William J. Rhead, MD, PhD
Titles Pediatric geneticist, Children's Hospital of Wisconsin; professor, Pediatrics and Pathology, Medical College of Wisconsin
Division Genetics
Research interests Genetic diseases/genomics
Study interests Human fatty acid oxidation disease, mitochondrial disease, newborn screening.
Education Medical degree, University of California, San Diego, 1974; doctorate, University of California, San Diego, 1974; residency, North Carolina Memorial Hospital, Chapel Hill, 1977; fellowships, Research, University of California, San Diego, 1975, and Human Genetics and Pediatrics, Yale University School of Medicine, New Haven, Conn. 1979.
Certifications Pediatrics, Human Genetics (Clinical Genetics and Clinical Biochemical Genetics).
Honors Noel Raine Prize, Society for the Study of Inborn Errors of Metabolism, 1983; Best Doctors in America, 1992, 1994, 1998, 2003.
Representative publications
- Brix AE, Elgavish A, Nagy TR, Gower BA, Rhead WJ, Wood PA. Evaluation of Liver Fatty Acid Oxidation in the Leptin Deficient Obese Mouse. Molecular Genetics and Metabolism. 2002; 75(3):219-226.
- Koch R, Burton B, Hoganson G, Peterson R, Rhead W, Rouse B, Scott R, Wolff J, Guttler F, Nelson M, de la Cruz F, Coldwell J, Erbe R, Geraghty MT, Shear C, Thomas J, Azen C. Phenylketonuria in Adulthood: A Collaborative Study. Journal of Inheritated Metabolic Disease. 2002; 25(5):333-346.
- Brix AE, Elgavish A, Nagy TR, Gower BA, Rhead WJ, Wood PA. Evaluation of Fatty Acid Oxidation in the Leptin Deficient Obese Mouse. Molecular Genetics and Metabolism. 2002; 75:219-26.
- Cox KM, Hamm DA, Millington DS, Matern D, Vockley J, Rinaldo R, Pinkert CA, Rhead WJ, Lindsey R, Wood PA. Gestational, Pathologic and Biochemical Differences between very Long-chain Acyl-CoA Dehydrogenase Deficiency and Long-chain Acyl-CoA Dehydrogenase Deficiency in the Mouse. Human Molecular Genetics. 2001; 10(19) 2069-76.
- Koch R, Burton B, Hoganson G, Peterson R, Rhead W, Rouse B, Scott R, Wolff J, Stern AM, Guttler F, Neslon M, DeLaCruz F, Coldwell J, Erbe R, Geraghty MT, Shear C, Thomas J, Azen C. Phenylketonuria in Adulthood: A Collaborative Study. Journal of Inherited Metabolic Diseases. 2002; 25:333-346.
- Rhead WJ. Introduction to Symposium, Washington D.C., on Mitochondrial Myopathies and Disorders of the Electron Transport Chain in Man: A Molecular and Clinical Update. Pediatric Research. 1990; 28:524.
- Roettger V, Marshall T, Amendt B, Rhead WJ. Multiple Acyl-Coenzyme A Dehydrogenase Disorder (MAD) Responsive to Riboflavin: Biochemical Studies in Fibroblasts. In New Developments in Fatty Acid Oxidation, Paul Coates and Kay Tanaka, eds. 1992; 375:317-326.
- Gordon JA, Heller SK, Rhead WJ, Watkins PA, Spector AA. Formation of a Novel Arachidonic Acid Metabolite in Peroxisomes. Prostaglandins, Leukotrienes and Essential Fatty Acids. 1995; 52:77-81.
- Rhead WJ. Inborn Errors of Metabolism in Present Knowledge. In Nutrition, Ziegler and Filer, eds., seventh edition. ILSI Press, Washington, D.C., 1996; 623-629.
- Lysaught MT, Milhollin L, Peirce R, Getchell J, Rhead W, Susanin J, Anderson J, Murray JC. A Pilot Test of DNA-based Analysis Using Anonymized Newborn Screening Cards. In Iowa, Stored Tissue Samples: Ethical Legal, and Public Policy Implications. R.F. Weir, ed., University of Iowa Press, Iowa City, 1998; 3-31.
- Rhead WJ, Irons M. The Call from the Newborn Screening Laboratory: Frustration in the Afternoon. Pediatric Clinics of North America. 2004.
Grants
- Study of Fabrazyme in Patients with Fabry Disease, Genzyme, Inc., principal investigator.
- Recombinant Human Alpha-L-Induronidase, Genzyme, Inc., principal investigator.
- Clinical Trial of Replagal Enzyme Replacement Therapy, Transkarotic Therapy, Inc., principal investigator.
- Congential Disorders Program, State of Wisconsin, principal investigator.
- Statewide Genetics Services Network, State of Wisconsin, principal investigator.
Contact Children's Research Institute 8701 Watertown Plank Road Wauwatosa, WI 53226 Phone: (414) 266-2979 Fax: (414) 266-1616 E-mail: wrhead@mcw.edu

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