IntellxxDNA

08/13/2026

We want the best for your patients AND your practice.

A genomic report doesn’t add more noise to an already full picture. 

It adds a different kind of insight, one that can only come from a patient’s DNA, to help you see what may be contributing that standard workups can’t show you.

🧬 Want to see how an IntellxxDNA genomics report helped a patient reverse autoimmune disease? Check the Autoimmune Case Study in our links.

08/11/2026

GCH1, the little known “big sister” to MTHFR. Have you heard of it?

It’s part of the same pathway as MTHFR, but often overlooked, even though it can play a bigger role in mental health.

Ineffective GCH1 lowers BH4 (tetrahydrobiopterin) and the body’s ability to produce key neurotransmitters, like serotonin and dopamine, and also nitric oxide which can contribute to anxiety, depression, ADHD, and even self-injurious behavior, PMDD, or symptoms seen in autism.

For patients who haven’t responded the way you’d expect, this is a piece of information you need. It’s another layer of the biology behind what they’re experiencing.

IntellxxDNA gives you this and so much more in their Mental Wellness Report.

Visit us at our Start Here page to learn more.

08/10/2026

When someone tells our co-founder Carol they’re not using IntellxxDNA in their practice yet. 😅 (bold move.)

We get it. Adding something new to your practice takes time, but if you’ve got a case where something’s just not adding up, like a gap that the standard workup wouldn’t catch, we know exactly what would help- an IntellxxDNA Genomic report.

Curious to learn what is getting clinicians of a variety of specialties excited to bring to their patients’ care?

Visit our Start Here page to get the scoop.

08/07/2026

What changed to get her pregnant — at 41?

Eight years of trying.

When Dr. Hausman-Cohen looked at this patient’s genomics, a different picture emerged: her body wasn’t recycling CoQ10 efficiently, and her platelets were more likely to clot than they should be.

Two contributing factors that never would have shown up in standard labs. For other patients, the recipes for fertility were completely different.

With a plan built around what her genomics revealed, she became a mom at 41.

This is what IntellxxDNA Women’s Health genomics reports can offer when the answers to women’s health and infertility aren’t in the usual places: not a guess, but a clearer picture of what may be contributing.

Follow for more genomic breakthroughs brought to patients with IntellxxDNA reports.

07/30/2026

The hallway between sessions was its own kind of education. 🧬

Grateful for the exhibitors who showed up in Austin and gave clinicians real tools to keep learning.

Go check them out, we’ll tag them below.
Researched Nutritionals Nutramax Laboratories EnlyteRX Auro Wellness Longevity Launch Labs The Mold Pros Inc. Canada RNA Biocehmical Inc. Your Online Supplement Dispensary HANS | AI for Functional Medicine Grand Ave Pharmacy PDLabs Neuro Nutrients Advanced Humeomics SSRP Institute SALT Health | Root-Cause Medicine Practice Pure Pharmacy

07/26/2026

07/24/2026

Day one is here. 🧬

The IntellxDNA Annual Conference on Applied Genomics. Changing how you practice medicine.

Years ago, this conference started as an idea, a room where clinicians could find the missing piece when something wasn’t adding up.

This year, we’re welcoming our largest group yet: 240 attendees who are here because they know genomics can help find that missing piece.

That’s the part that gets co-founder Carol every year. Watching this community show up, share stories, ask the right questions, and gain valuable knowledge and insight along the way. That’s the whole point.

Grateful doesn’t quite cover it. Let’s get into it.

07/23/2026

You already know this moment: a family asking what’s actually contributing to their child’s autism diagnosis, and “it’s genetic” doesn’t feel like a full answer.

Here’s why: true single-gene causes are identified in only about 10–20% of children with autism. For the other 80%, there isn’t one genetic variant to point to.

What the research increasingly shows is interaction, multiple gene variants interacting with each other and with environmental exposures, food, and toxicants over time.

This is often where the picture gets more clear: when variants linked to autism are considered alongside those tied to gut inflammation and detoxification, a more complete pattern starts to emerge, and that’s where a more confident next step can begin.

🧬 Follow us for more genomic insights.

07/21/2026

Longevity isn’t just “live longer.”

For your patients, it’s living better, sharper cognition, stronger cardiometabolic health, a body that keeps pace with their life.

But what’s standing in the way is different for every patient. For one, it might be cognitive decline. For another, cardiac risk. For someone else, bone or ocular health.

There’s no one-size-fits-all path, which means there shouldn’t be a one-size-fits-all workup. 🧬

Genomics is one more piece of the puzzle, helping you begin to understand what may be contributing to your patient’s health picture — so you can build a more targeted, individualized plan.

Quality of life > quantity of years.

Visit intellxxdna.com to see how the platform supports this work.

07/14/2026

Life is simply better with genomics you can actually use.

Here’s the problem: most genomic testing was never built for this moment. Broad sequencing hands you more data than direction. Consumer tests were built for curiosity, not care.

Neither one was built for the room you’re actually in, with a patient in front of you, and no clear next step.

IntellxxDNA was built differently: as a clinical decision support platform, structured around how care actually happens.

What that looks like, in practice:
* Over 800 clinically significant SNPs evaluated, organized across multiple pathways per topic
* Validated for accuracy, and trusted by both researchers and medical practitioners
* Structured to support clinical decision-making, not just surface a list of variants
* Patient data is never sold
* Typical turnaround under 4 weeks

This isn’t about collecting more data and giving you information you don’t know what to do with.

It’s about genomics organized for the moment you actually need it. In the room, with the patient in front of you.

See the difference for yourself.
Schedule a platform tour through the link in our bio.