Micheline Merlin

GPIHBP1 C89F Neomutation and Hydrophobic C-Terminal Domain G175R Mutation in Two Pedigrees with Severe Hyperchylomicronemia

Sybil Charrière, Noël Peretti, Sophie Bernard et al. · The Journal of Clinical Endocrinology & Metabolism · 2011 · 57 citations · Full text

Severe hypertriglyceridaemia in Type II diabetes: involvement of apoC-III Sst-I polymorphism, LPL mutations and apo E3 deficiency

Christophe Marçais, Sophie Bernard, Micheline Merlin et al. · Diabetologia · 2000 · 35 citations · Full text

Severe Hypertriglyceridaemia, Metabolic Syndrome, Metabolic Disorder +8

Association of APOA5 −1131T>C and S19W gene polymorphisms with both mild hypertriglyceridemia and hyperchylomicronemia in type 2 diabetic patients

Sybil Charrière, Sophie Bernard, Mahdi Aqallal et al. · Clinica Chimica Acta · 2008 · 31 citations

Metabolic Syndrome, Genetic Determinant, Diabetes Epidemiology +14

Modulation of phenotypic expression of APOA5 Q97X and L242P mutations

Sybil Charrière, C. Cugnet, Myriam Guitard et al. · Atherosclerosis · 2009 · 26 citations

Apoa5 Q97x, Allelic Variant, Molecular Physiology +9