P. Pierre

<i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Nelly Burnichon, Alberto Cascón, Francesca Schiavi et al. · Clinical Cancer Research · 2012 · 321 citations · Full text

Positive Impact of Genetic Test on the Management and Outcome of Patients With Paraganglioma and/or Pheochromocytoma

Alexandre Buffet, Laurène Ben Aim, Sophie Leboulleux et al. · The Journal of Clinical Endocrinology & Metabolism · 2019 · 118 citations · Full text

Role of adiponectin receptors, AdipoR1 and AdipoR2, in the steroidogenesis of the human granulosa tumor cell line, KGN

P. Pierre, Pascal Froment, Didier Négre et al. · Human Reproduction · 2009 · 78 citations · Full text

Significant prevalence of NR3C1 mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR Study

Géraldine Vitellius, Séverine Trabado, Christine Hoeffel et al. · European Journal of Endocrinology · 2018 · 43 citations

X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

Elodie Fiot, Delphine Zénaty, Priscilla Boizeau et al. · European Journal of Endocrinology · 2019 · 42 citations