Morcom L, Xia W, Xu Z, et al. DNA damage burden causes selective CUX2 neuron loss in neuroinflammation. Nature. 2026. doi:10.1038/s41586-026-10310-3
Publications
Hemeryck J, De Moor N, Ezzat D, et al. Blood Pressure Genetic Risk and Incident Hypertension at 2 to 7 Years Post Partum. JAMA cardiology. 2026. doi:10.1001/jamacardio.2026.0363
de la Cruz FF, Varkaris A, Patel PS, et al. Acquired On-Target Alterations Drive Clinical Resistance to p53-Y220C Reactivators. Cancer discovery. 2026;16(4):677-685. doi:10.1158/2159-8290.CD-25-1761
Hreha TN, Manson AL, Collins CA, et al. Single-nucleus transcriptomics illuminates sex differences during murine Escherichia coli pyelonephritis. Communications biology. 2026. doi:10.1038/s42003-026-09946-8
Zhang Z, Ho YJ, Fang X, et al. A convergent uPAR-positive tumor ecosystem creates broad vulnerability to CAR T cell therapy. Cell. 2026. doi:10.1016/j.cell.2026.03.002
Adam KR, Suhail A, Kuchroo VK, Vignali DAA. Inhibitory receptor agonists: Emerging strategies in immune modulation. The Journal of experimental medicine. 2026;223(4). doi:10.1084/jem.20241217
Global, regional, and national burden of meningitis, its risk factors, and aetiologies, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023. The Lancet. Neurology. 2026. doi:10.1016/S1474-4422(26)00101-8
Gutierrez C, Kwok M, Ruthen N, et al. Mutant ribosomal protein RPS15 drives B cell malignancy through oxidative stress and genomic instability. Nature communications. 2026. doi:10.1038/s41467-026-70655-1
Avila MN, Jung S, Satterstrom K, et al. Deleterious coding variation associated with autism is shared across ancestries. Nature medicine. 2026. doi:10.1038/s41591-026-04228-6
Wu Y, Zheng Z, Thibaut L, et al. Genome-wide fine-mapping improves identification of causal variants. Nature genetics. 2026. doi:10.1038/s41588-026-02549-3