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Hernández-Arciga U, Kim JK, Fisher JL, et al. Mutation in IR or IGF1R produces features of long-lived mice while maintaining metabolic health. JCI insight. 2025;10(24). doi:10.1172/jci.insight.189683

Çevrim Ç, Hilgert NJ, Kaage AM, et al. Induction of menstruation in mice reveals the regulation of menstrual shedding. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.08.681007

Audam TN, Schmandt B, Huang Y, et al. The Coronary Artery Disease Risk Locus Modulates Vascular Cell-State Transitions via Enhancer-Driven Regulation of . bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.18.689066

Rao I, Kellis M, Tanigawa Y. sc4D: spatio-temporal single-cell transcriptomics analysis through embedded optimal transport identifies joint glial response to Alzheimer’s disease pathology. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.19.689166

Kunorozva L, Valliere J, Chen CY, et al. From Normal Variation in Sleep to Clinical Sleep Disorders: Genetic Insights from Over One Million Individuals. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.21.25340447

Sevilla-González M, Wang N, Hanson PA, et al. Dissecting Genetic and Environmental Determinants of Plasma Molecular Signatures and Their Link to Type 2 Diabetes Risk. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.26.25341007

Hirayama S, Al-Inaya Y, Bryan ME, et al. Clinical validation of an HPV whole genome sequencing assay for molecular residual disease detection in HPV-associated head and neck cancer patients treated with surgery. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.24.25340887

Taylor K, Huerta-Chagoya A, Wang X, et al. Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.24.25340878

van Vugt JJFA, Zwamborn RAJ, Dolzhenko E, et al. The role of disease-associated short tandem repeats in amyotrophic lateral sclerosis. Brain communications. 2025;7(6):fcaf482. doi:10.1093/braincomms/fcaf482

Hsiao JC, Warui DM, Kwon JJ, et al. Deep Mutational Scanning of FDX1 Identifies Key Structural Determinants of Lipoylation and Cuproptosis. Nature communications. 2025. doi:10.1038/s41467-025-67869-0