Nihar
@niharb
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Postdoc at UCL. Eyes are so cool, man.
Canada and/or the UK
Joined September 2008
Love a good beeswarm! Our demographics paper is up! Congrats to all that worked so hard!
This multicenter cohort study examines the relationship between demographic factors and the age at first keratoplasty in a genetically refined group of individuals with Fuchs endothelial corneal dystrophy (FECD). https://t.co/RWhsYJH6bz
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I'm slowly migrating off of here onto bluesky https://t.co/xYpoYnmQCx I really hope i can find a similar scientific community there!
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Thank you for awarding me runner up in the Research Excellence award! The @UCLeye annual ECR symposium is always a wonderful day
A huge congratulations to all of our prize winners today! It has been absolute joy for the committee to provide a space for you all to share the fantastic work you have been doing - we are so proud of the talent and drive of our ECRs at the institute @UCLeye. Thank you!
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So grateful to all the patients who donate their corneal tissue and enable our research. Primary patient endothelial cells making the cover of the May issue of @PLOSGenetics with our paper. So cool to see our work front and center
Very excited to see @niharb image on the front cover of @PLOSGenetics this month. Amazing work Nihar! https://t.co/U4n0lX1YtO
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Proud to finally get this work out. Couldn't have done it without such a great team 🎉
Excited to our new paper in @PLOSGenetics
https://t.co/DkV02guWJr…@niharb worked tirelessly to get this across the line with much support and collaboration from NZ, @NathanTear @AmandaSadan, @ChristinaZarou, @aaron_r_j, @aszabo08, @Ismail_Moghul, Szi Kay, and many others!
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@niharb presenting her really nice transcriptomics work on elucidating Fuchs Endothelial Cell Dystophy mechanisms, a very common #TCF4 triplet repeat expansion mediated disease. More excellent output from @aliceedavidson lab #ESHG2023. Check out poster P03.13.A!
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Deciphering novel TCF4-driven molecular origins and mechanisms underlying a common triplet repeat expansion-mediated disease https://t.co/6xhDjSNcSm
#bioRxiv
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I'm so happy to share the preprint for some of the work I've been doing in my post-doc with @aliceedavidson ! https://t.co/VvmVbBrTwK It was so much fun to dig into so many different types of transcriptomic data
biorxiv.org
The predominant cause of Fuchs endothelial corneal dystrophy (FECD) is a CTG repeat expansion (termed CTG18.1) situated within an intron of the transcription factor encoding gene, TCF4 . Here we use...
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