Welcome to the Department of Human Genetics
In human genetics, we combine application-oriented research at the highest level 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, we investigate the complex molecular relationships in human genetics. 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 genotype and phenotype.
We use our findings to clarify genetic diseases. We are the point of contact for patients and families with suspected rare diseases as part of our genetic ambulance. 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 a university hospital, we are committed to teaching students and providing practice-oriented further training for doctors and researchers in order to ensure modern medical care.