Nelson CP, Goel A, Butterworth AS, et al. Association analyses based on false discovery rate implicate new loci for coronary artery disease. Nat Genet. 2017;49(9):1385-1391. doi:10.1038/ng.3913
Lazaridis I, Mittnik A, Patterson N, et al. Genetic origins of the Minoans and Mycenaeans. Nature. 2017;548(7666):214-218. doi:10.1038/nature23310
Gray KJ, Kovacheva VP, Mirzakhani H, et al. Gene-Centric Analysis of Preeclampsia Identifies Maternal Association at . Hypertension. 2018;72(2):408-416. doi:10.1161/HYPERTENSIONAHA.117.10688
Wang X, He L, Goggin SM, et al. High-resolution genome-wide functional dissection of transcriptional regulatory regions and nucleotides in human. Nat Commun. 2018;9(1):5380. doi:10.1038/s41467-018-07746-1
Márquez-Luna C, Loh PR, South Asian Type 2 Diabetes (SAT2D) Consortium, Consortium STD 2, Price AL. Multiethnic polygenic risk scores improve risk prediction in diverse populations. Genet Epidemiol. 2017;41(8):811-823. doi:10.1002/gepi.22083
Medina-Gomez C, Kemp JP, Trajanoska K, et al. Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. Am J Hum Genet. 2018;102(1):88-102. doi:10.1016/j.ajhg.2017.12.005
Goto A, Chen BH, Chan KHK, et al. Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African American, Hispanic American, and European American postmenopausal women in the US. J Diabetes. 2018;10(6):524-533. doi:10.1111/1753-0407.12648
Wang X, Srivastava Y, Jankowski A, et al. DNA-mediated dimerization on a compact sequence signature controls enhancer engagement and regulation by FOXA1. Nucleic Acids Res. 2018;46(11):5470-5486. doi:10.1093/nar/gky259
Renneville A, Ben Abdelali R, Chevret S, et al. Clinical impact of gene mutations and lesions detected by SNP-array karyotyping in acute myeloid leukemia patients in the context of gemtuzumab ozogamicin treatment: results of the ALFA-0701 trial. Oncotarget. 2014;5(4):916-32. doi:10.18632/oncotarget.1536
Pashos EE, Park Y, Wang X, et al. Large, Diverse Population Cohorts of hiPSCs and Derived Hepatocyte-like Cells Reveal Functional Genetic Variation at Blood Lipid-Associated Loci. Cell Stem Cell. 2017;20(4):558-570.e10. doi:10.1016/j.stem.2017.03.017