IntellxxDNA Puts Personalized, Evidence-Based Genomic Insights at Your Fingertips
Uncover root causes and untangle medical mysteries with the power of DNA.
“Doctors are held to a higher standard than biohackers and ancestry testing when it comes to genomics. You have to vet your tests and tools and give your patients that knowledge and choice.“
Dr. Sharon Hausman-Cohen
IntellxxDNA in the Media
IntellxxDNA & Your Practice
Save Time & Money for Your Patients
Save time and money with each patient interaction by being able to find and treat root causes based on each patient’s unique genomics.
Make Evidence-Based Decisions
Research in our database is unbiased, significant, and scientifically supported. Owned & operated by M.Ds, our focus is on bringing you the most researched interventions.
Get Real & Personalized Patient Results
Join thousands of physicians using personalized genomic medicine to treat the root causes of patient problems, uncovering solutions they didn’t imagine were possible.
Give Exceptional Levels of Care to All
With detailed discussions of over 700 SNPs and 10,000 references, you’ll be able to deliver molecular-level healing to a variety of patients.
The IntellxxDNA Clinical Decision Support Tool
Our genomics reports are ordered from within our advanced CDST. With detailed discussions of over 700 SNPs and over 10,000 references, our platform provides clinicians with comprehensive, accessible medical reports and scientific explanations of specific genomic patient data. IntellxxDNA puts the world of medical genomics research and functional medicine interventions at your fingertips.
What Sets Us Apart
Accuracy and Integrity of Research
Released only to licensed health care professionals, our reporting and analytics follow strict guidelines that ensure only studies with excellent scientific evidence and appropriate confidence levels are included. Utilizing our proprietary analytical methodology, IntellxxDNA provides clinicians with unbiased, scientifically current data reflecting potential additive risks and benefits that are clinically significant and scientifically supported.
The Convergence of Traditional, Functional and Integrative Medicine
Our personalized reports help clinicians understand gene function and explore potential prevention and intervention strategies. One key feature of our reports is our detailed discussions of potential interventions, which include elements from integrative and functional medicine as well as traditional medicine. Clinical reports are divided into health risk and benefit categories, where genomic single nucleotide polymorphisms (SNPs) are grouped to show risks and benefits. As a Clinical Decision Support Tool, IntellxxDNA gives you enough information about potential interventions, including information about supplement mechanisms, studies and dosing, so that you can truly develop informed, targeted plans.
A Look Inside Our Genomics Reports
A Sampling of IntellxxDNA™ Core Reports
Brain Optimization Report
The exciting Brain Optimization Report is designed to optimize your cognition, memory and overall brain health. It focuses on helping you to understand the reversible and modifiable causes of memory loss from brain fog to dementia, including vascular dementia, hippocampal atrophy and ischemic factors. There are hundreds of variants in our DNA that affect cognition. This report also includes nutrigenomics, inflammation, detox, hormones and methylation factors that contribute to brain health. Although the well-known APOE e4 gene variant is highlighted in this report, it is only one piece of a complex puzzle. This report is being used by functional and integrative medical physicians and researchers across the country including Dr. Dale Bredesen, author of End of Alzheimer’s, and other published researchers across the country.
Over 500 clinically significant gene variants are analyzed and linked to research within 21 different organized topics allowing clinicians to provide a highly individualized health plan to optimize quality of life and achieve health goals.
Key panels focus on the following:
- Cognition and Memory
- Brain Inflammation and Blood Brain Barrier Permeability
- Brain Ischemia
- Extensive Brain Nutrient Panels
- Extensive Detoxification Panels
- Hormones
- Homocysteine and Methylation
- Mitochondrial Factors
CLINICIANS: Request a demo
Medical Overview Report
Our Medical Overview Report arms you with the information you need as a clinician to help your patients address and reverse chronic health issues.
Society has accepted that as we age chronic illnesses such as cardiac disease, diabetes, osteoporosis and obesity are inevitable. However, when underlying contributing factors are made clear and addressed, chronic disease can generally be prevented and often reversed.
Our Medical Overview Report gives you the information you need to guide your patients toward a healthy lifestyle, and allows you to develop a personalized prevention or treatment plan. Without genomics, there is no way of knowing who is not able to make enough nitric oxide for opening the blood vessels, who cannot properly open their insulin channels to lower their blood sugar, who does not convert thyroid hormone to its active form in their brain, or who needs extra vitamin K2 in order to keep the calcium in their bones where it belongs; not in their arteries where it can contribute to heart disease. These are just some of the hundreds of pearls that can help you personalize your care. When a patient knows that your recommendation to cut down saturated fat in their diet or take curcumin to lower inflammation is a specific recommendation for them based on their genes, they are more compliant and achieve better outcomes.
The Medical Overview Report also helps you to better understand metabolic pathways related to anesthesia, iron, blood clotting factors and other nutrients, which will improve quality of life. It may even help prevent major healthcare events.
Over 300 clinically significant gene variants are analyzed and linked to research within 20 different organized topics allowing your clinician to provide a highly individualized health plan to optimize your quality of life and achieve your health goals.
Key panels focus on the following:
- Anesthesia Response
- Blood Clots
- Cardiac Disease
- Diabetes
- Gluten, Dairy, Histamine, Nut Tolerance
- Key Elements of Methylation, Nutrition and Detox
- Macular Degeneration
- Melanoma/Skin Cancer
- Obesity
- Thyroid
CLINICIANS: Request a demo
PLEASE NOTE, OUR POPULAR EXECUTIVE COMBINATION REPORT INCLUDES BOTH BRAIN OPTIMIZATION AND MEDICAL OVERVIEW REPORTS
Mental Wellness Report
Our Mental Wellness Report focuses on the saying “Happy Brain, Happy Life!” Understanding and balancing brain neurotransmitters is key to having the mental performance and sense of calm central to a happy and productive life.
Understanding how your DNA contributes to your mental wellness, can help you or your child optimize your attention and focus, optimize your body’s response to stress and anxiety, reduce cravings for things like sugar, alcohol, nicotine, and even gambling or drugs.
Over 250 clinically significant gene variants are analyzed and linked to research within 20 different organized topics allowing your clinician to provide a highly individualized health plan to optimize your quality of life and achieve your health goals.
Key panels focus on the following:
- Addiction and Substance Use
- ADHD Stimulant Response
- Anxiety and Stress Vulnerability
- Attention and Focus
- Obsession, Rumination and Compulsions
- Extensive Brain Nutrient Panels
- Extensive Detoxification Panels
- Hormones
- Homocysteine and Methylation
- Endocannabinoid Binding and Response
- Heavy Metal and Detox
CLINICIANS: View Webinar | Request a demo
Neurodevelopmental Report
Our Neurodevelopmental Report is comprised of the Mental Wellness Report along with the supplementary Neurodevelopmental panels. The genomics in these panels cover topics that relate to glutamate, neural connectivity, GABA receptors, mitochondrial factors, cell signaling, and more. This unique combination of topics is ideal for individuals with neurodevelopmental issues such as Autism Spectrum Disorder, Asperger’s, PANDAS, and PANS.
This report was used to obtain the excellent outcomes observed in a pilot study in Australia. The publication in the Journal of Personalized Medicine, “Genomics as a Clinical Decision Support Tool: Successful Proof of Concept for Improved ASD Outcomes,” features four patient cases and how their genomics targeted their treatment.
Our report is specifically designed to help untangle contributing factors to ASD, PANS/PANDAS, ADHD, OCD, anxiety, and other pediatric neurodevelopmental conditions. As with all of our reports, the Neurodevelopmental Report is designed to help clinicians identify root causes and create a plan using targeted potential interventions to provide an individualized health plan.
- Autism Spectrum Contributing Pathways
- Neurodevelopmental Research
- PANDAS/PANS
- Extensive Inflammation and Immune-Related Pathways
- Gluten Intolerance and Other Gut Related Pathways
- Anxiety and Stress Vulnerability
- Attention and Focus
- ADHD Stimulant Response
- Obsession, Rumination and Compulsions
- And all other pathways included in our Mental Wellness Report
CLINICIANS: Request a demo
Common Questions
Below are the answers to the questions we hear most from clinicians.
Want to know more? Contact info@intellxxdna.com for assistance.
I want to know more about the integrity of your research.
Released only to licensed health care professionals, our reporting and analytics follow strict guidelines that ensure only studies with good statistical data, reproducibility and appropriate confidence intervals are included. IntellxxDNA™ provides clinicians with highly accurate data reflecting potential additive risks information utilized in the development of IntellxxDNA™ reports comes from peer reviewed studies in the published medical literature. We aim to include only information of the highest clinical significance which is scientifically proven and supported by highly significant p values.
Genomic analysis can be complex and lengthy. Our reports focus on significant results and present the results in a format that allows clinicians to easily access data. All SNPs and other information within our reports including potential intervention and prevention strategies for addressing SNPs are referenced, so that you as a clinician can easily review any articles of interest and confirm our findings.
I want to know about your genomic reports.
For many health care professionals, two barriers to entry into utilizing genomic intelligence are time and complexity. IntellxxDNA™ reports distill dense information into an organized, color-coded structure to facilitate ease of use. Each result provides the clinician with scientific explanations and well-researched, evidence-based potential intervention strategies to support clinical decision-making.
We invite you to schedule a personalized tour with us to review a Sampler Report.
The field of genomics is complex and quickly evolving. How do you support clinician training?
IntellxxDNA™ has training video modules and other materials in development that our clinicians may access. These instructional support tools are designed to expand their knowledge base regarding gene function and implication within potential interventions. Topics include:
- Genomic Consultation Topics and Best Practices
- Safety Considerations
- Genomics Overview
- Disease State Spotlights: Modules focused on gene function, and potential preventions/interventions, within specific, complex disease states.
- Cognition and other case studies to show you IntellxxDNA™ reports in action.
Help me understand differences in genomic tests.
Direct-To-Consumer Genotype Tests
You may have seen commercials for companies that provide DNA tests and health reports to the general public, often piggybacking on the public’s interest in genealogy and ancestry. We appreciate that their marketing efforts have brought the concept of genomics and health into the public eye, however the tests and reports that they deliver to the public are not medically comprehensive. These tests only show variants relayed through selected, single SNPs, which don’t tell the whole story from a clinical perspective.
Commercial Exome Tests
Some companies conduct whole genomic or exome sequencing – meaning they sequence all of your genes. Exome sequencing is a good choice if you are looking for a rare genetic illness, and you need to identify very large deletions or insertions. Examples of genetic illnesses include Huntington’s disease or genetic forms of breast cancer (i.e. BRCA). However, current exome reports do not tend to highlight gene interactions, role of variants, or potential modulation strategies. They are also cost prohibitive for routine use.
IntellxxDNA™ Clinical Tests & Analytic Reports
Created by clinicians for clinicians, IntellxxDNA™ is a clinical decision support tool that provides genomic data and analytics based on gene-to-gene and gene-to-environment interactions through SNP technology.
Whereas most commercial tests focus on just a few alleles or single SNPs, our technology and proprietary methodology dives into the interplay within multiple SNPs, as well as the role that minor alleles play in gene function. IntellxxDNA™’s reporting provides analytics on SNP variables and pairs these findings with odds ratios, a critical factor in clinical decision-making.
IntellxxDNA™’s data and analytics look at the complex intricacies of a patient’s genomic profile and how small variations within their DNA affect their quality of life and health risks. We include evidence-based, well-researched potential intervention strategies – encompassing environment, lifestyle, nutrition, supplements and medications. These components make our reports accessible and actionable for ease-of-use in clinical decision-making.
I want to utilize the IntellxxDNA™ clinical decision support tool in my practice. How do I establish an account?
We only offer accounts to licensed health care professionals. To become an IntellxxDNA™ clinician, you will be required to provide proof of licensure. Once approved, you will receive login instructions to your dedicated clinician dashboard. This dashboard will be your portal to your patients' reporting, training and support materials and other information of assistance.
Click here to request a new account.
Or email us at info@intellxxdna.com, and a member of our team will help you establish your account.