Recent Episodes...

In the second installment of our Alexion-sponsored series, Dr. Kathryn Dahir explores the complex genetics of HPP, why disease severity varies so widely, and the challenges of predicting symptoms.

Explore AI in genetics, emerging genome mapping technology with Nabsys, and the future of genetic research and publishing through our live podcast recording co-hosted with Wiley's Advanced Genetics.

Renowned gene-editing expert Dr. Kiran Musunuru explores CRISPR’s journey from edited embryos in China to the personalized treatment he helped develop for Baby KJ.

With 4 precision treatments now approved or in late-stage development, we explore how the expanding achondroplasia treatment landscape could shape growth, body proportionality, function, and family decision-making.

Monisha Sebastin explains how the Global Directory of Genetics and Genomics Professionals connects genetics professionals worldwide to support patient care and collaboration.

Dr. Jennifer Brown and her daughter Lillian Isabella explore the realities of PKU, from food and family life to mental health and independence.

Pioneering prenatal genetics researcher Dr. Diana Bianchi shares what the IDENTIFY study is revealing about unexpected cancer signals in cfDNA screening.

Genetic counselor Amy Patterson kicks off our three-part hypophosphatasia (HPP) series explaining the disorder and diagnosis.

Alongside his wife, Liz, Art shares how family health history and genetic testing finally connected the clues, and inspired their mission for earlier detection and advocacy.

Dr. Madhuri Hegde and Mackenzie Mosera Derby kick off a new series on the health economics of genetic testing, starting with insurance coverage and barriers to access.