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Plos One|November 25, 2015
What Is the Best NGS Enrichment Method for the Molecular Diagnosis of Monogenic Diabetes and Obesity?Julien Philippe, Mehdi Derhourhi, Emmanuelle Durand, et al.Plos One|May 12, 2017
Characterization of a Bvg-regulated fatty acid methyl-transferase in Bordetella pertussisAlex Rivera-Millot, Elodie Lesne, Luis Solans, et al.Human Genetics|February 3, 2009
Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scansYohan Bossé, François Bacot, Alexandre Montpetit, et al.Genes and Immunity|November 18, 2023
Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. studyFrédéric Fumeron, Gilberto Velho, Fawaz Alzaid, et al.La Tunisie Medicale|December 19, 2012
Familial early-onset diabetes is not a typical MODY in several Tunisian patientsAbdelbasset Amara, Molka Chadli-Chaieb, Hela Ghezaiel, et al.Diabetes & Metabolism|December 23, 2023
Dominant PDX1 deficiency causes highly penetrant diabetes at different ages, associated with obesity and exocrine pancreatic deficiency: Lessons for precision medicineYoussef Kouidrat, Lauriane Le Collen, Martine Vaxillaire, et al.BMC Medical Genetics|March 4, 2011
Bio-Repository of DNA in stroke (BRAINS): a study protocolSunaina Yadav, Renata Schanz, Ankita Maheshwari, et al.Scientific Reports|November 22, 2019
Contribution of rare coding mutations in CD36 to type 2 diabetes and cardio-metabolic complicationsDavid Meyre, Edward J Andress, Tanmay Sharma, et al.Diabetes Care|August 12, 2008
Predicting diabetes: clinical, biological, and genetic approaches: data from the Epidemiological Study on the Insulin Resistance Syndrome (DESIR)Beverley Balkau, Céline Lange, Leopold Fezeu, et al.Pediatric Diabetes|September 24, 2017
A novel NEUROG3 mutation in neonatal diabetes associated with a neuro-intestinal syndromeSuna Hancili, Amélie Bonnefond, Julien Philippe, et al.Pageof 50