Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry

Overview of attention for article published in JAMA Network Open, March 2019

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This genetic association study uses whole-exome sequencing to identify genetic variants associated with the risk of Alzheimer…

Genetic association study using whole-exome sequencing shows rare mutations in NOTCH3 and different copy number of a TREM2…

Different mutations in the same gene or variable dose of a particular mutation may be associated with dissimilar types of…

Researchers have identified two, extremely rare genetic variants linked to Alzheimer disease (AD) for the first time. These…

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