Nguyen T, Koesterer R, Haydarlou P, et al. Empirically determined baseline masking strategies and other considerations for gene-level burden tests. Nature genetics. 2026. doi:10.1038/s41588-026-02597-9
Metabolism Program
Tyshkovskiy A, Kholdina D, Davitadze M, et al. Universal transcriptomic hallmarks of mammalian ageing and mortality. Nature. 2026. doi:10.1038/s41586-026-10542-3
Li E, Yuan Y, Sun H, et al. Oxytocin signaling in adipocytes is required for normal milk fat production. Cell metabolism. 2026. doi:10.1016/j.cmet.2026.03.013
Cromer SJ, Cobran EK, Iyer HS, et al. Incorporating polygenic risk scores and social determinants of health across populations: Considerations and best practices in research. American journal of human genetics. 2026. doi:10.1016/j.ajhg.2026.02.007
Bartell E, Lin K, Tsuo K, et al. Genetics of skeletal proportions across two different populations. American journal of human genetics. 2026. doi:10.1016/j.ajhg.2026.02.015
Meisel JD, Joshi PR, Spelbring AN, et al. Mutations in mitochondrial ferredoxin FDX2 suppress frataxin deficiency. Nature. 2025. doi:10.1038/s41586-025-09821-2
Deutsch AJ, Bell AS, Michalek DA, et al. Development and Validation of a Type 1 Diabetes Multi-Ancestry Polygenic Score. Diabetes. 2025. doi:10.2337/db25-0772
Zhou Y, Ahsan FM, Emans SW, Soukas AA. The nuclear pore complex connects energy sensing to transcriptional plasticity in longevity. Molecular cell. 2025. doi:10.1016/j.molcel.2025.08.035
Marutani E, Miranda M, Durham TJ, et al. Hypoxia ameliorates neurodegeneration and movement disorder in a mouse model of Parkinson’s disease. Nature neuroscience. 2025. doi:10.1038/s41593-025-02010-4
Gupta R, Durham TJ, Chau G, et al. Mechanism of age-related accumulation of mitochondrial DNA mutations in human blood. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.05.25.655566