Jacques Young

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al. · Nature Genetics · 2003 · 830 citations

Life Sciences, Genetics, Molecular Genetics +9

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé, Luís Teixeira, Jacqueline Levilliers et al. · PLoS Genetics · 2006 · 452 citations · Full text

Life Sciences, Endocrinology, Genetics +16

Neurosteroids: 3 alpha-hydroxy-5 alpha-pregnan-20-one and its precursors in the brain, plasma, and steroidogenic glands of male and female rats.

C. Corpéchot, Jacques Young, M Calvel et al. · Endocrinology · 1993 · 344 citations

Life Sciences, Biochemistry, Endocrinology +12

Ketoconazole in Cushing's Disease: Is It Worth a Try?

Frédéric Castinetti, Laurence Guignat, Pauline Giraud et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 287 citations · Full text

Medicine, Endocrinology, Pharmacology +9

Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (<i>TCF2</i>) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5

Christine Bellanné‐Chantelot, Séverine Clauin, Dominique Chauveau et al. · Diabetes · 2005 · 273 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17