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 · 825 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +3

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

Catherine Dodé, Luís Teixeira, Jacqueline Levilliers et al. · PLoS Genetics · 2006 · 451 citations · Full text

Kallmann Syndrome Combines, Human Growth, Genetics +21

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

Hormonal Contraceptive, Fertility, Ria Procedure +27

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 · 283 citations · Full text

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 · 270 citations · Full text

Genetics, Pathology, Molecular Genetics +16