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Mathieu Quinodoz

@mquinodoz.bsky.social

Reposted by Mathieu Quinodoz

IOB - Institute of Molecular and Clinical Ophthalmology Basel @iobswiss.bsky.social · 09/01/2026

🧬 Major breakthrough: IOB researchers identify new genetic cause of inherited blindness in overlooked RNA genes. The discovery solves decades-old diagnostic mystery and opens new pathways for many patients worldwide. ➡️ www.nature.com/articles/s41... #AcademicBlueSky #Genetics #VisionResearch #IRDs

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Reposted by Mathieu Quinodoz

IOB - Institute of Molecular and Clinical Ophthalmology Basel @iobswiss.bsky.social · 17/09/2025

🧬 How can we navigate the genetic complexity of inherited retinal diseases? Our new paper in @ajhgnews.bsky.social presents RetiGene, a curated atlas of IRD genes, built with @erdc-team.bsky.social, to support diagnosis, research and therapy. 👉 bit.ly/467U1S9 #AcademicBlueSky #IRDs #VisionResearch

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Reposted by Mathieu Quinodoz

Carlo Rivolta @carlorivolta.bsky.social · 09/06/2025

Happy to announce that the preprint about Retigene, our new gene atlas for inherited retinal diseases, is now on-line. www.biorxiv.org/content/10.1...

biorxiv.org

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)

Inherited retinal diseases (IRDs) are rare disorders, typically presenting as Mendelian traits, that result in stationary or progressive visual impairment. They are characterized by extensive genetic ...

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