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About Luna Genetics

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meet the team

Luna Genetics was founded by physicians and scientists who believed there was a better, safer, and earlier way to test for fetal abnormalities.

The Luna team developed a novel approach called the Luna Prenatal Test. The Luna Prenatal Test uniquely captures fetal trophoblast cells in maternal blood early in pregnancy and uses advanced DNA analysis to detect a range of genetic abnormalities, including Down syndrome, trisomy 13, trisomy 18, and many smaller chromosomal abnormalities.

Luna Genetics

Team Leadership

Luna Genetics

Scientific Advisory Board

Our Mission

Our mission is to revolutionize prenatal genetic testing by providing safer, more accurate, and earlier results.

Our Vision

We envision the Luna Prenatal Test as the next generation in prenatal testing for an earlier and safer diagnosis of genetic abnormalities in pregnancy.

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Luna Genetics


"This test is incredible and will supplant cell-free NIPTs in short order.

Hope the company has the bandwidth to test what is likely to become a flood of samples. The fact that it’s a diagnostic and can take the place of amnio/CVS is a really big deal. Even couples who are enthusiastic about genetic testing have some reservations about these tests due to their invasive nature. The Luna Test changes this."

~Mark Zylka, Ph.D. researcher at UNC working on prenatal CRISPR treatment for Angelman syndrome
"If I’d had the option to take the Luna Prenatal Test to avoid the wait, I would not have hesitated.

After receiving an abnormal screening result from my noninvasive prenatal test (NIPT), I had to wait two months until I could undergo amniocentesis. It turned out the NIPT result was a false positive, but the months of waiting to get a normal diagnostic result on the health of my growing fetus were the two most difficult months of my life."

~Kim S., mother who experienced amniocentesis following an abnormal NIPT result.

See What Makes Our Test Better

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Luna Genetics

Team Photos

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