Juanita Neira, is a Clinical and Biochemical Geneticist with a focus on inborn errors of metabolism (IEM), including urea cycle disorders, fatty acid oxidation defects, and congenital disorders of glycosylation. She has participated in research studies for therapeutics and new managements for IEM's and lysosomal storage disorders. Currently, she is involved with the Newborn Screening Long-Term Follow-Up Program for the state of Georgia. Dr.Neira has joined the national consortia of disorders of glycosylation (FCDGC). This collaboration involves a multicenter effort to define the natural history of these conditions, which is crucial for improving patient outcomes.

Additionally, she is particularly interested in Potocki-Lupski Syndrome and Smith-Magenis Syndrome. She has been involved has particular interest in projects that lead to new gene discoveries. As a Hispanic individual, she is deeply committed to advocating for Hispanic and minority populations, striving to help them overcome barriers within the healthcare system.