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Michael P. Whyte

Shriners Hospital for Children

2001 South Lindbergh Boulevard

St. Louis

Missouri 63131

[email]@shrinenet.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Shriners Hospital for Children, 2001 South Lindbergh Boulevard, St. Louis, Missouri 63131. 2011 - 2012
  • Center for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children; St. Louis, Missouri, 63131; Division of Bone and Mineral Diseases, USA. 2002 - 2012
  • Shriners Hospital for Children, St. Louis, Missouri, USA. 2010
  • Division of Bone and Mineral Diseases, Washington University School of Medicine at Barnes-Jewish Hospital, and Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children, USA. 2009
  • Division of Bone and Mineral Diseases, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid, Box 8301, USA. 2005 - 2006

References

  1. Resorptive hypercalcemia in post-essential thrombocythemia myelofibrosis: treatment with denosumab. Khoury, N., Chang, J., Gru, A.A., Whyte, M.P. J. Clin. Endocrinol. Metab. (2012) [Pubmed]
  2. Enzyme-replacement therapy in life-threatening hypophosphatasia. Whyte, M.P., Greenberg, C.R., Salman, N.J., Bober, M.B., McAlister, W.H., Wenkert, D., Van Sickle, B.J., Simmons, J.H., Edgar, T.S., Bauer, M.L., Hamdan, M.A., Bishop, N., Lutz, R.E., McGinn, M., Craig, S., Moore, J.N., Taylor, J.W., Cleveland, R.H., Cranley, W.R., Lim, R., Thacher, T.D., Mayhew, J.E., Downs, M., Millán, J.L., Skrinar, A.M., Crine, P., Landy, H. N. Engl. J. Med. (2012) [Pubmed]
  3. Fibrodysplasia ossificans progressiva: Middle-age onset of heterotopic ossification from a unique missense mutation (c.974G > C, p.G325A) in ACVR1. Whyte, M.P., Wenkert, D., Demertzis, J.L., Dicarlo, E.F., Westenberg, E., Mumm, S. J. Bone Miner. Res. (2011) [Pubmed]
  4. Skeletal fluorosis from brewed tea. Izuora, K., Twombly, J.G., Whitford, G.M., Demertzis, J., Pacifici, R., Whyte, M.P. J. Clin. Endocrinol. Metab. (2011) [Pubmed]
  5. Camurati-engelmann disease: Unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. Whyte, M.P., Totty, W.G., Novack, D.V., Zhang, X., Wenkert, D., Mumm, S. J. Bone Miner. Res. (2011) [Pubmed]
  6. Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders. Whyte, M.P., Kempa, L.G., McAlister, W.H., Zhang, F., Mumm, S., Wenkert, D. J. Bone Miner. Res. (2010) [Pubmed]
  7. 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. J. Bone Miner. Res. (2010) [Pubmed]
  8. Physiological role of alkaline phosphatase explored in hypophosphatasia. Whyte, M.P. Ann. N. Y. Acad. Sci. (2010) [Pubmed]
  9. Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasia. Whyte, M.P., Wenkert, D., McAlister, W.H., Mughal, M.Z., Freemont, A.J., Whitehouse, R., Baildam, E.M., Coburn, S.P., Ryan, L.M., Mumm, S. J. Bone Miner. Res. (2009) [Pubmed]
  10. Atypical femoral fractures, bisphosphonates, and adult hypophosphatasia. Whyte, M.P. J. Bone Miner. Res. (2009) [Pubmed]
  11. Bisphosphonate-induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceases. Whyte, M.P., McAlister, W.H., Novack, D.V., Clements, K.L., Schoenecker, P.L., Wenkert, D. J. Bone Miner. Res. (2008) [Pubmed]
  12. Adult hypophosphatasia treated with teriparatide. Whyte, M.P., Mumm, S., Deal, C. J. Clin. Endocrinol. Metab. (2007) [Pubmed]
  13. Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levels. Whyte, M.P., Singhellakis, P.N., Petersen, M.B., Davies, M., Totty, W.G., Mumm, S. J. Bone Miner. Res. (2007) [Pubmed]
  14. Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling. Whyte, M.P. Ann. N. Y. Acad. Sci. (2006) [Pubmed]
  15. Clinical practice. Paget's disease of bone. Whyte, M.P. N. Engl. J. Med. (2006) [Pubmed]
  16. Skeletal fluorosis and instant tea. Whyte, M.P., Essmyer, K., Gannon, F.H., Reinus, W.R. Am. J. Med. (2005) [Pubmed]
  17. Misinterpretation of osteodensitometry with high bone density: BMD Z > or = + 2.5 is not "normal". Whyte, M.P. J. Clin. Densitom (2005) [Pubmed]
  18. Heritable disorders of the RANKL/OPG/RANK signaling pathway. Whyte, M.P., Mumm, S. J. Musculoskelet. Neuronal. Interact (2004) [Pubmed]
  19. Marrow cell transplantation for infantile hypophosphatasia. Whyte, M.P., Kurtzberg, J., McAlister, W.H., Mumm, S., Podgornik, M.N., Coburn, S.P., Ryan, L.M., Miller, C.R., Gottesman, G.S., Smith, A.K., Douville, J., Waters-Pick, B., Armstrong, R.D., Martin, P.L. J. Bone Miner. Res. (2003) [Pubmed]
  20. Bisphosphonate-induced osteopetrosis. Whyte, M.P., Wenkert, D., Clements, K.L., McAlister, W.H., Mumm, S. N. Engl. J. Med. (2003) [Pubmed]
  21. Familial expansile osteolysis (excessive RANK effect) in a 5-generation American kindred. Whyte, M.P., Reinus, W.R., Podgornik, M.N., Mills, B.G. Medicine. (Baltimore) (2002) [Pubmed]
  22. Osteoprotegerin deficiency and juvenile Paget's disease. Whyte, M.P., Obrecht, S.E., Finnegan, P.M., Jones, J.L., Podgornik, M.N., McAlister, W.H., Mumm, S. N. Engl. J. Med. (2002) [Pubmed]
 
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