New guidance co-led by University of Otago researchers could help more people with suspected inherited diseases receive a ...
A study from Karolinska Institutet shows that genetic testing can identify germline predisposition underlying childhood ...
Rare genetic diseases can go years, or even decades, without diagnosis. Standard testing often misdiagnoses these diseases, ...
Partnership with RISE will expand access to genomic testing for families with unresolved rare genetic conditions ...
Morning Overview on MSN
Connecticut limits who genetic testing companies can share customers’ DNA data with starting Oct. 1
Starting Thursday, October 1, Connecticut companies that sell DNA tests directly to consumers will operate under a new set of limits on what they can do with the results. Under Public Act 26-64, the ...
Falling sequencing costs, scalable NGS, robust patient registries and advanced bioinformatics enable higher test volumes, sharper diagnoses and personalized care.Dublin, Sept. (GLOBE NEWSWIRE) -- ...
The pilot could cut brain tumour diagnosis from weeks to days, with results available in under 2 hours during surgery.
The Lancet Oncology Commission on accelerating equitable access to cancer genomics and precision oncology provides an important framework defining indicators that health systems can and should measure ...
University of Nottingham innovation to drive NHS rollout of ultra-rapid brain tumour genetic testing
A groundbreaking ultra-rapid method of genetically diagnosing brain tumours, developed by researchers at the University of Nottingham and Nottingham University Hospitals Trust, is set to benefit ...
A world-first test developed by researchers at the Garvan Institute of Medical Research has identified the genetic cause of ...
Breast cancer genetic testing identified pathogenic variants in 4.7% of 3,515 patients through an NHS clinician-light pathway.
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