Key Publications
Biobank participation and returning research results: perspectives from a deliberative engagement in South Side Chicago
Patients' views on incidental findings from clinical exome sequencing
Incidental findings of therapeutic misconception in biobank-based research
Attitudes of African-American parents about biobank participation and return of results for themselves and their children
Engaging African-Americans about biobanks and the return of research results
Was it worth it? Patients' perspectives on the perceived value of genomic-based individualized medicine
Living kidney donors who develop kidney failure: excerpts of their thoughts
A systematic literature review of individuals' perspectives on privacy and genetic information in the United States
How do patients describe their disabilities? A coding system for categorizing patients' descriptions
Standards and legacies: Pragmatic constraints on a uniform gene nomenclature
NON-PEER REVIEWED
Biosociality: Where Diagnosis Intersects with Community
“Individualized: an ethnography of translation in a genomics clinic”
Translating Medicine Part III: Interview with Colin Halverson
NEW SOVEREIGNTIES AND THE TRANSLATION OF CLINICAL AUTHORITY
Titles & Appointments
- Assistant Professor of Medicine
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Education
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Research