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    Researchers saw monogenic disease-related mutations in almost 11 percent of infants’ genomes, prompting further testing and management, including for family members.

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    • #BabySeq Project Unearths Actionable #GeneticVariants Impacting Infants, Parents https://t.co/jvvgPHYzFE Actionability of unanticipated #monogenic disease risks in #newborn #genomicscreening: Findings from the BabySeq Project @RobertCGreen https://t.co/egKsBCoeoE #GeneticTesting… https://t.co/v2gjLyRml8 https://t.co/LedaL6Ysit

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    Researchers used exome sequencing data for hundreds of thousands of individuals to identify rare coding variants and genes associated with three cognitive functional traits.

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    • #Cognitive Functions Linked to Rare Coding Variants in #Sequencing Study https://t.co/7vdMug0g5F #Exome #UK_Biobank #WES The impact of rare #protein-coding genetic variation on adult #cognitivefunction @NatureGenet https://t.co/NJn7nxfChE #cognition #intelligence #intellect… https://t.co/dhHLCAleJW https://t.co/fvstamHe9G

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    Clopidogrel is less effective at preventing subsequent strokes in patients with certain variations in the CYP2C19 gene and testing could aid treatment selection.

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    • Great to see UK's NICE endorse this use of pharmacogenomics for patients with stroke and TIA. 32% of individuals in UK have elevated risk of subsequent stroke when given clopidogrel rather than platelet inhibitors not impacted by CYP2C19. https://t.co/5JN0H9mQdv