Jean‐Claude Carel

Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54

Nicolás de Roux, Emmanuelle Génin, Jean‐Claude Carel et al. · Proceedings of the National Academy of Sciences · 2003 · 2.4K citations · Full text

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

Factors Associated with Early Remission of Type I Diabetes in Children Treated with Cyclosporine

Pierre-François Bougnères, Jean‐Claude Carel, Luís Castaño et al. · New England Journal of Medicine · 1988 · 329 citations

Obesity, Metabolic Syndrome, Early Remission +11

11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations

Irène Netchine, Sylvie Rossignol, Marie‐Noëlle Dufourg et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 312 citations · Full text

Long-Term Mortality after Recombinant Growth Hormone Treatment for Isolated Growth Hormone Deficiency or Childhood Short Stature: Preliminary Report of the French SAGhE Study

Jean‐Claude Carel, Emmanuel Écosse, F Landier et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 290 citations · Full text