NIH-funded research R01 grant

Integrative computational and lab approaches to better predict cardiovascular risk from genes and variants

Official title: Integrative computational-experimental approaches for cardiovascular risk assessment

Funded at Brigham and Women's Hospital · NIH-11365365 · Data updated 2026-11-12

Aiming to combine big patient data with fast lab tests to understand how rare gene changes affect cholesterol and heart disease risk.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionBrigham and Women's Hospital
NIH-funded
Lab location1 site (Boston, United States)
Project startJuly 15, 2026
Project endJune 30, 2028
Funding year2026
Award (this year)$1,789,824
NIH project number1R01HL181570-01A1
Project IDNIH-11365365 on NIH RePORTER

Who could benefit from this research

Could help

People with genetic variants affecting LDL cholesterol or cardiovascular risk, and those who have elevated LDL-C or a family history of CVD.

Less likely to help

Individuals without relevant genetic variants or those not contributing samples to functional studies may not benefit directly.

What this research studies

This project will merge large human data sets with high-throughput lab screening to map rare coding variants that influence LDL cholesterol and cardiovascular risk. Using computational methods and CRISPR-based screens, researchers will connect genetic signals to actual biological effects relevant to patients. The work seeks to improve individualized risk assessments and potential clinical interventions by translating genetic findings into clearer variant interpretations. The team will address the challenge that many rare variants are hard to classify and may not be well represented in population studies. Outcomes could lead to better prediction of who is at higher risk and how to tailor prevention or treatment strategies.

Why it matters

Potential benefit: If successful, this work could improve the accuracy of personal heart-attack risk predictions and guide targeted therapies based on a person’s genetic variants.

How similar studies have gone: Prior studies show that combining population data with functional assays can clarify variant effects, but applying this at scale across lipid-related genes is still emerging.

Where this research is happening

  • Brigham and Women's Hospital
    Boston, United States
    Active

Researchers

  • Principal investigator: Cassa, Christopher — Brigham and Women's Hospital
  • Study coordinator: Cassa, Christopher

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.