- By Amanda Sheldon
- Posted February 28, 2018
Finding the Missing Link of Heart Disease in Families: Familial Hypercholesterolemia (FH)
Many people have friends and family members who tell stories of losing their father when he was 40, or having a mother who had a heart attack in her 30s. These same people may even know that they have high cholesterol, and sometimes are told it is inherited. What they don’t know is that this condition could be familial hypercholesterolemia (FH)…
- By Jessica Profato, MS, CGC
- Posted February 15, 2018
Using Family History to Guide Cancer Prevention
There are many factors that impact your patients’ risk to develop certain cancers, including whether or not they have a family history of the disease, which can significantly impact the likelihood they may develop cancers such as breast, colorectal, and prostate. Individuals with a strong family history of cancer may have a hereditary cancer…
- By Aaron Schmidt
- Posted February 12, 2018
Science in 60 - Genetic Testing and Familial Hypercholesterolemia - (FH)
Editor’s Note: Science in 60 is a new video series from Ambry in which our researchers will give a brief overview of how genetic testing can help everyone understand disease. In this inaugural segment, Ambry genetic counselor Tami Johnston, MS CGC, looks at how genetic testing can improve the diagnoses and treatment plans for patients with…
- By Beth Kuhn
- Posted January 30, 2018
How I Got Ahead of Cancer After Learning About My BRCA2 Gene Mutation
After watching my mom and aunt battle bilateral breast cancer - which included chemotherapy, radiation, mastectomies (surgical removal of the breast(s)), and all the physical and emotional anguish that accompanies it – I learned that I carry a BRCA2 gene mutation. It runs in our family. I was told that my inherited BRCA2 mutation…
- By David Pfeifer
- Posted December 18, 2017
Have a Little Heart: The Growing Segment of Cardiovascular Genetics
From consumers, to physicians to genetic counselors, the importance of heart health is taking center stage in genetics. Clinicians from all specialties are recognizing the benefits of cardiovascular genetic testing; inherited arrhythmias, cardiomyopathies, thoracic aortic aneurysms, and familial hypercholesterolemia are becoming more commonly discussed…
- By Aaron Schmidt
- Posted December 18, 2017
Ambry Celebrates a Milestone Year
Ambry Celebrates a Milestone Year Ambry is looking forward to an exciting 2018, after experiencing a year of reaching important milestones and seeing many changes in 2017. From joining the Konica Minolta family, to the launch of our paired testing in our mission to understand all disease, to say it was a busy year is an understatement. Test Launches…
- By Jessica Profato, MS, CGC
- Posted December 6, 2017
How Ambry Affected Hereditary Cancer Testing in 2017
It has been an exciting and busy year at Ambry Genetics, packed with steps forward on our path towards understanding all human disease. We have continued our dedication, not only to quality testing, but to innovation, research, and patient advocacy. As we reach the end of 2017, we look forward to an even more impactful 2018 and working together…
- By Eve Mart
- Posted November 20, 2017
Genetic Testing May Have Changed Things for My Mom
*Editor's Note: In honor of Family History Day, which is on Thanksgiving, Eve Mart is sharing the story how hereditary cancer has shaped her relationship with her mother, and how genetic testing may have been able to help change the course of her mother's health. I often tell women “be your own best advocate”, and I truly mean it.…
- By Taylor Leigh
- Posted November 10, 2017
Why Genetic Counselors are Integral to Ambry
In our more than 20 years of operation, Ambry has come a long way. Looking back, it’s important to remember that we would not be “Ambry Genetics” without our genetic counselors. Ambry is built on the foundation of quality genetic testing that helps people find answers – and genetic counselors have been with us from the beginning, working…
- By Desiree Magee
- Posted November 8, 2017
Genetic Counselors: Companions on the Journey to Rare Disease Diagnosis
Our daughter Daphne started missing developmental milestones at around 6 months of age. She was unable to sit on her own and unwilling to eat baby food. We started down the path of diagnosis, which was long and exhausting and went like this: First, we went to our pediatrician to document our initial concerns and obtain referrals for a physical…