Massimo showed us all what the very best of humanity can achieve working together to achieve a common goal. Join us 8:00pm next Monday 21/5 on @AustralianStory to help #finishthemission https://t.co/6ozEzehOhZ
Massimo’s Mission has LIFT OFF! Massimo's Mission, a clinical & research program in childhood leukodystrophies, is recruiting Aus patients facing challenges in obtaining a confirmed genetic diagnosis for a suspected leukodystrophy. More: https://t.co/0oV1LsOYqb @missionmassimo
Today in @WIRED: read the amazing story of a scientist, our own @ryanjtaft, who volunteered to help solve a family's genetic mystery and began his quest to bring DNA sequencing to kids who need answers: https://t.co/TWI2rAGiAB @missionmassimo
Not all heroes wear capes. Great story in @WIRED about the inspiring quest of @ryanjtaft & @illumina “to bring a genome to every kid who needs one” and use genomic #sequencing to give hope & answers to families facing rare genetic disease. #GenomicMedicine https://t.co/pgCWQ5rXEs
Study from @RadyGenomics shows progress in scaling up rapid (under 24 hours) AI-powered diagnosis with genome sequencing of seriously ill infants. Clinicians can used saved time to better plan care. In @ScienceTM
https://t.co/UVzTKtaOK9
The Govt is providing $25m to help establish a new national Drug Discovery Centre that aims to turn scientific discoveries into new medicines faster through advanced robotics. @WEHI_research
https://t.co/i3qke9e2J1
$25M support from #MRFF for a national Drug Discovery Centre at @WEHI_research that will increase Australia's capacity for developing new medicines, announced today by @GregHuntMP
We are thrilled to share the announcement of $3 million of Federal Government funding for Massimo’s Mission. A touching tribute to honour Massimo’s legacy and support pioneering research to finish the mission he started. https://t.co/9x8CXo5WvI #finishthemission#missionmassimo
100,000 Genomes Project has hit its target. One in four participants with rare diseases received a diagnosis for the first time ending the "diagnostic odyssey" for many families. Next step is 'close the loop' to clinical treatments. #finishthemission https://t.co/UrEMxHKfCK
Excellent example of how an early diagnosis allowed clinicians and researchers to offer a precision treatment for a better patient outcome. Also highlights the growing need for n=1 clinical trials for newly discovered rare diseases. https://t.co/tS92bTB900 #finishthemission
Great work from Prof Ernst Wolvetang @AIBNatUQ showing how the same technologies used to model rare diseases can provide valuable insights to common diseases like Alzheimer's Disease. https://t.co/rkwir2Rdhu