Truong B, Ruan Y, Haidermota S, et al. Modification of coronary artery disease clinical risk factors by coronary artery disease polygenic risk score. Med (New York, N.Y.). 2024. doi:10.1016/j.medj.2024.02.015
Publications
Wang Y, He Y, Shi Y, et al. Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.04.002
Vilhjálmsson BJ. Towards fair and clinically relevant polygenic predictions. Trends in genetics : TIG. 2024. doi:10.1016/j.tig.2024.04.002
Luo K, Peters BA, Moon JY, et al. Metabolic and inflammatory perturbation of diabetes associated gut dysbiosis in people living with and without HIV infection. Genome medicine. 2024;16(1):59. doi:10.1186/s13073-024-01336-1
Baudic M, Murata H, Bosada FM, et al. TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications. 2024;15(1):3380. doi:10.1038/s41467-024-47739-x
Rosenthal ZC, Fass DM, Payne C, et al. Epigenetic modulation through BET bromodomain inhibitors as a novel therapeutic strategy for progranulin-deficient frontotemporal dementia. Scientific reports. 2024;14(1):9064. doi:10.1038/s41598-024-59110-7
Miller AB, Rodriguez FH, Langenbucher A, et al. Leukemia circulation kinetics revealed through blood exchange method. Communications biology. 2024;7(1):483. doi:10.1038/s42003-024-06181-x
Vaidya A, Chen RJ, Williamson DFK, et al. Demographic bias in misdiagnosis by computational pathology models. Nature medicine. 2024;30(4):1174-1190. doi:10.1038/s41591-024-02885-z
Claussnitzer M, Parikh VN, Wagner AH, et al. Minimum information and guidelines for reporting a multiplexed assay of variant effect. Genome biology. 2024;25(1):100. doi:10.1186/s13059-024-03223-9
Yoon J, Zhang YM, Her C, et al. The immune-evasive proline-283 substitution in influenza nucleoprotein increases aggregation propensity without altering the native structure. Science advances. 2024;10(16):eadl6144. doi:10.1126/sciadv.adl6144