Jesse M. Hunter

Jesse M. Hunter's work centers on clinical and molecular genetics, particularly the use of exome sequencing to diagnose rare genetic diseases in children, including rapid diagnosis in newborns and characterization of rare disease-causing gene variants. This research combines patient-based genetic testing with laboratory studies of protein function to understand how specific mutations cause disease. Prospective students would likely engage with both clinical genomics data analysis and functional biochemical experiments.

Publication output was modest and variable from 2017-2023 (1-5 papers/year) but increased sharply in 2024-2025, suggesting a recent growth phase in research activity.

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