A podcast about RetiGene is now available on Spotify! open.spotify.com/episode/6WVx...
@iobswiss.bsky.social @erdc-team.bsky.social #IRDs #VisionResearch
@erdc-team.bsky.social
A podcast about RetiGene is now available on Spotify! open.spotify.com/episode/6WVx...
@iobswiss.bsky.social @erdc-team.bsky.social #IRDs #VisionResearch
A podcast about RetiGene is now available on Spotify! open.spotify.com/episode/6WVx...
@iobswiss.bsky.social @erdc-team.bsky.social #IRDs #VisionResearch
Excellent meeting last week in Nijmegen! Thanks a lot Susanne for the excellent organization and for serving as Chair of the ERDC for so many years! We are all very much indebted to you.
18.09.2025 11:58 β π 1 π 1 π¬ 0 π 1𧬠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.
π bit.ly/467U1S9
#AcademicBlueSky #IRDs #VisionResearch
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...
09.06.2025 10:35 β π 12 π 5 π¬ 4 π 0Big blue skies in Salt Lake City
06.05.2025 03:43 β π 1 π 0 π¬ 0 π 0@karkam.bsky.social (#1919) presented exciting discoveries on AP-5 disease at at #ARVO2025 This is a novel Lysosomal Macular Dystrophy and also defines a new RPE disease. Great collaboration of the ERDC www.erdc.info @carlorivolta.bsky.social
#maculardystrophy #lysosomal #AP5 #RPEdisease
A great start to #ARVO2025 in Salt Lake City!
We kicked off the week with the biannual meeting of the European Retinal Disease Consortium (ERDC) www.erdc.info
𧬠Collaboration drives progress - together, we are stronger π§¬
#ERDC #retinalresearch #collaboration #ARVO2025
RNA xkcd.com/3056
26.02.2025 14:58 β π 17863 π 2561 π¬ 154 π 171New hope for inherited vision loss
IOB researchers (@karkam.bsky.social, @carlorivolta.bsky.social, @mquinodoz.bsky.social, @abimoye.bsky.social) identify AP5Z1, AP5M1, AP5B1 mutations, revealing new causes of macular dystrophy.
π www.cell.com/ajhg/fulltex...
#AcademicBlueSky #Ophthalmology