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This is personalized medicine.

Genomics intelligence is a health care professional's ultimate clinical decision support tool.


IntellxxDNA™ provides licensed health care professionals with genomic intelligence to support cutting-edge clinical decision-making. Our custom DNA array (chip) and proprietary methodology produces well-researched, easy-to-understand genomic reporting that details risks, benefits and evidence-based potential intervention  strategies – encompassing environment, lifestyle, nutrition, supplements and medications.

 

IntellxxDNA™ Supports Clinicians

Insight into gene function, and the ability to create an individualized health plan in response, offers the most targeted, personalized route to helping your patients achieve health goals.  It all starts with a DNA test kit.

Has your patient already conducted a 23andMe test?

Upload their data into the IntellxxDNA™ analytic tool, and when results are delivered to you, you can schedule consulting appointments to review results and formulate prevention and intervention plans. 

Keep in mind, however, that IntellxxDNA™ reports run from 23andMe data will not be as comprehensive as reports run from IntellxxDNA™ test kits. Our test kits are processed on our custom, research-grade array and deliver a depth and breadth of analysis appropriate for clinical decision-making

Your patient doesn't have a 23andMe data file?

Access more in-depth reporting by having your patients undergo DNA testing using the IntellxxDNA™ test kit. Our saliva test kits are processed on our custom, research-grade array.  This array, or chip, provides exceptional depth and breadth of analytics and potential intervention recommendations that aren't accessible through direct-to-consumer tests.  Our goal is to fully support your clinical decision-making. 

 IntellxxDNA Authorized Clnician

Doctor Patient Genomics Consulting

Converging Traditional and Personalized Medicine
Our reporting capabilities enable clinicians to “get under the hood,” and investigate each patient’s unique genomic profile. Clinical reports are divided into health risk categories, where genomic single nucleotide polymorphisms (SNPs) are grouped to show risks and benefits. Our personalized reports help clinicians understand gene function and explore potential prevention and intervention strategies available within functional and integrative medicine as well as and conventional medicine. Genomically targeted potential nutrition and lifestyle recommendations are referenced and discussed in detail.

Intellxx DNA Genomic Chip

Demanding Accuracy and Integrity of 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. Utilizing our proprietary analytical methodology, IntellxxDNA™ provides clinicians with scientifically current data reflecting potential additive risks and benefits that are clinically significant and scientifically supported.

 

Genomics Training for Physicians

Expanding A Clinician's Knowledge Base
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 translating gene function and supporting science for both clinician and patient. Well-researched, evidence-based potential intervention strategies support YOUR clinical decision-making.  We also provide training resources within our clinician dashboard so that you can learn any time, any place.

Evidence-Based. Research-Centric. Action-Enabled.

Below are common inquiries that we receive from clinicians. Let us know how we can assist you. Contact clinician@intellxxdna.com for assistance.

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. Due to the quality of our custom chip and the proprietary methodology that our research team employs, 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.

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 order a free Sampler Report so that you can review an example. Contact us at info@intellxxDNA.com and we'll have a member of our team contact you.

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.

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.

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 clinician@intellxxdna.com, and a member of our team will help you establish your account.

Absolutely! However, reports run off of 23andMe data are not be as comprehensive as reports run using IntellxxDNA™ test kits. Our test kits are processed on a custom array that provides a depth and breadth of information not accessed from 23andMe results.

Training Information. The Latest Research. Get it all in your email.

We are busy clinicians and researchers, and we, too, dislike being bombarded by too much email. Therefore, we only send email newsletters periodically, and only when there is valuable content to share.  You are also always welcome to opt out.  Our goal is to provide information to support your practice.

About Our Privacy Policy

IntellxxDNA™ is committed to safeguarding the personal data of our clinicians, patients, and anyone who visits our website or dashboards. Our research, analytics, reporting and marketing practices adhere to strict privacy and integrity principles, including: enabling informed consent; empowering individuals through choices; and protecting and safeguarding information according to the highest industry standards, including HIPAA.  Our Privacy Policy is available under our About page or access it here: IntellxxDNA Privacy Policy.

IntellxxDNA Logo Genomics Medicine

Curious As To What Is Inside?

We have three great report options:

This exciting report is designed to help licensed prescribers to understand the modifiable causes of memory loss. This report provides clinicians with genomic resources for the implementation of a cognitive impairment reversal protocol. In addition to the well-known APOE ԑ4 variant, there are many additional genes and SNPs which can contribute to memory loss. Genes highlighted in this report relate to numerous pathways of inflammation, clearance of amyloid, hormone related pathways, nutritional factors, detoxification pathways and more. Our report addresses over 100 SNPs found to affect cognition. Referenced potential interventions are provided. Some of these combinations of SNPs have been found to increase or decrease the risk of Alzheimer’s from 20% to 500%.
Designed especially for naturopaths, certified nutritionists, dieticians, chiropractors and acupuncturists, this report is similar to our Alzheimer’s and Cognitive Health Report but does not include prescription interventions. In addition to classic cognitive and nutrient pathways, we’ve included histamine intolerance, blood sugar and insulin resistance panels. All the information needed for a cognitive impairment reversal protocol is included plus 100s of other nutritionally related SNPs. The potential interventions of this report focus on nutrition, supplementation and lifestyle modifications.
Designed specifically for MDs, DOs, NPs, PA’s and other licensed prescribers, this report focuses on common medical issues affecting your patient’s health and quality of life. Our 20-panel report includes information on heart disease, diabetes, obesity, osteoporosis, anesthesia tolerance, thyroid, homocysteine/methylation, histamine/DAO, vitamin D and many other pathways. With over 250 referenced SNPs analyzed we are sure you will find this to be the most comprehensive and clinically relevant report available.

 

The ultimate self-care is better health care.

Help your patients take a pro-active and preventive approach to their health through advanced, actionable, accessible genomics intelligence. The IntellxxDNA™ clinical decision support tool enables you to deliver in-depth personalized care to improve patient satisfaction and improve outcomes.

Qualified clinicians are eligible to receive a free 6 panel sampler report using 23andMe data. Click on the button below to request an account and get more information.  After requesting an account, you will need to respond to the email asking you to confirm your account.  You will then be able to “order” a free sampler using 23andMe data for yourself or a patient.  If you do not have access to a patient’s or your own 23andMe data, we can give you a sampler report based on a test patient’s data.

 

 

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