Genetic Cancer Testing with Ambry

We partner with Ambry Genetics to provide comprehensive genetic analysis tailored to your personal and family medical background. This advanced screening evaluates your hereditary risk for certain types of cancer; empowering you to make proactive, informed decisions about your long-term health management.

Ambry Genetics specializes in analyzing specific genes linked to inherited cancer risks. Their advanced multi-gene panels evaluate mutations associated with common hereditary conditions; including BRCA1 and BRCA2 genes related to breast and ovarian cancers, Lynch syndrome genes related to colon and endometrial cancers, and other high-risk indicators.

The collection process is entirely non-invasive, requiring only a quick in-office blood draw or saliva sample. This sample undergoes state-of-the-art laboratory analysis, and within weeks, a highly detailed genomic report is generated to outline any relevant findings or mutations.

Identifying genetic variations early can guide vital life decisions. The results provide a clear roadmap for your preventative healthcare; allowing us to implement targeted screenings, introduce lifestyle adjustments, or coordinate early clinical interventions safely.

Advanced genomic profiles are only valuable when thoughtfully interpreted; Dr. Baker uses her extensive background as a double board-certified diagnostician to translate complex genetic panels into clear, practical clinical insights rather than standard, automated data summaries.

We do not treat genetic markers in isolation; your hereditary risks are directly integrated into a comprehensive internal medicine framework that considers your lifestyle, current physiology, and long-term longevity goals.

If an elevated mutation or hereditary risk is identified, you have an engaged physician in your corner; Dr. Baker remains personally involved beyond the initial visit to guide you, support your family, and coordinate necessary specialist screenings.