Atrial fibrillation is the most common heart arrhythmia in humans. This condition increases the risk of heart failure, stroke, dementia and death, and current treatments have suboptimal efficacy and carry side effects. Looking ...
Oct 21, 2019
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Two Leicester sisters who had their entire genomes sequenced in the hope of finding answers to their family history of breast cancer have learned they both carry a genetic variant that significantly increases their risk of ...
Sep 27, 2019
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Scientists have published a novel computational framework for highly accurate and targeted Non-Invasive Prenatal genetic Testing (NIPT) assay, which enables the application of cost-effective TAC-seq laboratory method in clinical ...
Aug 14, 2019
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In a Finnish study that included researchers from UCLA, the DNA from nearly 20,000 people was harnessed to identify genetic mutations that may increase the risk of diabetes, high cholesterol and other diseases and conditions.
Aug 2, 2019
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A team of Swedish and British scientists have studied the heritability of dog ownership using information from 35,035 twin pairs from the Swedish Twin Registry. The new study suggests that genetic variation explains more ...
May 17, 2019
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Inside cells DNA is tightly wrapped around proteins and packed in a complex, 3-D structure called chromatin. Chromatin not only protects genetic material from damage, but also organizes the entire genome by regulating the ...
Jan 29, 2019
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Children's heads expand steadily to accommodate their growing brains, and doctors routinely measure head circumference during the first years of life to assess healthy brain development. Children from around the world follow ...
Jan 21, 2019
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Approximately 98 percent of the human genome is made up of noncoding DNA, including enhancers, promoters, and other elements that regulate gene activity. The methods for studying these regions tend to be expensive, labor-intensive, ...
Dec 21, 2018
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Searching the entire genome, a Yale research team has identified a gene that when eliminated can spur regeneration of axons in nerve cells severed by spinal cord injury.
Apr 10, 2018
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When doctors can't find a diagnosis for patient's disease, they turn to genetic detectives. Equipped with genomic sequencing technologies available for less than 10 years, these sleuths now routinely search through a patient's ...
Aug 10, 2017
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