FGF-23 in patients with end-stage renal disease on hemodialysis

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

Kenneth E. White, W. Evans, Jeffery L.H. O'Riordan et al. · Nature Genetics · 2000 · 1.5K citations

Life Sciences, Genetics, Molecular Genetics +12

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

Takashi Shimada, S. Mizutani, Takanori Muto et al. · Proceedings of the National Academy of Sciences · 2001 · 1.5K citations · Full text

Medicine, Oncology, Pathobiology +17

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

Fiona Francis, Steffen Hennig, Bernd Korn et al. · Nature Genetics · 1995 · 1.1K citations

Life Sciences, Genetics, Molecular Genetics +11

Increased Circulatory Level of Biologically Active Full-Length FGF-23 in Patients with Hypophosphatemic Rickets/Osteomalacia

Y. Yamazaki, Ryo Okazaki, Minako Shibata et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 675 citations

Medicine, Endocrinology, Pathobiology +14

Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23

Kenneth E. White, Gwénaëlle Carn, Bettina Lorenz‐Depiereux et al. · Kidney International · 2001 · 497 citations · Full text

Medicine, Genetics, Molecular Genetics +12