Deciphering the biological pathways behind rare genetic diseases often involves assembling a team of specialists to work closely with the family members of those affected.
A new study shows connections between genetics, biomarkers in the blood, and mental disorders - opening new avenues to understand the causes of mental illness and find new treatments.
Genetic analysis of caribou populations reveals that some groups are genetically more predisposed to migrating than others. But human activities are affecting these behaviours.
Non-alcoholic fatty liver disease is surprisingly common, affecting about one in four adults. Eating processed foods and sugary drinks can increase the risk of developing the disease.
The numbat is one of the Tasmanian tiger’s closest surviving relatives. And its newly sequenced genome raises the possibility of piecing together the genetic code of its extinct fellow marsupial.
Cases of the Omicron sub-variant BA.2 are now in Australia. While there’s no evidence it causes more severe disease than the original Omicron, early research suggests it’s more transmissible.
A medical genomics professor reflects on how lab simulations offer some advantages for student learning, but developing the muscle memory of performing hands-on lab work is important.
DNA and mRNA vaccines produce a different kind of immune response than traditional vaccines, allowing researchers to tackle some previously unsolvable problems in medicine.
Visiting Professor in Biomedical Ethics, Murdoch Children's Research Institute; Distinguished Visiting Professor in Law, University of Melbourne; Uehiro Chair in Practical Ethics, University of Oxford