faculty photo

 

John C. Carey, MD, MPH

Professor
Education
  • Villanova University - B.A. Social Sciences
  • Georgetown University - M.D.
  • San Francisco General Hospital - Pediatrics Internship
  • University of California, San Francisco - Pediatrics Residency
  • University of California, Berkeley - M.P.H.
  • University of California, San Francisco - Fellowship, Genetics and Dysmorphology
Board Certifications
  • Pediatrics
  • Medical Genetics
Current Appointments
  • Staff - Univeristy of Utah, Primary Children's Medical Center, Shriner's
  • Director Pregnancy Riskline - Utah State Department of Health
  • Professor - University of Utah, Department of Pediatrics
  • Adjunct Professor - University of Utah, OB/Gyn & School of Nursing
  • Vice-Chair Academic Enterprise - University of Utah, Department of Pediatrics
  • Editor-in-Chief - American Journal of Medical Genetics
Research
  • Shriner Foundation Multi-Center Study of Outcome of Tibial Dysplasia in NF1 Patients
  • Centers for Disease Control Utah Center for Birth Defects Research & Prevention
  • NIH/NICHP Nutrient Markers, Genes and Orofacial Clefts
  • Centers for Disease Control Cooperative Agreement for EDHI Tracking and Research with Other Newborn Screening Programs.
  • Centers for Disease Control Surveillance of Birth Defects in Utah
More Recent Publications [Search PubMed for Additional Publications]
  • Maternal exposure to statins and risk for birth defects: a case-series approach.
    Petersen EE, Mitchell AA, Carey JC, Werler MM, Louik C, Rasmussen SA, National Birth Defects Prevention Study
    Am J Med Genet A
  • Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement.
    Stevenson DA, Carey JC, Coburn SP, Ericson KL, Byrne JL, Mumm S, Whyte MP
    J Clin Endocrinol Metab
  • Spectrum of epilepsy and EEG patterns in Wolf-Hirschhorn syndrome: experience with 87 patients.
    Battaglia A, Filippi T, South ST, Carey JC
    Am J Med Genet Part C Semin in Med Genet
  • Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russel-Silver phenotype.
    South ST, Whitby H, Maxwell T, Aston E, Brothman AR, Carey JC
    Am J Med Genet A
  • Bone mineral density in children with neurofibromatosis type 1.
    Stevenson DA, Murray M, Viskochil DH, Carey JC, Moyer-Mileur LJ
    J Pediatr Orthop