Goleen Samari

Associate Professor of Population and Public Health Sciences

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Overview

Goleen Samari is a population health demographer and Associate Professor in the Department of Population and Public Health Sciences whose research focuses on social inequities and health. Dr. Samari examines how racism, gender inequities, and migration-based inequities shape population and reproductive health both domestically and globally with a particular focus on communities in or from the Middle East and North Africa. She focuses on issues related to immigrant health, women’s health, and sexual and reproductive health and rights. She was the first to draw attention to racialization of religious minorities and Islamophobia as a public health issue. She is also one of a handful of public health researchers examining women’s empowerment, gender equity, and reproductive health in the Middle East and North Africa. Her recent work includes a measure of structural xenophobia in the U.S. at the state level, the Immigrant Policy Climate index, that can be leveraged to understand the health implications of exclusionary and inclusive immigration contexts. Her research remains focused on understanding and alleviating intersectional structural determinants of health. Cutting across all her research areas is an interest in the way social science constructs are measured and mixed methods that guide the research process. Her research has been published in several journals including Social Science & Medicine and the American Journal of Public Health, and her editorials and Op-Eds have been published in local and national newspapers. She is recognized as a thought leader on the population and reproductive health effects of discrimination for Muslim, Middle Eastern, and immigrant communities and has received a few notable honors for her contributions to health equity research.

Education and Training

  • University of Texas at Austin, Austin — 08/2017 — Postdoctoral Training in Population Studies
  • UCLA, Los Angeles — PhD — 06/2015 — Public Health & Demography
  • UCLA, Los Angeles — MPH — 06/2010 — Community Health Sciences
  • UCLA, Los Angeles — MA — 06/2010 — Islamic Studies
  • University of Texas at Austin, Austin — BA — 05/2007 — Plan II Honors
  • University of Texas at Austin, Austin — BA — 05/2007 — Middle Eastern Studies

Publications

  • Medicaid Expansion and Severe Maternal Morbidity During Delivery Hospitalizations. Obstet Gynecol. 2026 Aug 27.. View in PubMed
  • Maternal epigenetic signatures are associated with small for gestational age births among black women. Epigenet Insights. 2026; 19:e009.. View in PubMed
  • Experiences of Discrimination and DNA Methylation Among Black Nulliparous Women. J Racial Ethn Health Disparities. 2026 Jun 25.. View in PubMed
  • Epigenome-wide DNA methylation and spontaneous preterm birth among pregnant black women. Clin Epigenetics. 2026 May 24; 18(1).. View in PubMed
  • Transforming academic public health mentorship: implementation and expansion of MOSAIC. Front Public Health. 2025; 13:1640606.. View in PubMed
  • Implementation and sustainability of mentorship for public health student success. Front Public Health. 2025; 13:1657044.. View in PubMed
  • Blood Transfusions for Pregnancy Loss in Texas Before and After Abortion Bans, 2017‒2023. Am J Public Health. 2025 Nov; 115(11):1887-1894.. View in PubMed
  • Promoting More Equitable Global Health Research, Education, and Community Partnerships: The Efforts of One US‑Based Academic Institution. Ann Glob Health. 2025; 91(1):31.. View in PubMed
  • Reduced odds of severe maternal morbidity associated with the US Affordable Care Act dependent coverage provision. Am J Obstet Gynecol MFM. 2025 Jun; 7(6):101668.. View in PubMed
  • Epigenomic pathways from racism to preterm birth: secondary analysis of the Nulliparous Pregnancy Outcomes Study: monitoring Mothers-to-be (nuMoM2b) cohort study in the USA to examine how DNA methylation mediates the relationship between multilevel racism and preterm birth in black women: a study protocol. BMJ Open. 2025 Mar 04; 15(3):e091801.. View in PubMed