Whyte, Michael P
Author affiliations appear on pp. 15–20
5 papers on CoChatORCID 0000-0002-8755-8490
Most cited papers
- Verified
Atypical subtrochanteric and diaphyseal femoral fractures: Second report of a task force of the American Society for Bone and Mineral Research
Shane, E., Burr, D., Abrahamsen, B., Adler, R. A., Brown, T. D., Cheung, A. M., Cosman, F., Curtis, J. R., Dell, R., Dempster, D. W., et al. (2014) · Journal of Bone and Mineral Research
Bone health and osteoporosis researchBone health and treatments
Cited by 2,147
- Verified
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
Watts, G. D. J., Wymer, J., Kovach, M. J., Mehta, S. G., Mumm, S., Darvish, D., Pestronk, A., Whyte, M. P., & Kimonis, V. E. (2004) · Nature Genetics
Genetic Neurodegenerative DiseasesAmyotrophic Lateral Sclerosis Research
Cited by 1,391
- Verified
Atypical subtrochanteric and diaphyseal femoral fractures: Report of a task force of the american society for bone and mineral Research
Shane, E., Burr, D., Ebeling, P. R., Abrahamsen, B., Adler, R. A., Brown, T. D., Cheung, A. M., Cosman, F., Curtis, J. R., Dell, R., et al. (2010) · Journal of Bone and Mineral Research
Bone health and osteoporosis researchBone health and treatments
Cited by 1,116
- Verified
Paget’s disease of bone and genetic disorders of RANKL/OPG/RANK/NF-κB signaling.
WHYTE, M. P. (2006) · Annals of the New York Academy of Sciences
Bone Metabolism and DiseasesOsteomyelitis and Bone Disorders Research
Cited by 95
- Verified
Dysosteosclerosis presents as an “Osteoclast-Poor” form of osteopetrosis: Comprehensive investigation of a 3-year-old girl and literature review
Whyte, M. P., Wenkert, D., McAlister, W. H., Novack, D. V., Nenninger, A. R., Zhang, X., Huskey, M., & Mumm, S. (2010) · Journal of Bone and Mineral Research
Bone Metabolism and DiseasesDermatological and Skeletal Disorders
Cited by 43
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