Distinct impaired regulation of SOCS3 and long and short isoforms of the leptin receptor in visceral and subcutaneous fat of lean and obese women
Seron, K.
Corset, L.
Vasseur, F.
Boutin, P.
Gomez-Ambrosi, J.
Salvador, J.
Fruhbeck, G.
Froguel, P.
Karin Seron
Seron Karin
ORCID: 0000-0002-9667-133X
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Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults
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Expression and functional assessment of candidate type 2 diabetes susceptibility genes identify four new genes contributing to human insulin secretion.
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Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
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The case for too little melatonin signalling in increased diabetes risk.
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A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk
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Decreased STARD10 Expression Is Associated with Defective Insulin Secretion in Humans and Mice.
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Hepatic DPP4 DNA Methylation Associates With Fatty Liver
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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.
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KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.
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Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
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Detection of human adaptation during the past 2000 years.
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Impact of statistical models on the prediction of type 2 diabetes using non-targeted metabolomics profiling.
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Endoplasmic Reticulum Stress Links Oxidative Stress to Impaired Pancreatic Beta-Cell Function Caused by Human Oxidized LDL.
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The Difficult Journey from Genome-wide Association Studies to Pathophysiology: The Melatonin Receptor 1B (MT2) Paradigm.
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Genomic insights into the origin of farming in the ancient Near East.
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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.
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The genetic architecture of type 2 diabetes.
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Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
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Eating Behavior, Low-Frequency Functional Mutations in the Melanocortin-4 Receptor (MC4R) Gene, and Outcomes of Bariatric Operations: A 6-Year Prospective Study
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Interaction between GPR120 p.R270H loss-of-function variant and dietary fat intake on incident type 2 diabetes risk in the D.E.S.I.R. study.
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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index.
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KAT2B Is Required for Pancreatic Beta Cell Adaptation to Metabolic Stress by Controlling the Unfolded Protein Response
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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
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Induction of TDO2 and IDO2 in Liver by High-Fat Feeding in Mice: Discrepancies with Human Obesity.
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New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
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Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
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Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
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What Is the Best NGS Enrichment Method for the Molecular Diagnosis of Monogenic Diabetes and Obesity?
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The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
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Genetic association analyses highlight biological pathways underlying mitral valve prolapse
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The kynurenine pathway is activated in human obesity and shifted toward kynurenine monooxygenase activation
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Genetic variants in LEP, LEPR, and MC4R explain 30% of severe obesity in children from a consanguineous population
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Directional dominance on stature and cognition in diverse human populations
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A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array
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Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study
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The loss-of-function PCSK9 p.R46L genetic variant does not alter glucose homeostasis
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Contribution of the low-frequency, loss-of-function p.R270H mutation in FFAR4 (GPR120) to increased fasting plasma glucose levels
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Association of gene variants with susceptibility to type 2 diabetes among Omanis
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Genetic studies of body mass index yield new insights for obesity biology
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New genetic loci link adipose and insulin biology to body fat distribution
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Rare and Common Genetic Events in Type 2 Diabetes: What Should Biologists Know?
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Genetic Determinants of Leucocyte Telomere Length in Children: a Neglected and Challenging Field
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Biological interpretation of genome-wide association studies using predicted gene functions
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RFX6 Regulates Insulin Secretion by Modulating Ca2+ Homeostasis in Human beta Cells
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Beneficial effect of a high number of copies of salivary amylase AMY1 gene on obesity risk in Mexican children
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Defining the role of common variation in the genomic and biological architecture of adult human height
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Identification of Two Novel Loss-of-Function SIM1 Mutations in Two Overweight Children with Developmental Delay
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Weight loss independent association of TCF7 L2 gene polymorphism with fasting blood glucose after Roux-en-Y gastric bypass in type 2 diabetic patients
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Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes
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Fine-scale human genetic structure in Western France
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Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index
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Placental antiangiogenic prolactin fragments are increased in human and rat maternal diabetes
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Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR study
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A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity
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Common Genetic Variants and Risk of Brain Injury After Preterm Birth
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Gene-Lifestyle Interaction and Type 2 Diabetes: The EPIC InterAct Case-Cohort Study
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Characterization of human variants in obesity-related SIM1 protein identifies a hot-spot for dimerization with the partner protein ARNT2
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Role of the Unfolded Protein Response in beta Cell Compensation and Failure during Diabetes
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Quality control and conduct of genome-wide association meta-analyses
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Beneficial Metabolic Effects of Rapamycin Are Associated with Enhanced Regulatory Cells in Diet-Induced Obese Mice
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Multi-ethnic fine-mapping of 14 central adiposity loci
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A Central Role for GRB10 in Regulation of Islet Function in Man
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Low copy number of the salivary amylase gene predisposes to obesity
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Comment On: Valette et al. Melanocortin-4 Receptor Mutations and Polymorphisms Do Not Affect Weight Loss after Bariatric Surgery. PLOS ONE 2012; 7(11):E48221
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CDKN2B expression and subcutaneous adipose tissue expandability: Possible influence of the 9p21 atherosclerosis locus
10.1016/j.bbrc.2014.03.075
Role of Ink4a/Arf Locus in Beta Cell Mass Expansion under Physiological and Pathological Conditions
10.1155/2014/873679
Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study
10.1016/S2213-8587(13)70059-7
Pluripotent Stem Cells as a Potential Tool for Disease Modelling and Cell Therapy in Diabetes
10.1007/s12015-014-9503-6
Alternative human liver transcripts of TCF7L2 bind to the gluconeogenesis regulator HNF4 alpha at the protein level
10.1007/s00125-013-3154-z
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
10.1038/ng.2897
Adipose tissue in obesity-related inflammation and insulin resistance: cells, cytokines, and chemokines.
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Direct Estimates of Natural Selection in Iberia Indicate Calcium Absorption Was Not the Only Driver of Lactase Persistence in Europe
10.1093/molbev/msu049
Novel LEPR Mutations in Obese Pakistani Children Identified by PCR-Based Enrichment and Next Generation Sequencing
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Leveraging Cross- Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms
10.1016/j.cell.2013.10.058
Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity
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Coffee and tea consumption, genotype- based CYP1A2 and NAT2 activity and colorectal cancer risk- Results from the EPIC cohort study
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Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates
10.1371/journal.pgen.1003919
Peroxisome Proliferator-activated Receptor gamma Regulates Genes Involved in Insulin/Insulin-like Growth Factor Signaling and Lipid Metabolism during Adipogenesis through Functionally Distinct Enhancer Classes
10.1074/jbc.M113.526996
The SH2B1 obesity locus and abnormal glucose homeostasis: Lack of evidence for association from a meta-analysis in individuals of European ancestry
10.1016/j.numecd.2013.05.001
Highly Sensitive Diagnosis of 43 Monogenic Forms of Diabetes or Obesity Through One-Step PCR-Based Enrichment in Combination With Next-Generation Sequencing
10.2337/dc13-0698
Meal Frequencies Modify the Effect of Common Genetic Variants on Body Mass Index in Adolescents of the Northern Finland Birth Cohort 1986
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GUESS-ing Polygenic Associations with Multiple Phenotypes Using a GPU-Based Evolutionary Stochastic Search Algorithm
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Genome-wide association study identifies three novel loci for type 2 diabetes
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Parental history of type 2 diabetes, TCF7L2 variant and lower insulin secretion are associated with incident hypertension. Data from the DESIR and RISC cohorts
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Next-generation sequencing for identifying new genes in rare genetic diseases: many challenges and a pinch of luck
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Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics
10.1016/j.ajhg.2013.06.011
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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Association between large detectable clonal mosaicism and type 2 diabetes with vascular complications
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Mechanisms behind the immediate effects of Roux-en-Y gastric bypass surgery on type 2 diabetes
10.1186/1742-4682-10-45
Are C-Reactive Protein Associated Genetic Variants Associated with Serum Levels and Retinal Markers of Microvascular Pathology in Asian Populations from Singapore?
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Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features
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Changes in levels of peripheral hormones controlling appetite are inconsistent with hyperphagia in leptin-deficient subjects
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Evidence for tuning adipocytes ICER levels for obesity care.
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Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
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Common variants near BDNF and SH2B1 show nominal evidence of association with snacking behavior in European populations
10.1007/s00109-013-1027-z
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
10.1038/ng.2606
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci
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Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family
10.1016/j.diabet.2013.02.007
Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity
10.1371/journal.pone.0058048
From obesity genetics to the future of personalized obesity therapy
10.1038/nrendo.2013.57
The TGR5 gene is expressed in human subcutaneous adipose tissue and is associated with obesity,Weight loss and resting metabolic rate
10.1016/j.bbrc.2013.03.031
Macrophage Gene Expression in Adipose Tissue is Associated with Insulin Sensitivity and Serum Lipid Levels Independent of Obesity
10.1002/oby.20443
Integration of clinical data with a genome-scale metabolic model of the human adipocyte
10.1038/msb.2013.5
What Is the Contribution of Two Genetic Variants Regulating VEGF Levels to Type 2 Diabetes Risk and to Microvascular Complications?
10.1371/journal.pone.0055921
Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels
10.1007/s00125-013-2875-3
Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts
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Analysis of the contribution of FTO, NPC1, ENPP1, NEGR1, GNPDA2 and MC4R genes to obesity in Mexican children
10.1186/1471-2350-14-21
Blood Microbiota Dysbiosis Is Associated with the Onset of Cardiovascular Events in a Large General Population: The DESIR Study
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Improved Protocol For Laser Microdissection Of Human Pancreatic Islets From Surgical Specimens
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Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
10.1038/ng.2500
Adipose Tissue Resting Energy Expenditure and Expression of Genes Involved in Mitochondrial Function Are Higher in Women than in Men
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Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes
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Seventy-five genetic loci influencing the human red blood cell
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Estimation of Newborn Risk for Child or Adolescent Obesity: Lessons from Longitudinal Birth Cohorts
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Genome-Wide Association Study for Type 2 Diabetes in Indians Identifies a New Susceptibility Locus at 2q21
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New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
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Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
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Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population
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A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site
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Response to comment on: Marquez et al. Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. Diabetes 2012;61:524-530.
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A Genome-Wide Association Study Identifies GRK5 and RASGRP1 as Type 2 Diabetes Loci in Chinese Hans
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Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
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TCF7L2 rs7903146 impairs islet function and morphology in non-diabetic individuals
10.1007/s00125-012-2660-8
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
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GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetes
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Interleukin-7 Regulates Adipose Tissue Mass and Insulin Sensitivity in High-Fat Diet-Fed Mice through Lymphocyte-Dependent and Independent Mechanisms
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Dynamic hydroxymethylation of deoxyribonucleic acid marks differentiation-associated enhancers
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Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene
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Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits
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Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases
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The Interplay of Variants Near LEKR and CCNL1 and Social Stress in Relation to Birth Size
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Glucose-Dependent Regulation of NR2F2 Promoter and Influence of SNP-rs3743462 on Whole Body Insulin Sensitivity
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Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity
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Tryptophan metabolism activation by indoleamine 2,3-dioxygenase in adipose tissue of obese women: an attempt to maintain immune homeostasis and vascular tone
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A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
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Genome-Wide Association for Abdominal Subcutaneous and Visceral Adipose Reveals a Novel Locus for Visceral Fat in Women
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The lessons of early-onset monogenic diabetes for the understanding of diabetes pathogenesis
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Circadian Gene Variants and Susceptibility to Type 2 Diabetes: A Pilot Study
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A genome-wide association meta-analysis identifies new childhood obesity loci
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Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals
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High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families
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European genetic variants associated with type 2 diabetes in North African Arabs
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Loss-of-Function Mutations in MC4R Are Very Rare in the Greek Severely Obese Adult Population
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A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations
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No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels
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Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
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KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
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A Genome-Wide Association Study Identifies rs2000999 as a Strong Genetic Determinant of Circulating Haptoglobin Levels
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Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations
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Multicohort Genomewide Association Study Reveals a New Signal of Protection Against HIV-1 Acquisition
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Alcohol consumption and risk of type 2 diabetes in European men and women: influence of beverage type and body size The EPIC-InterAct study
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Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma
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Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human
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Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes
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A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
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Parent-Offspring Correlations in Pedometer-Assessed Physical Activity
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Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations
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Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes Risk
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Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity
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Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
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New gene functions in megakaryopoiesis and platelet formation
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Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children
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Human Mutation within Per-Arnt-Sim (PAS) Domain-containing Protein Kinase (PASK) Causes Basal Insulin Hypersecretion
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Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
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Low Water Intake and Risk for New-Onset Hyperglycemia
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Identification of a Variable Number of Tandem Repeats Polymorphism and Characterization of LEF-1 Response Elements in the Promoter of the IDO1 Gene
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The Lin28/let-7 Axis Regulates Glucose Metabolism
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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
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Effects of Genetic Susceptibility for Type 2 Diabetes on the Evolution of Glucose Homeostasis Traits Before and After Diabetes Diagnosis Data From the DESIR Study
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Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes
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Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
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ITIH-5 Expression in Human Adipose Tissue Is Increased in Obesity
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Characterization of the human SLC30A8 promoter and intronic enhancer
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A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes
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Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes
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Association of Sirtuin 1 (SIRT1) Gene SNPs and Transcript Expression Levels With Severe Obesity
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Systems medicine and integrated care to combat chronic noncommunicable diseases
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Common Variants in FTO, MC4R, TMEM18, PRL, AIF1 and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population
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Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC Study
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Number of children and change in markers of metabolic health over 9-years in men and women. Data from the DESIR study
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Accurate Single-Nucleotide Polymorphism Allele Assignment in Trisomic or Duplicated Regions by Using a Single Base-Extension Assay with MALDI-TOF Mass Spectrometry
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Disruption of a Novel Kruppel-like Transcription Factor p300-regulated Pathway for Insulin Biosynthesis Revealed by Studies of the c.-331 INS Mutation Found in Neonatal Diabetes Mellitus
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Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes
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famCNV: copy number variant association for quantitative traits in families
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Replication of 13 obesity loci among Singaporean Chinese, Malay and Asian-Indian populations
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Dietary fat intake and polymorphisms at the PPARG locus modulate BMI and type 2 diabetes risk in the D.E.S.I.R. prospective study
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Association of Genetic Loci With Glucose Levels in Childhood and Adolescence A Meta-Analysis of Over 6,000 Children
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Chromosome 19p13.3 Deletion in a Patient With Macrocephaly, Obesity, Mental Retardation, and Behavior Problems
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Endospanins Regulate a Postinternalization Step of the Leptin Receptor Endocytic Pathway
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Dairy Consumption and the Incidence of Hyperglycemia and the Metabolic Syndrome Results from a French prospective study, Data from the Epidemiological Study on the Insulin Resistance Syndrome (DESIR)
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Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic Traits
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Differential coexpression analysis of obesity-associated networks in human subcutaneous adipose tissue
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Metabolic health, obesity and 9-year incidence of peripheral arterial disease: The DESIR study
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Investigation of the HIN200 Locus in UK SLE Families Identifies Novel Copy Number Variants
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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
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Bio-Repository of DNA in stroke (BRAINS): A study protocol
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Childhood Obesity Is Associated with Shorter Leukocyte Telomere Length
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TCF7L2 splice variants have distinct effects on beta-cell turnover and function
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Obesity-susceptibility loci have a limited influence on birth weight: a meta-analysis of up to 28,219 individuals
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Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations
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Influence of blood glucose on heart rate and cardiac autonomic function. The DESIR study
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Investigation of Mendelian forms of obesity holds out the prospect of personalized medicine
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Screening Low-Frequency SNPS From Genome-Wide Association Study Reveals a New Risk Allele for Progression to AIDS
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Molecular Diagnosis of Neonatal Diabetes Mellitus Using Next-Generation Sequencing of the Whole Exome
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Lack of Association of CD36 SNPs With Early Onset Obesity: A Meta-Analysis in 9,973 European Subjects
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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
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Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
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Mean and yearly changes in blood pressure with age in the metabolic syndrome: the DESIR study
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Common Variants at 10 Genomic Loci Influence Hemoglobin A(1C) Levels via Glycemic and Nonglycemic Pathways
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A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
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Evaluation of A2BP1 as an Obesity Gene
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The emerging genetics of type 2 diabetes
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Multiple-Cohort Genetic Association Study Reveals CXCR6 as a New Chemokine Receptor Involved in Long-Term Nonprogression to AIDS
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Interactions of Dietary Whole-Grain Intake With Fasting Glucose- and Insulin-Related Genetic Loci in Individuals of European Descent A meta-analysis of 14 cohort studies
10.2337/dc10.1150
Genetic and Functional Assessment of the Role of the rs13431652-A and rs573225-A Alleles in the G6PC2 Promoter That Are Strongly Associated With Elevated Fasting Glucose Levels
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Expression of the selenoprotein S (SELS) gene m subcutaneous adipose tissue and SELS genotype are associated with metabolic risk factors
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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
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Monogenic forms of diabetes mellitus: an update.
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cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs
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Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups
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Association of common variants in NPPA and NPPB with blood pressure does not translate into kidney damage in a general population study
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Inferring combined CNV/SNP haplotypes from genotype data
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Genetic Variability at the Six Transmembrane Protein of Prostate 2 Locus and the Metabolic Syndrome: The Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) Study
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Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
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Evidence for leptin receptor isoforms heteromerization at the cell surface
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Inflammatory Role of Toll-Like Receptors in Human and Murine Adipose Tissue
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MTNR1B G24E Variant Associates With BMI and Fasting Plasma Glucose in the General Population in Studies of 22,142 Europeans
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High Baseline Insulin Levels Associated With 6-Year Incident Observed Sleep Apnea
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Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French population
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Meta-analysis and functional effects of the SLC30A8 rs13266634 polymorphism on isolated human pancreatic islets
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Study of TNF alpha-308G/A and IL6-174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population
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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
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Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
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Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population
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Evaluating the Association of FAAH Common Gene Variation with Childhood, Adult Severe Obesity and Type 2 Diabetes in the French Population
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TCF7L2 rs7903146-macronutrient interaction in obese individuals' responses to a 10-wk randomized hypoenergetic diet
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PLCL1 rs7595412 variation is not associated with hip bone size variation in postmenopausal Danish women
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Parental origin of sequence variants associated with complex diseases
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Insulin Gene Mutations Resulting in Early-Onset Diabetes: Marked Differences in Clinical Presentation, Metabolic Status, and Pathogenic Effect Through Endoplasmic Reticulum Retention
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Genome-wide association study identifies five loci associated with lung function
10.1038/ng.501
Clinical Heterogeneity in Monogenic Diabetes Caused by Mutations in the Glucokinase Gene (GCK-MODY)
10.2337/dc09-0681
Early Detrimental Metabolic Outcomes of rs17300539-A Allele of ADIPOQ Gene Despite Higher Adiponectinemia
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Obesity-related Polymorphisms and Their Associations With the Ability to Regulate Fat Oxidation in Obese Europeans: The NUGENOB Study
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Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design?
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The Imprinted Gene Neuronatin Is Regulated by Metabolic Status and Associated With Obesity
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MODY7 Gene, KLF11, Is a Novel p300-dependent Regulator of Pdx-1 (MODY4) Transcription in Pancreatic Islet beta Cells
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Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals
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Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03)
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Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia
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Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians
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Genetic Variant m HK1 Is Associated With a Proanemic State and A1C but Not Other Glycemic Control-Related Traits
10.2337/009-0652
Tenomodulin Is Highly Expressed in Adipose Tissue, Increased in Obesity, and Down-Regulated during Diet-Induced Weight Loss
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Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations
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Improved donor/acceptor BRET couples for monitoring beta-arrestin recruitment to G protein-coupled receptors.
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Insulin Storage and Glucose Homeostasis in Mice Null for the Granule Zinc Transporter ZnT8 and Studies of the Type 2 Diabetes-Associated Variants
10.2337/db09-0551
The genetic contribution to non-syndromic human obesity
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A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism
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The role of ghrelin and ghrelin-receptor gene variants and promoter activity in type 2 diabetes
10.1530/EJE-09-0122
Sex hormone-binding globulin predicts the incidence of hyperglycemia in women: interactions with adiponectin levels
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Center Effect on Ankle-Brachial Index Measurement when Using the Reference Method (Doppler and Manometer): Results From a Large Cohort Study
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Common Variation in SIM1 Is Reproducibly Associated With BMI in Pima Indians
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Several obesity- and nutrient-related gene polymorphisms but not FTO and UCP variants modulate postabsorptive resting energy expenditure and fat-induced thermogenesis in obese individuals: the NUGENOB Study
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Linkage Disequilibrium Mapping of the Replicated Type 2 Diabetes Linkage Signal on Chromosome 1q
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The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects
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Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study
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Regulation of carboxylesterase 1 (CES1) in human adipose tissue
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G-allele of Intronic rs10830963 in MTNR1B Confers Increased Risk of Impaired Fasting Glycemia and Type 2 Diabetes Through an Impaired Glucose-Stimulated Insulin Release Studies Involving 19,605 Europeans
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A Rare Variant in the Visfatin Gene (NAMPT/PBEF1) Is Associated With Protection From Obesity
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Functional and genetic analysis in type 2 diabetes of Liver X receptor alleles - a cohort study
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Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease
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TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia
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ALK7 expression is specific for adipose tissue, reduced in obesity and correlates to factors implicated in metabolic disease
10.1016/j.bbrc.2009.03.014
Combined effects of MC4R and FTO common genetic variants on obesity in European general populations
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Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction
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Evaluating the association of common APOA2 variants with type 2 diabetes
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Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans
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Common genetic variation near MC4R is associated with eating behaviour patterns in European populations
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Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity
10.1038/oby.2008.589
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
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Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height
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Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02)
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A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk
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Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan population
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Is Obesity Our Genetic Legacy?
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The Q121 Variant of ENPP1 May Protect From Childhood Overweight/obesity in the Italian Population
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Estrogen receptor alpha gene variants associate with type 2 diabetes and fasting plasma glucose
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A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature
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Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements
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The FTO gene is associated with adulthood obesity in the Mexican population
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Predicting Diabetes: Clinical, Biological, and Genetic Approaches Data from the Epidemiological Study on the Insulin Resistance Syndrome (DESIR)
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Effect of ENPP1/PC-1-K121Q and PPAR gamma-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population
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Common nonsynonymous variants in PCSK1 confer risk of obesity
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Prevalence of melanocortin-4 receptor deficiency in Europeans and their age-dependent penetrance in multigenerational pedigrees
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The common P446L polymorphism in GCAR inversely modulates fasting glucose and triglyceride levels and reduces type 2 diabetes risk in the DESIR prospective general French population
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Genetic analysis of Kruppel-like zinc finger 11 variants in 5864 Danish individuals: Potential effect on insulin resistance and modified signal transducer and activator of transcription-3 binding by promoter variant-1659G \textgreater C
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The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies
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Post Genome-Wide Association Studies of Novel Genes Associated with Type 2 Diabetes Show Gene-Gene Interaction and High Predictive Value
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Common variants near MC4R are associated with fat mass, weight and risk of obesity
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Common genetic variation near MC4R is associated with waist circumference and insulin resistance
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Inflammation is associated with a decrease of lipogenic factors in omental fat in women
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A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels
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Monogenic diabetes in the young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetes
10.1210/er.2007-0024
Long-term follow-up of oral glucose tolerance test-derived glucose tolerance and insulin secretion and insulin sensitivity indexes in subjects with glucokinase mutations (MODY2)
10.2337/dc07-2017
Evaluation of the association of IGF2BP2 variants with type 2 diabetes in French Caucasians
10.2337/db07-1789
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans
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INS VNTR is not associated with childhood obesity in 1,023 families: A family-based study
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Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations
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Strong association of common variants in the CDKN2A/CDKN2B region with type 2 diabetes in French Europids
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A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults
10.2337/db07-1547
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population
10.1093/hmg/ddn070
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity
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Evaluating the association of common PBX1 variants with type 2 diabetes
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Neonatal hyperglycaemia and abnormal development of the pancreas
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Effects of TCF7L2 polymorphisms on obesity in European populations
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Meta-analysis of 23 type 2 diabetes linkage studies from the international type 2 diabetes linkage analysis consortium
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Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: A report from the French ND (Neonatal Diabetes) Study Group
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Analysis of novel risk loci for type 2 diabetes in a general French population: the DESIR study
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The EBPP1 K121Q polymorphism is associated with type 2 diabetes in European populations: Evidence from an updated meta-analysis in 42,042 subjects
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Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations
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Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids
10.1007/s00125-007-0857-z
Association analysis indicates that a variant GATA-binding site in the PIK3CB promoter is a cis-acting expression quantitative trait locus for this gene and attenuates insulin resistance in obese children
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Lack of association between the Pro(12)Ala polymorphism of the PPAR-gamma 2 gene and type 2 diabetes mellitus in the Qatari consanguineous population
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A single-nucleotide polymorphism in the p110 beta gene promoter is associated with partial protection from insulin resistance in severely obese adolescents
10.1210/jc.2007-1822
Alcohol consumption and risk of type 2 diabetes in European men and women: influence of beverage type and body size The EPIC-InterAct study (vol 272, pg 358, 2012)
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High prevalence of leptin and melanocotin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families (vol 106, pg 121, 2012)
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KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron (vol 44, pg 458, 2012)
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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (vol 42, pg 579, 2010)
10.1038/ng0411-388b
Response to the letter to the editor: "HIF-1 alpha protein rather than mRNA as a marker of hypoxia in adipose tissue in obesity," by Trayhurn et al.
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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)
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Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia (vol 41, pg 1110, 2009)
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Silencing of OB-RGRP in mouse hypothalamic arcuate nucleus increases leptin receptor signaling and prevents diet-induced obesity
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Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population
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Missense mutations in the TGM2 gene encoding transglutaminase 2 are found in patients with early-onset type 2 diabetes. Mutation in brief no. 982. Online.
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Minor contribution of SMAD7 and KLF10 variants to genetic susceptibility of type 2 diabetes
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Neonatal diabetes: a disease linked to multiple mechanisms
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ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study
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Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity
10.1210/jc.2006-2316
Analysis of KLF transcription factor family gene variants in type 2 diabetes
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Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases
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Type 2 diabetes whole-genome association study in four populations: The DiaGen consortium
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Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity
10.1186/1471-2350-8-44
TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population
10.1186/1471-2350-8-37
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity
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Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene
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Variation in FTO contributes to childhood obesity and severe adult obesity
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TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis
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Examining the candidacy of ghrelin as a gene responsible for variation in adult stature in a United Kingdom population with type 2 diabetes
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New ABCC8 mutations in relapsing neonatal diabetes and clinical features
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Coexistence in the same family of both focal and diffuse forms of hyperinsulinism
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Preadipocyte response and impairment of differentiation in an inflammatory environment
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Activating transcription factor 6 (ATF6) sequence polymorphisms in type 2 diabetes and pre-diabetic traits
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Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes - Association analyses in 9,518 subjects
10.2337/db06-0930
A genome-wide association study identifies novel risk loci for type 2 diabetes
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Targeted disruption of AdipoR1 and AdipoR2 causes abrogation of adiponectin binding and metabolic actions
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Two Caucasian families with the hepatocyte nuclear factor-1 alpha mutation Tyr218Cys
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A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese population
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Leptin receptor genotype at Gln223Arg is associated with body composition, BMD, and vertebral fracture in postmenopausal Danish women
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Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects
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Comment on "A common genetic variant is associated with adult and childhood obesity"
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No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases
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Adiponectin, type 2 diabetes and the metabolic syndrome: lessons from human genetic studies.
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No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects
10.1007/s00125-006-0505-z
Genotype-by-nutrient interactions assessed in European obese women - A case-only study
10.1007/s00394-006-0619-6
TCF7L2 variation predicts hyperglycentia incidence in a French general population - The Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) study
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Epistasis between type 2 diabetes susceptibility loci on chromosomes 1q21-25 and 10q23-26 in northern Europeans
10.1111/j.1469-1809.2006.00289.x
Impact of a CART promoter genetic variation on plasma lipid profile in a general population
10.1016/j.ymgme.2006.08.012
Transcription factor TCF7L2 genetic study in the French population - Expression in human beta-cells and adipose tissue and strong association with type 2 diabetes
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Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French Caucasians
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Genetics of obesity and the prediction of risk for health
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Variation within the gene encoding the upstream stimulatory factor 1 does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence of linkage to chromosome 1q
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Polymorphisms in the glucokinase-associated, dual-specificity phosphatase 12 (DUSP12) gene under chromosome 1q21 linkage peak are associated with type 2 diabetes
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Distinct impaired regulation of SOCS3 and long and short isoforms of the leptin receptor in visceral and subcutaneous fat of lean and obese women
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Genetic polymorphisms and weight loss in obesity: A randomised trial of hypo-energetic high-versus low-fat diets
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Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses
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Analysis of common PTPN1 gene variants in type 2 diabetes, obesity and associated phenotypes in the French population
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Hepatocyte nuclear factor-4 alpha P2 promoter haplotypes are associated with type 2 diabetes in the Japanese population
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Genetic basis of maturity-onset diabetes of the young
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The INS VNTR locus does not associate with smallness for gestational age (SGA) but interacts with SGA to increase insulin resistance in young adults
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A POMC variant implicates beta-melanocyte-stimulating hormone in the control of human energy balance
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Obesity susceptibility CART gene polymorphism contributes to bone remodeling in postmenopausal women
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Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1
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Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes
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GAD2: A polygenic contribution to genetic susceptibility for common obesity?
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Absence of an association between the polymorphisms in the genes encoding adiponectin receptors and type 2 diabetes
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Hypoadiponectinaemia and high risk of type 2 diabetes are associated with adiponectin-encoding (ACDC) gene promoter variants in morbid obesity: evidence for a role of ACDC in diabesity
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Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population
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Implication of the Pro 12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French population
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Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function
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The genetics of human obesity
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Effect of common polymorphisms in the HNF4 alpha promoter on susceptibility to type 2 diabetes in the French Caucasian population
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Is glutamate decarboxylase 2 (GAD2) a genetic link between low birth weight and subsequent development of obesity in children?
10.1210/jc.2004-1468
The EIF2AK3 gene region and type 1 diabetes in subjects from South India
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Single nucleotide polymorphisms of protein tyrosine phosphatase 1B gene are associated with obesity in morbidly obese French subjects
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A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetes.
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Understanding the rising incidence of type 2 diabetes in adolescence
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Insulin/Foxo1 pathway regulates expression levels of adiponectin receptors and adiponectin sensitivity
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A promoter polymorphism in CD36 is associated with an atherogenic lipid profile in a French general population
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GAD2 on chromosome 10p12 is a candidate gene for human obesity
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Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation
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Impaired multimerization of human adiponectin mutants associated with diabetes - Molecular structure and multimer formation of adiponectin
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A meta-analysis of four European genome screens (GIFT consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes
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PAI-1 polymorphisms modulate phenotypes associated with the metabolic syndrome in obese and diabetic Caucasian population
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Cloning of adiponectin receptors that mediate antidiabetic metabolic effects
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Islet-brain1/C-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease
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Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians
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Does the-11377 promoter variant of APM1 gene contribute to the genetic risk for Type 2 diabetes mellitus in Japanese families?
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Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations
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Let science speak for itself
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Increased Hepatic PDGF-AA Signaling Mediates Liver Insulin Resistance in Obesity-Associated Type 2 Diabetes
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