Astrid U. Meysing

Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

Nelly Pitteloud, James S. Acierno, Astrid U. Meysing et al. · Proceedings of the National Academy of Sciences · 2006 · 246 citations · Full text

Human Growth, Genetics, Gynecology +17

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

Nelly Pitteloud, Astrid U. Meysing, Richard Quinton et al. · Molecular and Cellular Endocrinology · 2006 · 197 citations

Fibrosis, Developmental Biology, Mendelian Disorder +12

Reversible Kallmann Syndrome, Delayed Puberty, and Isolated Anosmia Occurring in a Single Family with a Mutation in the Fibroblast Growth Factor Receptor 1 Gene

Nelly Pitteloud, James S. Acierno, Astrid U. Meysing et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 160 citations · Full text

<i>GNRHR</i>Mutations in a Woman with Idiopathic Hypogonadotropic Hypogonadism Highlight the Differential Sensitivity of Luteinizing Hormone and Follicle-Stimulating Hormone to Gonadotropin-Releasing Hormone

Astrid U. Meysing, Haruhiko Kanasaki, Grégoy Y. Bédécarrats et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 57 citations

C-peptide and insulin, but not C19-steroids, support the predictive value of body mass index on leptin in serum of premenopausal women

F. Geisthövel, Astrid U. Meysing, Georg Brabant · Human Reproduction · 1998 · 18 citations · Full text

Serum Leptin, Gynecology, Multiple Regression +22