Race-Based Care and Beliefs Regarding the Etiology of Racial Differences in Health Outcomes by Okah, Ebiere, Cronholm, Peter F., Crow, Brendan, Persaud, Anitra, Westby, Andrea, Bonham, Vence L.

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Engagement and Education of the Sickle Cell Disease Community: What Sickle Cell Disease Patients and Parents Want to Know about CRISPR Genome Editing by Desine, Stacy, Hollister, Brittany, Persaud, Anitra, Bonham, Vence L.

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The Role of the Health Care Provider in Building Trust Between Patients and Precision Medicine Research Programs by Persaud, Anitra, Bonham, Vence L.

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Insights into the skin microbiome of sickle cell disease leg ulcers by Byeon, Julia, Blizinsky, Katherine D., Persaud, Anitra, Findley, Keisha, Lee, Jung‐Jin, Buscetta, Ashley J., You, Shuo, Bittinger, Kyle, Minniti, Caterina P., Bonham, Vence L., Grice, Elizabeth A.

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The Meaning of Informed Consent: Genome Editing Clinical Trials for Sickle Cell Disease by Desine, Stacy, Hollister, Brittany M., Abdallah, Khadijah E., Persaud, Anitra, Hull, Sara Chandros, Bonham, Vence L.

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