Improving genomic testing access for newborns in Texas
Official title: MAGNET: MAKING GENOMICS ACCESSIBLE FOR NEWBORNS IN TEXAS
Funded at Baylor College of Medicine · NIH-10993905 · Data updated 2026-11-12
This study is working to make sure that all newborns in underserved areas of Texas, especially in Hispanic communities, can get important genetic testing to help diagnose health issues early, using a special service that connects families with genetic experts for support.
Quick facts
| Grant type | R01 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | Baylor College of Medicine NIH-funded |
| Lab location | 1 site (Houston, United States) |
| Project start | September 25, 2024 |
| Project end | July 31, 2029 |
| Funding year | 2024 |
| Award (this year) | $705,600 |
| NIH project number | 1R01HG013428-01A1 |
| Project ID | NIH-10993905 on NIH RePORTER |
Who could benefit from this research
✓Could help
Ideal candidates for this research are newborns, particularly those born in underserved regions of Texas, who may require genetic evaluation and testing.
✕Less likely to help
Patients who are not newborns or those who already have access to genetic testing and care in their local area may not benefit from this research.
What this research studies
This research aims to enhance access to genomic testing for newborns in underserved areas of Texas, particularly in predominantly Hispanic regions. By utilizing advanced genomic technologies like whole genome and RNA sequencing, the project seeks to provide timely diagnoses for sick newborns who currently lack access to genetic expertise. The approach includes a remote consultation service, Consultagene, to connect families with genetic specialists, thereby improving the quality of care and reducing health disparities. The goal is to ensure that all newborns, regardless of their location, can benefit from the latest advancements in genomic medicine.
Why it matters
Potential benefit: If successful, this research could lead to earlier and more accurate diagnoses for newborns, enabling timely and personalized medical interventions.
How similar studies have gone: Other research has shown success in improving access to genomic medicine through remote consultation and advanced testing, indicating that this approach has potential for significant impact.
Where this research is happening
-
Baylor College of Medicine
Houston, United States Active
Researchers
- Principal investigator: Lee, Brendan — Baylor College of Medicine
- Study coordinator: Lee, Brendan
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About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page.