NIH-funded research R01 grant

Understanding how genes shape endometriosis severity using single-cell multi-omics

Official title: Disentangling the genetic mechanisms of endometriosis severity with single-cell multi-omics

Funded at University of Texas Hlth Science Center · NIH-11324620 · Data updated 2026-11-12

Researchers will map how genetic and epigenetic factors contribute to different severities of endometriosis to help improve diagnosis and future treatments for people living with the condition.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Texas Hlth Science Center
NIH-funded
Lab location1 site (San Antonio, United States)
Project startSeptember 1, 2024
Project endMay 31, 2029
Funding year2026
Award (this year)$691,810
NIH project number5R01HD114855-03
Project IDNIH-11324620 on NIH RePORTER

Who could benefit from this research

Could help

Individuals with endometriosis across different disease stages who have consented to participate in genomic and epigenomic analyses.

Less likely to help

Patients not represented in the study cohort or those without endometriosis may not directly benefit.

What this research studies

This project looks at endometriosis, a painful and often fertility‑related condition, by studying how gene regulation changes across individual cells in high‑ and low‑severity cases. Using advanced single‑cell epigenomics and multi-omics approaches, the team will profile landscapes of gene regulation and identify allele‑specific effects that differ by disease stage. They will also build genetic predictors that could forecast outcomes for patients based on their unique biology. The study leverages a large well‑annotated cohort to connect molecular patterns with clinical features, with the aim of revealing mechanisms that drive disease severity. The ultimate goal is to lay groundwork for personalized strategies in diagnosis and management tied to a patient’s molecular profile.

Why it matters

Potential benefit: If successful, the findings could lead to better stage-specific understandings of endometriosis and pave the way for personalized diagnostics and targeted therapies.

How similar studies have gone: Previous work has mapped gene expression in endometriosis and endometrioma, with growing evidence that molecular patterns relate to disease stage.

Where this research is happening

  • University of Texas Hlth Science Center
    San Antonio, United States
    Active

Researchers

  • Principal investigator: Lawrenson, Kate — University of Texas Hlth Science Center
  • Study coordinator: Lawrenson, Kate

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.