Graduate Student Research Assistant
Current• Leading a collaboration with an international pharmaceutical company to develop a disease modifying treatment for Huntington’s Disease (HD), using CRISPR-Cas gene editing technology. Involves early R&D (molecular biology), in vitro studies in human cell lines, HD mouse models, and larger animal models. • Mentoring, teaching, and managing 5 undergraduate research assistants. • Applying conditionally controlled optogenetic and small molecule domains to CRISPR systems.• Increasing the safety of genome editing technologies.• Developing unbiased CRISPR off-target detection methods that increase ease of implementation while decreasing cost compared to current methods.