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My Top Tips For Explaining Complex Genomic Information To Patients As a practitioner, explaining complex genomic information to patients can be a challenge. While the science is intricate, your role is to translate these insights into actionable, patient-friendly guidance. Effective communication ensures patients understand their results and feel empowered to take charge of their health. […]

To avoid overwhelm, start with these key SNPs and pathways: MTHFR (C677T, A1298C), MTR, TCN2: Affects folate metabolism and methylation.

How Genes Interact with Diet, Lifestyle, and the Environment: A Functional Approach The genetic code is often referred to as the blueprint for the body, but it’s not a static destiny. Instead, genes interact dynamically with diet, lifestyle, and environmental factors, shaping how that blueprint is expressed. This interaction provides opportunities to optimise health outcomes

Legal implications that practitioners should be aware of when working with genetic information include: Privacy and Confidentiality: Practitioners must comply with data privacy laws, such as GDPR in Europe, HIPAA in the U.S., or the Australian Privacy Principles, which require secure handling, storage, and sharing of genetic information. Genetic data is considered sensitive information, so

What are SNPs, and why are they important in clinical practice? SNPs, or single nucleotide polymorphisms, are the most common type of genetic variation. They occur when a single nucleotide (one of the basic structural units of DNA, represented by the letters A, T, C, and G) is replaced with another at a specific position

Genomics enables practitioners to move beyond symptom-based treatment to address the root causes of health issues. By understanding a patient’s genetic predispositions and how these interact with lifestyle and environmental factors, practitioners can:

Genetics refers to the study of individual genes and their role in inheritance—how traits and conditions are passed down from one generation to the next. For example, genetics examines how mutations in the BRCA1 gene may increase the risk of breast cancer. Genomics, on the other hand, is a broader field that examines all of

Genomic testing offers profound insights into a patient’s unique genetic makeup, helping identify specific areas where they may need support. However, with the depth and detail these tests provide, the information can sometimes feel overwhelming for patients. As a practitioner, it’s important to present these findings in a way that is both accessible and empowering,

Integrating genetic, blood, and organic acid testing into patient care can provide profound insights into an individual’s health. However, to make the most of these tests, it’s essential to follow a strategic approach. Here’s a breakdown of the critical first steps for practitioners to ensure that they’re identifying, prioritising, and addressing the key health insights

The Role of Reverse T3 in Thyroid Dysfunction: A Practical Guide for Practitioners Reverse T3 (rT3) plays a crucial role in thyroid health, often serving as a marker of the body’s response to stress, illness, or metabolic dysregulation. While rT3 is biologically inactive, it competes with active T3 for receptor binding, effectively slowing metabolic activity.