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Natural history of elderly-onset inflammatory bowel disease: a population-based cohort study

Gut, 2014-03, Vol.63 (3), p.423-432

2014

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Are anxiety and depression associated with cognition and cardiovascular function in young male and female adults?

PloS one, 2023-10, Vol.18 (10), p.e0292246-e0292246

2023

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A Novel Rare Missense Variation of the NOD2 Gene: Evidences of Implication in Crohn’s Disease

International journal of molecular sciences, 2019-02, Vol.20 (4), p.835

2019

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GAD2 on chromosome 10p12 is a candidate gene for human obesity

PLoS biology, 2003-12, Vol.1 (3), p.E68-E68

2003

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Hypoadiponectinemia Is Associated With Progression Toward Type 2 Diabetes and Genetic Variation in the ADIPOQ Gene Promoter

Diabetes care, 2006-07, Vol.29 (7), p.1645-1650

2006

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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

Biochemical and biophysical research communications, 2006-10, Vol.348 (4), p.1232-1238

2006

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A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1

Annals of neurology, 2002-11, Vol.52 (5), p.666-670

2002

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Epidemiology of inflammatory bowel diseases: New insights from a French population-based registry (EPIMAD)

Digestive and liver disease, 2013-02, Vol.45 (2), p.89-94

2013

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Gene/environment interaction in the susceptibility of Crohn's disease patients to aluminum

The Science of the total environment, 2022-12, Vol.850, p.158017-158017, Article 158017

2022

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Adiponectin and its receptors: Partners contributing to the “vicious circle” leading to the metabolic syndrome?

Pharmacological research, 2006-06, Vol.53 (6), p.478-481

Vasseur, Francis

2006

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Impaired multimerization of human adiponectin mutants associated with diabetes. Molecular structure and multimer formation of adiponectin

The Journal of biological chemistry, 2003-10, Vol.278 (41), p.40352-40363

2003

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Growth Pattern in Paediatric Crohn Disease Is Related to Inflammatory Status

Journal of pediatric gastroenterology and nutrition, 2016-12, Vol.63 (6), p.637-643

2016

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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

Journal of human genetics, 2010-04, Vol.55 (4), p.227-231

2010

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Usability flaws of medication-related alerting functions: A systematic qualitative review

Journal of biomedical informatics, 2015-06, Vol.55, p.260-271

2015

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La loi Jardé et la recherche en santé travail : quelles démarches préalables aux enquêtes en santé au travail ?

Archives des maladies professionnelles et de l'environnement, 2020-11, Vol.81 (6), p.830-836

2020

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Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians

Human molecular genetics, 2002-10, Vol.11 (21), p.2607-2614

2002

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Nutritional Status and Growth in Pediatric Crohn's Disease: A Population-Based Study

The American journal of gastroenterology, 2010-08, Vol.105 (8), p.1893-1900

2010

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Su1876 - A Combination of Clinical, Serological and Genetic Factors Predicts Complicated Disease Course in Paediatric-Onset Crohn's Disease: Results from a Population-Based Study

Gastroenterology (New York, N.Y. 1943), 2018-05, Vol.154 (6), p.S-616-S-616

2018

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Adiponectin, type 2 diabetes and the metabolic syndrome: lessons from human genetic studies

Expert reviews in molecular medicine, 2006-11, Vol.8 (27), p.1-12

2006

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Msh2 c. 1022t>c, p. Leu341pro is a founder pathogenic variation and a major cause of lynch syndrome in the north of france

Genes chromosomes & cancer, 2019-08, Vol.59 (2), p.111-118

2019

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Diagnosing Rare Inherited Disorders Using Targeted Next Generation Sequencing in Patients with Early-Onset Inflammatory Bowel Disease: A Population Based Study

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S983-S983

2017

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Tu1832 - Diagnosing Rare Inherited Disorders Using Targeted Next Generation Sequencing in Patients with Early-Onset Inflammatory Bowel Disease: A Population Based Study

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S983-S983

2017

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Positional Candidate Gene Analysis of Lim Domain Homeobox Gene (Isl-1) on Chromosome 5q11-q13 in a French Morbidly Obese Population Suggests Indication for Association With Type 2 Diabetes

Diabetes (New York, N.Y.), 2002-05, Vol.51 (5), p.1640-1643

2002

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Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease Patients

Scientific reports, 2016-07, Vol.6 (1), p.29636-29636, Article 29636

2016

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A Novel Rare Missense Variation of the NOD2 Gene: Evidencesof Implication in Crohn's Disease

International journal of molecular sciences, 2019-02, Vol.20 (4)

2019

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Natural history of elderly-onset inflammatory bowel disease: a population-based cohort study

Are anxiety and depression associated with cognition and cardiovascular function in young male and female adults?

A Novel Rare Missense Variation of the NOD2 Gene: Evidences of Implication in Crohn’s Disease

GAD2 on chromosome 10p12 is a candidate gene for human obesity

Hypoadiponectinemia Is Associated With Progression Toward Type 2 Diabetes and Genetic Variation in the ADIPOQ Gene Promoter

Distinct impaired regulation of SOCS3 and long and short isoforms of the leptin receptor in visceral and subcutaneous fat of lean and obese women

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1

Epidemiology of inflammatory bowel diseases: New insights from a French population-based registry (EPIMAD)

Gene/environment interaction in the susceptibility of Crohn's disease patients to aluminum

Adiponectin and its receptors: Partners contributing to the “vicious circle” leading to the metabolic syndrome?

Impaired multimerization of human adiponectin mutants associated with diabetes. Molecular structure and multimer formation of adiponectin

Growth Pattern in Paediatric Crohn Disease Is Related to Inflammatory Status

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

Usability flaws of medication-related alerting functions: A systematic qualitative review

La loi Jardé et la recherche en santé travail : quelles démarches préalables aux enquêtes en santé au travail ?

Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians

Nutritional Status and Growth in Pediatric Crohn's Disease: A Population-Based Study

Su1876 - A Combination of Clinical, Serological and Genetic Factors Predicts Complicated Disease Course in Paediatric-Onset Crohn's Disease: Results from a Population-Based Study

Adiponectin, type 2 diabetes and the metabolic syndrome: lessons from human genetic studies

Msh2 c. 1022t>c, p. Leu341pro is a founder pathogenic variation and a major cause of lynch syndrome in the north of france

Diagnosing Rare Inherited Disorders Using Targeted Next Generation Sequencing in Patients with Early-Onset Inflammatory Bowel Disease: A Population Based Study

Tu1832 - Diagnosing Rare Inherited Disorders Using Targeted Next Generation Sequencing in Patients with Early-Onset Inflammatory Bowel Disease: A Population Based Study

Positional Candidate Gene Analysis of Lim Domain Homeobox Gene (Isl-1) on Chromosome 5q11-q13 in a French Morbidly Obese Population Suggests Indication for Association With Type 2 Diabetes

Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease Patients

A Novel Rare Missense Variation of the NOD2 Gene: Evidencesof Implication in Crohn's Disease

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