Kany S, Rämö JT, Hou C, et al. Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk. Nature genetics. 2025. doi:10.1038/s41588-025-02397-7
Publications
Small AM, Yang TY, Itoh S, et al. Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction. Nature genetics. 2025. doi:10.1038/s41588-025-02417-6
Yu H, Zhou J, Li L, et al. Simulated patient systems powered by large language model-based AI agents offer potential for transforming medical education. Communications medicine. 2025. doi:10.1038/s43856-025-01283-x
Gurjao C, Cazaubiel J, Tan C, et al. Germline predisposition to oncogenic alkylating damage in colorectal cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2025. doi:10.1158/1055-9965.EPI-25-1006
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
PMCID
PMC12667862
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
PMCID
PMC12667831
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
PMCID
PMC12668089
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
PMCID
PMC12668077
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
PMCID
PMC12668118
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
PMCID
PMC12668067