Meaghan Wall
@wall_meaghan
ID: 2765920482
25-08-2014 10:28:16
174 Tweet
192 Followers
351 Following
Phenomenal study led by Prof Zornitza Stark & involving many Australian Genomics geneticists - rapid acute care diagnostic genomics impacting health care for so many families. Greatly looking forward to her presentation International Congress of Genetics 2023! 👋🧬🏥 Murdoch Children's Research Institute (MCRI)
Thank you RARE Revolution Magazine for shining a light on the importance of #NewbornScreening. We’re proud to be able to provide this service to Victorian babies & families at VCGS Victorian Clinical Genetics Services (VCGS) Seb Lunke Ronda Greaves
The Australian Acute Care Genomics program report shows that integrating rapid whole genome sequencing and multiomic analyses informs diagnoses and treatment decisions in a prospective cohort of 290 critically ill infants & children. Prof Zornitza Stark Seb Lunke nature.com/articles/s4159…
Ira Deveson showing the power of long reads for repeat expansion, even for complex repeats like CANVAS. Game changer #ESHG2023 , now we need to bring it into #dxlabs
The NSW Sudden Cardiac Arrest Registry is up! We aim to recruit all families with SCA aged 1-50 years in NSW. Follow our lab socials (clinicalgenomicslab) for info and please RT! Garvan Institute of Medical Research NSW Ambulance Heart Foundation NSW Health Baker Institute ACvA Greg Page
Interested in the ethical and practical issues of genomic newborn screening? Check out our new paper! Prof. Ainsley Newson 💉💉💉💉💉 Julian Savulescu Biomedical Ethics Research Group UniMelb MDHS dovepress.com/articles.php?a…
We spoke to Prof Zornitza Stark at Australian Genomics about The Acute Care Genomics program - where whole genome sequencing is combined with multiomics to improve diagnostic outcomes for people with rare diseases. Read the interview! brnw.ch/21wC3Qc #raredisease
Congratulations AIMBRAIN team. It’s a privilege to act in support of this pioneering work. VCGS salutes your leadership and vision ANZCHOG 🎗️ RCD Foundation Jordan R. Hansford
Today marks a significant milestone towards equitable healthcare in Australia. MCRI and Victorian Clinical Genetics Services (VCGS) are proud to support giving people access to vital genetic information, enabling them to make more informed decisions about family planning.
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 Prof Zornitza Stark, Lilian Downie and many others.
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 Murdoch Children's Research Institute (MCRI). Read about what we are screening for and how it compares internationally 👇👇👇
🤗 Absolutely thrilled to see our #AcuteCare Australian Genomics work featured nature together with ExeterGenomes Rady Genomics euan ashley 🧬⏱️🤗 nature.com/articles/d4158…