G. Velho

S. Hadjadj, M. Marre, R. Roussel, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Expression of phosphoenolpyruvate carboxykinase gene in human adipose tissue: induction by rosiglitazone and genetic analyses of the adipocyte-specific region of the promoter in type 2 diabetes.

G. Velho, F. Fouque, E. Duplus, 2003, Biochimie.

Genetics of macrovascular complications in diabetes

G. Velho, F. Fumeron, A. F. Reis, 2006, Current diabetes reports.

Diagnosis of Hyperglycemia in a Cohort of Brazilian Subjects

M. T. Ghiringhello, J. Vieira, G. Velho, 2007, Diabetes Care.

Dynamic Changes in Renal Function Are Associated With Major Cardiovascular Events in Patients With Type 2 Diabetes

V. Rigalleau, S. Hadjadj, M. Marre, 2016, Diabetes Care.

Dairy consumption is associated with lower plasma dihydroceramides in women from the D.E.S.I.R. cohort.

B. Balkau, M. Marre, R. Roussel, 2020, Diabetes & metabolism.

Subject Index Vol. 57, Suppl. 1, 2001

Margaret S. McGill, M. Knip, D. Dunger, 2004, Hormone Research in Paediatrics.

Evidence for 100% 13C NMR visibility of glucose in human skeletal muscle

R. Roussel, P. Carlier, G. Velho, 1997, Magnetic resonance in medicine.

Polymorphism of the glycogen synthase gene and non-insulin-dependent diabetes mellitus.

P. Froguel, H. Zouali, G. Velho, 1993, The New England journal of medicine.

The lactase persistence genotype is associated with body mass index and dairy consumption in the D.E.S.I.R. study.

B. Balkau, O. Lantieri, M. Marre, 2013, Metabolism: clinical and experimental.

Leukocyte Telomere Length, DNA Oxidation, and Risk of Lower-Extremity Amputation in Patients With Long-standing Type 1 Diabetes

S. Hadjadj, M. Marre, R. Roussel, 2020, Diabetes Care.

ACE I/D Polymorphism, Plasma ACE Levels, and Long-term Kidney Outcomes or All-Cause Death in Patients With Type 1 Diabetes

S. Hadjadj, M. Marre, R. Roussel, 2021, Diabetes Care.

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.

B. Balkau, M. Marre, R. Roussel, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Relationship between renal capacity to reabsorb glucose and renal status in patients with diabetes.

S. Hadjadj, M. Marre, R. Roussel, 2020, Diabetes & metabolism.

Plasma Copeptin and Risk of Lower-Extremity Amputation in Type 1 and Type 2 Diabetes

S. Hadjadj, M. Marre, R. Roussel, 2019, Diabetes Care.

Plasma copeptin and chronic kidney disease risk in 3 European cohorts from the general population.

Lyanne M. Kieneker, O. Melander, B. Balkau, 2018, JCI insight.

Variations in the vitamin D-binding protein (Gc locus) and risk of type 2 diabetes mellitus in French Caucasians.

C. Bellanné-Chantelot, D. Dubois-Laforgue, G. Velho, 2001, Metabolism: clinical and experimental.

Lipoprotein(a) in Diabetic Patients and Normoglycemic Relatives in Familial NIDDM

P. Froguel, G. Velho, D. Néel, 1993, Diabetes Care.

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

J. Beckmann, J. Weissenbach, K. Clément, 1992, Nature.

Association of a variant in exon 31 of the sulfonylurea receptor 1 (SUR1) gene with type 2 diabetes mellitus in French Caucasians

C. Bellanné-Chantelot, G. Velho, J. Timsit, 2000, Human Genetics.

Genetic analyses of glucose transporter genes in French non-insulin-dependent diabetic families.

P. Froguel, H. Zouali, S. Lesage, 1997, Diabetes & metabolism.

Insulin receptor substrate (IRS-1) gene polymorphisms in French NIDDM families

P. Froguel, H. Zouali, G. Velho, 1993, The Lancet.

Glucagon revisited: Coordinated actions on the liver and kidney.

L. Bankir, G. Velho, N. Bouby, 2018, Diabetes research and clinical practice.

Maturity-Onset Diabetes of the Young (MODY): Genetic and Clinical Characteristics

G. Velho, J. Robert, 2004, Hormone Research in Paediatrics.

Mutations in the insulin promoter factor-1 gene in late-onset type 2 diabetes mellitus.

C. Bellanné-Chantelot, D. Dubois-Laforgue, G. Velho, 2000, European journal of endocrinology.

Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the young.

M. Vaxillaire, H. Zouali, S. Lesage, 1993, The Journal of clinical investigation.

A polymorphism in the promoter of UCP2 gene modulates lipid levels in patients with type 2 diabetes.

C. Bellanné-Chantelot, G. Velho, J. Timsit, 2004, Molecular genetics and metabolism.

- Cell Genes and Diabetes : Quantitative and Qualitative Differences in the Pathophysiology of Hepatic Nuclear Factor-1 and Glucokinase Mutations

T. Frayling, A. Hattersley, S. Ellard, 2001 .

Leptin Levels, β-Cell Function, and Insulin Sensitivity in Families with Congenital and Acquired Generalized Lipoatropic Diabetes1

G. Velho, S. Purisch, V. C. Pardini, 1998 .

Leptin levels, beta-cell function, and insulin sensitivity in families with congenital and acquired generalized lipoatropic diabetes.

G. Velho, S. Purisch, V. C. Pardini, 1998, The Journal of clinical endocrinology and metabolism.

Glucose-induced insulin hypersecretion in lipid-infused healthy subjects is associated with a decrease in plasma norepinephrine concentration and urinary excretion.

A. Girard, G. Velho, C. Magnan, 2001, The Journal of clinical endocrinology and metabolism.

HNF 1 α Mutations Are Present in Half of Clinically Defi ned MODY Patients in South-Brazilian Individuals

B. Grandchamp, G. Velho, J. Gross, 2008 .

Allelic variation in exon 18 of the sulfonylurea receptor 1 (SUR1) gene, insulin secretion and insulin sensitivity in nondiabetic relatives of type 2 diabetic subjects.

P. Froguel, G. Velho, E. Hani, 2002, Diabetes & metabolism.

Genetic determinants of type 2 diabetes mellitus: lessons learned from family studies.

P. Froguel, G. Velho, P. Passa, 1993, Diabete & metabolisme.

Maturity-onset diabetes of the young.

P. Froguel, G. Velho, 1994, Current opinion in pediatrics.

Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR ): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians

M. Permutt, P. Boutin, P. Froguel, 1998, Diabetologia.

Beta-cell secretory defect caused by mutations in glucokinase gene

K. Clément, A. Hattersley, P. Froguel, 1992, The Lancet.

HNF1alpha controls renal glucose reabsorption in mouse and man.

P. Froguel, M. Yaniv, M. Pontoglio, 2000, EMBO reports.

Mutation screening in 18 Caucasian families suggest the existence of other MODY genes

P. Boutin, G. Charpentier, P. Froguel, 1998, Diabetologia.

Maturity Onset Diabetes of the Young (Mody)

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Prevalence of maturity-onset diabetes of the young mutations in Brazilian families with autosomal-dominant early-onset type 2 diabetes.

C. Bellanné-Chantelot, G. Velho, R. Moises, 2001, Diabetes care.

MODY sub-types in a panel of Spanish families with early onset diabetes mellitus , and to assess phenotypic differences in patients with the different subtypes of MODY . Research design and methods Subjects

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Molecular Genetics of Maturity-onset Diabetes of the Young

P. Froguel, G. Velho, 1999, Trends in Endocrinology & Metabolism.

Adipocyte Reprogramming by the Transcriptional Coregulator GPS2 Impacts Beta Cell Insulin Secretion

R. Roussel, E. Treuter, G. Velho, 2020, Cell reports.

Medical Genetics of MODYs

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Genetic, metabolic and clinical characteristics of maturity onset diabetes of the young.

P. Froguel, G. Velho, 1998, European journal of endocrinology.

Structure/function studies of human beta-cell glucokinase. Enzymatic properties of a sequence polymorphism, mutations associated with diabetes, and other site-directed mutants.

P. Froguel, M. Vaxillaire, G. Velho, 1993, The Journal of biological chemistry.

Proposed involvement of adipocyte glyceroneogenesis and phosphoenolpyruvate carboxykinase in the metabolic syndrome.

G. Velho, F. Fouque, J. Tordjman, 2005, Biochimie.

Differential prognostic burden of cardiovascular disease and lower-limb amputation on the risk of all-cause death in people with long-standing type 1 diabetes

V. Rigalleau, S. Hadjadj, M. Marre, 2022, Cardiovascular Diabetology.

Vasopressin and diabetic nephropathy

R. Roussel, L. Bankir, G. Velho, 2017, Current opinion in nephrology and hypertension.

Genetic determinants of non-insulin-dependent diabetes mellitus: strategies and recent results.

P. Froguel, G. Velho, 1997, Diabetes & metabolism.

Non‐severe hypoglycaemia is associated with weight gain in patients with type 1 diabetes: Results from the Diabetes Control and Complication Trial

M. Marre, R. Roussel, G. Velho, 2018, Diabetes, obesity & metabolism.

Vasopressin and hydration play a major role in the development of glucose intolerance and hepatic steatosis in obese rats

O. Melander, V. Paradis, R. Roussel, 2015, Diabetologia.

Specific insulin and proinsulin secretion in glucokinase-deficient individuals.

H. Blanché, J. Vieira, G. Velho, 1999, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

The Ala45Thr polymorphism of NEUROD1 is associated with type 1 diabetes in Brazilian women.

J. Vieira, G. Velho, J. Gross, 2005, Diabetes & metabolism.

Plasma concentrations of 8-hydroxy-2′-deoxyguanosine and risk of kidney disease and death in individuals with type 1 diabetes

S. Hadjadj, M. Marre, R. Roussel, 2018, Diabetologia.

Vasopressin and metabolic disorders: translation from experimental models to clinical use

G. Velho, Kazuaki Nakamura, N. Bouby, 2017, Journal of internal medicine.

Glucose tolerance and insulin secretion, morbidity, and death in patients with cystic fibrosis.

G. Velho, I. Sermet, E. Bismuth, 2008, The Journal of pediatrics.

Leukocyte telomere length, allelic variations in related genes and risk of coronary heart disease in people with long-standing type 1 diabetes

S. Hadjadj, M. Marre, R. Roussel, 2022, Cardiovascular Diabetology.

Acute and chronic hyperglycemic effects of vasopressin in normal rats: involvement of V1A receptors.

O. Melander, R. Roussel, L. Bankir, 2017, American journal of physiology. Endocrinology and metabolism.

Primary pancreatic beta-cell secretory defect caused by mutations in glucokinase gene in kindreds of maturity onset diabetes of the young

K. Clément, P. Froguel, H. Zouali, 1992, The Lancet.

Non-sense mutation of glucokinase gene

M. Permutt, P. Froguel, G. Velho, 1993, The Lancet.

The Gly482Ser polymorphism in the peroxisome proliferator-activated receptor-γ coactivator-1 gene is associated with hypertension in type 2 diabetic men

C. Bellanné-Chantelot, D. Dubois-Laforgue, G. Velho, 2004, Diabetologia.

ABCG8 polymorphisms and renal disease in type 2 diabetic patients.

S. Hadjadj, M. Marre, R. Roussel, 2015, Metabolism: clinical and experimental.

Fetal hemoglobin levels are related to metabolic control in diabetic subjects.

G. Velho, S. Purisch, V. C. Pardini, 1999, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Erratum: Human glucokinase gene: Isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin- dependent (type 2) diabetes mellitus (Proc. Natl. Acad. Sci. USA (August 15, 1992) 89 (7698-7702))

M. Stoffel, P. Froguel, I. Weber, 1992 .

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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Two novel mutations in the EIF2AK3 gene in children with Wolcott–Rallison syndrome

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Impaired hepatic glycogen synthesis in glucokinase-deficient (MODY-2) subjects.

P. Froguel, K. Petersen, G. Shulman, 1996, The Journal of clinical investigation.

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.

J. Beckmann, M. Permutt, M. Stoffel, 1993, The New England journal of medicine.

An Automated Fluorescent Single-Strand Conformation Polymorphism Technique for Screening Mutations in the Hepatocyte Nuclear Factor-1α Gene (Maturity-Onset Diabetes of the Young)

P. Boutin, P. Froguel, M. Vaxillaire, 1997, Diabetes.

An Automated Fluorescent Single-Strand Conformation Polymorphism Technique for Screening Mutations in the Hepatocyte Nuclear Factor-la Gene (Maturity-Onset Diabetes of the Young) Boutin, Jean Claude Chevre, El Habib Hani, Ramon Gomis, Victor C. Pardini,

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A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q

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Linkage disequilibrium with HLA-DRB1-DQB1 haplotypes explains the association of TNF-308G>A variant with type 1 diabetes in a Brazilian cohort.

G. Velho, E. Pavin, L. Canani, 2015, Gene.

Determination of peritoneal glucose kinetics in rats: implications for the peritoneal implantation of closed-loop insulin delivery systems

P. Froguel, G. Reach, G. Velho, 1989, Diabetologia.

Body-weight variability and risk of cardiovascular outcomes in patients with type 1 diabetes: a retrospective observational analysis of data from the DCCT/EDIC population

G. Varoquaux, J. Vie, R. Roussel, 2022, Cardiovascular Diabetology.

Maturity-onset diabetes of the young (MODY), MODY genes and non-insulin-dependent diabetes mellitus.

P. Froguel, G. Velho, 1997, Diabetes & metabolism.

SGLT2 inhibitors and lower limb complications: the diuretic-induced hypovolemia hypothesis

R. Roussel, G. Velho, K. Mohammedi, 2021, Cardiovascular Diabetology.

T-cadherin gene variants are associated with nephropathy in subjects with type 1 diabetes

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T-cadherin gene variants are associated with nephropathy in subjects with type 1 diabetes.

S. Hadjadj, M. Marre, R. Roussel, 2017, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

A missense mutation in the glucagon receptor gene is associated with non–insulin–dependent diabetes mellitus

G. Velho, C. Carcassi, C. Carcassi, 1995, Nature Genetics.

The N363S polymorphism in the glucocorticoid receptor gene is associated with overweight in subjects with type 2 diabetes mellitus

R. Roussel, C. Bellanné-Chantelot, G. Velho, 2003, Clinical endocrinology.

Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10.

J. Terwilliger, D. Weeks, G. Lathrop, 1997, Human molecular genetics.

Antibodies to Bovine Serum Albumin in Brazilian Children and Young Adults With IDDM

J. Vieira, G. Velho, S. R. Ferreira, 1996, Diabetes Care.

Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5.

M. Jadoul, Jacques Young, C. Bellanné-Chantelot, 2005, Diabetes.

Insertion/deletion polymorphism of the angiotensin-converting enzyme gene is strongly associated with coronary heart disease in non-insulin-dependent diabetes mellitus.

F. Cambien, P. Froguel, H. Blanché, 1994, Proceedings of the National Academy of Sciences of the United States of America.

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

B. Balkau, P. Froguel, O. Lantieri, 2012, International Journal of Obesity.

Genetic Studies of the Sulfonylurea Receptor Gene Locus in NIDDM and in Morbid Obesity Among French Caucasians

K. Clément, M. Permutt, C. Dina, 1997, Diabetes.

Glutathione peroxidase-1 gene (GPX1) variants, oxidative stress and risk of kidney complications in people with type 1 diabetes.

S. Hadjadj, M. Marre, H. Le Nagard, 2016, Metabolism: clinical and experimental.

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

J. Beckmann, J. Weissenbach, K. Clément, 1992, Nature.

Plasma concentrations of lipoproteins and risk of lower-limb peripheral artery disease in people with type 2 diabetes: the SURDIAGENE study

V. Rigalleau, S. Hadjadj, M. Marre, 2021, Diabetologia.

HNF1alpha mutations are present in half of clinically defined MODY patients in South-Brazilian individuals.

B. Grandchamp, G. Velho, J. Gross, 2008, Arquivos brasileiros de endocrinologia e metabologia.

Diagnosis and Management of Maturity-Onset Diabetes of the Young

C. Bellanné-Chantelot, G. Velho, J. Timsit, 2005, Treatments in endocrinology.

beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations.

T. Frayling, A. Hattersley, S. Ellard, 2001, Diabetes.

HNF1α controls renal glucose reabsorption in mouse and man

P. Froguel, M. Yaniv, M. Pontoglio, 2000 .

Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice.

P. Froguel, K. Polonsky, S. Bonner-Weir, 1998, The Journal of clinical investigation.

13C/31P NMR studies of glucose transport in human skeletal muscle.

R. Roussel, P. Carlier, G. Velho, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families

P. Froguel, I. Weber, H. Blanché, 1997, Diabetologia.

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.

B. Balkau, M. Marre, J. Tichet, 2010, The Journal of clinical endocrinology and metabolism.

Sex-specific associations of variants in regulatory regions of NADPH oxidase-2 (CYBB) and glutathione peroxidase 4 (GPX4) genes with kidney disease in type 1 diabetes

G. Velho, M. Marre, G. Velho, 2013, Free radical research.

Comparison between copeptin and vasopressin in a population from the community and in people with chronic kidney disease.

B. Balkau, O. Lantieri, M. Marre, 2014, The Journal of clinical endocrinology and metabolism.

Allelic variations in the vitamin D receptor gene, insulin secretion and parents' heights are independently associated with height in obese children and adolescents.

G. Velho, S. Villares, N. Bellili-Muñoz, 2012, Metabolism: clinical and experimental.

Search for a Third Susceptibility Gene for Maturity-Onset Diabetes of the Young: Studies With Eleven Candidate Genes

J. Beckmann, M. Stoffel, P. Froguel, 1994, Diabetes.

T-cadherin gene variants are associated with type 2 diabetes and the Fatty Liver Index in the French population.

B. Balkau, M. Marre, J. Tichet, 2017, Diabetes & metabolism.

Vitamin D receptor gene polymorphisms are associated with obesity in type 2 diabetic subjects with early age of onset.

C. Bellanné-Chantelot, D. Dubois-Laforgue, G. Velho, 2001, European journal of endocrinology.

Lower extremity arterial disease in patients with diabetes: a contemporary narrative review

V. Rigalleau, M. Marre, R. Roussel, 2018, Cardiovascular Diabetology.

Sulfonylurea receptor -1 (SUR1): genetic and metabolic evidences for a role in the susceptibility to type 2 diabetes mellitus.

G. Velho, A. Reis, André F. Reis, 2002, Diabetes & metabolism.

Glucose Metabolism in 105 Children and Adolescents After Pancreatectomy for Congenital Hyperinsulinism

F. Brunelle, G. Velho, J. Saudubray, 2012, Diabetes Care.

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

S. Hadjadj, M. Marre, H. Le Nagard, 2015, Cardiovascular Diabetology.

Glucokinase as pancreatic beta cell glucose sensor and diabetes gene.

M. Permutt, P. Froguel, G. Velho, 1993, The Journal of clinical investigation.

Plasma Copeptin and Decline in Renal Function in a Cohort from the Community: The Prospective D.E.S.I.R. Study

B. Balkau, M. Marre, R. Roussel, 2015, American Journal of Nephrology.

Plasma Adrenomedullin and Allelic Variation in the ADM Gene and Kidney Disease in People With Type 2 Diabetes

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Tissue kallikrein deficiency, insulin resistance, and diabetes in mouse and man.

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Association of Circulating Biomarkers (Adrenomedullin, TNFR1, and NT-proBNP) With Renal Function Decline in Patients With Type 2 Diabetes: A French Prospective Cohort

S. Hadjadj, S. Ragot, R. Roussel, 2016, Diabetes Care.

Genetic determinants of type 2 diabetes.

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Association of circulating levels of nicotinamide phosphoribosyltransferase (NAMPT/Visfatin) and of a frequent polymorphism in the promoter of the NAMPT gene with coronary artery disease in diabetic and non-diabetic subjects

J. Vieira, G. Velho, F. Crispim, 2013, Cardiovascular Diabetology.

O R I G I N a L I N V E S T I G a T I O N Open Access

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Association of ADIPOQ variants, total and high molecular weight adiponectin levels with coronary artery disease in diabetic and non-diabetic Brazilian subjects.

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Renal dysfunction in HNF 1 α / MODY 3 deficiency scientific reports

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Glucokinase mutations associated with non-insulin-dependent (type 2) diabetes mellitus have decreased enzymatic activity: implications for structure/function relationships.

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Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu(UUR) gene

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In vivo NMR evidence for moderate glucose accumulation in human skeletal muscle during hyperglycemia.

R. Roussel, P. Carlier, G. Velho, 1996, The American journal of physiology.

Allelic variations in superoxide dismutase-1 (SOD1) gene are associated with increased risk of diabetic nephropathy in type 1 diabetic subjects.

S. Hadjadj, M. Marre, R. Roussel, 2011, Molecular genetics and metabolism.

Angiotensin converting enzyme insertion/deletion polymorphism is associated with increased adiposity and blood pressure in obese children and adolescents.

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Effect of a diabetic environment in utero on predisposition to type 2 diabetes

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Impact of morbid obesity on the kidney function of patients with type 2 diabetes.

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Allelic variations in the CYBA gene of NADPH oxidase and risk of kidney complications in patients with type 1 diabetes.

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Association of Serum Concentration of TNFR1 With All-Cause Mortality in Patients With Type 2 Diabetes and Chronic Kidney Disease: Follow-up of the SURDIAGENE Cohort

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Prognostic Values of Inflammatory and Redox Status Biomarkers on the Risk of Major Lower-Extremity Artery Disease in Individuals With Type 2 Diabetes

V. Rigalleau, S. Hadjadj, M. Marre, 2018, Diabetes Care.

The evaluation of off-loading using a new removable oRTHOsis in DIABetic foot (ORTHODIAB) randomized controlled trial: study design and rational

M. Dolz, V. Rigalleau, F. Tubach, 2016, Journal of Foot and Ankle Research.

Association Between the ACE Insertion/Deletion Polymorphism and Risk of Lower-Limb Amputation in Patients With Long-Standing Type 1 Diabetes.

V. Rigalleau, S. Hadjadj, G. Charpentier, 2021, Diabetes care.

Relationship Between Diabetic Retinopathy Stages and Risk of Major Lower-Extremity Arterial Disease in Patients With Type 2 Diabetes

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Lower limb events in individuals with type 2 diabetes: evidence for an increased risk associated with diuretic use

S. Hadjadj, M. Marre, S. Ragot, 2019, Diabetologia.

Prognostic value of plasma MR-proADM vs NT-proBNP for heart failure in people with type 2 diabetes: the SURDIAGENE prospective study

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Outpatient measurement of arterial stiffness in patients with type 2 diabetes and obesity

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Plasma Copeptin, AVP Gene Variants, and Incidence of Type 2 Diabetes in a Cohort From the Community.

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Plasma Copeptin and Renal Outcomes in Patients With Type 2 Diabetes and Albuminuria

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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.

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Plasma copeptin, kidney disease, and risk for cardiovascular morbidity and mortality in two cohorts of type 2 diabetes

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Lower-extremity amputation as a marker for renal and cardiovascular events and mortality in patients with long standing type 1 diabetes

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Linkage Analysis and Molecular Scanning of Glucokinase Gene in NIDDM Families

J. Beckmann, P. Froguel, H. Zouali, 1993, Diabetes.

Evaluating in vitro and in vivo the interference of ascorbate and acetaminophen on glucose detection by a needle-type glucose sensor.

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Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3).

G. Lathrop, R. Cox, G. Charpentier, 1997, Human molecular genetics.

Allelic variations in superoxide dismutase-1 (SOD1) gene and renal and cardiovascular morbidity and mortality in type 2 diabetic subjects.

M. Marre, R. Roussel, G. Velho, 2012, Molecular genetics and metabolism.

Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNALeu(UUR) Gene Mutation

P. Froguel, M. Byrne, J. Sturis, 1996, Diabetes.

Redox Genetic Risk Score and the Incidence of End-Stage Kidney Disease in People with Type 1 Diabetes

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Vitamin D endocrine system and the genetic susceptibility to diabetes, obesity and vascular disease. A review of evidence.

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Manganese Superoxide Dismutase (SOD2) Polymorphisms, Plasma Advanced Oxidation Protein Products (AOPP) Concentration and Risk of Kidney Complications in Subjects with Type 1 Diabetes

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Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes

S. Hadjadj, M. Marre, R. Roussel, 2013, Diabetologia.

Diabetes Complications in NIDDM Kindreds Linked to the MODY3 Locus on Chromosome 12q

G. Charpentier, P. Froguel, M. Vaxillaire, 1996, Diabetes Care.

In vitro and in vivo evaluation in dogs of a miniaturized glucose sensor.

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Strategies for calibrating a subcutaneous glucose sensor.

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Maternal diabetes alters birth weight in glucokinase-deficient (MODY2) kindred but has no influence on adult weight, height, insulin secretion or insulin sensitivity

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Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families.

P. Froguel, C. Bellanné-Chantelot, G. Velho, 2000, European journal of endocrinology.

Plasma proprotein‐convertase‐subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes

S. Hadjadj, M. Marre, S. Ragot, 2018, Diabetes, obesity & metabolism.

Plasma Copeptin, Kidney Outcomes, Ischemic Heart Disease, and All-Cause Mortality in People With Long-standing Type 1 Diabetes

S. Hadjadj, M. Marre, R. Roussel, 2016, Diabetes Care.

Antagonism of vasopressin V2 receptor improves albuminuria at the early stage of diabetic nephropathy in a mouse model of type 2 diabetes.

R. Roussel, L. Bankir, G. Velho, 2017, Journal of diabetes and its complications.

[MODY, a model of genotype/phenotype interactions in type 2 diabetes].

C. Bellanné-Chantelot, G. Velho, J. Timsit, 2003, Medecine sciences : M/S.

Six Mutations in the Glucokinase Gene Identified in MODY by Using a Nonradioactive Sensitive Screening Technique

P. Froguel, H. Blanché, P. Czernichow, 1994, Diabetes.

Adiponectin gene and cardiovascular risk in type 2 diabetic patients: a review of evidences.

G. Velho, F. Fumeron, A. Reis, 2007, Arquivos brasileiros de endocrinologia e metabologia.

CA repeat polymorphism in the glucose transporter GLUT 2 gene

P. Froguel, H. Zouali, F. Sun, 1991, Nucleic Acids Res..

Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations.

K. Clément, M. Stoffel, P. Froguel, 1994, The Journal of clinical investigation.

The Common −866G>A Variant in the Promoter of UCP2 Is Associated With Decreased Risk of Coronary Artery Disease in Type 2 Diabetic Men

M. Marre, G. Velho, J. Timsit, 2008, Diabetes.

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu(UUR) gene

P. Froguel, J. Maassen, R. Trembath, 1994, Diabetes.

Monocytopenia, monocyte morphological anomalies and hyperinflammation characterise severe COVID‐19 in type 2 diabetes

S. Germain, R. Roussel, G. Velho, 2020, EMBO molecular medicine.

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

B. Balkau, O. Lantieri, M. Marre, 2011, Diabetologia.

A standardized protocol to achieve normoglycaemia during labour and delivery in women with type 1 diabetes.

D. Dubois-Laforgue, G. Velho, J. Timsit, 2008, Diabetes & metabolism.

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.

M. Marre, R. Roussel, G. Velho, 2013, Diabetes & metabolism.

Monocyte class switch and hyperinflammation characterise severe COVID-19 in type 2 diabetes

R. Roussel, G. Velho, J. Gautier, 2020, medRxiv.

Allelic variations in the CYBA gene of NADPH oxidase and risk of kidney complications in patients with type 1 diabetes.

S. Hadjadj, M. Marre, R. Roussel, 2015, Free radical biology & medicine.

Arginine-Induced Insulin Release in Glucokinase-Deficient Subjects

K. Clément, P. Froguel, M. Vaxillaire, 1994, Diabetes Care.

Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families.

P. Froguel, C. Bellanné-Chantelot, G. Velho, 2000, European journal of endocrinology.

In vivo calibration of a subcutaneous glucose sensor for determination of subcutaneous glucose kinetics

Gérard Reach, G. Velho, Daniel R. Thévenot, 1988 .