Julie Sarfati

A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

Julie Sarfati, Anne Guiochon‐Mantel, Philippe Rondard et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 145 citations

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

Jacques Young, Corinne Métay, Jérôme Bouligand et al. · Human Reproduction · 2012 · 139 citations · Full text

The Prevalence of<i>CHD7</i>Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients

Séverine Marcos, Julie Sarfati, Chrystel Leroy et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 86 citations · Full text

Insulin-like Peptide 3 (INSL3) in Men With Congenital Hypogonadotropic Hypogonadism/Kallmann Syndrome and Effects of Different Modalities of Hormonal Treatment: A Single-Center Study of 281 Patients

Séverine Trabado, Luigi Maione, Hélène Bry‐Gauillard et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 51 citations · Full text

Sex Steroids, Precursors, and Metabolite Deficiencies in Men With Isolated Hypogonadotropic Hypogonadism and Panhypopituitarism: A GCMS-Based Comparative Study

Frank Giton, Séverine Trabado, Luigi Maione et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 50 citations · Full text