Add Yahoo as a preferred source to see more of our stories on Google. A study of over 1.2 million people has uncovered new genetic clues to dyslexia, shedding light on brain development and reading ...
Add Yahoo as a preferred source to see more of our stories on Google. A genetic cause for ME has been found for the first time, proving the illness is real. In a breakthrough that charities said ...
Myriad Genetics, Inc. announced a study indicating that the use of its online screening tool, MyGeneHistory®, alongside a virtual education program, significantly increased the completion rates for ...
A landmark study led by researchers with the Department of Veterans Affairs has uncovered new genetic insights into ...
A new genetic study of more than 50,000 obsessive-compulsive disorder (OCD) cases has linked around 250 genes to the condition, including more than two dozen identified as likely causal, in about 30 ...
The findings shed new light on human reproduction and suggest pathways for developing treatments to lower the risk of ...
Experts say the research could reveal more about the role of genetics in autism and lead to more personalized care. A new study has identified four biologically distinct subtypes of autism, each with ...
Euan Ashley's lab explores the intricate interactions of gene variants. Tiny "typos," or genetic mutations, can sneak into segments of DNA. Many of these are harmless, but some can cause health ...
Tired all the time? It might be in your DNA. A new study has uncovered striking genetic differences in people suffering from a devastating illness that causes extreme exhaustion, chronic pain and ...
A new study has revealed that those with myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS) have notable genetic differences from the general population. The DecodeME research team, led by ...
Reading determines almost all aspects of everyday life. Reading allows you to learn in school, to read signs, to read books, and talk to people. But for millions, reading is a constant struggle.
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