Rachel L Richesson, MPH, MP, PhD, FACMI
Clinical Professor of Learning Health Sciences
Medical School
[email protected]
Available to mentor
Rachel L Richesson, MPH, MP, PhD, FACMI
Clinical Professor
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Qualifications
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PhDThe University of Texas Health Science Center at Houston, Houston, TX, United States
2000 - 2003
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MS, Health InformaticsThe University of Texas Health Science Center at Houston, Houston, TX, United States
1998 - 2000
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MPH, Community Health PracticeThe University of Texas Health Science Center at Houston, Houston, TX, United States
1993 - 1995
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BS, ZoologyUniversity of Massachusetts Amherst, Amherst, MA, United States
1987 - 1992
Center Memberships
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Center MemberInstitute for Healthcare Policy and Innovation
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Center Membere-Health and Artificial Intelligence Initiative
Recent Publications
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Richesson R. 2026 May 29;PresentationPatient-Powered Interoperability Clinic: Designing Digital Health Tools with HL7 FHIR and Patient/Consumer Informed Data Flows
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Douthit B, Cummings J, Lanham M, Richesson R. 2026 May 29;PresentationAn APPetite for Better Health: Closing the Gap Between Health Apps, Data Access, and Patient Engagement
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Douthit B, Cummings J, Lanham M, Richesson R. 2026 May 29;PresentationAn APPetite for Better Health: Closing the Gap Between Health Apps, Data Access, and Patient Engagement
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Dullabh P, Boxwala A, Correa K, Richesson R, Leaphart D, Desai P. 2026 May 21;Proceeding / Abstract / PosterA General Taxonomy of Override Reasons for Patient-Centered Clinical Decision Support Recommendations
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Maniar K, Balczewski E, Hanauer D, Richesson R. 2026 May 18;Proceeding / Abstract / PosterExploring Coded Laboratory Data in the NIH All of Us Researcher Workbench Using Rare Disorder Exemplars
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2026 May 29;PresentationPrivacy, Trust, and Consent in Aging Research Recruitment
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Richesson R. 2026 May 29;PresentationAdvancing the Relevance and Scalability of Clinical Decision Support (CDS) Alerts Using a Taxonomy of Override Reasons
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Vaishnaw MS, Richesson R. Orphanet J Rare Dis, 2026 Feb 24;Journal ArticleA practical framework to approach the development and evaluation of patient registries for rare diseases.
DOI:10.1186/s13023-026-04270-0 PMID: 41731596