The Case Comprehensive Cancer Center will host a seminar series event Friday, April 13, from noon to 1 p.m. in the Iris S. and Bert L. Wolstein Research Building auditorium. The event will feature ...
Genetic risk models, including PREMMplus and BOADICEA/CanRisk, refine breast cancer risk assessment by incorporating genetic status and polygenic risk scores. Challenges in classifying gene variants, ...
A more predictive, preventive approach to medicine can enable more accurate population-level risk assessments and predictions ...
Standardize tumor classification and variant annotation for reproducible cohort building with COSMIC
Accurate interpretation of cancer genomics depends on standardized disease classification, tumor characterization and variant annotation. In this joint COSMIC and QIAGEN webinar, we show how ...
An international research consortium co-led by scientists from Vanderbilt University Medical Center, the University of Toronto and University of Pittsburgh has mapped the functional impact of more ...
A common genetic variant is linked to a doubled dementia risk for older men, a recent analysis in Neurology suggests. The study used data from Aspirin in Reducing Events in the Elderly (ASPREE), which ...
Rare genetic traits are features that are uncommon within the general population. They can lead to different observable features or to rare physical abilities. Rare genetic traits are typically ...
Genetic inheritance may sound straightforward: One gene causes one trait or a specific illness. When doctors use genetics, it’s usually to try to identify a disease-causing gene to help guide ...
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