Research output per year
Research output per year
Personal profile
Research interests
Bone and mineral research, bone and joint disorders, human genetics, skeletal dysplasias
Clinical interests
Bone and mineral research, bone and joint disorders, human genetics, skeletal dysplasias
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Dive into the research topics where William McAlister is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Periarticular calcifications containing giant pseudo-crystals of francolite in skeletal fluorosis from 1,1-difluoroethane “huffing”
Salles Rosa Neto, N., Englert, D., McAlister, W. H., Mumm, S., Mills, D., Veis, D. J., Burshell, A., Boyde, A. & Whyte, M. P., Jul 2022, In: Bone. 160, 116421.Research output: Contribution to journal › Article › peer-review
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Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V
Whyte, M. P., Aronson, J., McAlister, W. H., Weinstein, R. S., Wenkert, D., Clements, K. L., Gottesman, G. S., Madson, K. L., Stolina, M., Bijanki, V. N., Plotkin, H., Huskey, M., Duan, S. & Mumm, S., Apr 2021, In: Bone. 145, 115835.Research output: Contribution to journal › Article › peer-review
4 Scopus citations -
Non-endemic skeletal fluorosis: Causes and associated secondary hyperparathyroidism (case report and literature review)
Cook, F. J., Seagrove-Guffey, M., Mumm, S., Veis, D. J., McAlister, W. H., Bijanki, V. N., Wenkert, D. & Whyte, M. P., Apr 2021, In: Bone. 145, 115839.Research output: Contribution to journal › Article › peer-review
6 Scopus citations -
Vitamin B6 deficiency with normal plasma levels of pyridoxal 5′-phosphate in perinatal hypophosphatasia
Whyte, M. P., May, J. D., McAlister, W. H., Burgener, K., Cortez, S. R., Kreienkamp, R., Castro, O., Verzola, R., Zavala, A. S., McPherson, C. C., Gottesman, G. S., Ericson, K. L., Coburn, S. P. & Arbelaez, A. M., Sep 2021, In: Bone. 150, 116007.Research output: Contribution to journal › Article › peer-review
4 Scopus citations -
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
10 Scopus citations