MeSH tree: N02.421.308
Young breast cancer (BC) survivors (40 years or younger) without a pathogenic variant (PV) have a low risk for developing second primary BC (SPBC), according to a study published online April 11 in JAMA Oncology.
Apr 16, 2024
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Newborn genetic screening (NBGS) seeks to assist in the early identification of newborns at risk for severe genetic disorders. The integration of genomics into newborn screening represents a significant advancement, enhancing ...
Apr 2, 2024
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ChatGPT accurately answers questions about genetic syndromes, genetic testing, and counseling, according to a study presented at the Society of Gynecologic Oncology Annual Meeting on Women's Cancer, held from March 16 to ...
Mar 25, 2024
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A stem cell donation saves a leukemia sufferer's life. Five years later, the patient develops a chronic inflammatory bowel disease that occurs very rarely following a transplant. Researchers from the University of Basel and ...
Mar 19, 2024
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A QIMR Berghofer-led international team of scientists has unlocked the genetic secrets behind why some mothers are more likely than others to conceive twins.
Mar 14, 2024
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Genetic testing has become a more common way to diagnose and manage many neurologic conditions including dementia, Parkinson's disease and epilepsy, but a new study has found not everyone may have the same level of access ...
Mar 6, 2024
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Even as it's become clear that an inherited susceptibility to some cancers is more common than once thought, genetic testing of family members of cancer patients hasn't increased as much as experts had hoped. A new study ...
Feb 27, 2024
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A new University of Kentucky Markey Cancer Center study published in JCO Precision Oncology demonstrates a feasible way to expand germline genetic testing for patients with cancer.
Feb 26, 2024
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In a time of inactive workdays and rising obesity rates in America, most people don't know that what they eat, drink and how much they move can impact their risk for colorectal cancer, a highly preventable form of cancer ...
Feb 26, 2024
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A UC San Francisco-led study has for the first time identified genetic variants that predict whether patients will respond to treatment for preterm birth, a condition that affects one in 10 infants born in the United States.
Jan 23, 2024
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