Siobhan I. Davis
Publications by Year
Research Areas
Parathyroid Disorders and Treatments, Genetic Syndromes and Imprinting, Fibroblast Growth Factor Research, Bone and Dental Protein Studies, Heterotopic Ossification and Related Conditions
Most-Cited Works
- → Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism(2006)1,190 cited
- → Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice(2011)373 cited
- → Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation(2005)320 cited
- → Initial FGF23-Mediated Signaling Occurs in the Distal Convoluted Tubule(2009)234 cited
- → A Novel Recessive Mutation in Fibroblast Growth Factor-23 Causes Familial Tumoral Calcinosis(2005)222 cited
- → Analysis of the Biochemical Mechanisms for the Endocrine Actions of Fibroblast Growth Factor-23(2005)213 cited
- → Fibroblast Growth Factor-23 Mutants Causing Familial Tumoral Calcinosis Are Differentially Processed(2005)135 cited
- → The Role of Mutant UDP-N-Acetyl-α-d-Galactosamine-Polypeptide N-Acetylgalactosaminyltransferase 3 in Regulating Serum Intact Fibroblast Growth Factor 23 and Matrix Extracellular Phosphoglycoprotein in Heritable Tumoral Calcinosis(2006)119 cited
- → Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets(2008)71 cited
- → Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis(2008)55 cited