Margie Ream

Margie Ream's work focuses on pediatric (child) neurology, particularly newborn screening for rare genetic and metabolic disorders such as Krabbe disease, adrenoleukodystrophy, metachromatic leukodystrophy, and mucopolysaccharidosis type II. Much of the work also addresses training and education for child neurology residents, including genomics curricula and program design. This research combines clinical genetics, neurodevelopmental outcomes, and medical education topics relevant to how rare neurological conditions in infants and children are detected and treated.

Publication output has grown over the last decade, rising from about 1 paper per year in 2017 to a steady 7-8 papers per year from 2021 onward.

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