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Ying K, Tyshkovskiy A, Moldakozhayev A, et al. Autonomous AI Agents Discover Aging Interventions from Millions of Molecular Profiles. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2023.02.28.530532

Song BJ, Ge Y, Nicolella A, et al. Elevated synaptic PKA activity and abnormal striatal dopamine signaling in mutant mice, a genetic model of schizophrenia and bipolar disorder. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2024.09.24.614783

Wang B, Kabir D, Clark CR, Choi KW, Smoller JW. Extracting social determinants of health from electronic health records: development and comparison of rule-based and large language models-based methods. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.15.25339520

Galea B, Reid J, Gooley S, et al. Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.17.25340194

Shilova L, Sens D, Aliyeva A, et al. REECAP: Contrastive learning of retinal aging reveals genetic loci linking morphology to eye disease. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.19.25340555

Cirnigliaro M, Lowe JK, Flynn-Carroll AO, et al. Common and rare variant genetic contributions in African Americans with autism. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.18.25340532

Gould SI, Acosta J, Bielo LB, et al. A functional map of CDK-drug interactions at single amino acid resolution. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.02.685764

García-Marín LM, Ceja Z, Parasuraman A, et al. Genome-wide analysis in over 1.6 million participants uncovers 147 loci associated with obstructive sleep apnoea. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.08.25339824

Miller GA, Roman A, Glettig M, et al. Simulation and empirical evaluation of biologically-informed neural network performance. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.13.687845

Cheng YHH, Sedeño-Cortés AE, Ranchalis JE, et al. Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.07.25339764