Siobhan I. Davis - Concepedia

Author

Siobhan I. Davis

Indiana University – Purdue University Indianapolis

Also Known As

S I Davis, Siobhan I Davis, Siobhan I. Davis

Publications

Citations

H-Index

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All Affiliations

Indiana University – Purdue University Indianapolis Indiana University School of Medicine Trinity College Dublin University of Missouri–Kansas City St. James's Hospital

About

Siobhan I. Davis is an author at Indiana University – Purdue University Indianapolis specializing in medicine, cell biology, and tumor biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	2.2K
2	Cell Biology	3	3	589
3	Health Sciences	1	1	1.2K
4	Biochemistry	1	1	1.2K
5	Cellular Physiology	1	1	233

Siobhan I. Davis

Publications

Citations

H-Index

Page 1

	Year	Citations
Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism Jian Q. Feng, Leanne M. Ward, Shiguang Liu, Nature Genetics BiochemistryPhysiologyOsteocalcinMetabolismMedicine	2006	1.2K
Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice Emily Farrow, Xijie Yu, Lelia J. Summers, Proceedings of the National Academy of Sciences	2011	367
Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation Kenneth E. White, J. M. Segura Cabral, Siobhan I. Davis, The American Journal of Human Genetics Developmental BiologyBone Morphogenic ProteinGeneticsBone ElongationBone Remodeling	2005	320
Initial FGF23-Mediated Signaling Occurs in the Distal Convoluted Tubule Emily Farrow, Siobhan I. Davis, Lelia J. Summers, Journal of the American Society of Nephrology Distal Convoluted TubuleFgf23 InjectionRenal InflammationFgf23 BioactivityCellular Physiology	2009	233
A Novel Recessive Mutation in Fibroblast Growth Factor-23 Causes Familial Tumoral Calcinosis Tobias E. Larsson, Xijie Yu, Siobhan I. Davis, The Journal of Clinical Endocrinology & Metabolism Renal PathologyParathyroid DiseasePathologyFgf23 ConcentrationsTumor Biology	2005	221
Analysis of the Biochemical Mechanisms for the Endocrine Actions of Fibroblast Growth Factor-23 Xijie Yu, Omar A. Ibrahimi, Regina Goetz, Endocrinology	2005	212
Fibroblast Growth Factor-23 Mutants Causing Familial Tumoral Calcinosis Are Differentially Processed Tobias E. Larsson, Siobhan I. Davis, Holly J. Garringer, Endocrinology Tumor BiologyCancer PathologyFamily MembersVitamin D MetabolismMedicine	2005	135
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 Holly J. Garringer, Corinne Fisher, Tobias E. Larsson, The Journal of Clinical Endocrinology & Metabolism	2006	118
Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets Emily Farrow, Siobhan I. Davis, Leanne M. Ward, Bone Genetic DisorderGeneticsMolecular BiologyMolecular GeneticsDmp1 Mutants	2008	68
Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis Holly J. Garringer, Mahdi Malekpour, Fatemehsadat Esteghamat, American Journal of Physiology-Endocrinology and Metabolism	2008	55

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