Bio
Marcus J. Miller, PhD FACMG, is an ABMGG certified clinical biochemical geneticist that oversees the Biochemical Genetics Laboratory at Indiana University School of Medicine. Prior to this position, Dr. Miller was an assistant professor at Baylor College of Medicine and an assistant director within the Baylor Genetics Laboratories. Dr. Miller’s research interests focus on improving the diagnosis and management of patients with inborn errors of metabolism.
Key Publications
Miller, M.J., Luu, S.M, Graham, B. H. (2021) “Acute Hyperammonemia, Lactic Acidosis, and Ketoacidosis in a Developmentally Normal Child” Clin Chm: 67-11.
Miller M.J., Cusmano-Ozog K, Oglesbee D, & Young S (2020) “Laboratory analysis of acylcarnitines, 2020 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG).” Genet Med:1-10.
Griffin, C., Z. Ammous, G. H. Vance, B. H. Graham and M. J. Miller (2019). "Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometry." J Chromatogr B Analyt Technol Biomed Life Sci 1128: 121786, PMID31518899
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
Burrage, L.C, Miller, M.J., Wong, L.J., Kennedy, A.D., Sutton, V.R., Sun, Q., Elsea, S.H., Graham, B.H. (2015) “Elevations of C14:1 and C14:2 Plasma Acylcarnitines in Fasted Children: A Diagnostic Dilemma” Journal of Pediatrics, PMID26602010
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.
Titles & Appointments
- Assistant Professor of Clinical Medical & Molecular Genetics
- Director, IU Biochemical Genetics Laboratory
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Education
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Professional Organizations
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Board Certifications