Deafness genetics' reseach group in Hearing & Genes, headed by Prof. dr. Hannie Kremer and Dr. Ronald Pennings, aims to unravel the genetic landscape of hereditary hearing loss and determine and understand genotype-phenotype correlations. The gained insights are being employed for the development of therapeutic interventions in the closely associated research team headed by dr. Erwin van Wijk and dr. Erik de Vrieze.
The candidate will be embedded in the Department of Human Genetics within the Radboudumc (Nijmegen, the Netherlands), which is internationally renowned for its research and diagnostics of a variety of genetic and genomic disorders. The Department offers an exciting working environment with enthusiastic people from many parts of the world enjoying high quality research.
Radboud university medical center is a university medical center for patient care, scientific research, and education in Nijmegen. Radboud university medical center strives to be at the forefront of shaping the healthcare of the future. We do this in a person-centered and innovative way, and in close collaboration with our network. We want to have a significant impact on healthcare. We want to improve with each passing day, continuously working towards better healthcare, research, and education. And gaining a better understanding of how diseases arise and how we can prevent, treat, and cure them, day in and day out. This way, every patient always receives the best healthcare, now and in the future. Because that is why we do what we do.
Read more about our strategy and what working at Radboud university medical center means. Our colleagues would be happy to tell you about it. #weareradboudumc
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