Economics of Genomics and Precision Medicine Unit
Economics of Genomics and Precision Medicine Unit
@eigen-uom.bsky.social
Generating health economics evidence to support cost-effective and value-based implementation of genomics and precision medicine. Melbourne Health Economics, The University of Melbourne
44 followers21 following35 posts
What is the value of genomic testing for Atrial Fibrillation? A new study led by Lizzy Liu and Ilias Goranitis found people highly value genomic testing for AF,at $2,900 for symptomatic patients and $2,600 for at risk relatives, with predicted uptake of 82% if publicly funded. go.unimelb.edu.au/xzr2
New publication 🎉 A systematic review of preferences for additional findings from genomic testing, led by Daniel Sheen with A/Prof Ilias Goranitis, is now published in the European Journal of Human Genetics. Read more: www.nature.com/articles/s41...
PhD opportunity in Health Economics: Quantifying the Value of Advanced Cell Therapy for Long-term Autoimmune Conditions: CAR-T Cell Therapy for Systemic Lupus Erythematosus. Led by the Uni of Manchester with a 12-month placement at UniMelb. More here: findanexpert.unimelb.edu.au/opportunity/...
PhD opportunity in Health Economics: Real world evaluation methods for health technology assessment of genomic technologies. Joint PhD based at the University of Melbourne with a minimum 12-month stay at the University of Manchester. More info here: findanexpert.unimelb.edu.au/opportunity/...
PhD opportunity in Health Economics: Evaluate the value, feasibility and sustainability of PERSONA, a precision prevention program for breast and ovarian cancer. Methods include early HTA, micro-costing and DCEs. More info here: findanexpert.unimelb.edu.au/opportunity/...
Determining the value of genomics in healthcare” is now published in Nature Medicine. Led by A/Prof Ilias Goranitis, the paper brings together international co-authors to examine how the value of genomics can be assessed. Read the full article: www.nature.com/articles/s41...
What a fantastic achievement! Congratulations to @zornitza.bsky.social, @iliasgoranitis.bsky.social and team on the publication of the BabyScreen+ genomic newborn screening study, out today in Nature Medicine.
🤗 Out now @naturemedicine.bsky.social results of our genomic NBS study BabyScreen+ 👶🧬 👉 www.nature.com/articles/s41... 1,000 babies WGS using existing cards 600+ conditions 13 day TAT 16 diagnoses (vs 1 in std NBS) High clinical impact High parental acceptability
Economics of Genomics and Precision Medicine Unit reposted
(1/4) INVITATION: Applying #MendelianRandomization in #HealthEconomics - Bridging #Genomics & #CostEffectiveness 🗓️ Tues 16 Sept ⏰8-9 AM UTC / 9-10 AM BST / 6-7 PM AEST 📍Online, download the calendar invite here: healtheconomics.org/event/applyi...
Economics of Genomics and Precision Medicine Unit reposted
(1/4) INVITATION: Webinar exploring distributional cost-effectiveness analysis (#DCEA) for advancing #healthequity 🗓️ Date & time: 6-7pm Wed 8 Oct EDT / 10-11pm Wed 8 Oct UTC / 9-10am Thurs 9 Oct AEDT 📍 Online, download the calendar invitation here: healtheconomics.org/event/advanc...
📢 New publication in The European Journal of Health Economics! The paper assesses the psychometric performance CHU9D proxy version compared with the PedsQL in Australian children aged 0–7 years with congenital colorectal conditions. Read our findings: link.springer.com/article/10.1...
Recently our team conducted two #DCEs as part of the BabyScreen+ program to elicit the Australian public’s preferences, values, and priorities for genomic newborn screening (gNBS) and its implementation. Read more here: sciencedirect.com/science/arti...
A few weeks ago, @iliasgoranitis.bsky.social presented at the Pan American Health Organisation webinar series. The webinar explored the challenges and opportunities of incorporating genomic innovations into health systems. youtube.com/watch?v=cPQr...
A few weeks ago, @iliasgoranitis.bsky.social presented at the Pan American Health Organisation webinar series. The webinar explored the challenges and opportunities of incorporating genomic innovations into health systems. youtube.com/watch?v=cPQr...
Links to the papers referenced in the presentation are included below. 📄 pubmed.ncbi.nlm.nih.gov/32266555/ 📄 pubmed.ncbi.nlm.nih.gov/39522058/ 📄 pubmed.ncbi.nlm.nih.gov/32024983/ 📄 pubmed.ncbi.nlm.nih.gov/32371919/ 📄 nature.com/articles/s41... 📄 pubmed.ncbi.nlm.nih.gov/32839572/
🔬 Excited to share our latest work: "The Cost Effectiveness of Genomic Medicine in Cancer Control", in collaboration with Cancer Australia and @who.int.
Preferences like testing uptake, treatment adherence, and trust in the healthcare system are key to evaluating genomic medicine. Ignoring them can bias cost-effectiveness and policy relevance. 🔎 Read the paper our team supported: rdcu.be/eaJBy
How has publicly funded genetic and genomic tests been used in Australia? Read our recent study on test utilisation and MBS funding here: www.nature.com/articles/s41...
Cancer Australia recently launched the National Framework for Genomics in Cancer Control, a major step toward integrating genomics into routine cancer care for all Australians. Read the Framework: canceraustralia.gov.au/key-initiati...
Our team is proud to have led the health economics component of the evidence review that informed this Framework. Read our evidence review: canceraustralia.gov.au/sites/defaul...
Our recent micro-costing paper found that proteomics offers a more cost-effective solution with broader applications compared to respiratory chain enzymology for mitochondrial disorders in Australia. Read more of our findings here: ojrd.biomedcentral.com/articles/10....
Exciting research in #genomic_newborn_screening (gNBS)! Ilias and Riccarda contributed to this paper exploring public perspectives on which conditions should be included in #gNBS. Read more here: link.springer.com/article/10.1...
Our team, in collaboration with @ausgenomics.bsky.social, identified priority indicators for assessing the value of #genomic_testing in #rare_diseases, an important step toward standardising evidence generation. Read more here: pubmed.ncbi.nlm.nih.gov/38459833/
An interesting paper from our team on #additional_findings in #genomic_sequencing. We report results from a #DCE exploring parental preferences for the process of returning additional findings and the value placed on this analysis for children with rare conditions. Read more here: rdcu.be/dyDkq
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