genetics
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St. Jude Hospital Found Genetic Mutations In Cancer
Sep 22
Scientists from St. Jude’s Children’s Hospital have created a roadmap of the genetic mutations present in the most common childhood cancer, acute lymphoblastic leukemia (ALL). The St. Jude Children’s Research Hospital study is the first to supply a comprehensive view of the genomics of all subtypes of ALL. The work serves as a f...
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Oldest Case of Klinefelter Syndrome Discovered
Sep 15
Skull by Pixabay on Pexels Australian National University wrote that the oldest case of a rare genetic condition has been discovered in a 1,000-year-old skeleton from Portugal. Klinefelter syndrome gives men an extra X chromosome. What is Klinefelter Syndrome? Mayo Clinic explains that it is a genetic condition that results when a boy is bor...
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DNA Analysis Sheds Light On Victims Of 12th Century Violence
Sep 13
In 2004, workers on a construction site in Norwich, England, stumbled upon an 800-year-old well as they prepared the ground for a new shopping center. Inside the well, MyHeritage reported, they uncovered a heartbreaking and chilling sight: the remains of 17 people, including 6 adults and 11 children. A study titled: “Genomes from a medie...
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23andMe Launches Rare Disease Study
Sep 8
Listening to those with a rare disease, a common refrain is that they often feel isolated, unheard, and alone. But, they’re not alone, 23andMe says. Much to Learn While each rare disease is by definition uncommon - affecting fewer than 200,000 people - there are more than 7,000 known rare diseases. There are more than 300 million peopl...
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23andMe Announces A New Genetic Study On Pneumonia
Aug 25
23andMe announced that a new genetic study identified five regions in the human genome associated with susceptibility to pneumonia, a leading cause of death worldwide. Published in the journal Nature Communications, the study also found a surprising link between the risk of pneumonia and psychiatric conditions, such as schizophrenia, bipola...
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Mount Sinai Launches Genetics Project With Regeneron
Aug 23
Mount Sinai Health System and the Ichan School of Medicine at Mount Sinai have launched a new human genome sequencing research project called the Mount Sinai Million Health Discoveries Program with Regeneron Genetics Center (RGC), part of the industry-leading, New-York-based biotechnology company Regeneron. The Program aims to enroll o...
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Study On Side Effects of Parkinson’s Medication
Aug 11
23andMe posted information on a new genetic study that may help those looking for ways to avert some of the troubling side effects of a common medication used to treat Parkinson’s disease. Parkinson’s is sometimes treated with medication that increases dopamine activity in the brain. In some patients, that triggers impulsivity, such as ...
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Researchers Seek Genetic Causes of Parkinson’s
Jul 26
New research by Yale researchers offers important clues about the genetic causes of Parkinson’s disease. In two new papers, scientists provide insight into the function of a protein called VPS13C, one of the molecular suspects underlying Parkinson’s, a disease marked by uncontrollable movements including tremors, stiffness, and loss of bal...
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23andMe Updated Report for People with Asian Ancestry
Jun 21
23andMe updated its report on an inherited condition characterized by mild to profound hearing loss. The update to 23andMe’s Nonsyndomic Hearing Loss and Deafness, DFNB1 (GJB1-Related) Carrier Status Report adds six variants that improve the coverage of the test for people with East Asian, Southeast Asian, and South Asian ancestry. “We ...
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23andMe Has A Study About Long COVID
Jun 1
In what is among the largest studies of long COVID to date, researchers at 23andMe confirm that it disproportionately impacts women, and being diagnosed with depression or anxiety is associated with more than a two-fold increase in risk for the condition. The study also found that about half of those with persistent symptoms are experiencing ...