Michael P. Whyte

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 et al. · Nature Genetics · 2004 · 1.4K citations · Full text

Medicine, Genetics, Neurology +13

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 et al. · Journal of Bone and Mineral Research · 2010 · 1.1K citations

Medicine, Orthopaedic Surgery, Orthopedic Surgery +15

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 et al. · Proceedings of the National Academy of Sciences · 1983 · 622 citations · Full text

Life Sciences, Biochemistry, Genetics +17

Enzyme-Replacement Therapy in Life-Threatening Hypophosphatasia

Michael P. Whyte, Cheryl R. Greenberg, Nada Salman et al. · New England Journal of Medicine · 2012 · 566 citations · Full text

Medicine, Pediatrics, Pharmacotherapy +17

Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis

Anne E. Hughes, Stuart H. Ralston, John Marken et al. · Nature Genetics · 2000 · 484 citations

Medicine, Molecular Genetics, Pathobiology +14