Genetics
Insurers banned from jacking up premiums based on your genes
People who undergo genetic testing for medical purposes will never be obliged to share their results with insurers, and insurers will not be allowed to ask.
- by Natassia Chrysanthos
Latest
Sasha has a disease so rare, it doesn’t have a name
An ultra-rare genetic mutation has seven-year-old Sasha Lipworth regressing into infancy. Her diagnosis this month gives her a front-row seat to the future of medicine.
- by Angus Thomson
Sydney family seek treatment for daughter with ultrarare disease
Scientists this month identified the specific mutation causing Sasha Lipworth's regression into infancy, a first step towards an RNA therapy that could correct these issues in the future.
Why Sydney scientists kept two livers alive in a box for a week
The world-first study used an organ-preserving machine nicknamed a “liver in a box” that could revolutionise the way scientists trial medicines.
- by Angus Dalton
Will a revolutionary DNA-editing tool end disease – or threaten humanity?
When US biochemist Jennifer Doudna discovered the key for editing DNA, she opened scientific frontiers full of promise – and peril.
- by Greg Callaghan
The genetic ‘crystal ball’: Would you want to know which disease will kill you?
Your risk of cancer, heart attack and Alzheimer’s could be revealed with a swab of saliva. But the burgeoning DNA technology has significant flaws.
- by Angus Dalton
Exclusive
Healthcare
‘Years my kids didn’t have’: Boost to Australian gene therapy development
When Megan Maack’s two children were diagnosed with childhood dementia, it took years for a drug that could help to be available in Australia.
- by Mary Ward
Gene therapy, blood transfusions, stool monitoring: The Sydneysiders trying to escape death
Tech billionaire Bryan Johnson is convinced he’ll be able to cheat death. His “Don’t Die” movement has hit Australia, and Sydneysiders are signing up to his regime.
- by Amber Schultz
Louise says genetic testing saved her life. But others are being put off
Concerns about how life insurance deals with genetic testing are deterring people from getting important tests. Even the industry welcomes government intervention.
- by Natassia Chrysanthos
It’s free and essential for planning a pregnancy, but few know this test exists
Carrier screening could have saved Elizabeth Tierney the heartache of losing her infant son. Tests for three of the most common and serious genetic conditions will now be eligible for bulk-billing.
- by Angus Thomson
How Amelia found the woman who had saved her life
Looking through the results of a DNA database, Amelia Lewis was confused to see a “self” or “twin” living in the United States.
- by Laura Banks
Original URL: https://www.smh.com.au/topic/genetics-jr4