Before Heather became the Lynch Syndrome expert that she is today, Heather started her career working with BRCA1 and BRCA2. She’s published many papers on Lynch Syndrome cascade testing, including MSI, immunohistochemistry (IHC) and germline sequencing. Heather has been working in cancer genetics as a counselor and researcher for over twenty years. “Her real-world experience with MSI testing…was inspiring.” “I was so excited to have Heather on campus because it helped put all the work we are doing on MSI into context,” says Promega Director of Clinical Diagnostics Heather Tomlinson. On July 31, we hosted Heather and her colleagues Paul Goodfellow, Ph.D., and Rachel Pearlman, MS, LGC, for a day of learning and lively conversations about microsatellite instability (MSI), Lynch Syndrome and the future of cancer genetic testing. She is currently the Associate Director of the Division of Human Genetics at The Ohio State University Comprehensive Cancer Center. Heather is a world leader in cancer genetics and has devoted most of her career to research on Lynch Syndrome detection. It’s almost like speaking several different languages.” “You have to explain what’s going on – DNA mismatch repair, autosomal dominant inheritance – in a way they’ll understand. “Your patient might not have a high school education, or might have a PhD,” Heather says. As a genetic counselor, she works with many patients who have recently been diagnosed with a cancer syndrome or hereditary predisposition to cancer.įor Heather, one of the biggest challenges is explaining complex information about genetics and DNA to a specific patient in language that they will understand. Heather Hampel, MS, LGC, leads difficult conversations for a living.
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