Kreeger LJ, Honnuraiah S, Maeker S, Shea S, Fishell G, Goodrich L. An anatomical and physiological basis for flexible coincidence detection in the auditory system. eLife. 2025;13. doi:10.7554/eLife.100492
Publications
, Koehler AN, Vegas AJ. At The Interface: Small-Molecule Inhibitors of Soluble Cytokines. Chemical reviews. 2025. doi:10.1021/acs.chemrev.4c00469
Yates J, Van Allen EM. New horizons at the interface of artificial intelligence and translational cancer research. Cancer cell. 2025;43(4):708-727. doi:10.1016/j.ccell.2025.03.018
Baluapuri A, Zhao NC, Marina RJ, et al. Integrator loss leads to dsRNA formation that triggers the integrated stress response. Cell. 2025. doi:10.1016/j.cell.2025.03.025
Rodrigues FM, Terekhanova N V, Imbach KJ, et al. Precision proteogenomics reveals pan-cancer impact of germline variants. Cell. 2025. doi:10.1016/j.cell.2025.03.026
Livesey BJ, Badonyi M, Dias M, et al. Guidelines for releasing a variant effect predictor. Genome biology. 2025;26(1):97. doi:10.1186/s13059-025-03572-z
Mahuron KM, Shahid O, Sao P, et al. Single-Cell Analyses Reveal a Functionally Heterogeneous Exhausted CD8+ T-cell Subpopulation That Is Correlated with Response to Checkpoint Therapy in Melanoma. Cancer research. 2025;85(8):1424-1440. doi:10.1158/0008-5472.CAN-23-3918
Venkatesh SS, Wittemans LBL, Palmer DS, et al. Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum. Nature genetics. 2025. doi:10.1038/s41588-025-02156-8
Martin-Geary AC, Blakes AJM, Dawes R, et al. Systematic identification of disease-causing promoter and untranslated region variants in 8040 undiagnosed individuals with rare disease. Genome medicine. 2025;17(1):40. doi:10.1186/s13073-025-01464-2
Deutsch AJ, Udler MS. Phenotypic and genetic diversity in diabetes across populations. The Journal of clinical endocrinology and metabolism. 2025. doi:10.1210/clinem/dgaf234