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Critically, integrating genomic and molecular data has uncovered fundamental mechanisms of patient heterogeneity, such as the discovery that a diurnal BMAL1-HIF2A complex regulates myocardial vulnerability to injury, providing a molecular rationale for the long-observed circadian patterns of MI severity and opening the door to chronopharmacologytiming interventions for maximum efficacy (Ruan et al., 2025)

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Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy