Strausz S, Broberg M, Jones SE, et al. Genetic associations between serotonin receptor 1F () regulatory variation and sleep apnoea in non-obese individuals: insights from GWAS and eQTL analyses. The European respiratory journal. 2025;66(3). doi:10.1183/13993003.01778-2024
Publications
Jassim A, Nimmervoll B V, Terranova S, et al. Gene context drift identifies drug targets to mitigate cancer treatment resistance. Cancer cell. 2025;43(9):1608-1621.e9. doi:10.1016/j.ccell.2025.06.005
Gupta S, Mistry K, Alikhan FM, et al. Urinary C-X-C-motif ligand 9 (CXCL9) in immune checkpoint inhibitor-associated acute interstitial nephritis. Kidney international. 2025;108(3):491-496. doi:10.1016/j.kint.2025.05.029
Nadeu F, Shuai S, Clot G, et al. Disease-specific U1 spliceosomal RNA mutations in mature B-cell neoplasms. Leukemia. 2025;39(9):2076-2086. doi:10.1038/s41375-025-02667-7
Cho J, Woo S, Hwang SH, et al. A Multimodal Predictive Model for Chronic Kidney Disease and Its Association With Vascular Complications in Patients With Type 2 Diabetes: Model Development and Validation Study in South Korea and the U.K. Diabetes care. 2025;48(9):1562-1570. doi:10.2337/dc25-0355
Wieder N, D’Souza EN, Dawes R, Chan A, Martin-Geary A, Whiffin N. The role of untranslated region variants in Mendelian disease: a review. European journal of human genetics : EJHG. 2025;33(9):1096-1105. doi:10.1038/s41431-025-01905-x
La YP, Di Bello DT, Escobar MLM, et al. Genetic variation at PPM1H predicts mobilization efficiency in stem cell donors. Blood advances. 2025;9(18):4683-4686. doi:10.1182/bloodadvances.2024015246
Orbach R, Maio N, Butterfield RJ, et al. BCS1L-Associated Disease: 5’-UTR Variant Shifts the Phenotype Towards Axonal Neuropathy. Annals of clinical and translational neurology. 2025;12(9):1834-1845. doi:10.1002/acn3.70108
Kumar KH, Rubinacci S, ZÓ§llner S. MetaGLIMPSE: Meta Imputation of Low Coverage Sequencing Data for Modern and Ancient Genomes. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.06.24.660721
Chatterjee E, Betti MJ, Sheng Q, et al. The extracellular vesicle transcriptome provides tissue-specific functional genomic annotation relevant to disease susceptibility in obesity. Cell genomics. 2025;5(9):100925. doi:10.1016/j.xgen.2025.100925