About the department


The Department of Medical Genetics is Norway’s largest medical genetics department with over 200 employees. The department is responsible for diagnostics of rare and inherited diseases, and the main activities are clinical genetic testing, genetic counselling including assistance in connection with prenatal diagnosis, genetic laboratory diagnostics, and genetic research and teaching. The department also runs a national research infrastructure for high-throughput DNA sequencing at the Norwegian Consortium for Sequencing and Personalized Medicine (www.norseq.org). 

The research section is run in collaboration with Institute of Clinical Medicine at the University of Oslo. Several research groups are working in various fields of medical genetics, including breast cancer, the genetics of autoimmune, neurological, cardiovascular and psychiatric disorders, epigenetics causes of disease, as well as groups focusing on bioinformatics and system evolution. 

By harnessing state of the art sequencing technology our department aims to develop a platform that will take diagnosis and treatment to the next level by providing personalized medicine for the Norwegian population.

Report Department of Medical Genetics 2022/2023

Report Department of Medical Genetics 2020/2021