NIH-funded research NIH-funded research

Understanding genetic risks for blood cancers

Official title: Myeloid Malignancy Variant Curation Expert Panel

Funded at Northwestern University at Chicago · NIH-10887719 · Data updated 2026-11-12

This study is looking at specific genetic changes that might make people more likely to develop certain blood cancers, and it aims to help patients and their families understand their risks better and find more personalized ways to manage their health.

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionNorthwestern University at Chicago
NIH-funded
Lab location1 site (Chicago, United States)
Project startApril 20, 2021
Project endJune 30, 2027
Funding year2024
Award (this year)$322,766
NIH project number2U24CA258118-05
Project IDNIH-10887719 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research include individuals with a family history of myeloid malignancies or those who have been diagnosed with related blood cancers.

Less likely to help

Patients without a genetic predisposition to myeloid malignancies or those with unrelated health conditions may not benefit from this research.

What this research studies

This research focuses on identifying genetic variants that predispose individuals to myeloid malignancies, which are types of blood cancers. The project involves a collaborative effort to curate and classify these genetic variants, particularly those in genes like RUNX1, DDX41, and GATA2. By developing standardized rules for variant curation, the research aims to improve the understanding of how these genetic factors contribute to cancer risk. Patients and families may benefit from this work through better risk assessment and personalized management strategies.

Why it matters

Potential benefit: If successful, this research could lead to improved identification of individuals at risk for myeloid malignancies, enabling earlier detection and tailored treatment options.

How similar studies have gone: Previous research has successfully identified genetic variants associated with blood cancers, indicating that this approach has potential for meaningful advancements.

Where this research is happening

  • Northwestern University at Chicago
    Chicago, United States
    Active

Researchers

  • Principal investigator: Godley, Lucy Ann — Northwestern University at Chicago
  • Study coordinator: Godley, Lucy Ann

Related research

Other NIH-funded projects on the same topics.

  • Myeloid Cancer Gene Variant Curation Expert Panel

    A patient-facing group creates and shares trusted rules for interpreting genetic variants that raise the risk of blood cancers, helping families understand their test results.

    NIH research Northwestern University · Chicago, United States · NIH-11384370

  • Genetic variant review team for myeloid blood cancers

    Experts are reviewing inherited genetic changes that raise the risk of myeloid blood cancers so patients and families get clearer test results and care guidance.

    NIH research Northwestern University · Chicago, United States · NIH-11124044

  • Creating a bone marrow model to study a genetic platelet disorder and its cancer risks

    This study is looking at a rare genetic condition that affects blood platelets and can increase the risk of blood cancers, and it's for people with this condition; the researchers want to create a mini version of bone marrow to better understand the disease and find new ways to help reduce the risk of leukemia.

    NIH research Boston Children's Hospital · Boston, United States · NIH-11011813

  • Detecting cancer risk and treatment response in NF1 nerve tumors using cfDNA markers

    A doctor-led study will test blood-based DNA markers to detect when NF1-related nerve tumors become malignant and to monitor how well treatment is working.

    NIH research Mayo Clinic Rochester · Rochester, United States · NIH-11452312

  • Epigenetic Basis for Controlling Aggressive IDH-Mutant Gliomas

    Aims to understand and shape the epigenetic changes in IDH-mutant brain tumors to restrain their growth, which could lead to new, targeted treatment options for patients.

    NIH research State University New York Stony Brook · Stony Brook, United States · NIH-11449546

  • US–East Africa center to prevent and detect virus-linked cancers in people with HIV

    This program builds a US–East Africa research network to train local investigators and improve prevention, earlier detection, and faster connection to care for virus-related cancers in people with HIV.

    NIH research University of California, San Francisco · San Francisco, United States · NIH-11410166

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.