The Leader in DNA-Targeted Precision Medicine
Uncover root causes & actionable treatment plans that deliver life-changing outcomes
Explore Longer Discussions in the Media on IntellxxDNA’s Life-Changing Impact
Matthew D. Taylor
Matthew D. Taylor, MD
INDEX HEALTH
Cardiometabolic, Gastrointestinal Health, Functional Immunology, Anxiety & Depression, Genomics
“This is a test that everyone can benefit from, particularly those with an undiagnosed or unexplained syndrome. It is a test to understand a person’s physiology and story, not to diagnose pathology. It takes medicine of the average to medicine of the individual in a way unparalleled by other similar lab services.”
Dr. Angela O’Neil
Dr. Angela O’Neil
NEXT LEVEL CONCIERGE CARE
Former Mayo Clinic Physician and Assistant Dean of the Mayo Medical School. Board-Certified in both Family Medicine and Integrative Medicine and certified in Functional Medicine.
“Using IntellxxDNA clinical decision support tool, I can get a true picture of a patient’s future risks, and more importantly, how we can work together to modify them.”
Dr. Sandeep Kapoor
Dr. Sandeep Kapoor
FOUNDER OF KAPOOR MEDICAL
Specializing in Internal and Geriatric Medicine. Certified Practitioner with the Institute for Functional Medicine (IFM)
“After integrating genomics for Alzheimer’s into my practice, I discovered that IntellxxDNA provides a road map for all my patients and enables me to prevent and treat a host of other medical conditions as well. IntellxxDNA Genomics has helped me discover the “Ah-hah” moments that were pivotal in optimizing the health of my patients and some of them have coined it ‘magic.’”
Laura Lile, MD, RPh
Laura Lile, MD, RPh
FOUNDER AND CEO OF LILE WELLNESS PARTNERS
Recipient of the 2023 Distinguished Alumni Award at The Ohio State University
Board-certified in Family Practice and Compounding Pharmacy
“For several decades, my medical practice has been primarily dedicated to preventative healthcare and enhancing longevity. With dual credentials as a compounding pharmacist and a medical doctor, I maintain a discerning approach when it comes to recommending supplements and medical interventions. The IntellxxDNA Clinical Decision Support Tool stands out as the most extensive and pragmatic resource I have integrated into our medical practice. It has profoundly transformed our approach to patient care, enabling us to offer precise, tailored recommendations rooted in each patient’s unique genetic profile. This tool represents revolutionary advancements in our field of medicine!”
Dr. Aunna Herbst
Dr. Aunna Herbst
CHIEF MEDICAL OFFICER, SALT HEALTH
Previous IFM Faculty at the Cleveland Clinic and author of Functional Medicine in Primary Care: Together We Will Get You Better, and contributing author to the new Functional Medicine textbook.
“The benefit of IntellxxDNA is that in 30 minutes, my patient and I were able to figure out what took me 7 years of trial and error. IntellxxDNA is a huge asset to the practice of functional medicine.”
Dr. Robert Sheeler
Dr. Robert Sheeler
NEXT LEVEL CONCIERGE CARE
Former Clinical Practice Chair for the Department of Family Medicine at the Mayo Clinic. Former Family Medicine Clerkship Director and professor at the Mayo Medical School. Board-Certified in both Family Medicine and Integrative Medicine and certified in Functional Medicine
“IntellxxDNA genomic testing is the single most valuable test I have ever ordered. It gives me the precision needed to prevent and reverse disease.”
Dr. Emily Gutierrez, DNP, CPNP, APRN, PMHS, IFM-CP
Dr. Emily Gutierrez, DNP, CPNP, APRN, PMHS, IFM-CP
FOUNDER OF NEURONUTRITION ASSOCIATES
IFM Trained, Mental Health Specialist. Dr. Gutierrez specializes in children with neurodevelopmental issues including Autism, PANDAS and ADHD. She is the author of the book The Parent’s Roadmap to Autism: A Functional Approach
“His IQ went up from 54 to 70, so he was no longer officially classified as intellectually impaired and could move to a mainstream school. WOW! How could it get better than this? You must be thrilled with your work…IntellxxDNA is really the most impactful tool I have used. I am so glad I switched!”
Dr. Penelope McDonnell, ND
Dr. Penelope McDonnell, ND
NATUROPATHIC PARTNERS
“Recently, when I finished reviewing a patient’s IntellxxDNA results, the patient said, “Everyone should be doing this!” and I couldn’t agree more. I can’t recommend this test more highly – it has changed the way I practice and treat for the better and the improved patient results are proof!”
Dr. Eduardo Maristany
Dr. Eduardo Maristany
NAPLES CENTER FOR FUNCTIONAL MEDICINE
Board Certified internal medicine physician and an Institute of Functional Medicine Certified Practitioner
“Finally, the future is here! As a functional medicine physician and genomics researcher, I’m honored to use IntellxxDNA as an evidence-based compass, to provide precise recommendations unique to each patient.”
Roberta Van Zant, D.O.
Roberta Van Zant, D.O.
FOUNDER, VAN ZANDT MEDICAL GROUP, S.C.
Board certified in Family Medicine and Osteopathy. Functional and Integrative Medicine Trained.
“IntellxxDNA has elevated the game in healthcare by providing a precise, well researched, and clinically useful tool that allows you to hit the ground running in the application of genomic medicine for your patients and their health concerns.”
What is precision genomics?
Genomics is the study of very small changes in a person’s DNA. Each of us has about 25,000 different genes made up of approximately 3 billion DNA nucleotides or units. Subtle variations in this DNA are not only what make us look different from one another, but also create subtle health differences by changing the instructions for everything our cells make and do; how we make hormones, handle inflammation and what nutrients we need more or less of. These changes translate to health effects that can be modified, when understood.
Powerful precision medicine that brings life-changing benefits to patients
The IntellxxDNA™ Clinical Decision Support Platform is a powerful, proprietary genomic research and intelligence platform, which provides comprehensive, accessible medical reporting and scientific explanations of an individual patient’s gene functions.
Our support of the clinical decision-making process helps to guide prevention and intervention strategies that enable cutting-edge, personalized medical and nutritional treatments.