The Neurogenetics Lab ION
@IonSynapse
Followers
935
Following
811
Statuses
373
The Neurogenetics lab @UCLION led by Professor Henry Houlden is dedicated to discovering new genes and disease mechanisms linked to neurological disorders
London, England
Joined December 2015
RT @FahrBeyond: Want to find out more about #Fahrs Disease/ #PFBC? Then take a look at the videos from our latest webinar? @camrarediseas…
0
2
0
RT @Rahema_UCL: It was a pleasure to visit the Aga Khan Hospital in Dar es Salaam, Tanzania 🇹🇿 to explore how genetic research can advance…
0
7
0
RT @RMaroofian: As part of 2 parallel studies, we delineated a new subtype of neurodevelopmental disorder linked to biallelic GTF3C3 varian…
0
3
0
RT @VioricaChelban: Top level data from @AlterityT Therapeutics ATH434 Phase 2 Trial Results in Multiple System Atrophy
0
3
0
RT @VioricaChelban: Delighted to invite you to the Multiple System Atrophy Symposium 2025. With an excellent group of speakers covering dia…
0
6
0
RT @RMaroofian: NDUFA13, a mitochondrial complex I subunit, was linked to complex I deficiency in only 3 patients. We now report 10 more, e…
0
3
0
RT @UCLIoN: Read all about our Neurogenetics Lab's collaboration with Little House of Science @lhouseofscience to host an engaging day of n…
0
6
0
Check out the latest article from the ION-DRI Newsletter about our lab. Learn more about our ongoing research & the work we're doing to better understand the genetic mechanisms behind neurological diseases! 🧬🧠 @UCLIoN @UCLBrainScience @UKDRI
0
7
17
RT @RMaroofian: Back in 2013, we identified KPTN as a cause of NDD, though its function was unclear. By 2017, it was revealed as part of KI…
0
2
0
RT @arianna_tucci: Come and join the lab! we have a position available to work on the analysis of short and long-read DNA and RNA sequencin…
0
10
0
RT @StephanieEfthy1: Renee Lin from my team and Prof Paola Nicolaides presenting a genetic and clinical overview from 162 NCBRS patients at…
0
1
0
RT @UCLBrainScience: Listen to Prof. Sir John Hardy (@UCLIoN) talk about the future of identifying, detecting and treating Alzheimer’s dis…
0
8
0
RT @Brain1878: RBL2 dysfunction disrupts cell-cycle gene expression and has been linked to a severe neurodevelopmental disorder. Aughey et…
0
8
0
RT @RMaroofian: TRMT1 & TRMT1L modify tRNAs, essential for protein production. Their modifications are crucial for tRNA stability & functio…
0
5
0
RT @RMaroofian: In 2021, we identified a rare VWA1 founder mutation in UK & Western European populations, linked to neuromuscular disorder…
0
1
0
RT @GIMJournal: As 2024 draws to a close, make sure to check out some highlights from GIM's EIC Robert D. Steiner, MD, FACMG in this year's…
0
3
0
RT @FahrBeyond: 🚨EXCITING NEWS🚨 Hold the date of 29th January 2025, we will be holding a webinar with @amitbatla, clinical lead for #Fahrs…
0
3
0
Join us for the 3rd MSA Research Symposium on Fri 25th April 2025, focused on the prodromal stage, diagnosis & management of MSA. Hear from experts Dr. Horacio Kaufmann, Prof. Tom Foltynie & Andrew Singleton. Register now for early bird tickets! @UCLIoN
0
8
6
Dr Viorica Chelban recently attended the PMFG Summit in Doha, Qatar where she presented latest advancements in Neurogenetics & Rare Diseases @VioricaChelban @UCLBrainScience @UCLIoN @SidraMedicine #PMFG2024
0
1
9
Merry Christmas from our lab! 🎄 Wishing everyone a joyful and well-deserved Christmas break, filled with peace and happiness. Here’s to a fantastic start to 2025 – we can’t wait to see what the year ahead brings! 🥂✨ @UCLIoN @UCLBrainScience @uclh
0
3
29