Could routine eye scans become a new way to detect diseases early, just like mammograms do for breast cancer? We think so! One of the largest eye studies reveals new insights thanks to brilliant science by @_vickijackson@MelanieBahlo and team.
https://t.co/75jd8A5mXW
📢 Last chance!!
⏱️Earlybird registration ends tomorrow: Friday 21st June!
🖱️Don't miss out on our special discounted rates, register today: https://t.co/Tg5JIdShmg
🗓️ We are pleased to announce the extension of the Earlybird Registration deadline until Friday 21 June!
🙌 All abstracts are currently under review and your result will be received prior to the earlybird deadline.
🖱️ Register now: https://t.co/nx98JHyGdk
🙏 Thanks to everyone who submitted an abstract! The GeneMappers committee are currently reviewing submissions and looking forward to putting together an exciting program!
In the meantime, don't forget to take advantage of our earlybird registration rates! 👇
📢 Abstract deadline has been extended!!
📅 You now have until Monday 20th May to submit your abstract for GeneMappers 2024.
🖱️ Head to https://t.co/nx98JHy8nM for the abstract submission portal, and registration.
We are now inviting abstract submissions for GeneMappers 2024!
Head to https://t.co/F6GtuTW3Ct to submit your abstract, or to find out more about the conference.
We are excited to announce the 2024 Genemappers Conference will be held in Christchurch, in Aotearoa New Zealand!
Mark your calendars now!
🗓️19- 21 AUGUST 2024
Our new preprint on multi-omic AI-enabled retinal thickness analysis is up. Exciting work with @aaronylee. Analysis co-led by @_VickiJackson, @robbie_bonelli Yue Wu (UWA) & co-authors. https://t.co/1RnSaJhE1m
I guess this is the first study to investigate rare variant associations of Parkinson's disease at a genome-wide scale (7,184 PD cases, 6,701 proxy-cases, and 51,650 healthy controls).
https://t.co/EWvpNG7dPm
There are just 23 days remaining to get your #GeneMappers2023 abstract submitted!
Submit today at: https://t.co/EWkdkgQUOy
Here are 3 reasons why you should:
🆕paper from the Speech and Language team at MCRI, identifying new genes for severe childhood #speech disorder | @MCRI_SpeechLang
Published open access in @molpsychiatry 👉 https://t.co/t5qt6mcKhx
New! Genome sequencing in 70 children with speech apraxia implicates multiple genes & highlights roles of chromatin regulation pathways in the developing brain in this trait. Led by @MCRI_SpeechLang/@WEHI_research & published open access in @molpsychiatry:
https://t.co/VmOfMDbv18
On acknowledging the disconnect between what seems good and what is good, when it comes to the environment.
Always an informative read from @_HannahRitchie in @WorksInProgMag
https://t.co/HWf63h6MOA