Olivier Chabre

Genetic Testing in Pheochromocytoma or Functional Paraganglioma

Laurence Amar, Jérôme Bertherat, Éric Baudin et al. · Journal of Clinical Oncology · 2005 · 680 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

The European Registry on Cushing's syndrome: 2-year experience. Baseline demographic and clinical characteristics

Elena Valassi, Alicia Santos, Maria Yaneva et al. · European Journal of Endocrinology · 2011 · 392 citations · Full text

Medicine, Endocrinology, Internal Medicine +11

Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

Luis Jaime Castro‐Vega, Alexandre Buffet, Aguirre A. de Cubas et al. · Human Molecular Genetics · 2013 · 391 citations

Life Sciences, Genetics, Oncology +13

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

Hélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano et al. · Nature Genetics · 2012 · 337 citations · Full text

Medicine, Genetics, Nephrology +17

Aryl Hydrocarbon Receptor-Interacting Protein Gene Mutations in Familial Isolated Pituitary Adenomas: Analysis in 73 Families

Adrian F. Daly, Jean-François Vanbellinghen, Sok Kean Khoo et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 324 citations · Full text

Medicine, Endocrinology, Genetics +14