Marcus J. Miller, PhD FACMG, is an ABMGG certified clinical biochemical geneticist and clinical molecular geneticists that oversees the Biochemical Genetics Laboratory  and the Molecular Genetics Laboratory at the Indiana University School of Medicine.   Dr. Miller’s research focuses on advancing laboratory testing for genetic disease and improving the diagnosis and management of patients with inborn errors of metabolism. 

Luna, C., Griffin, C, and Miller, M. J. (2022). " A clinically validated method to separate and quantify underivatized acylcarnitines and carnitine metabolic intermediates using mixed-mode chromatography with tandem mass spectrometry" J Chromatogr A. 1663: 462749

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