Katrin Õunap is a leading Estonian clinical geneticist specializing in rare diseases and
metabolic disorders.
In this episode Katrin delves into her journey into genetics, starting with her early career and unexpected shift into genetics after Estonia's independence from the Soviet Union. She recounts her pivotal role in introducing newborn screening for phenylketonuria (PKU) in Estonia, emphasizing the collaboration and learning experiences that shaped her path.
The discussion covers Katrin's research in Estonia and abroad, including her significant work in the U.S. with the Center of Mendelian Genomics at Harvard University, aiming to solve unsolved genetic disease cases.
Today Katrin is a professor in Clinical Genetics at the Institute of Clinical Medicine, at the University of Tartu. She is also the Head of the Department of Clinical Genetics, at Tartu University Hospital.
At the podcast we talk about:
Sign up to receive occasional emails with new episodes, updates and behind-the-scenes content from the Beyond BAFF podcast: https://mailchi.mp/balticamericanfreedomfoundation/podcast-list
Learn more about the scholarship opportunities provided by the Baltic-American Freedom Foundation to help Baltic Scientists fund their research in the United States: www.balticamericanfreedomfoundation.org
