Integrated RP2 Research
Decoding Mechanisms
Advancing Therapies
InsightRP2 unites clinical data, AI, and molecular research to uncover disease mechanisms of RP2-associated retinitis pigmentosa and to develop targeted, innovative therapies.
Multidisciplinary Research
InsightRP2 Project
InsightRP2 is a multidisciplinary research project at the Department of Human Genetics of the University Medical Center Göttingen that focuses on a rare form of the inherited retinal disease retinitis pigmentosa (RP) caused by mutations in the RP2 gene. Its goal is to better understand the disease mechanisms underlying RP2-associated RP and to pave the way for future gene-based therapies.
Creating
knowledge together.
Complementary expertise and diverse perspectives driving new scientific insights.
Measurability
through AI.
AI‑based analysis of retinal images enabling quantitative assessment of disease progression.
Patients
in focus.
Translation of novel therapeutic approaches based on gene replacement and genome editing.
Precision
meets research.
Molecular studies in retinal models revealing specific disease mechanisms
