G. Chabrier

The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with Paragangliomas

Nelly Burnichon, V. Rohmer, Laurence Amar et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 370 citations · Full text

RET mutations in exons 13 and 14 of FMTC patients.

Alessandra Bolino, Isabelle Schuffenecker, Yin Luo et al. · PubMed · 1995 · 222 citations

SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome

Naresh K. Hanchate, Paolo Giacobini, Pierre Lhuillier et al. · PLoS Genetics · 2012 · 210 citations · Full text

Familial Medullary Thyroid Carcinoma with Noncysteine RET Mutations: Phenotype-Genotype Relationship in a Large Series of Patients

Patricia Niccoli‐Sire, Arnaud Murat, V. Rohmer et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 150 citations

Phenotype-genotype Relationship, Somatic Variant, Genetic Disorder +12

Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey

Claire Bouvattier, Laure Esterle, Peggy Renoult-Pierre et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 112 citations · Full text