About 40% of East Asians suffer from alcohol intolerance, known as "Asian Flush Syndrome," caused by an ALDH2 genetic ...
A systematic review of 52 scientific papers submitted to a world-leading clinical genetics journal from multiple scientists ...
The FDA proposes new rules allowing mutation-specific gene therapies to qualify for approval despite extremely small patient ...
Researchers use long-read genome sequencing to discover 33% more structural variants and 38% more tandem repeats linked to autism spectrum disorder.
Koala populations with low genetic diversity are actually recovering by "reshuffling" their genes to remove harmful mutations ...
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Long-read whole genome sequencing uncovers new genetic variants linked to autism
Researchers at the University of California San Diego have identified new genetic variants associated with autism spectrum disorder (ASD) by using long-read whole genome sequencing (LR-WGS), an ...
Discover the molecular mechanisms behind severe blood clots linked to specific COVID-19 vaccines, revealing crucial insights for future vaccine safety.
For women who undergo a mastectomy, reconstruction is treated almost as a given. We speaks to seven women proudly defying the status quo.
Researchers have devised a new tool for discerning between naturally occurring viral outbreaks and those resulting from lab ...
Research is shaking up how we think about evolution, suggesting there's a level of predictability influenced by genes and genetic history.
Many of us might reach for the hair dye the moment those first grey hairs appear. But a new study suggests we may be covering up one of the body's most ingenious defences against cancer.
Researchers have discovered that mutations in the FOXJ3 gene act as a "master switch" failure, disrupting how the brain builds its layers and leading to FCD, a primary cause of drug-resistant epilepsy ...
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