ӳ��ý

Publications

DispatchMAS: fusing taxonomy and artificial intelligence agents for emergency medical services.

Li X, Yu H, Wang W, et al. DispatchMAS: fusing taxonomy and artificial intelligence agents for emergency medical services. BMC emergency medicine. 2026;26(1). doi:10.1186/s12873-026-01540-9

Global burden of adverse effects of medical treatment from 1990 to 2021: a Global Burden of Disease Study 2021.

Global burden of adverse effects of medical treatment from 1990 to 2021: a Global Burden of Disease Study 2021. The Korean journal of internal medicine. 2026;41(2):350-366. doi:10.3904/kjim.2025.278

Early-Onset Digestive System Cancers: Risk Factors and Clinicopathological and Molecular Features Across Organ Sites.

Nakazawa N, Ugai S, Kondo A, et al. Early-Onset Digestive System Cancers: Risk Factors and Clinicopathological and Molecular Features Across Organ Sites. Cancer science. 2026. doi:10.1111/cas.70363

De novo mutations and environmental modifiers: lessons from neural tube defects.

Li HY, Shen Y, Vong KI, Kahle KT, Gleeson JG. De novo mutations and environmental modifiers: lessons from neural tube defects. Trends in genetics : TIG. 2026. doi:10.1016/j.tig.2026.01.011

Distinct malignant cell states and myeloid glutamate signaling associated with aggressive pancreatic neuroendocrine tumors.

Arbesfeld-Qiu JM, Cho JW, Nguyen PTT, et al. Distinct malignant cell states and myeloid glutamate signaling associated with aggressive pancreatic neuroendocrine tumors. Clinical cancer research : an official journal of the American Association for Cancer Research. 2026. doi:10.1158/1078-0432.CCR-25-2565

Combining Genomics With Lipid and Inflammatory Biomarkers to Predict Coronary Artery Disease Risk: UK Biobank Study.

Farah R, Kim MS, Truong B, et al. Combining Genomics With Lipid and Inflammatory Biomarkers to Predict Coronary Artery Disease Risk: UK Biobank Study. Journal of the American College of Cardiology. 2026. doi:10.1016/j.jacc.2026.01.076

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Brünger T, Krey I, Kim S, et al. Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification. medRxiv : the preprint server for health sciences. 2026. doi:10.64898/2026.03.05.26347086

PMCID

PMC12976905

Mapping the heritability of disease: a nationwide study.

Auning J, Trabjerg BB, Dreier JW, Vilhjálmsson BJ, Christensen J. Mapping the heritability of disease: a nationwide study. Nature communications. 2026. doi:10.1038/s41467-026-69991-z

A blueprint for local and distal invasion programs in glioblastoma.

Chanoch-Myers R, Hara T, Greenwald AC, et al. A blueprint for local and distal invasion programs in glioblastoma. Nature communications. 2026. doi:10.1038/s41467-026-70470-8

Detecting chromatin state alterations in PBMCs associated with Type 2 Diabetes Mellitus.

Afarani MM, Gupta R, Uhler C, Fetian I, Shivashankar G V. Detecting chromatin state alterations in PBMCs associated with Type 2 Diabetes Mellitus. Communications medicine. 2026. doi:10.1038/s43856-026-01513-w