Ardissino M, Paraboschi EM, Lambert SA, et al. Polygenic Prediction of Recurrent Events After Early-Onset Myocardial Infarction. Circulation. Genomic and precision medicine. 2024:e004687. doi:10.1161/CIRCGEN.124.004687
Wang M, Lee-Kim VS, Atri DS, et al. Rare, Damaging DNA Variants in CORIN and Risk of Coronary Artery Disease: Insights From Functional Genomics and Large-Scale Sequencing Analyses. Circ Genom Precis Med. 2021;14(5):e003399. doi:10.1161/CIRCGEN.121.003399
Wardell CP, Fujita M, Yamada T, et al. Genomic characterization of biliary tract cancers identifies driver genes and predisposing mutations. J Hepatol. 2018;68(5):959-969. doi:10.1016/j.jhep.2018.01.009
Deelen P, Menelaou A, van Leeuwen EM, et al. Improved imputation quality of low-frequency and rare variants in European samples using the ’Genome of The Netherlands’. Eur J Hum Genet. 2014;22(11):1321-6. doi:10.1038/ejhg.2014.19
Lettre G, Hirschhorn JN. Small island, big genetic discoveries. Nat Genet. 2015;47(11):1224-5. doi:10.1038/ng.3426
Lander ES, Botstein D. Consanguinity and heterogeneity: cystic fibrosis need not be homogeneous in Italy. Am J Hum Genet. 1986;39(2):282-3.