ACDC/adiponectin polymorphisms are associated with severe childhood and adult obesity
Bouatia-Naji, N.
Meyre, D.
Lobbens, S.
Seron, K.
Fumeron, F.
Balkau, B.
Heude, B.
Jouret, B.
Scherer, P. E.
Dina, C.
Weill, J.
Froguel, P.
Diabetes, 2006
Nabila Bouatia-Naji
Bouatia-Naji Nabila
ORCID: 0000-0001-5424-2134
Mitral valve disease-morphology and mechanisms.
10.1038/nrcardio.2015.161
Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.
10.1097/HJH.0000000000000625
Genetic association analyses highlight biological pathways underlying mitral valve prolapse.
10.1038/ng.3383
Mutations in DCHS1 cause mitral valve prolapse.
10.1038/nature14670
A central role for GRB10 in regulation of islet function in man.
10.1371/journal.pgen.1004235
[New genetic determinants of glycemic traits: insights in biological pathways of glucose homeostasis].
10.1051/medsci/20143001008
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
10.1038/ng.2610
Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels.
10.1007/s00125-013-2875-3
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
10.1038/ng.2500
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.
10.1038/ng.2385
Dietary factors impact on the association between CTSS variants and obesity related traits.
10.1371/journal.pone.0040394
Impact of common variation in bone-related genes on type 2 diabetes and related traits.
10.2337/db11-1515
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
10.1038/ng.2274
No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels.
10.2337/db11-0973
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.
10.1038/ng.2218
A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels.
10.1371/journal.pone.0032327
Association between FTO variant and change in body weight and its interaction with dietary factors: the DiOGenes study.
10.1038/oby.2012.49
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes.
10.1038/ng.1053
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
10.2337/db11-0415
Association of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children.
10.2337/db10-1575
Genetic polymorphisms in the hypothalamic pathway in relation to subsequent weight change--the DiOGenes study.
10.1371/journal.pone.0017436
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
10.1038/ng.686
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
10.1038/ng.685
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.
10.2337/db10-0502
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.
10.2337/db10-0389
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.
10.1038/ng.567
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
10.1038/ng.520
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.
10.1038/ng.521
Genome-wide association study identifies five loci associated with lung function.
10.1038/ng.501
Early detrimental metabolic outcomes of rs17300539-A allele of ADIPOQ gene despite higher adiponectinemia.
10.1038/oby.2009.403
[Inputs from the genetics of fasting glucose: lessons for diabetes].
10.1051/medsci/20092511897
Genetic variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traits.
10.2337/db09-0652
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.
10.2337/db08-1660
Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction.
10.1007/s00125-009-1299-6
Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height.
10.1530/EJE-08-0794
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.
10.1038/ng.277
Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan population.
10.1016/j.diabet.2008.06.005
A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels.
10.1126/science.1156849
INS VNTR is not associated with childhood obesity in 1,023 families: a family-based study.
10.1038/oby.2008.209
Association analysis of the IGF1 gene with childhood growth, IGF-1 concentrations and type 1 diabetes.
10.1007/s00125-008-0970-7
ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study.
10.1007/s00125-007-0787-9
Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity.
10.1186/1471-2350-8-44
ACDC/adiponectin polymorphisms are associated with severe childhood and adult obesity.
10.2337/diabetes.55.02.06.db05-0971
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes.
10.1038/ng1604
Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas
10.1210/clinem/dgz168
Chromatin Accessibility of Human Mitral Valves and Functional Assessment of MVP Risk Loci.
10.1161/circresaha.120.317581
National French Registry of Spontaneous Coronary Artery Dissections: Prevalence of Fibromuscular Dysplasia and Genetic Analyses.
10.4244/eij-d-20-01046
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.
10.1161/circgen.120.003030
Rare Loss-of-function Mutations of PTGIR are enriched in Fibromuscular Dysplasia.
10.1093/cvr/cvaa161
Genetic Study of PHACTR1 and Fibromuscular Dysplasia, Meta-Analysis and Effects on Clinical Features of Patients: The ARCADIA-POL Study.
10.1161/hypertensionaha.120.14793
[Genetics provides a link between cardiovascular diseases predominantly afflicting women].
10.1051/medsci/2019119
A plasma proteogenomic signature for fibromuscular dysplasia.
10.1093/cvr/cvz219
Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city.
10.1016/j.dsx.2019.02.024
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals.
10.1038/s41598-019-45823-7
Primary cilia defects causing mitral valve prolapse.
10.1126/scitranslmed.aax0290
Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse.
10.1161/circgen.119.002497
Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection.
10.1016/j.jacc.2018.09.085
Spontaneous coronary artery dissections and fibromuscular dysplasia: Current insights on pathophysiology, sex and gender.
10.1016/j.ijcard.2018.11.023
Fibromuscular Dysplasia and Its Neurologic Manifestations: A Systematic Review.
10.1001/jamaneurol.2018.2848
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.
10.1371/journal.pgen.1006367
The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city.
10.1016/j.ijcard.2016.10.027
The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma.
10.1210/jc.2016-2103
Top Advances in Functional Genomics and Translational Biology for 2015.
10.1161/circgenetics.116.001421
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
10.1038/ncomms10023
Genetic risk of type 2 diabetes in populations of the African continent: A systematic review and meta-analyses.
10.1016/j.diabres.2016.01.003
Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.
10.3390/jcdd2030176
Karin Seron
Seron Karin
ORCID: 0000-0002-9667-133X
Identification of class II ADP-ribosylation factors as cellular factors required for hepatitis C virus replication
10.1111/cmi.12572
Khaya grandifoliola C.DC: a potential source of active ingredients against hepatitis C virus in vitro
10.1007/s00705-016-2771-5
Characterization of Hepatitis C Virus Interaction with Heparan Sulfate Proteoglycans
10.1128/jvi.03647-14
Claudin-6 and Occludin Natural Variants Found in a Patient Highly Exposed but Not Infected with Hepatitis C Virus (HCV) Do Not Confer HCV Resistance In Vitro
10.1371/journal.pone.0142539
Plant extracts from Cameroonian medicinal plants strongly inhibit hepatitis C virus infection in vitro
10.3389/fmicb.2015.00438
Polyphenols Inhibit Hepatitis C Virus Entry by a New Mechanism of Action
10.1128/jvi.01473-15
Identification of Conserved Residues in Hepatitis C Virus Envelope Glycoprotein E2 That Modulate Virus Dependence on CD81 and SRB1 Entry Factors
10.1128/jvi.01402-14
Potent antiviral activity of Solanum rantonnetii and the isolated compounds against hepatitis C virus in vitro
10.1016/j.jff.2014.09.022
Structure-activity studies of (-)-epigallocatechin gallate derivatives as HCV entry inhibitors
10.1016/j.bmcl.2014.07.051
(-)-Epigallocatechin-3-gallate is a new inhibitor of hepatitis C virus entry
10.1002/hep.24803
Hepatitis C Virus and Natural Compounds: A New Antiviral Approach?
10.3390/v4102197
Endospanins Regulate a Postinternalization Step of the Leptin Receptor Endocytic Pathway
10.1074/jbc.M111.224857
Identification of a dominant endoplasmic reticulum-retention signal in yellow fever virus pre-membrane protein
10.1099/vir.0.015339-0
Silencing of OB-RGRP in mouse hypothalamic arcuate nucleus increases leptin receptor signaling and prevents diet-induced obesity
10.1073/pnas.0706671104
ACDC/adiponectin polymorphisms are associated with severe childhood and adult obesity
10.2337/diabetes.55.02.06.db05-0971
Distinct impaired regulation of SOCS3 and long and short isoforms of the leptin receptor in visceral and subcutaneous fat of lean and obese women
10.1016/j.bbrc.2006.07.068
Genetic study of the CD36 gene In a French diabetic population
10.1016/s1262-3636(07)70143-x
GAD2 on chromosome 10p12 is a candidate gene for human obesity
10.1371/journal.pbio.0000068
Molecular cloning, functional complementation in Saccharomyces cerevisiae and enzymatic properties of phosphatidylinositol synthase from the protozoan parasite Toxoplasma gondii
10.1046/j.1432-1327.2000.01749.x
Disruption of six novel genes from the left arm of chromosome XV of Saccharomyces cerevisiae and basic phenotypic analysis of the generated mutants
10.1002/(sici)1097-0061(19990115)15:1<73::aid-yea341>3.0.co;2-q
Efficient transcription obtained by a new procedure of the tRNA-like structure of turnip yellow mosaic virus by a template-dependent and specific viral RNA polymerase
10.1016/s0166-0934(96)02166-0
Efficient transcription obtained by a new procedure of the tRNA-like structure of turnip yellow mosaic virus by a template-dependent and specific viral RNA polymerase (vol 64, pg 181, 1997)
10.1016/s0166-0934(96)02249-5
Expression of the 69K movement protein of turnip yellow mosaic virus in insect cells
10.1006/viro.1996.0246
Gene expression from viral RNA genomes
10.1007/bf00039391
Vascular movement of plant viruses
10.1094/mpmi-9-0435
IN-VITRO TRANSCRIPTS OF TURNIP YELLOW MOSAIC-VIRUS ENCOMPASSING A LONG 3' EXTENSION OR PRODUCED FROM A FULL-LENGTH CDNA CLONE HARBORING A 2 KB-LONG PCR-AMPLIFIED SEGMENT ARE INFECTIOUS
10.1016/s0923-2516(06)80049-x
Entry and release of hepatitis C virus in polarized human hepatocytes.
10.1128/jvi.00478-17
An ecological approach to discover new bioactive extracts and products: the case of extremophile plants.
10.1111/jphp.12728
Identification of a New Benzimidazole Derivative as an Antiviral against Hepatitis C Virus.
10.1128/jvi.00404-16
Middle East respiratory syndrome coronavirus infection is inhibited by griffithsin.
10.1016/j.antiviral.2016.07.011
Theaflavins, polyphenols of black tea, inhibit entry of hepatitis C virus
10.1101/325126
Viral hepatitis in the Peruvian Amazon: Ethnomedical context and phytomedical resource.
10.1016/j.jep.2020.112735
Functional Carbon Quantum Dots as Medical Countermeasures to Human Coronavirus.
10.1021/acsami.9b15032
Dehydrojuncusol, a Natural Phenanthrene Compound Extracted from Juncus maritimus, Is a New Inhibitor of Hepatitis C Virus RNA Replication.
10.1128/jvi.02009-18
Theaflavins, polyphenols of black tea, inhibit entry of hepatitis C virus in cell culture.
10.1371/journal.pone.0198226
Correction for Belouzard et al., "Entry and Release of Hepatitis C Virus in Polarized Human Hepatocytes".
10.1128/jvi.00309-18
Plant extracts from Cameroonian medicinal plants strongly inhibit hepatitis C virus infection in vitro.
10.3389/fmicb.2015.00488
A yeast t-SNARE involved in endocytosis.
10.1091/mbc.9.10.2873
Large scale screening discovers clofoctol as an inhibitor of SARS-CoV-2 replication that reduces COVID-19-like pathology
10.1101/2021.06.30.450483
Frederic Fumeron
Fumeron Frederic
ORCID: 0000-0002-7916-4619
L'adiponectine
10.3166/sda.23.3-12
Genetics of the Human Obesities
10.1007/978-2-8178-0343-2_24
Obésité : d’un syndrome monogénique exceptionnel aux interactions entre gènes multiples et environnement nutritionnel
10.1051/ocl.2003.0109
Iron intake in obese menstruating women
10.1016/0168-8227(90)90178-v
Predicting diabetes: Clinical, biological, and genetic approaches
10.2337/dc08-0368
Association of apolipoprotein ɛ4 allele with hypertriglyceridemia in obesity
10.1111/j.1399-0004.1988.tb02873.x
Nine-year incident diabetes is predicted by fatty liver indices: The French D.E.S.I.R. study
10.1186/1471-230X-10-56
Dairy product consumption, calcium intakes, and metabolic syndrome-related factors over 5 years in the STANISLAS study
10.1016/j.nut.2012.08.013
ABCA1 single nucleotide polymorphisms on high-density lipoprotein- cholesterol and overweight: The D.E.S.I.R. study
10.1038/oby.2006.217
Sex-dependent associations of leptin with metabolic syndrome-related variables: The stanislas study
10.1038/oby.2009.156
Extensive association analysis between the CETP gene and coronary heart disease phenotypes reveals several putative functional polymorphisms and gene-environment interaction
10.1002/1098-2272(200007)19:1<64::AID-GEPI5>3.0.CO;2-E
Decreased insulin secretion and increased risk of type 2 diabetes associated with allelic variations of the WFS1 gene: The data from epidemiological study on the insulin resistance syndrome (DESIR) prospective study
10.1007/s00125-010-1989-0
Association of a functional 5-HT transporter gene polymorphism with anorexia nervosa and food intake [3]
10.1038/sj.mp.4000824
LEPR gene polymorphisms: Associations with overweight, fat mass and response to diet in women
10.1046/j.1365-2362.2001.00843.x
ABCG8 polymorphisms and renal disease in type 2 diabetic patients
10.1016/j.metabol.2015.03.005
High baseline insulin levels associated with 6-year incident observed sleep apnea
10.2337/dc09-1901
Comparison between copeptin and vasopressin in a population from the community and in people with chronic kidney disease
10.1210/jc.2014-2295
Are the same clinical risk factors relevant for incident diabetes defined by treatment, fasting plasma glucose, and HbA1c ?
10.2337/dc10-1581
Allelic variations of the vitamin D receptor (VDR) gene are associated with increased risk of coronary artery disease in type 2 diabetics: The DIABHYCAR prospective study
10.1016/j.diabet.2012.11.004
Lack of association between dietary alcohol and HDL-cholesterol concentrations in obese women
10.1016/0021-9150(90)90018-E
Potential risks associated with increased plasma plant-sterol levels
10.1016/j.diabet.2014.11.003
Adiponectin Gene Polymorphisms and Adiponectin Levels Are Independently Associated with the Development of Hyperglycemia during a 3-Year Period: The Epidemiologic Data on the Insulin Resistance Syndrome Prospective Study
10.2337/diabetes.53.4.1150
Association of ADIPOQ genetic variants and plasma adiponectin isoforms with the risk of incident renal events in type 2 diabetes
10.1093/ndt/gfp771
GUESS-ing Polygenic Associations with Multiple Phenotypes Using a GPU-Based Evolutionary Stochastic Search Algorithm
10.1371/journal.pgen.1003657
Antidepressant medication use and trajectories of fasting plasma glucose, glycated haemoglobin, β-cell function and insulin sensitivity: A 9-year longitudinal study of the D.E.S.I.R. cohort
10.1093/ije/dyv153
Studies on an Isolated West Indies Population: I. Analysis of HLA Genotypes
10.1111/j.1399-0039.1981.tb00709.x
Death, end-stage renal disease and renal function decline in patients with diabetic nephropathy in French cohorts of type 1 and type 2 diabetes
10.1007/s00125-015-3785-3
Associations of the 344 T>C and the 3097 G>A polymorphisms of CYP11B2 gene with hypertension, type 2 diabetes, and metabolic syndrome in a French population
10.1038/ajh.2010.44
Plasma extracellular superoxide dismutase concentration, allelic variations in the SOD3 gene and risk of myocardial infarction and all-cause mortality in people with type 1 and type 2 diabetes
10.1186/s12933-014-0163-2
Association of the G-2548A polymorphism in the 5′ region of the LEP gene with overweight
10.1017/S0003480000008277
Plasma copeptin, AVP gene variants, and incidence of type 2 diabetes in a cohort from the community
10.1210/jc.2016-1113
Apolipoprotein B signal peptide polymorphism and plasma LDL-cholesterol response to low-calorie diet
10.1038/sj.ijo.0802648
Plasma copeptin and renal outcomes in patients with type 2 diabetes and albuminuria
10.2337/dc13-0683
Allelic variations in superoxide dismutase-1 (SOD1) gene and renal and cardiovascular morbidity and mortality in type 2 diabetic subjects
10.1016/j.ymgme.2012.04.023
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
10.1210/jc.2010-0026
Plasma Dihydroceramides Are Diabetes Susceptibility Biomarker Candidates in Mice and Humans
10.1016/j.celrep.2017.02.019
Contribution of the low-frequency, loss-of-function p. R270H mutation in FFAR4 (GPR120) to increased fasting plasma glucose levels
10.1136/jmedgenet-2015-103065
Lack of association between genetic variations of apo A-I - C-III - A- IV gene cluster and myocardial infarction in a sample of European male: ECTIM study
10.1016/S0021-9150(99)00066-0
Patterns of Alcohol Consumption and Cardiovascular Risk in Northern Ireland and France
10.1016/j.annepidem.2007.01.017
Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: The DESIR prospective study
10.1007/s00109-009-0548-y
Intensifying glycaemic control with insulin reduces adiponectin and its HMW isoform moderately in type 2, but not in type 1, diabetes
10.1016/j.diabet.2010.12.001
Lack of plasmatic beta-endorphin response to a gastronomic meal in healthy humans
10.1016/0031-9384(91)90354-Q
Association of vitronectin and plasminogen activator inhibitor-1 levels with the risk of metabolic syndrome and type 2 diabetes mellitus
10.1160/TH11-03-0179
Phytosterols: Focus on ANSES guidelines | Phytostérols: un point sur les recommandations de l'ANSES
10.1016/j.cnd.2015.02.004
Les aliments fonctionnels contenant des phytostérols ou des phytostanols: quels bénéfices, quels risques
10.1016/j.pranut.2015.12.009
Association of ACACB gene polymorphism (rs2268388, G > A) with type 2 diabetes and end stage renal disease in Pakistani Punjabi population
10.1016/j.mgene.2017.02.003
Longitudinal association of antidepressant medication use with metabolic syndrome: Results of a 9-year follow-up of the D.E.S.I.R. cohort study
10.1016/j.psyneuen.2016.08.020
Effect of a moderate alcohol intake on the lipoproteins of normotriglyceridemic obese subjects compared with normoponderal controls
10.1016/0026-0495(92)90167-9
Weight change and changes in the metabolic syndrome as the French population moves towards overweight: The D.E.S.I.R. cohort
10.1093/ije/dyi281
Adiponectin multimers and ADIPOQ T45G in coronary artery disease in caribbean type 2 diabetic subjects of african descent
10.1038/oby.2009.441
Genetics of the human obesities | Génétique des obésités humaines
10.1007/s11690-013-0357-x
Low high density lipoprotein-2 concentrations in obese male subjects
10.1016/0021-9150(88)90163-3
Evidence for distinct effects of GH and IGF-I in the metabolic syndrome
10.1111/j.1464-5491.2007.02195.x
The common-866G> A variant in the promoter of UCP2 is associated with decreased risk of coronary artery disease in type 2 diabetic men
10.2337/db07-1292
Individual responses to dietary lipid changes | Réponse aux lipides de l'alimentation et profil géné tique
10.3166/sda.28.143-149
Plasma copeptin, kidney outcomes, ischemic heart disease, and all-cause mortality in people with long-standing type 1 diabetes
10.2337/dc16-1003
Glutathione peroxidase-1 gene (GPX1) variants, oxidative stress and risk of kidney complications in people with type 1 diabetes
10.1016/j.metabol.2015.10.004
Association between endothelin receptor B nonsynonymous variants and melanoma risk
10.1093/jnci/dji253
Sex hormone-binding globulin predicts the incidence of hyperglycemia in women: Interactions with adiponectin levels
10.1530/EJE-09-0202
The functional c.-2G>C variant of the mineralocorticoid receptor modulates blood pressure, renin, and aldosterone levels
10.1161/HYPERTENSIONAHA.110.155630
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)
10.2337/dc10-1772
Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes
10.1007/s00125-013-3057-z
HLA and longevity
10.1111/j.1399-0039.1982.tb01436.x
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
10.1016/j.numecd.2016.04.010
Allelic variations in the CYBA gene of NADPH oxidase and risk of kidney complications in patients with type 1 diabetes
10.1016/j.freeradbiomed.2015.04.002
Manganese superoxide dismutase (SOD2) polymorphisms, plasma advanced oxidation protein products (AOPP) concentration and risk of kidney complications in subjects with type 1 diabetes
10.1371/journal.pone.0096916
ACDC/adiponectin polymorphisms are associated with severe childhood and adult obesity
10.2337/diabetes.55.02.06.db05-0971
Relationships between common polymorphisms of adenosine triphosphate-binding cassette transporter A1 and high-density lipoprotein cholesterol and coronary heart disease in a population with type 2 diabetes mellitus
10.1016/j.metabol.2008.08.009
Tissue kallikrein deficiency, insulin resistance, and diabetes in mouse and man
10.1530/JOE-13-0529
Interindividual variability in the cholesterol-lowering effect of supplementation with plant sterols or stanols
10.1093/nutrit/nuw059
HLA genotypes in familial Hodgkin's disease. Excess of HLA identical affected sibs
10.1016/0014-2964(80)90134-6
Presence of the french canadian deletion in a french patient with familial hypercholesterolemia
10.1056/NEJM199201023260117
Plasma adrenomedullin and allelic variation in the ADM gene and kidney disease in people with type 2 diabetes
10.2337/db14-1852
Urinary Sodium Concentration Is an Independent Predictor of All-Cause and Cardiovascular Mortality in a Type 2 Diabetes Cohort Population
10.1155/2017/5327352
Update on the ANSES (French agency for food, environmental and occupational health & safety) recommendations | Phytostérols: Un point sur les recommandations de l'ANSES
10.1051/ocl/2014051
Effects of Slight Plasma Glucose Decrease on Glycosylated Hemoglobin in Healthy Subjects during Caloric Restriction
10.1056/NEJM198510103131515
Comparative effects of several simple carbohydrates on erythrocyte insulin receptors in obese subjects
10.1016/0091-3057(86)90159-0
Plasma Copeptin and Decline in Renal Function in a Cohort from the Community: The Prospective D.E.S.I.R. Study
10.1159/000439061
Comment on: Park et al. Association of serum ferritin and the development of metabolic syndrome in middle-aged Korean men: A 5-year follow-up study. Diabetes Care 2012;35:2521-2526
10.2337/dc12-1803
Genetics of macrovascular complications in diabetes
10.1007/s11892-006-0028-5
T-cadherin gene variants are associated with type 2 diabetes and the Fatty Liver Index in the French population
10.1016/j.diabet.2016.05.005
Ferritin and transferrin are associated with metabolic syndrome abnormalities and their change over time in a general population: Data from an Epidemiological Study on the Insulin Resistance syndrome (DESIR)
10.2337/dc06-2312
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
10.1038/ijo.2011.91
Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study
10.2337/db07-0615
Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: The Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) study
10.2337/dc06-0093
Prognostic value of the insertion/deletion polymorphism of the ACE gene in type 2 diabetic subjects: Results from the non-insulin-dependent diabetes, hypertension, microalbuminuria or proteinuria, cardiovascular events, and ramipril (DIABHYCAR), diabete de type 2, nephropathie et genetique (DIAB2NEPHROGENE), and survie, diabete de type 2 et genetique (SURDIAGENE) studies
10.2337/dc07-2079
The PPARG Pro12Ala polymorphism is associated with a decreased risk of developing hyperglycemia over 6 years and combines with the effect of the APM1 G-11391A single nucleotide polymorphism: The Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) Study
10.2337/diabetes.55.04.06.db05-0676
Association between HLA-B18 and the Familial-Obesity Syndrome
10.1056/NEJM198109103051120
Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French Caucasians
10.2337/db06-0337
Dynamic changes in renal function are associated with major cardiovascular events in patients with type 2 diabetes
10.2337/dc15-2607
Polymorphism in the fractalkine receptor CX3CR1 as a genetic risk factor for coronary artery disease
10.1182/blood.V97.7.1925
The lactase persistence genotype is associated with body mass index and dairy consumption in the D.E.S.I.R. study
10.1016/j.metabol.2013.04.006
Adiponectin gene variants, adiponectin isoforms and cardiometabolic risk in type 2 diabetic patients
10.1111/jdi.12133
The loss-of-function PCSK9 p.R46L genetic variant does not alter glucose homeostasis
10.1007/s00125-015-3659-8
Role of liver metastasis on nitrogen balance in enterally fed cancer patients | Les métastases hépatiques ont-elles un rôle néfaste sur la positivation du bilan azoté sous nutrition entérale chez les patients cancéreux ?
10.1016/S0985-0562(05)80023-8
The CETP TaqIB polymorphism is associated with the risk of sudden death in type 2 diabetic patients
10.2337/dc07-0869
Association of common variants in NPPA and NPPB with blood pressure does not translate into kidney damage in a general population study
10.1097/HJH.0b013e328338a901
Increased plasma adiponectin concentrations are associated with microangiopathy in type 1 diabetic subjects
10.1007/s00125-005-1747-x
Novel polymorphisms in the 5' region of the LEP gene: Association with leptin levels and response to low-calorie diet in human obesity
10.2337/diabetes.47.3.487
Dairy products and the metabolic syndrome in a prospective study, desir
10.1080/07315724.2011.10719990
Serotonin transporter gene polymorphism and myocardial infarction: Etude Cas-Témoins de l'Infarctus du Myocarde (ECTIM)
10.1161/01.CIR.0000022603.92986.99
Analysis of novel risk loci for type 2 diabetes in a general French population: The D.E.S.I.R. study
10.1007/s00109-007-0295-x
Allelic variations in superoxide dismutase-1 (SOD1) gene are associated with increased risk of diabetic nephropathy in type 1 diabetic subjects
10.1016/j.ymgme.2011.08.033
Hyperadiponectinemia is independent of kidney function, diabetes duration, and control in type 1 diabetic patients without microangiopathy
10.1210/jc.2010-1835
Génétique des obésités humaines
10.1007/978-2-8178-0332-6_24
Adiponectin gene and cardiovascular risk in type 2 diabetic patients: a review of evidences
10.1590/s0004-27302007000200003
T-cadherin gene variants are associated with nephropathy in subjects with type 1 diabetes
10.1093/ndt/gfx071
Endogenous opiates and energy balance
10.1126/science.7063865
De l'obésité au diabète de type 2 : épidémiologie et physiopathologie
10.3166/sda.25.339-347
Lipoprotein Lipase Gene Variants and Coronary Risk
10.1161/01.cir.97.25.2588
La T-cadhérine, troisième récepteur de l’adiponectine : structure et rôle en santé humaine
10.1007/s11690-017-0586-5
Dietary fat, energy density and BMI: a case of a missing flower?
10.1038/sj.ijo.0800736
BIRTHWEIGHT DIFFERENCE IN MONOZYGOUS TWINS FOLLOWED BY DIFFERENCE IN DEVELOPMENT OF BODY WEIGHT
10.1016/s0140-6736(82)90359-2
Dairy consumption, systolic blood pressure, and risk of hypertension: Mendelian randomization study.
10.1136/bmj.j1000
Fine-scale human genetic structure in Western France.
10.1038/ejhg.2014.175
Blood microbiota dysbiosis is associated with the onset of cardiovascular events in a large general population: the D.E.S.I.R. study.
10.1371/journal.pone.0054461
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.
10.1007/s00125-012-2756-1
Low water intake and risk for new-onset hyperglycemia.
10.2337/dc11-0652
Number of children and change in markers of metabolic health over 9-years in men and women. Data from the DESIR study.
10.1016/j.diabet.2011.04.006
Influence of blood glucose on heart rate and cardiac autonomic function. The DESIR study.
10.1111/j.1464-5491.2010.03222.x
Metabolic health, obesity and 9-year incidence of peripheral arterial disease: the D.E.S.I.R. study.
10.1016/j.atherosclerosis.2011.02.032
Hemoglobin A1c and fasting plasma glucose levels as predictors of retinopathy at 10 years: the French DESIR study.
10.1001/archophthalmol.2010.353
Mean and yearly changes in blood pressure with age in the metabolic syndrome: the DESIR study.
10.1038/hr.2010.180
Center effect on ankle-brachial index measurement when using the reference method (Doppler and manometer): results from a large cohort study.
10.1038/ajh.2009.78
Urinary albumin excretion is a risk factor for diabetes mellitus in men, independently of initial metabolic profile and development of insulin resistance. The DESIR Study.
10.1097/hjh.0b013e328310ddff
5-HT2A receptor gene polymorphism is associated with food and alcohol intake in obese people.
10.1038/sj.ijo.0801253
Extensive association analysis between the CETP gene and coronary heart disease phenotypes reveals several putative functional polymorphisms and gene-environment interaction.
10.1002/1098-2272(200007)19:1<64::aid-gepi5>3.0.co;2-e
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPI.
10.1161/01.atv.19.4.862
Hind III polymorphism of the lipoprotein lipase gene and plasma lipid response to low calorie diet.
10.1038/sj.ijo.0800401
Alcohol intake modulates the effect of a polymorphism of the cholesteryl ester transfer protein gene on plasma high density lipoprotein and the risk of myocardial infarction.
10.1172/jci118207
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
10.1016/s1474-4422(17)30327-7
Erratum.
10.1093/ndt/gfx290
Plasma PCSK9 and Cardiovascular Events in Type 2 Diabetes
10.1111/dom.13181
Dairy Consumption and Body Mass Index Among Adults: Mendelian Randomization Analysis of 184802 Individuals from 25 Studies.
10.1373/clinchem.2017.280701
Non-severe hypoglycemia is associated with weight gain in patients with type 1 diabetes: Results from the Diabetes Control and Complication Trial.
10.1111/dom.13197
Plasma copeptin and chronic kidney disease risk in 3 European cohorts from the general population.
10.1172/jci.insight.121479
Plasma copeptin, kidney disease, and risk for cardiovascular morbidity and mortality in two cohorts of type 2 diabetes.
10.1186/s12933-018-0753-5
Prognostic value of plasma MR-proADM vs NT-proBNP for heart failure in people with type 2 diabetes: the SURDIAGENE prospective study.
10.1007/s00125-018-4727-7
Dairy consumption is associated with lower plasma dihydroceramides in women from the D.E.S.I.R. cohort.
10.1016/j.diabet.2019.06.002
Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study.
10.1001/jamanetworkopen.2019.10915
Plasma Copeptin and Risk of Lower-Extremity Amputation in Type 1 and Type 2 Diabetes.
10.2337/dc19-1062
New roles for prokineticin 2 in feeding behavior, insulin resistance and type 2 diabetes: Studies in mice and humans.
10.1016/j.molmet.2019.08.016
Plasma Apelin and Risk of Type 2 Diabetes in a Cohort From the Community.
10.2337/dc19-1865
Relationship between renal capacity to reabsorb glucose and renal status in patients with diabetes.
10.1016/j.diabet.2020.03.002
Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood.
10.1007/s10654-020-00638-z
Plasma total adiponectin and changes in renal function in a cohort from the community: the prospective Data from an Epidemiological Study on the Insulin Resistance Syndrome study.
10.1093/ndt/gfaa228
Effects of acyl-coenzyme A binding protein (ACBP)/diazepam-binding inhibitor (DBI) on body mass index.
10.1038/s41419-021-03864-9
Barbara Heude
Heude Barbara
ORCID: 0000-0002-1565-1629
Email: barbara.heude@inserm.fr
Persistent maternal depressive symptoms trajectories influence children's IQ: The EDEN mother-child cohort.
10.1002/da.22552
Early oral exposure to house dust mite allergen through breast milk: Apotential risk factor for allergic sensitization and respiratory allergies in children
10.1016/j.jaci.2016.07.021
Rapid Early Growth May Modulate the Association Between Birth Weight and Blood Pressure at 5 Years in the EDEN Cohort Study.
10.1161/hypertensionaha.116.07529
Prospective associations between energy balance-related behaviors at 2 years of age and subsequent adiposity: the EDEN mother-child cohort.
10.1038/ijo.2016.138
Social Withdrawal Behaviour at One Year of Age Is Associated with Delays in Reaching Language Milestones in the EDEN Mother-Child Cohort Study.
10.1371/journal.pone.0158426
A Novel Method to Describe Early Offspring Body Mass Index (BMI) Trajectories and to Study Its Determinants.
10.1371/journal.pone.0157766
Transcriptomic signatures of villous cytotrophoblast and syncytiotrophoblast in term human placenta.
10.1016/j.placenta.2016.06.001
Dietary acrylamide intake during pregnancy and anthropometry at birth in the French EDEN mother-child cohort study.
10.1016/j.envres.2016.05.019
Maternal weight prior and during pregnancy and offspring's BMI and adiposity at 5-6years in the EDEN mother-child cohort
10.1111/ijpo.12145
Re: "Maternal Caffeine Intake During Pregnancy and Child Cognition and Behavior at 4 and 7 Years of Age".
10.1093/aje/kww027
DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis.
10.1016/j.ajhg.2016.02.019
Early risk factors for posterior crossbite and anterior open bite in the primary dentition.
10.2319/102715-723.1
Fish Intake in Pregnancy and Child Growth: A Pooled Analysis of 15 European and US Birth Cohorts.
10.1001/jamapediatrics.2015.4430
Early determinants of food liking among 5y-old children: a longitudinal study from the EDEN mother-child cohort
10.1186/s12966-016-0342-5
Growth monitoring as an early detection tool: a systematic review.
10.1016/s2213-8587(15)00392-7
Association of postpartum depressive symptoms and urinary incontinence. A cohort study
10.1016/j.ejogrb.2015.12.028
DOHaD: epidemiological researches
10.1051/medsci/20163201005
Early growth characteristics and the risk of reduced lung function and asthma: A meta-analysis of 25,000 children.
10.1016/j.jaci.2015.08.050
Multidimensionality of the relationship between social status and dietary patterns in early childhood: longitudinal results from the French EDEN mother-child cohort
10.1186/s12966-015-0285-2
Effects of Antenatal Maternal Depression and Anxiety on Children's Early Cognitive Development: A Prospective Cohort Study
10.1371/journal.pone.0135849
Cohort Profile: The EDEN mother-child cohort on the prenatal and early postnatal determinants of child health and development.
10.1093/ije/dyv151
Impact on obstetric outcome of third-trimester screening for small-for-gestational-age fetuses
10.1002/uog.14755
Gender-specific factors associated with shorter sleep duration at age 3years
10.1111/jsr.12308
Maternal Depression Trajectories and Children's Behavior at Age 5 Years
10.1016/j.jpeds.2015.03.002
Maternal tobacco smoking in pregnancy and children's socio-emotional development at age 5: The EDEN mother-child birth cohort study
10.1016/j.eurpsy.2015.03.005
Should the WHO growth charts be used in France?
10.1371/journal.pone.0120806
Dietary patterns track from infancy to preschool age: cross-sectional and longitudinal perspectives.
10.3945/jn.114.201988
Associations Between Genetic Obesity Susceptibility and Early Postnatal Fat and Lean Mass An Individual Participant Meta-analysis
10.1001/jamapediatrics.2014.1619
Postnatal Weight and Height Growth Modeling and Prediction of Body Mass Index as a Function of Time for the Study of Growth Determinants
10.1159/000362203
Air Pollution During Pregnancy and Childhood Cognitive and Psychomotor Development Six European Birth Cohorts
10.1097/ede.0000000000000133
Predicting changes in language skills between 2 and 3 years in the EDEN mother-child cohort
10.7717/peerj.335
Preterm birth, infant weight gain, and childhood asthma risk: a meta-analysis of 147,000 European children
10.1016/j.jaci.2013.12.1082
Fish intake during pregnancy, fetal growth, and gestational length in 19 European birth cohort studies
10.3945/ajcn.113.067421
Ambient air pollution and low birthweight: a European cohort study (ESCAPE)
10.1016/s2213-2600(13)70192-9
Does consideration of larger study areas yield more accurate estimates of air pollution health effects? An illustration of the bias-variance trade-off in air pollution epidemiology
10.1016/j.envint.2013.07.005
Modifiable exposures to air pollutants related to asthma phenotypes in the first year of life in children of the EDEN mother-child cohort study
10.1186/1471-2458-13-506
Breastfeeding Duration, Social and Occupational Characteristics of Mothers in the French 'EDEN Mother-Child' Cohort
10.1007/s10995-012-1053-4
Exposure to food contaminants during pregnancy
10.1016/j.scitotenv.2013.03.100
Impact of objectively measured sedentary behaviour on changes in insulin resistance and secretion over 3 years in the RISC study: Interaction with weight gain
10.1016/j.diabet.2012.12.006
Breastfeeding Duration and Cognitive Development at 2 and 3 Years of Age in the EDEN Mother-Child Cohort
10.1016/j.jpeds.2012.11.090
Infant feeding patterns over the first year of life: influence of family characteristics
10.1038/ejcn.2012.200
Association between maternal blood cadmium during pregnancy and birth weight and the risk of fetal growth restriction: The EDEN mother-child cohort study
10.1016/j.reprotox.2012.09.002
Pregnancy exposure to atmospheric pollutants and placental weight: An approach relying on a dispersion model
10.1016/j.envint.2012.06.013
Specific role of maternal weight change in the first trimester of pregnancy on birth size
10.1111/j.1740-8709.2012.00423.x
Depression and anxiety in women during pregnancy and neonatal outcome: Data from the EDEN mother-child cohort
10.1016/j.earlhumdev.2012.01.014
Perinatal risk factors and social withdrawal behaviour
10.1007/s00787-012-0250-4
Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes Risk
10.2337/db11-0728
Parent-Offspring Correlations in Pedometer-Assessed Physical Activity
10.1371/journal.pone.0029195
Maternal depression, socioeconomic position, and temperament in early childhood: The EDEN mother-child cohort
10.1016/j.jad.2011.09.018
Association of the Pro12Ala and C1431T variants of PPARgamma and their haplotypes with susceptibility to gestational diabetes.
10.1210/jc.2011-0381
Maternal weight change before pregnancy in relation to birthweight and risks of adverse pregnancy outcomes
10.1007/s10654-011-9599-9
Higher Cord C-Peptide Concentrations Are Associated With Slower Growth Rate in the 1st Year of Life in Girls but Not in Boys
10.2337/db10-1189
Discordant time trends in maternal body size and offspring birthweight of term deliveries in France between 1972 and 2003: data from the French National Perinatal Surveys
10.1111/j.1365-3016.2010.01188.x
Determinants of neonatal weight loss in term-infants: specific association with pre-pregnancy maternal body mass index and infant feeding mode
10.1136/adc.2010.185546
Determinants of early ponderal and statural growth in full-term infants in the EDEN mother-child cohort study
10.3945/ajcn.2010.29292
Parental body size and early weight and height growth velocities in their offspring
10.1016/j.earlhumdev.2010.06.001
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
10.1371/journal.pgen.1000916
Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population
10.1038/oby.2009.468
Early Detrimental Metabolic Outcomes of rs17300539-A Allele of ADIPOQ Gene Despite Higher Adiponectinemia
10.1038/oby.2009.403
Cognitive restraint, uncontrolled eating and emotional eating: correlations between parent and adolescent
10.1111/j.1740-8709.2008.00164.x
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
10.1038/ng.301
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk
10.1038/ng.277
A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature
10.1111/j.1469-1809.2008.00484.x
Ghrelin receptor gene polymorphisms and body size in children and adults
10.1210/jc.2008-0366
Common nonsynonymous variants in PCSK1 confer risk of obesity
10.1038/ng.177
INS VNTR is not associated with childhood obesity in 1,023 families: A family-based study
10.1038/oby.2008.209
Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations
10.1093/hmg/ddn089
Association analysis of the IGF1 gene with childhood growth, IGF-1 concentrations and type 1 diabetes
10.1007/s00125-008-0970-7
Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity
10.1210/jc.2006-2316
Relationship between gamma-glutamyltransferase and fat mass in a general population of 8-17 years old children. The FLVS II study
10.1016/j.diabet.2007.03.008
Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity
10.1186/1471-2350-8-44
Study of association between common variation in the insulin-like growth factor 2 gene and indices of obesity and body size in middle-aged men and women
10.1210/jc.2006-1948
Cardiovascular risk factor levels and their relationships with overweight and fat distribution in children: The Fleurbaix Laventie Ville Sante II study
10.1016/j.metabol.2006.12.006
A genome-wide association study identifies novel risk loci for type 2 diabetes
10.1038/nature05616
Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects
10.1007/s00125-006-0555-2
High plasma leptin predicts an increase in subcutaneous adiposity in children and adults
10.1038/sj.ejcn.1602579
Serum adiponectin is related to plasma high-density lipoprotein cholesterol but not to plasma insulin-concentration in healthy children: the FLVS II study
10.1016/j.metabol.2006.04.015
Growth curves of anthropometric indices in a general population of French children and comparison with reference data
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The insulin gene variable number of tandem repeat: Associations and interactions with childhood body fat mass and insulin secretion in normal children
10.1210/jc.2005-2055
ACDC/adiponectin polymorphisms are associated with severe childhood and adult obesity
10.2337/diabetes.55.02.06.db05-0971
Reliability of bioimpedance analysis compared with other adiposity measurements in children: The FLVS II Study
10.1016/s1262-3636(07)70228-8
Anthropometric relationships between parents and children throughout childhood: the Fleurbaix-Laventie Ville Sante Study
10.1038/sj.ijo.0802920
INS VNTR class genotype and indexes of body size and obesity: population-based studies of 7,999 middle-aged men and women.
10.2337/diabetes.54.9.2812
Changes in physical activity explain paradoxical relationship between baseline physical activity and adiposity changes in adolescent girls: the FLVS II study
10.1038/sj.ijo.0802992
Is glutamate decarboxylase 2 (GAD2) a genetic link between low birth weight and subsequent development of obesity in children?
10.1210/jc.2004-1468
VNTR polymorphism of the insulin gene and childhood overweight in a general population
10.1038/oby.2004.56
Time trend in height, weight, and obesity prevalence in school children from Northern France, 1992-2000
10.1016/s1262-3636(07)70032-0
Modelling the growth curve of Maine-Anjou beef cattle using heteroskedastic random coefficients models
10.1051/gse:2002016
Emotional, behavioral and social difficulties among high-IQ children during the preschool period: Results of the EDEN mother-child cohort
10.1016/j.paid.2016.02.014
Maternal depression and child development: evidence from an EDEN cohort
10.1016/j.eurpsy.2015.09.101
Pregnancy and birth cohort resources in Europe: a large opportunity for aetiological child health research (vol 27, pg 393, 2013)
10.1111/ppe.12079
The Dietary n6:n3 Fatty Acid Ratio during Pregnancy Is Inversely Associated with Child Neurodevelopment in the EDEN Mother-Child Cohort
10.3945/jn.113.178640
Pre-Pregnancy Body Mass Index and Weight Gain During Pregnancy: Relations with Gestational Diabetes and Hypertension, and Birth Outcomes
10.1007/s10995-011-0741-9
Evolution of Obesity Prevalence in France An Age-Period-Cohort Analysis
10.1097/EDE.0b013e3181d5bff5
Ages and Stages Questionnaire at 3 Years for Predicting IQ at 5-6 Years
10.1542/peds.2016-2798
10.1542/peds.2016-2798.
Breastfeeding, Polyunsaturated Fatty Acid Levels in Colostrum and Child Intelligence Quotient at Age 5-6 Years
10.1016/j.jpeds.2016.12.039
Do developmental milestones at 4, 8, 12 and 24 months predict IQ at 5-6 years old? Results of the EDEN mother-child cohort
10.1016/j.ejpn.2016.11.001
Early factors related to carbohydrate and fat intake at 8 and 12 months: results from the EDEN mother-child cohort
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Factors Associated with Breastfeeding Initiation: A Comparison between France and French-Speaking Canada
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Relationship between early language skills and the development of inattention/hyperactivity symptoms during the preschool period: Results of the EDEN mother-child cohort
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The Influence of Meteorological Factors and Atmospheric Pollutants on the Risk of Preterm Birth
10.1093/aje/kww141
Influence of infant feeding patterns over the first year of life on growth from birth to 5years
10.1111/ijpo.12213
Prenatal Exposure to Phenols and Growth in Boys
10.1097/ede.0000000000000132
Returning to Work One Year After Childbirth: Data from the Mother-Child Cohort EDEN
10.1007/s10995-012-1147-z
Trends in urinary incontinence in women between 4 and 24 months postpartum in the EDEN cohort
10.1111/1471-0528.13545
Phthalate pregnancy exposure and male offspring growth from the intra-uterine period to five years of age
10.1016/j.envres.2016.08.033
Predictors of persistent maternal depression trajectories in early childhood: results from the EDEN mother-child cohort study in France
10.1017/s003329171500015x
Health effects of ambient air pollution: Do different methods for estimating exposure lead to different resifts?
10.1016/j.envint.2014.02.001
Gestational Exposure to Urban Air Pollution Related to a Decrease in Cord Blood Vitamin D Levels
10.1210/jc.2012-1943
Influence of fetal and parental factors on intrauterine growth measurements: results of the EDEN mother-child cohort
10.1002/uog.9006
Maternal Exposure to Nitrogen Dioxide during Pregnancy and Offspring Birth Weight: Comparison of Two Exposure Models
10.1289/ehp.0901509
Cord serum 25-hydroxyvitamin D and risk of early childhood transient wheezing and atopic dermatitis
10.1016/j.jaci.2013.05.017
To which extent social withdrawal at the age of 1 year is associated with IQ at 5-6 years old? Results of the EDEN mother-child cohort
10.1007/s00787-017-0988-9
Joint Bayesian weight and height postnatal growth model to study the effects of maternal smoking during pregnancy
10.1002/sim.7407
Standards or References: A Central Question for Growth Monitoring?
10.1111/ppe.12394
To which mixtures are French pregnant women mainly exposed? A combination of the second French total diet study with the EDEN and ELFE cohort studies
10.1016/j.fct.2017.11.016
Early postnatal growth and neurodevelopment in children born moderately preterm or small for gestational age at term: A systematic review
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Pregnancy exposure to atmospheric pollution and meteorological conditions and placental DNA methylation.
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Air pollution exposure during pregnancy and symptoms of attention deficit and hyperactivity disorder in children in Europe.
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Prenatal diet and children's trajectories of hyperactivity-inattention and conduct problems from 3 to 8 years: the EDEN mother-child cohort.
10.1111/jcpp.12898
Survey highlights important discrepancies between definitions of paediatric abnormal growth taught to medical students in 23 European countries.
10.1111/apa.14266
Developmental milestones at one year for the offspring of mothers with congenital hypothyroidism: a population-based study
10.1530/eje-17-0855
In-utero exposure to phenols and phthalates and the intelligence quotient of boys at 5 years.
10.1186/s12940-018-0359-0
Sleep and its relation to cognition and behaviour in preschool-aged children of the general population: a systematic review.
10.1111/jsr.12636
Night-waking and behavior in preschoolers: a developmental trajectory approach.
10.1016/j.sleep.2017.10.008
Maternal nutritional determinants of colostrum fatty acids in the EDEN mother-child cohort.
10.1016/j.clnu.2017.10.007
Prenatal exposure to glycol ethers and cryptorchidism and hypospadias: a nested case-control study.
10.1136/oemed-2017-104391
Prenatal Exposure to Nonpersistent Endocrine Disruptors and Behavior in Boys at 3 and 5 Years.
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Mediation and modification of genetic susceptibility to obesity by eating behaviors.
10.3945/ajcn.117.157396
Priority target conditions for algorithms for monitoring children's growth: Interdisciplinary consensus.
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Ages and Stages Questionnaire at 3 Years for Predicting IQ at 5-6 Years.
10.1542/peds.2016-2798
Night-waking trajectories and associated factors in French preschoolers from the EDEN birth-cohort.
10.1016/j.sleep.2016.09.008
The association between linoleic acid levels in colostrum and child cognition at 2 and 3 y in the EDEN cohort.
10.1038/pr.2015.50
Pregnancy and birth cohort resources in europe: a large opportunity for aetiological child health research.
10.1111/ppe.12060
Postnatal weight and height growth velocities at different ages between birth and 5 y and body composition in adolescent boys and girls.
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Cognitive decline and fatty acid composition of erythrocyte membranes--The EVA Study.
10.1093/ajcn/77.4.803
Are selection criteria for healthy pregnancies responsible for the gap between fetal growth in the French national Elfe birth cohort and the Intergrowth‐21st fetal growth standards?
10.1111/ppe.12526
Association between genetic obesity susceptibility and mother‐reported eating behaviour in children up to 5 years
10.1111/ijpo.12496
Response to Letter to the Editor: “Algorithms to Define Abnormal Growth in Children: External Validation and Head-to-Head Comparison”
10.1210/jc.2019-00564
Which modifiable prenatal factors mediate the relation between socio‐economic position and a child's weight and length at birth?
10.1111/mcn.12878
Dietary Inflammatory Index and Non-Communicable Disease Risk: A Narrative Review
10.3390/nu11081873
An association between maternal weight change in the year before pregnancy and infant birth weight: ELFE, a French national birth cohort study
10.1371/journal.pmed.1002871
Deriving the Dietary Approaches to Stop Hypertension (DASH) Score in Women from Seven Pregnancy Cohorts from the European ALPHABET Consortium
10.3390/nu11112706
Breastfeeding initiation or duration and longitudinal patterns of infections up to 2 years and skin rash and respiratory symptoms up to 8 years in the EDEN mother–child cohort
10.1111/mcn.12935
Measuring Child Socio-Economic Position in Birth Cohort Research: The Development of a Novel Standardized Household Income Indicator
10.3390/ijerph17051700
Association between Dietary Intake of One-Carbon Metabolism Nutrients in the Year before Pregnancy and Birth Anthropometry
10.3390/nu12030838
Urban environment during early-life and blood pressure in young children
10.1016/j.envint.2020.106174
Dietary Quality and Dietary Inflammatory Potential During Pregnancy and Offspring Emotional and Behavioral Symptoms in Childhood: An Individual Participant Data Meta-analysis of Four European Cohorts.
10.1016/j.biopsych.2020.10.008
Cord Serum Cytokines at Birth and Children’s Anxiety-Depression Trajectories From 3 to 8 Years: The EDEN Mother–Child Cohort
10.1016/j.biopsych.2020.10.009
Prenatal Diet and Children's Trajectories of Anxiety and Depression Symptoms from 3 to 8 Years: The EDEN Mother-Child Cohort
10.1093/jn/nxaa343
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.
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Breast milk n-3 long-chain polyunsaturated fatty acids and blood pressure: an individual participant meta-analysis
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Prenatal Exposure to Perfluoroalkyl Substances Associated With Increased Susceptibility to Liver Injury in Children.
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Association of Fish Consumption and Mercury Exposure During Pregnancy With Metabolic Health and Inflammatory Biomarkers in Children.
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Gestational weight gain charts for different body mass index groups for women in Europe, North America, and Oceania.
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Domain-specific physical activity and sedentary behavior during pregnancy and postpartum depression risk in the French EDEN and ELFE cohorts.
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Is Handedness at Five Associated with Prenatal Factors?
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Associations between Children’s Genetic Susceptibility to Obesity, Infant’s Appetite and Parental Feeding Practices in Toddlerhood
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Placental DNA methylation signatures of maternal smoking during pregnancy and potential impacts on fetal growth
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