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Jiang H, Tang B, Li K, et al. iRUNNER: A Baseline Mutation Burden Regression for Identifying Gene Interaction Between Rare Variants for Diseases. Genomics, proteomics & bioinformatics. 2025. doi:10.1093/gpbjnl/qzaf135

Bai J, Lyu Q, Tan J, et al. High-throughput screen uncovers key regulators of 3D genome architecture. bioRxiv : the preprint server for biology. 2025. doi:10.64898/2025.12.09.693120

Basuroy T, Grubb T, Sadagopan A, et al. BCL-X Dependence is a Subtype Agnostic Actionable Feature of Difficult-to-Treat Kidney Cancers. bioRxiv : the preprint server for biology. 2025. doi:10.64898/2025.12.10.693422

Amin N, Kaushik P, Belbasis L, et al. Proteomic profiling of Alzheimer’s disease and Vascular dementia reveals unique underlying signatures. medRxiv : the preprint server for health sciences. 2025. doi:10.64898/2025.12.08.25341836

Zhao Z, Xu W, Feng EY, et al. PCMT1 generates the C-terminal cyclic imide degron on CRBN substrates. Nature chemical biology. 2025. doi:10.1038/s41589-025-02106-9

Jajoo A, Balakundi V, Chatzinakos C, et al. Leveraging genomic and transcriptomic data of diverse ancestry to uncover mechanisms of psychiatric risk in the adult and developing brain. Nature communications. 2025. doi:10.1038/s41467-025-67941-9

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Wan J, Saatcioglu HD, Ellis H, et al. MAPK Pathway Mutations Emerge in Mutant-IDH1 Inhibitor-Resistant Cholangiocarcinoma and Attenuate the Interferon Response. Clinical cancer research : an official journal of the American Association for Cancer Research. 2025. doi:10.1158/1078-0432.CCR-25-3284

Sabol AL, Mengiste AA, Sreekanth V, et al. Anti-CRISPR-mediated continuous directed evolution of CRISPR-Cas9 in human cells. bioRxiv : the preprint server for biology. 2025. doi:10.64898/2025.12.11.693673