Research Output per year
Research Output per year
Personal profile
Research interests
Heritable disorders of bone and mineral metabolism - including diagnosis, natural history, and treatment. Dysplastic skeletal diseases - including high bone mass, accelerated bone turnover, and osteolytic skeletal disease. Physiological role of alkaline phosphatase, osteoprotegerin, and RANK-Ligand action in bone biology.
Areas of Clinical Interest
Diagnosis and treatment of heritable disorders of bone and mineral metabolism, bone disease in adults and children, mineral disease, osteogenesis imperfecta, rickets, osteopetrosis, hypophosphatasia, hypophosphatemia, genetics, vitamin D-resistant rickets, metabolic and dysplastic bone disease in children, chondrodysplasia, pseudohypoparathyroidism, juvenile osteoporosis
Fingerprint
Dive into the research topics where Michael Whyte is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 10 Similar Profiles
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Research Output
-
Pharmacodynamics of asfotase alfa in adults with pediatric-onset hypophosphatasia
Seefried, L., Kishnani, P. S., Moseley, S., Denker, A. E., Watsky, E., Whyte, M. P. & Dahir, K. M., Jan 2021, In: Bone. 142, 115664.Research output: Contribution to journal › Article › peer-review
Open Access -
Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation
Mumm, S., Gottesman, G. S., Wenkert, D., Campeau, P. M., Nenninger, A., Huskey, M., Bijanki, V. N., Veis, D. J., Barnes, A. M., Marini, J. C., Stolina, M., Zhang, F., McAlister, W. H. & Whyte, M. P., Jan 2020, In: Bone. 130, 115047.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANK
Iwamoto, S. J., Rothman, M. S., Duan, S., Baker, J. C., Mumm, S. & Whyte, M. P., Apr 2020, In: Bone. 133, 115224.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Genetics of Skeletal Disorders
Hannan, F. M., Newey, P. J., Whyte, M. P. & Thakker, R. V., 2020, Handbook of Experimental Pharmacology. Springer Science and Business Media Deutschland GmbH, p. 325-351 27 p. (Handbook of Experimental Pharmacology; vol. 262).Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review
-
Growth curves for children with X-linked hypophosphatemia
Mao, M., Carpenter, T. O., Whyte, M. P., Skrinar, A., Chen, C. Y., Martin, J. S. & Rogol, A. D., Oct 1 2020, In: Journal of Clinical Endocrinology and Metabolism. 105, 10, p. 1-7 7 p.Research output: Contribution to journal › Article › peer-review
Open Access