Rashedi S, Leyva H, Hamade N, et al. Fibrinolytic Therapy for Thromboembolic Diseases: Approved Indications and Future Directions. Journal of the American College of Cardiology. 2025;86(14):1065-1087. doi:10.1016/j.jacc.2025.07.061
Publications
Cole JB, Dahlström EH, Fermin D, et al. Genome-Wide Association Study of Quantitative Kidney Function in 52,531 Individuals with Diabetes Identifies Five Diabetes-Specific Loci. Journal of the American Society of Nephrology : JASN. 2025;36(10):1939-1953. doi:10.1681/ASN.0000000718
DÃaz LA, Alazawi W, Agrawal S, et al. High inherited risk predicts age-associated increases in fibrosis in patients with MASLD. Journal of hepatology. 2025;83(4):849-859. doi:10.1016/j.jhep.2025.04.035
Graves OK, Kang J, Li H, et al. Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative delirium. Molecular psychiatry. 2025;30(10):4690-4699. doi:10.1038/s41380-025-03063-4
Graves OK, Kang J, Li H, et al. Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative delirium. Molecular psychiatry. 2025;30(10):4690-4699. doi:10.1038/s41380-025-03063-4
Belak L, James K, Rana M, et al. Association of Health-Related Social Needs With Adverse Pregnancy Outcomes Among Black and Latina Individuals. Obstetrics and gynecology. 2025;146(4):541-543. doi:10.1097/AOG.0000000000005999
Urnov F, Kassim S, Musunuru K, et al. Advancing gene-editing platforms to improve the viability of rare-disease therapeutics: key insights from a 2024 Scientific Exchange hosted by ARM, ISCT, and Danaher. Cytotherapy. 2025;27(10):1151-1163. doi:10.1016/j.jcyt.2025.06.010
Pauken KE, Markson SC, Conway TS, et al. PD-1 regulates tumor-infiltrating CD8+ T cells in both a cell-intrinsic and a cell-extrinsic fashion. The Journal of experimental medicine. 2025;222(10). doi:10.1084/jem.20230542
Honecker J, Paffenholz D, Jungmann J, et al. FoundationOne CDx and FoundationOne Heme Detect Epstein-Barr Virus with High Sensitivity and Specificity. The Journal of molecular diagnostics : JMD. 2025;27(10):920-935. doi:10.1016/j.jmoldx.2025.06.002
Itchaki G, Bai H, Tiao G, et al. Rare germline variant in NFATC4 associated with familial CLL. Leukemia. 2025;39(10):2547-2550. doi:10.1038/s41375-025-02713-4