Kenneth E. White - Concepedia

Author

Kenneth E. White

Indiana University – Purdue University Indianapolis ORCID

Also Known As

K E White, K White, K. E. WHITE, K. E. White, K. White, K.E White, K.E. White, Kathryn E. White, Kenneth E White, Kenneth E. White

204

Publications

14K

Citations

H-Index

Concepts

All Affiliations

Indiana University – Purdue University Indianapolis Indiana University School of Medicine Johns Hopkins University Dartmouth College Massachusetts General Hospital

About

Kenneth E. White is an author at Indiana University – Purdue University Indianapolis specializing in medicine, cell biology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	39	7.8K
2	Health Sciences	9	9	2K
3	Biochemistry	9	9	3.1K
4	Natural Sciences	8	8	1.8K
5	Engineering	1	1	14

Kenneth E. White

Publications

12.5K

Citations

H-Index

Page 1

	Year	Citations
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 Kenneth E. White, W. Evans, Jeffery L.H. O'Riordan, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2000	1.5K
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
Fibroblast Growth Factor 23 in Oncogenic Osteomalacia and X-Linked Hypophosphatemia Kenneth B. Jonsson, R Zahradnik, Tobias E. Larsson, New England Journal of Medicine	2003	907
FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wasting Mara Riminucci, Michael T. Collins, Neal S. Fedarko, Journal of Clinical Investigation	2003	640
Most Osteomalacia-associated Mesenchymal Tumors Are a Single Histopathologic Entity Andrew L. Folpe, Julie C. Fanburg–Smith, Steven D. Billings, The American Journal of Surgical Pathology Sinonasal HpcUrologyConventional HpcTumoral PathologyBone Morphogenic Protein	2004	639
Molecular Insights into the Klotho-Dependent, Endocrine Mode of Action of Fibroblast Growth Factor 19 Subfamily Members Regina Goetz, Andrew Beenken, Omar A. Ibrahimi, Molecular and Cellular Biology Aldo-keto ReductaseGlycobiologyCell ProliferationChemical BiologyCellular Physiology	2007	530
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23 Kenneth E. White, Gwénaëlle Carn, Bettina Lorenz‐Depiereux, Kidney International GeneticsAutosomal-dominant Hypophosphatemic RicketsFibroblast Growth FactorGenetic Disorder	2001	493
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis Shoji Ichikawa, Erik A. Imel, Mary L. Kreiter, Journal of Clinical Investigation GeneticsPathologyTumor BiologyVitamin D HomeostasisParathyroid Hormone	2007	471
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
MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia Peter Rowe, P A de Zoysa, Rong Dong, Genomics Bone DiseaseBone Morphogenic ProteinNew GeneTumors Causing OsteomalaciaPathology	2000	364

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