Nakata T, Li C, Mayassi T, et al. Genetic vulnerability to Crohn’s disease reveals a spatially resolved epithelial restitution program. Science translational medicine. 2023;15(719):eadg5252. doi:10.1126/scitranslmed.adg5252PubMedGoogle ScholarDOI
Publications
Vivelo C, Reilly KM, Widemann BC, et al. The Landscape of US and Global Rare Tumor Research Programs: A Systematic Review. The oncologist. 2023. doi:10.1093/oncolo/oyad285PubMedGoogle ScholarDOI
Hahn JW, Yang HR, Moon JS, et al. Global incidence and prevalence of autoimmune hepatitis, 1970-2022: a systematic review and meta-analysis. EClinicalMedicine. 2023;65:102280. doi:10.1016/j.eclinm.2023.102280PubMedGoogle ScholarDOI
Sturm D, Capper D, Andreiuolo F, et al. Author Correction: Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology. Nature medicine. 2023. doi:10.1038/s41591-023-02652-6PubMedGoogle ScholarDOI
Yao D, Binan L, Bezney J, et al. Scalable genetic screening for regulatory circuits using compressed Perturb-seq. Nature biotechnology. 2023. doi:10.1038/s41587-023-01964-9PubMedGoogle ScholarDOI
Pasanen A, Karjalainen MK, Zhang G, et al. Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. PLoS genetics. 2023;19(10):e1010982. doi:10.1371/journal.pgen.1010982PubMedGoogle ScholarDOI
Bang S, Shin YH, Ma X, et al. A Cardiolipin from Induces Antigen-Specific Cytokine Responses. Journal of the American Chemical Society. 2023. doi:10.1021/jacs.3c09734PubMedGoogle ScholarDOI
Wang Y, Kanai M, Tan T, et al. Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. Cell genomics. 2023;3(10):100408. doi:10.1016/j.xgen.2023.100408PubMedGoogle ScholarDOI
McAfee JC, Lee S, Lee J, et al. Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants. Cell genomics. 2023;3(10):100404. doi:10.1016/j.xgen.2023.100404PubMedGoogle ScholarDOI
Li T, Ferraro N, Strober BJ, et al. The functional impact of rare variation across the regulatory cascade. Cell genomics. 2023;3(10):100401. doi:10.1016/j.xgen.2023.100401PubMedGoogle ScholarDOI