Scientist Stories: Euan Ashley, Precision Medicine for Rare Childhood Disease

Born in Scotland, Dr. Ashley graduated with 1st class Honors in Physiology and Medicine from the University of Glasgow. He completed medical residency and a PhD at the University of Oxford before moving to Stanford University where he trained in cardiology, joining the faculty in 2006. His group is focused on the science of precision medicine. He is best known for his work helping establish the field of medical genomics. His team developed some of the earliest tools for the interpretation of the human genome in the context of human health. He founded the Clinical Genomics Program and the Center for Inherited Cardiovascular Disease at Stanford. He was the first co-chair of the steering committee of the national Undiagnosed Diseases Network. He was a recipient of the National Innovation Award from the American Heart Association and the NIH Director’s New Innovator Award. He was recognized by the Obama White House for his contributions to Personalized Medicine. In 2018, he was awarded the American Heart Association Medal of Honor for Genomic and Precision Medicine. He was appointed Stanford Associate Dean in 2019 and became the inaugural holder of the Roger and Joelle Burnell Chair in Genomics and Precision Health in 2021. In 2023, he became a Fellow of the John Simon Guggenheim Memorial Foundation. He is co-founder of three companies: Personalis ($PSNL), Deepcell, and Svexa. His first book The Genome Odyssey - Medical Mysteries and the Incredible Quest to Solve Them was released in 2021 and has been translated into multiple languages and distributed around the world. Father to three young-ish Americans, in his spare time, he pilots planes, tries to understand American football, plays jazz saxophone, and conducts research on the health benefits of single malt Scotch whisky.

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