Yardena Tenenbaum‐Rakover

Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3

Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Gertrud Eckstein et al. · The American Journal of Human Genetics · 2006 · 373 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Neuroendocrine Phenotype Analysis in Five Patients with Isolated Hypogonadotropic Hypogonadism due to a L102P Inactivating Mutation of GPR54

Yardena Tenenbaum‐Rakover, M. Commenges-Ducos, André Iovane et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 166 citations

Medicine, Endocrinology, Molecular Genetics +17

Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure

Yardena Tenenbaum‐Rakover, Ariella Weinberg‐Shukron, Paul Renbaum et al. · Journal of Medical Genetics · 2015 · 121 citations

Medicine, Genetics, Molecular Genetics +12

A Familial Thyrotropin (TSH) Receptor Mutation Provides in Vivo Evidence that the Inositol Phosphates/Ca2+ Cascade Mediates TSH Action on Thyroid Hormone Synthesis

Helmut Grasberger, Jacqueline Van Sande, Ahmad Hag-Dahood Mahameed et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 99 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

Sharona Tornovsky, Ana Crane, Karen E. Cosgrove et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 86 citations

Life Sciences, Genetics, Molecular Genetics +17