Actor and former professional wrestler Tyler Mane shares his male breast cancer diagnosis, the importance of self-advocacy, and why men need to know their hereditary cancer risk.
All in Interview
Melanie Hardy and Amy Shikany take listeners inside the American Board of Genetic Counselor’s (ABGC) board exam and explain how to prepare with the latest 2026 resources.
Our PKU series kicks off with Sarah Chamberlin and Ryan Miller, sharing the journey from newborn screening result to diagnosis, treatment, and family support.
Baylor Genetics’ Dr. Christine Eng and Chris Sands explore the power of whole genome sequencing when paired with multi-omic technology, like long-read sequencing, optical genome mapping, and RNA sequencing.
Siblings Dan and Faith share their family’s experience with Sialidosis; from the decade-long hunt for a diagnosis to the groundbreaking research they are involved in.
See how tools like long read sequencing, RNA sequencing, MAVEs, and AI are ethically transforming WGS to make patients lives better.
Baylor Genetics’ Chief Medical Officer Dr. Christine Eng explains how RNA sequencing complements DNA testing to unlock diagnoses for rare disease patients.
How whole genome sequencing is transforming rare disease diagnosis in Brazil featuring MGI’s Victor Camillo and Neogenomica’s Dr. João Bosco Oliveira.
Listen to The Persistence Lab, a new podcast from AbbVie. Hosted by Kira Dineen, the series explores how scientists, patients, and experts look to solve some of the toughest challenges in medicine and health care, one step at a time.
Recorded live at Connecticut’s Darwin Day Event, we examine natural selection, horizontal gene transfer, and how Charles Darwin’s ideas continue to shape genomic science.
Clinical geneticist Dr. Amy Kritzer reveals why Fabry disease looks so different across sexes and what that means for diagnosis and treatment.
Drs. Yuming Hu and Elizabeth Bhoj on bridging research and real-world impact through scientific publishing.