The latest science,
tailored to you.

Our artificial intelligence correlates clinical experience with research in genetics, epigenetics and nutri-genomics.


Geneticists began mapping the human genome in 1990. Today, frequent discoveries continue to expand our understanding of what it means to be human. Nutri-Therapy™ uses groundbreaking technology to monitor the world’s largest genetic research database for new discoveries which may impact your health.


Each element of your lifestyle impacts how genetic possibilities become health realities. A series of simple lifestyle questions helps us understand what may be impacting your genetic expression.


Gathering DNA and lifestyle data is the first step, but the interpretation of that data is what’s most important. Nutri-Therapy™ is the first technology to correlate your DNA and lifestyle information with clinical experience, charting a personalized course toward optimal health.


Your personalized Nutri-Therapy™ report empowers you to make informed decisions based on your health realities.


No appointments necessary. Nutri-Therapy’s machine-learning technology always has your best interests in mind. We send updates directly to your inbox, based on the latest research.

I Have DNA Results.

Use your DNA test results from 23andMe, Ancestry, or FamilyTree to get your free Nutri-Therapy™ report.
Need DNA Testing? Click here.

*The Curos DNA test uses qualitative genotyping in the genomic DNA of adults from saliva for research purposes only. The test is used for reporting and interpreting genetic health opportunities. It is not intended to diagnose any disease, illness, sickness or otherwise. It is strictly for research purposes. Various factors, including the quality of your sample or your ethnicity may affect the relevance of each report and how your genetic health opportunities are interpreted. Each genetic health opportunity report (Nutri-Therapy™ report) describes if a person has variants associated with particular biological functions or lifestyle insight. The report never describes a person’s overall risk of developing any disease. The test is not intended to tell you anything about your current state of health, or to be used to make medical decisions, or determine any treatment, including whether you should take a medication, or how much of a medication you should take. Our reports can be used to determine health opportunities for research purposes and insights alone, but our test cannot determine if you have two copies of any genetic variant. These reports are not intended to tell you anything about your risk for developing a disease in the future, the health of your fetus, or your newborn child's risk of developing a particular disease later in life. Warnings and limitations: The test is not a substitute for visits to a licensed healthcare professional, for recommended screenings, or appropriate follow-up care. All information and results should be confirmed in a clinical setting before taking any medical action. For important information and limitations regarding each genetic health report, visit