Director, IU Biochemical Genetics Laboratory
Assistant Professor, Clinical Medical and Molecular Genetics
Professional Address: 975 W. Walnut St., IB 344, Indianapolis, IN 46202
Office Phone: 317-278-1140
Fax: 317-278-1616
E-mail: majamill@iu.edu
Board Certifications:
ABMGG, Clinical Biochemical Genetics
Areas of Specialization:
Inborn Errors of Metabolism
Clinical Metabolomics
Fatty Acid Oxidation Disorders
Carnitine Metabolism
Education:
Clinical Fellowship in Molecular Genetics, Baylor College of Medicine, Houston, TX
Clinical Fellowship in Biochemical Genetics, Baylor College of Medicine, Houston, TX
Ph.D., Genetics, University of Wisconsin, Madison, WI
B.S., Biology, Purdue University
Selected Articles:
Jain, M., Kennedy, A.D., Elsea S.H., Miller, M.J., (2017) “Analytes Related to Erythrocyte Metabolism are Reliable Biomarkers for Preanalytical Error Due to Delayed Plasma Processing in Metabolomics Studies” Clinica Chimica Acta, PMID28069401.
Miller, M.J., Bostwick, B.L., Kennedy, A.D., Taraka, D., Sun, Q., Sutton, V.R., Elsea, S.H., (2016) “Chronic oral L-carnitine supplementation drives marked plasma TMAO elevations in patients with organic acidemias despite dietary meat restrictions” Journal of Inherited Metabolic Disease Reports, PMID26936850
Miller, M.J., Burrage L.C., Gibson, J.B., Strenk, M.E., Lose, J.E, Bick, D.P., Elsea, S.H., Sutton, V.R., Sun, Q., Graham, B.H., Craigen, W.J., Zhang, W., Wong, L.C. (2015) “Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States” Molecular Genetics and Metabolism, 116(3): 139-145. PMID26385305
Miller, M.J, Kennedy, A.D., Eckhart, A.D., Burrage, L.C., Wulff, J.E., Miller, L.A.D., Milburn, M.V., Ryals, J.A., Beaudet, A.L., Sun, Q., Sutton, V.R., Elsea, S.H. (2015) “Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism.” Journal of Inherited Metabolic Disease, 38(6): 1029-1039. PMID25875217
Miller, M.J., Soler-Alfonso, C.R., Grund, J.E., Fang, P., Sun, Q., Elsea, S.H., Sutton, V.R. (2014). Improved standards for prenatal diagnosis of citrullinemia. Molecular Genetics and Metabolism, 112, 205-209.