VCGS is the NFP genetic and genomic services arm of @MCRI_for_kids & one of the largest contributors driving genetic healthcare, research and policy in Aus.
Thank you @AusHealthEcon for this honour! Many, many thanks to @AusGenomics for the support, leadership and nomination and to my @EiGEN_UoM team. Find out more about some of our work this morning on the organised session for novel applications of health economics in genomics!
Congratulations to Prof. llias Goranitis for winning this year’s AHES Policy Impact Prize! Although he couldn’t be there to collect the award, it’s a well-deserved recognition of his impactful work. Well done! #AHES2024
The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact. Delighted to be leading a new consortium to help make this happen, along with an awesome team of Australian and global partners: mcri.edu.au/news/funding-awa…
VCGS/MCRI and the Robert Connor Dawes Foundation were pleased to welcome Victorian Minister for Health, Mary-Anne Thomas to announce a subsidy for an advanced diagnostic test for brain tumours.
Read the full story: vcgs.org.au/news/brain-cance…@MCRI_for_kids@VicGovDH
Congratulations to Prof @ZornitzaS, Clinical Geneticist at VCGS, who has won the @humangenomeorg HUGO Chen Award of Excellence for accelerating rare disease diagnosis! 🔬🌟 #genetics#genomics
“Even with a two-, three-week turnaround time, that’s clearly still not fast enough....I was very keen to make it even faster.” #MCRI and @TeamVCGS Prof Zornitza Stark has discussed challenges & triumphs of rapid #genomic sequencing in @Nature⬇️|@ZornitzaSgo.nature.com/49CewVV
Hot off the press: Our BabyScreen list of over 600 actionable genes and conditions that we screen for in our #gNBS pilot now published: gimjournal.org/article/S1098…
Thanks to the great work of @ZornitzaS, @drlildownie and many others.
Genomic newborn screening is coming but what should we screen for? BabyScreen gene list and comparison with international newborn sequencing gene lists now published! @ZornitzaS@GenomeSebgimjournal.org/article/S1098…
Proud to be involved in delivering this exiting new study! Fully accredited WGS for over 600 conditions as part of this genomic new born screening pilot @MCRI_for_kids. Read about what we are screening for and how it compares internationally 👇👇👇
🎄Season’s greetings from the VCGS team! Wishing you a joyful and safe holiday season surrounded by friends and loved ones. Here’s to the opportunities and successes that lie ahead in 2024! 🎉
🎙 PODCAST: In this episode of The Good GP, Dr. @AlisonArchiba19, Group Leader of Reproductive Genetic Counseling at VCGS and Dr. Krystyna de Lange explore noninvasive prenatal testing (#NIPT), a screening method for #chromosome conditions in the fetus.
soundcloud.com/thegoodgp/non…
Be sure to register for the Clinical Informatics Symposium happening on Thu 7 Dec right after the @ABACBS conference in Brisbane! eventbrite.com.au/e/clinical…
🧬Exciting news! 3-condition genetic carrier screening will be subsidised by Medicare from 1 November 2023. 🧬
We offer information, genetic testing, and expert support to help you and your family make informed reproductive choices.🤰👶
Visit: vcgs.org.au/prenatal-genetic…