Official account of the Biomedical Ethics Research Group, Murdoch Children's Research Institute. Views expressed are our own and do not represent those of MCRI.
Check out our new paper where we analysed submissions sent to the Senate Committee that informed drafting of the Mitochondrial Donation Law Reform (Maeve’s Law) Bill 2021 @JemimaAllen_@DanyaVears@MCRI_for_kids @UniMelbMDHS https://t.co/kXXVv30gqC
Check out the new position statement by the Human Genetic Society of Australasia on Genetic Carrier Testing for Recessive Conditions led by @DanyaVears with @biomedethics@Amcinerneyleo @jacobs_chrisj and Jackie Boyle https://t.co/gGXNUimsVg
Shared just a snippet of our recent work yesterday at #ICG2023
Reanalysis of genomic data is so beneficial, but there are practical and ethical issues to consider #genechat
New research analysing the first porcine cardiac xenotransplantation, with BERG’s Chris Gyngell, @konstantinov_ie, @juliansavulescu, Prof Megan Munsie, Prof Misao Fujita, and Dr. Carrie Thiessen.
https://t.co/0CiLlnWPOh
Looking at some of the issues around overdiagnosis/misdiagnosis of ADHD through the lens of an ethicist. Great to work with @CPAGyngell and Jonathan Payne on this. Hope it stimulates conversation @UniMelbMDHS #ADHD https://t.co/YLIdqcyn0U
Huge thanks to the #ESHG2023 organisers for letting @CelineLewis23 and I on the decks at the conference party and to the attendees for bringing their best moves to the D-floor! We had the best time 😁
Rapid genomic testing poses many ethical challenges – we surveyed intensivists from around the world to see what they think. Read about their attitudes in our new paper out now! https://t.co/C9FUKUj0Qm
@MDPIOpenAccess@MCRI_for_kids@UniMelb
New Position Statement issued by @HGSAAustralasia providing guidance on genetic carrier testing for recessive conditions in adults and children https://t.co/EOX3SBBYZZ
Just out! Our postdoc @DanyaVears along with Isabelle Budin Ljosne and Nina Hallowell, led the development of a practical checklist for return of results from genomic research in the European context @UniMelb@MCRI_for_kids@CBMER_KULeuven
https://t.co/aVu7JOI39D
Should we offer secondary findings from #genomics in children? What do parents want to know?
Read our latest blog post outlining some of our recent research on this!
Data sharing is so important for #genomics - check out the next blog in our series on this topic!
In this piece, we explore the pros and cons of #bigdata sharing, and what the Australian public thinks about it!
Interested in clinician perspectives on decision-making in paediatric home mechanical ventilation? Check out this paper by Juliette Jeffreys, Mayukh Rahman, @DanyaVears@BigjohnMassie https://t.co/5bdbOVIpVE
Should children with hearing loss undergoing exome sequencing also be offered secondary findings? Lauren Notini @DanyaVears@ClaraGaff and @juliansavulescu asked health professionals offering this testing what they thought @MCRI_for_kids@UniMelb
https://t.co/17xhM8CmHg
Data sharing is essential for #genomics - the Australian public are mostly supportive, but concerned about how the data might be misused.
Read more in our recent study: https://t.co/9pqs7e3rl3