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Retinal diseases such as age-related macular degeneration (AMD), diabetic retinopathy, and inherited retinal disorders are leading causes of blindness worldwide. Traditional models (animal or 2D cell cultures) fail to fully replicate the complex structure, vascularization, and function of the human retina. Retinal organoids-on-chip offer a breakthrough: they recreate 3D retinal architecture, allow integration of microvasculature, and enable real-time functional studies through electrophysiology. This platform provides an unprecedented window into human retinal development, disease mechanisms, and potential therapeutic interventions.
This research will focus on addressing these critical challenges, helping to pioneer innovative solutions for vision preservation and restoration.
We are seeking a highly motivated PhD candidate for The European Research Council project to join an interdisciplinary project at the interface of bioengineering, neuroscience, and microfluidics. This project aims to develop vascularized retinal organoids-on-chip to study retinal physiology and retinal disease mechanisms.
The project combines cutting-edge stem cell biology, electrophysiology, and microfluidic organ-on-chip technology to create functional retinal models with integrated vasculature.
The PhD candidate will:
Key Responsibilities:
The candidate will be affiliated at the Department of Ophthalmology and perform experiments at the Department of Human Genetics. The candidate will be supervised by Dr. Zohreh Hosseinzadeh.
The Department of Ophthalmology of the Radboud University Medical Center is a global leader in the field of multifactorial and genetic retinal eye diseases. The research of the department is focused on retinal forms of blindness that affect large numbers of patients worldwide, especially inherited retinal degenerations (IRDs), such as retinitis pigmentosa, and age-related macular degeneration (AMD). Our aim is to develop personalized treatment and prevention options using metabolomics, natural history studies and genetic profiles combined with imaging parameters, and artificial intelligence.
The Department of Human Genetics is divided in multiple division all well known worldwide. The patient care (division clinical genetics) and genetic diagnostics (division genome diagnostics) performed within our department is hosted by an official and acclaimed Centre for Clinical Genetics. The division genome research performs groundbreaking research into the relationship between genes and diseases, as well as therapy development, notably concerning blindness and deafness, cancer, congenital anomalies, and mental handicaps. To identify and functionally characterize novel disease genes, we utilize a combination of biochemistry, genomics technologies, molecular biology, cell biology, and developmental systems such as iPSC model systems, Drosophila melanogaster, zebrafish and mouse.
Radboudumc is internationally renowned for its research and diagnostics on a variety of genetic disorders and the impact of personalized medicine. Both Departments offer an exciting working environment with enthusiastic people from many parts of the world, providing ample critical mass and a stimulating, collaborative atmosphere for high quality research.
Our ideal candidate:
Candidates should have a strong ambition to succeed in science, be result-oriented, and have strong communication skills (both orally and in writing) and a high English level to ensure efficient interaction within a multidisciplinary team. They should possess a critical scientific attitude and should be able to work both independently as well as in a team.
Please take this into account.



