The All of Us Research Program has analyzed the genes of 150,000 Americans. The results are coming in
Michelle Anderson recently learned her body metabolizes medicines more slowly than average.
Dec 13, 2022
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Michelle Anderson recently learned her body metabolizes medicines more slowly than average.
Dec 13, 2022
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Nine in 10 Australians would participate in preventive DNA screening for risk of medically actionable conditions, a new national survey has found.
Dec 1, 2022
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When COVID-19 vaccines were first rolled out in limited quantities in early 2021, each country had to decide the order in which its citizens would be vaccinated. How did decision-makers prioritize allocation of these vital ...
Nov 30, 2022
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The field of genomic science is rapidly advancing, with commercial genetic tests becoming affordable and popular.
Nov 29, 2022
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As published in the Journal of the American Medical Informatics Association, University of Minnesota researchers led a study evaluating federated learning variations for COVID-19 diagnosis in chest X-rays. Federated learning ...
Nov 17, 2022
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Researchers at Lund University in Sweden have identified one of the reasons why the childhood cancer neuroblastoma becomes resistant to chemotherapy. The findings are significant for how future treatments should be designed. ...
Nov 11, 2022
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Scientists have discovered the cause of a rare condition within a part of the genome that has been largely unexplored in medical genetics. A team at the University of Exeter has found genetic changes in a region that controls ...
Nov 7, 2022
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Tailoring the analysis of whole genome sequencing to individual patients could double the diagnostic rates of rare diseases, finds a new study led by UCL researchers.
Nov 7, 2022
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Findings from a new study published in Cell Reports, involving a collaborative effort between researchers at the Luikart Laboratory at Dartmouth's Geisel School of Medicine and the Weston Laboratory at the University of Vermont, ...
Nov 1, 2022
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Improving knowledge of Schaaf-Yang syndrome (SYS), an ultra-rare disease caused by mutations in the MAGEL2 gene, is the aim of the first clinical guideline aimed at health care professionals and families of children affected ...
Oct 26, 2022
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