TBX20 and myocardial infarction: Although genetic variation in TBX20 has been associated with a spectrum of congenital cardiac lesions relating to cardiac and vascular development (Chen et al, 2021), there have been increasing observations that genetic loci near TBX20 meet genome-wide significance for disease in adulthood including coronary artery disease (Koyama et al, 2020), myocardial infarction (Sakaue et al, 2021), blood pressure (Warren et al, 2017), and aortic dimension and distensibility (Benjamins et al, 2022; Pirruccello et al, 2022).