Match tier Likely match
Presence Formerly Arkansas
Last published 2025
Sources OpenAlex · ORCID
Refreshed 2026-10-06

Patricia Porter‐Gill

This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.

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Also affiliated: Dartmouth College (2012); University of Vermont (2012); National Institutes of Health (2009–2015); Arkansas Children's Hospital (1996–2025); United States Food and Drug Administration (2016); University of Utah (2003–2007); Huntsman Cancer Institute (2003–2005); Hospital Research Foundation (1998); National Human Genome Research Institute (2009–2012); Quality Biological (2011); Maine Medical Center (2012); Frederick National Laboratory for Cancer Research (2012); National Cancer Institute (2010–2015); Vermont Cancer Support Network (2012); Cancer Genetics (United States) (2012); Arkansas Children's Nutrition Center (2025); Center for Cancer Research (2012); Department of Health and Human Services (2014); Division of Cancer Epidemiology and Genetics (2011–2013)

Formerly Arkansas Affiliated with NCTR, UAMS through 2019; recent publications list Arkansas Children's Research Institute.

18 h-index 59 pubs 2,038 cited

  • Humans
  • Female
  • Male
  • Genetic Predisposition to Disease
  • Mutation
  • Polymorphism, Single Nucleotide
  • Gene Expression Regulation, Neoplastic
  • RNA, Messenger
  • MicroRNAs
  • Gene Expression Profiling
  • Urinary Bladder Neoplasms
  • Phenotype
  • Genetic Variation
  • Child
  • Antibodies, Monoclonal

Biography and Research Information

OverviewAI-generated summary

Patricia Porter‐Gill's research investigates the genetic underpinnings of disease, focusing on the identification of genetic variants and their association with disease risk and gene expression. Her work has explored the functional significance of genetic variations in conditions such as hepatitis C, melanoma, prostate cancer, and bladder cancer. She has also examined epigenetic modifications, including DNA methylation, in the context of cancer development, specifically in ovarian and endometrial cancers.

Porter‐Gill's publications include studies on the association of single nucleotide polymorphisms (SNPs) with gene expression in breast cancer and the identification of mutations in matrix metalloproteinase genes in melanoma. Her research also delves into the impact of genetic variants on viral clearance and cancer predisposition. With an h-index of 18, 59 publications, and over 2,000 citations, her work contributes to the understanding of complex genetic influences on human health.

Metrics

  • h-index: 18
  • Publications: 59
  • Citations: 2,038

Selected Publications

  • Data on the effect of heat and other technical variables on the detection of microRNAs in human serum (2019)
    Data in Brief 1 citation DOI OpenAlex
  • Effects of a 28-day dietary co-exposure to melamine and cyanuric acid on the levels of serum microRNAs in male and female Fisher 344 rats (2016)
    Food and Chemical Toxicology 11 citations DOI OpenAlex

View all publications on OpenAlex →

Collaboration Network

7 Collaborators 4 Institutions 1 Country

Top Collaborators

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