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Despite Barriers, Labs Starting to Report Suspected Cancer Risk Mutations Seen in Tumor Testing

Despite Barriers, Labs Starting to Report Suspected Cancer Risk Mutations Seen in Tumor Testing

by Caitlin Kingsley | Feb 6, 2020 | News

Paired tumor/germline testing is far from standard practice in cancer care, but some experts in the field are advocating that when patients have their tumors genomically profiled to determine precision medicine options, that is an opportunity to also evaluate them for...
Despite Barriers, Labs Starting to Report Suspected Cancer Risk Mutations Seen in Tumor Testing

Personalized Medicine in 2019: Options Increasing But Are They Reaching Patients?

by Caitlin Kingsley | Jan 2, 2020 | News

In 2019, the field of personalized medicine continued to grow with the market launch of more than two dozen drugs targeting novel genomic alterations and numerous genetic tests to determine whether patients are at risk for serious diseases like cancer, and whether...
Despite Barriers, Labs Starting to Report Suspected Cancer Risk Mutations Seen in Tumor Testing

My Gene Counsel Weighs in on Large-Scale Multigene Panel Study of Hereditary Cancer Risk

by Caitlin Kingsley | Sep 12, 2019 | News

Investigators at Ambry Genetics, the Mayo Clinic in Rochester, the University of Utah, and the University of California at Irvine have tapped into Ambry’s large collection of multigene panel test results to clarify hereditary cancer associations in high-risk...
Demystifying Genetics for Hereditary Breast and Ovarian Cancer Week

Demystifying Genetics for Hereditary Breast and Ovarian Cancer Week

by Caitlin Kingsley | Oct 2, 2018 | Multimedia

CURE Talks Cancer: Knowing Your Hereditary Risk

CURE Talks Cancer: Knowing Your Hereditary Risk

by Caitlin Kingsley | Sep 30, 2018 | Multimedia

In 2010, history was made when a Congressional resolution was passed to declare the first ever National Hereditary Breast and Ovarian Cancer Week and National Previvor Day to raise awareness about hereditary cancer. Millions of people carry an inherited mutation or...
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