Eye2Gene

Twitter story about our recent research preprint on developing @Eye2Gene an #AI for #IRD at @ucleye @MoorfieldsBRC . Preprint available here: researchsquare.com/article/rs-211… (1/n)

Do you support someone living with an inherited sight loss condition? Book your free place for the @RetinaUK CPD-accredited Professionals’ Conference on Friday, 19 September in London or online. Register here: retinauk.org.uk/event/professi…

Retinograd-AI: An Open-source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Dystrophies ow.ly/nuCg50W8nAB @npontikos #ophthalmology

Next-generation phenotyping of inherited retinal diseases: Eye2Gene (AI-driven algorithm). Better-than-expert accuracy for 63 common genetic causes. @ucl @npontikos @GeoMichalis @MaximilianPfau3 @sktywagner @riksag @KonBalaskas #NIH @NatMachIntell: brnw.ch/21wUfkJ

Congrats to the @Eye2Gene team on their new paper in @NatMachIntell! Developed at @UCL, this AI tool predicts genetic causes of inherited retinal diseases from eye scans, accelerating diagnosis & advancing gene therapy. Proud to support via @UCLTRO. bit.ly/4l7Ft9G

Researchers at @UCLeye and @MoorfieldsBRC have developed an artificial intelligence tool, Eye2Gene, that can predict the cause of genetic eye diseases. buff.ly/9yGY9c5

A.I. is improving the accuracy of medical diagnoses. Today for inherited retinal diseases [IRD] (Eye2Gene vs retinal experts) nature.com/articles/s4225…

Last week, we sponsored @UCLeye's Early Career Researchers Symposium. Chrissie Adams spoke about research #inclusion, highlighting our free on-demand training to help researchers with #PPIE and #EDI. Register here: buff.ly/atpRkI5 Read more🔗buff.ly/qw2re

We have supported an #AI tool that improves genetic diagnosis of inherited retinal disease, a leading cause of blindness in the UK. Published in Nature Machine Intelligence, @Eye2Gene offers a faster, scalable diagnosis & better than expert accuracy. 🔗buff.ly/7yYxCNG

Did you miss ERN-EYE webinar on "#Usher Syndrome"? Don't worry, the replay is now available! See all ERN-EYE webinars: ern-eye.eu/type-media/vid… youtu.be/rFalKBKcBu4?fe… #UsherSyndrome #ShareCareCure

AI segmentation for inherited retinal diseases from @william_woof @ThalesGuimares5 @MalenaDaich @riksag @MichalisGeorg @Ismail_Moghul @DunJackFu @DSumodhee @MariyaMoosajee @praveenjpatel @KonBalaskas @MichelMichaelid @npontikos @UCL_Retina doi.org/10.1016/j.xops… #AI4IRD

Excellent talk from @shahida_moosa highlighting the need for a global reference for phenotype variability in rare disease diagnosis. Featured Symposium (session 35) on AI to improve clinical diagnoses in Four Seasons Ballroom 2&3 #ASHG24 #AI #rarediseases

@Eye2Gene for next generation phenotyping of inherited retinal diseases using AI was highlighted by Ismail Moghul @UCLeye during the great Featured Symposium on Advanced in AI (session 35). #ASHG24 @GeneticsSociety #AI @npontikos

@elfridedebaere @Eye2Gene @UCLeye @GeneticsSociety Thank you @elfridedebaere ! It certainly looked like a great session, I am sure @Ismail_Moghul enjoyed it!

@npontikos will be presenting at the Genomics England Research Summit 2024 tomorrow at the Emerging Technologies Stage at 11:25: "Eye2Gene - next generation AI phenotyping to predict genetic diagnosis in inherited retinal disease" Looking forward to seeing you there! #GERS2024

Tomorrow is the big day! @UKEyeGenetics Annual Conference in #Liverpool @RCPhysicians! See you there! 👁🧬 @MariyaMoosajee @CecileMejecase @neeru_vallabh @cm_stanton @RCOphth

First speaker is @npontikos from @UCLeye sharing insights on his work using #AI to improve genetic diagnosis! #UKEGG2024

@william_woof presenting on his #IRD journey and on @eye2gene today at @RIWC24 @Retina_Int @fight_blindness 👏

@RIWC24 @Penn @Retina_Int @FightBlindness @NIBRT_ @OHSUNews @SparingVision @ugent @william_woof is that you? :)

Final #RIWC24 session for today💫 An incredible panel on the High unmet medical needs in retinal degenerations, with Prof Bennett @Penn, Avril Daly @Retina_Int, Dr Durham @FightBlindness, Mr Morrisey @NIBRT_, Prof Pennesi @OHSUNews, Dr Chung @SparingVision and Prof. Leroy @ugent.

🎃🎃 Fresh Off the Press 🎃🎃 👉Senior Loken syndrome is a #ciliopathy characterised by #Nephronophthisis and #RetinalDegeneration (commonly #LeberCongenitalAmaurosis). The gene associated with this condition is #NPHP5 (IQCB1).