Dron JS. The clinical utility of polygenic risk scores for combined hyperlipidemia. Current opinion in lipidology. 2023;34(2):44-51. doi:10.1097/MOL.0000000000000865
Publications
Sephton-Clark P, McConnell SA, Grossman N, et al. Similar evolutionary trajectories in an environmental isolate after human and murine infection. Proceedings of the National Academy of Sciences of the United States of America. 2023;120(2):e2217111120. doi:10.1073/pnas.2217111120
Lee H, Sanidas I, Dyson NJ, Lawrence MS. Chromatin-bound protein colocalization analysis using bedGraph2Cluster and PanChIP. STAR protocols. 2023;4(1):101991. doi:10.1016/j.xpro.2022.101991
Ding L, Wang Q, Martincuks A, et al. STING agonism overcomes STAT3-mediated immunosuppression and adaptive resistance to PARP inhibition in ovarian cancer. Journal for immunotherapy of cancer. 2023;11(1). doi:10.1136/jitc-2022-005627
Linder JE, Allworth A, Bland ST, et al. Returning integrated genomic risk and clinical recommendations: The eMERGE study. Genetics in medicine : official journal of the American College of Medical Genetics. 2023;25(4):100006. doi:10.1016/j.gim.2023.100006
Kwapong YA, Boakye E, Khan SS, et al. Association of Depression and Poor Mental Health With Cardiovascular Disease and Suboptimal Cardiovascular Health Among Young Adults in the United States. Journal of the American Heart Association. 2023;12(3):e028332. doi:10.1161/JAHA.122.028332
Vlasschaert C, Heimlich B, Rauh MJ, Natarajan P, Bick AG. Interleukin-6 Receptor Polymorphism Attenuates Clonal Hematopoiesis-Mediated Coronary Artery Disease Risk Among 451 180 Individuals in the UK Biobank. Circulation. 2023;147(4):358-360. doi:10.1161/CIRCULATIONAHA.122.062126
Kumar MS, Stallworth KM, Murthy AC, et al. Interactions between FUS and the C-terminal Domain of Nup62 are Sufficient for their Co-phase Separation into Amorphous Assemblies. Journal of molecular biology. 2023;435(6):167972. doi:10.1016/j.jmb.2023.167972
Georgakis MK, Anderson CD. Polygenic Risk Scores in the Clinic: A Case for Stroke Survivors. Neurology. 2023;100(15):693-695. doi:10.1212/WNL.0000000000206899
Li Q, Agrawal R, Schmitz-Abe K, et al. Reanalysis of clinical exome identifies the second variant in two individuals with recessive disorders. European journal of human genetics : EJHG. 2023. doi:10.1038/s41431-023-01291-2