ChIPseq Analyses of the BvgA Virulence Regulator of Bordetella pertussis.mSystems2020
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