Photo of Cary O. Harding, M.D.

Cary O. Harding M.D.

  • (503) 494-8307
    • Professor of Molecular and Medical Genetics School of Medicine
    • Molecular and Medical Genetics Graduate Program School of Medicine
    • Program in Molecular and Cellular Biosciences School of Medicine

Dr. Harding received his medical degree in 1987 from the University of Washington School of Medicine in Seattle. He completed his pediatrics residency and fellowship in molecular and medical genetics and pediatrics at the University of Wisconson in Madison. Dr. Harding is fluent in German.

  • Residency:

    • University of Wisconsin Hospital, Madison
  • Fellowship:

    • Fellowship in molecular and medical genetics and pediatrics, University of Wisconsin
  • Certifications:

    • National Board of Medical Examiners, 1988

Publications

  • "Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening" Molecular Genetics and Metabolism  2014
  • "Self-reported treatment-associated symptoms among patients with urea cycle disorders participating in glycerol phenylbutyrate clinical trials" Molecular Genetics and Metabolism September 1 2015
  • "Up to date knowledge on different treatment strategies for phenylketonuria" Molecular Genetics and Metabolism  2011
  • "Potential for misdiagnosis due to lack of metabolic derangement in combined methylmalonic aciduria/hyperhomocysteinemia (cblC) in the neonate" Journal of Perinatology August 2003
  • "Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency" Molecular Genetics and Metabolism September 2006
  • "Establishing a consortium for the study of rare diseases" Molecular Genetics and Metabolism  2010
  • "Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency" Molecular Genetics and Metabolism September 2005
  • "Ammonia control in children ages 2 months through 5 years with urea cycle disorders" Journal of Pediatrics June 2013
  • "Postchemotherapy hyperammonemic encephalopathy emulating ornithine transcarbamoylase (OTC) deficiency" Southern Medical Journal May 2008
  • "Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disorders" Molecular Genetics and Metabolism November 2012
  • "Sodium phenylbutyrate decreases plasma branched-chain amino acids in patients with urea cycle disorders" Molecular Genetics and Metabolism September 1 2014
  • "Phenylketonuria scientific review conference" Molecular Genetics and Metabolism  2014
  • "Normal fatty acid concentrations in young children with phenylketonuria" Topics in Clinical Nutrition October 2009
  • "Siblings with mitochondrial acetoacetyl-CoA thiolase deficiency not identified by newborn screening" Pediatrics July 2011
  • "Molecular Basis of Two-Exon Skipping (Exons 12 and 13) by c.1248+5g>a in OXCT1 Gene" Human Mutation March 2013
  • "'Mommy, why can't I have a hamburger like the other kids?'" Gene Therapy  2000
  • "Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate" Hepatology June 2013
  • "Urinary phenylacetylglutamine (U-PAGN) concentration as biomarker for adherence in patients with urea cycle disorders (UCD) treated with glycerol phenylbutyrate" Molecular Genetics and Metabolism Reports December 1 2015
  • "Leigh syndrome in an infant resulting from mitochondrial DNA depletion" Pediatric Neurology  2001
  • "Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey" Journal of Inherited Metabolic Disease  1999
  • "Low therapeutic threshold for hepatocyte replacement in murine phenylketonuria" Molecular Therapy August 2005
  • "Long-term survival in typical thanatophoric dysplasia type 1" American Journal of Medical Genetics, Part A June 27 1997
  • "Erratum" Genetics in Medicine May 8 2015
  • "A longitudinal study of urea cycle disorders" Molecular Genetics and Metabolism September 1 2014
  • "Aluminum toxicity" JAMA Pediatrics  1998
  • "Mice with genetic γ-glutamyl transpeptidase deficiency exhibit glutathionuria, severe growth failure, reduced life spans, and infertility" Journal of Biological Chemistry May 9 1997
  • "Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism" Molecular Genetics and Metabolism August 2013
  • "Effect of feeding, exercise, and genotype on plasma 3-hydroxyacylcarnitines in children with LCHAD deficiency" Topics in Clinical Nutrition October 2009
  • "γ-Glutamyl transferase (GGT) deficiency in the GGT(enu1) mouse results from a single point mutation that leads to a stop codon in the first ceding exon of GGT mRNA" Mutagenesis  1999
  • "Friedreich's ataxia associated with mitochondrial myopathy" Journal of Child Neurology June 2002

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