Michael P. Whyte - Concepedia

Author

Michael P. Whyte

Shriners Hospitals for Children - Erie ORCID

Also Known As

Elizabeth Kersh, Mariana, M P Whyte, M WHYTE, M Whyte, M. P. Whyte, M. Whyte, M. Whyte⁎, M.P. Whyte, M.P. Whyte⁎, MICHAEL P. WHYTE

673

Publications

28.8K

Citations

H-Index

211

Concepts

All Affiliations

Shriners Hospitals for Children - Erie Washington University in St. Louis Barnes-Jewish Hospital Shriners Hospitals for Children - St. Louis Mallinckrodt (United States)

About

Michael P. Whyte is an author at Shriners Hospitals for Children - Erie specializing in medicine, osteoporosis, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	54	134	11.8K
2	Health Sciences	28	37	3.3K
3	Arts	2	2	158
4	Education	1	1	29
5	Engineering	1	1	10

Michael P. Whyte

242

Publications

22.7K

Citations

H-Index

Page 1

	Year	Citations
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein Giles D. Watts, Jill Wymer, Margaret J. Kovach, Nature Genetics Mutant Valosin-containing ProteinAlzheimer's DiseaseInclusion Body MyopathyPathologyDegenerative Disease	2004	1.4K
Atypical subtrochanteric and diaphyseal femoral fractures: Report of a task force of the american society for bone and mineral Research Elizabeth Shane, David B. Burr, Peter R. Ebeling, Journal of Bone and Mineral Research	2010	1.1K
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. William S. Sly, David Hewett‐Emmett, Michael P. Whyte, Proceedings of the National Academy of Sciences Electrolyte DisorderCarbonic Anhydrase IiPathologyCerebral CalcificationOsteoporosis	1983	618
Enzyme-Replacement Therapy in Life-Threatening Hypophosphatasia Michael P. Whyte, Cheryl R. Greenberg, Nada Salman, New England Journal of Medicine	2012	554
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis Anne E. Hughes, Stuart H. Ralston, John Marken, Nature Genetics Bone DiseasePathologySignal PeptideSystems BiologyMedicine	2000	473
Burosumab Therapy in Children with X-Linked Hypophosphatemia Thomas O. Carpenter, Michael P. Whyte, Erik A. Imel, New England Journal of Medicine	2018	449
Bisphosphonate-Induced Osteopetrosis Michael P. Whyte, Deborah Wenkert, Karen L. Clements, New England Journal of Medicine	2003	446
Osteoprotegerin Deficiency and Juvenile Paget's Disease Michael P. Whyte, Sara E. Obrecht, Patrick M. Finnegan, New England Journal of Medicine	2002	440
Alkaline Phosphatase Knock-Out Mice Recapitulate the Metabolic and Skeletal Defects of Infantile Hypophosphatasia K N Fedde, Libby A. Blair, Julie Silverstein, Journal of Bone and Mineral Research	1999	394
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Jenny C. Taylor, Hilary C. Martin, Stefano Lise, Nature Genetics SequencingPsychiatryClinical GenomeGeneticsMedicine	2015	378

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