research overview Primary research focus has been on protein defects that cause inborn errors of metabolism, specifically those of the glycine cleavage enzyme system (GCS) which causes the disease nonketotic hyperglycinemia (NKH).
selected publications journal article Deep postnatal phenotyping of a new mouse model of nonketotic hyperglycinemia.. Journal of Inherited Metabolic Disease. 971-990. 2024 X-Linked Cobalamin Disorder ( HCFC1 ) Mimicking Nonketotic Hyperglycinemia With Increased Both Cerebrospinal Fluid Glycine and Methylmalonic Acid. Pediatric Neurology. 65-69. 2017 The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT.. Genetics in Medicine. 104-111. 2017 A kinetic-theory analysis of the scale-up of circulating fluidized beds. Powder Technology. 190-203. 2001
education and training Ph.D., University of Denver 2010 B.S., University of Colorado Boulder 2002 B.A., University of Colorado Boulder 2002