Researchers from Karolinska Institutet and Maastricht University have developed a technique that enables the examination of embryos for all known genetic abnormalities with a single test. The new method is more accurate and ...
Sep 2, 2024
0
51
By analyzing electronic health records, researchers at the University of California San Diego School of Medicine have identified hundreds of new genes associated with tobacco use disorder. They also identified hundreds of ...
Apr 17, 2024
0
40
Every human's genome has millions of genetic variants, but most have little to no effect, making it difficult for clinicians to make medical diagnoses based on genetic differences.
Dec 7, 2023
0
6
Cluster headache, one of the most painful diseases known to man, is genetically correlated with risk-taking behavior, ADHD, depression and musculoskeletal pain, and smoking is a causal risk factor, according to an article ...
Sep 8, 2023
0
13
To study the effects of childhood environments on adult health and well-being, researchers examined epigenetic profiles of children using algorithms developed in adults. They find that children growing up in more socioeconomically ...
Sep 6, 2023
0
20
More than 20 years ago, the human genome was first sequenced. While the first version was full of "holes" representing missing DNA sequences, the genome has been gradually improved in successive rounds. Each has increased ...
Aug 26, 2023
0
42
Epilepsy in infants ranges in severity and can leave caregivers with questions about their child's health. While genetic testing to help determine the cause of epilepsy is possible, comprehensive testing does not always happen ...
Aug 16, 2023
0
5
Much of the human genome is made of regulatory regions that control which genes are expressed at a given time within a cell. Those regulatory elements can be located near a target gene or up to 2 million base pairs away from ...
May 8, 2023
0
78
A team of investigators from Massachusetts General Hospital (MGH), a founding member of Mass General Brigham (MGB) and Mass General for Children (MGfC) has identified—for the first time—the mutation in a single non-coding ...
Feb 28, 2023
0
31
A collaborative study led by the University of Oxford as part of the UK's 100,000 Genomes Project, published in Nature Genetics today, has defined five new subgroups of the most common type of blood cancer, chronic lymphocytic ...
Nov 7, 2022
0
142
