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

Mutant Valosin-containing Protein, Alzheimer's Disease, Inclusion Body Myopathy +9

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

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 · 618 citations · Full text

Electrolyte Disorder, Carbonic Anhydrase Ii, Pathology +16

Enzyme-Replacement Therapy in Life-Threatening Hypophosphatasia

Michael P. Whyte, Cheryl R. Greenberg, Nada Salman et al. · New England Journal of Medicine · 2012 · 554 citations · Full text

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 · 473 citations

Bone Disease, Pathology, Signal Peptide +4