G. Simonin

Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty

Dominique Simon, Ibrahima Ba, Nancy Mekhail et al. · European Journal of Endocrinology · 2015 · 111 citations · Full text

Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms

Rachel Reynaud, F. Albarel, Alexandru Saveanu et al. · European Journal of Endocrinology · 2011 · 100 citations

PROKR2 Variants in Multiple Hypopituitarism with Pituitary Stalk Interruption

Rachel Reynaud, Sujatha A. Jayakody, Carine Monnier et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 86 citations · Full text

Improved metabolic control in diabetic adolescents using the continuous glucose monitoring system (CGMS)

P Schaepelynck-Bélicar, P Vague, G. Simonin et al. · Diabetes & Metabolism · 2003 · 77 citations

Obesity, Metabolic Syndrome, Diabetes Management +10

An Uncommon Phenotype with Familial Central Hypogonadism Caused by a Novel PROP1 Gene Mutant Truncated in the Transactivation Domain

Rachel Reynaud, Anne Barlier, Sophie Vallette-Kasic et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 62 citations