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  • Jesse E. Otero, Gary S. Gottesman, +7 authors Michael P Whyte
  • Medicine
  • Journal of bone and mineral research : the…
  • 2013 (First Publication: 1 February 2013)
  • Generalized arterial calcification (AC) of infancy (GACI) is an autosomal recessive disorder that features hydroxyapatite deposition within arterial elastic fibers. Untreated, approximately 85% ofExpand
  • Steven Mumm, Margaret Huskey, +7 authors Michael P Whyte
  • Medicine, Biology
  • American journal of medical genetics. Part A
  • 2014 (First Publication: 1 September 2014)
  • Multicentric carpotarsal osteolysis syndrome (MCTO), an autosomal dominant disorder that often presents sporadically, features carpal-tarsal lysis frequently followed by nephropathy and renalExpand
  • Steven Mumm, Margaret Huskey, +7 authors Michael P Whyte
  • Medicine
  • Journal of bone and mineral research : the…
  • 2015
  • Heritable forms of hypophosphatemic rickets (HR) include X-linked dominant (XLH), autosomal recessive, and autosomal dominant HR (from deactivating mutations in PHEX, DMP1 or ENPP1, and activatingExpand
  • Gary S. Gottesman, Katherine L. Madson, +4 authors Michael P Whyte
  • Medicine, Biology
  • American journal of medical genetics. Part A
  • 2016 (First Publication: 14 January 2016)
  • We report auricular ossification (AO) affecting the elastic cartilage of the ear as a newly recognized feature of osteoprotegerin (OPG)-deficiency juvenile Paget disease (JPD). AO and auricularExpand
  • Dawn R. Phillips, Donna M Griffin, +5 authors Katherine L. Madson
  • Medicine
  • Journal of pediatric rehabilitation medicine
  • 2018 (First Publication: 7 September 2018)
  • PURPOSE: To modify the Performance-Oriented Mobility Assessment-Gait (POMA-G) subtest and validate this modified POMA-G (mPOMA-G) in children with hypophosphatasia (HPP), a rare metabolic disorderExpand