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Email

hadley.smith@bcm.edu

Positions

Health Policy Fellow

Center for Medical Ethics and Health Policy
Houston, Texas United States

Research Associate

Center For Medical Ethics and Healthy Policy
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Houston, TX

Research Associate

Mol. & Human Gen./Admin.
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Houston, TX US

Education

PhD from The University of Texas Health Science Center School of Public Health

05/2019 - Houston

Health Economics

MPA from Texas A&M University

05/2015 - College Station, Texas

Health Policy Analysis

BS from Texas A&M University

College Station, Texas

Political Science, Genetics

Professional Interests

• Evaluation of clinical genomic sequencing, especially in newborn and pediatric populations
• Ethical, Legal, and Social Implications (ELSI) of genomics
• Public health genomics
• Health equity and precision medicine
• Child health and wellbeing
• Patient-centered outcomes
• Health outcome measurement
• Economic evaluation of health care programs
• Applied econometrics

Professional Statement

Hadley Stevens Smith is the Health Policy Fellow in the Center for Medical Ethics and Health Policy at ²ÝÁñÉçÇøÈë¿Ú. Dr. Smith is a health economist working at the intersection of health economics and the ethical, legal, and social implications (ELSI) of genomics. Her research examines precision medicine applications from patient-centered, clinical, and economic perspectives. Dr. Smith evaluates implementation of clinical genomics services using both quantitative and qualitative approaches. She is particularly interested in genomic sequencing of newborn and pediatric patient populations and assessment of family-level effects, including cascade screening of family members. She aims to inform policies that advance equitable and efficient implementation of genomic medicine to improve population health.

Additionally, Dr. Smith incorporates her training in public health and health policy to study equity and access issues in genomic medicine and co-leads a journal club on Social Determinants of Health, Medicine, and Ethics.

Dr. Smith earned a PhD in Health Economics from the University of Texas Health Science Center at Houston School of Public Health. She also holds a Master of Public Service and Administration with a concentration in Health Policy Analysis from the Bush School of Government and Public Service at Texas A&M University. Dr. Smith received her Bachelor of Science in Political Science with a minor in Genetics from Texas A&M University. She has also completed a Certificate in Genetics and Genomics from the Stanford University Center for Professional Development.

Selected Publications

• Pereira S, Smith HS, Frankel LA, Christensen KD, Islam R, Robinson JO, Genetti CA, Blout Zawatsky CL, Zettler B, Parad RB, Waisbren SE, Beggs AH, Green RC, Holm IA, McGuire AL "." JAMA Pediatrics.;175(11):1132–1141. Pubmed PMID:
• Smith HS, Brothers KB, Knight SJ, Ackerman SL, Rini C, Veenstra DL, McGuire AL, Wilfond BS, Malek J. "." American Journal of Human Genetics. 2021 Nov 4;108(11)
• Smith HS, Franciskovich R, Lewis AM, Gerard A, Littlejohn RJ, Nugent K, Rodriguez J, Streff H "." Genet Med. 2021 May;23:950–955.
• 23. Smith HS, Swint JM, Lalani SR, Yamal JM, de Oliveira Otto MC, Castellanos S, Taylor A, Lee BH, Russell HV "." Genet Med. 2019 Jan;21(1) Pubmed PMID:

Funding

An ELSI-Integrated Evaluation of the Family-Level Utility of Pediatric Genomic Sequencing - #K99HG011491

Grant funding from National Human Genome Research Institute

The goal of the proposed research is to investigate how clinical genomic sequencing impacts families of pediatric patients. This research will develop an empirically informed framework of normative values important to families of pediatric patients, including ethical, legal, and social implications (ELSI), which will then be used to elicit preferences for features of sequencing from a nationally representative sample of parents in the US. The results of this work will lead to a measure of family utility that integrates ELSI and can be used in a decision analytic model to assess the impact of genomic sequencing and the importance of including family- level ELSI considerations in such analyses.

Health-related quality of life and family well-being in pediatric patients with genetic conditions and their families: A scoping review of the literature

(02/15/2022 - 02/14/2023) Family Wellbeing Research Network (FAM-NET) Research Scholars Corp

The objective of this project is to systematically describe empirical literature on health-related quality of life measurement in pediatric patients with genetic conditions and their family members and on family well-being measurement in the context of genetic conditions.

Value ethics: Mapping strategies for value assessment and reimbursement of gene therapies for rare diseases

Center for ELSI Resources and Analysis

This Working Group will engage a broad range of stakeholders in developing guidance for ethically justified and patient-centered value assessment and reimbursement strategies for gene therapies.