In the Department of Human Genetics, we combine outstanding application-focused research with professional patient care.

Our international and interdisciplinary research teams investigate the effects of genomic and epigenetic changes on the development of cells, organs and diseases using state-of-the-art technology and innovative methods. Our scientific findings make an important contribution to the understanding of ultra-rare genetic diseases, the identification of risk factors for cancer and the correlation between genotypes and phenotypes.

We use our research findings to help diagnose and treat genetic diseases. We are the point of contact for patients and families with suspected rare diseases as part of our genetic clinic. Our accredited diagnostic laboratories use a wide range of cytogenetic and molecular genetic methods. We handle the entire process from sample preparation to data collection, evaluation and medical interpretation in the field of rare diseases and in the genetic diagnosis of hematological tumors.

As an university hospital, we are committed to teaching students and providing practice-oriented continuing education for physicians and researchers in order to ensure modern medical care.