Philippe Froguel
Affiliations: | Lille 2 |
Area:
Diabetes, Obesity, Monogenic forms, NGSGoogle:
"Philippe Froguel"Children
Sign in to add traineeSuzanne Lesage | grad student | 1996 | UPMC Univ Paris 6 |
El Habib Hani | grad student | 1997 | UPMC Univ Paris 6 |
Amar Abderrahmani | grad student | 1999 | University Lille 1 |
Jean-Claude Chèvre | grad student | 2000 | UPMC Univ Paris 6 |
Sophie Dupont | grad student | 2000 | University Lille 1 |
Corinne Lacquemant | grad student | 2000 | University Lille 1 |
Jérôme Delplanque | grad student | 2002 | University Lille 1 |
Séverine Dubois | grad student | 2002 | Université Paris 7 |
Mouna Houari-barat | grad student | 2002 | Université Paris 5 |
Céline Populaire | grad student | 2004 | Lille 2 |
Christopher G. Bell | grad student | 2006 | Imperial College |
Maya Ghoussaini | grad student | 2006 | Lille 2 |
Nabila Bouatia Naji | grad student | 2006 | Lille 2 |
Ruth Gutierrez-aguilar | grad student | 2007 | Lille 2 |
Fanny Stutzmann | grad student | 2009 | Lille 2 |
Johan Bacart | grad student | 2010 | Lille 2 |
Julien Philippe | grad student | 2014 | Lille 2 |
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Publications
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Folon L, Baron M, Scherrer V, et al. (2024) Pathogenic, Total Loss-of-Function DYRK1B Variants Cause Monogenic Obesity Associated With Type 2 Diabetes. Diabetes Care |
Dance A, Fernandes J, Toussaint B, et al. (2023) Exploring the role of purinergic receptor P2RY1 in type 2 diabetes risk and pathophysiology: Insights from human functional genomics. Molecular Metabolism. 101867 |
Kouidrat Y, Collen LL, Vaxillaire M, et al. (2023) Dominant PDX1 deficiency causes highly penetrant diabetes at different ages, associated with obesity and exocrine pancreatic deficiency: lessons for precision medicine. Diabetes & Metabolism. 101507 |
Johanns M, Haas JT, Raverdy V, et al. (2023) Time-of-day-dependent variation of the human liver transcriptome and metabolome is disrupted in MASLD. Jhep Reports : Innovation in Hepatology. 6: 100948 |
Meulebrouck S, Scherrer V, Boutry R, et al. (2023) Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas. Diabetologia |
de Las Fuentes L, Schwander KL, Brown MR, et al. (2023) Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci. Frontiers in Genetics. 14: 1235337 |
Fumeron F, Velho G, Alzaid F, et al. (2023) Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. study. Genes and Immunity. 24: 303-308 |
Gao W, Liu L, Huh E, et al. (2023) Human GLP1R variants affecting GLP1R cell surface expression are associated with impaired glucose control and increased adiposity. Nature Metabolism |
Saeed S, Khanam R, Janjua QM, et al. (2023) High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor. Cell Reports. Medicine. 101187 |
Orioli L, Canouil M, Sawadogo K, et al. (2023) Identification of myokines susceptible to improve glucose homeostasis after bariatric surgery. European Journal of Endocrinology. 189: 409-421 |