Gupta A, Jayasinghe K, Majmundar A, et al. Next-generation nephrology: part 2-mainstreaming genomics in nephrology, a global perspective. Pediatric nephrology (Berlin, Germany). 2025;40(9):2779-2793. doi:10.1007/s00467-025-06711-7
Publications
Moscardini EH, Hudson CC, Kumar D, et al. Latent Trajectories of Depressive Symptoms During a Transdiagnostic Partial Hospitalization Program. Behavior therapy. 2025;56(2):334-351. doi:10.1016/j.beth.2024.05.008
Argentieri A, Amin N, Nevado-Holgado AJ, et al. Integrating the environmental and genetic architectures of aging and mortality. Nature medicine. 2025;31(3):1016-1025. doi:10.1038/s41591-024-03483-9
de Geus MB, Wu CY, Dodge H, et al. Unbiased CSF Proteomics in Patients With Idiopathic Normal Pressure Hydrocephalus to Identify Molecular Signatures and Candidate Biomarkers. Neurology. 2025;104(5):e213375. doi:10.1212/WNL.0000000000213375
Hill SY, Edenberg HJ, Corvin A, et al. Whole Genome Sequencing of Pedigrees With High Density of Substance Use and Psychiatric Disorders: A Meeting Report. Genes, brain, and behavior. 2025;24(1):e70017. doi:10.1111/gbb.70017
Hou L, Hsu A, Luo H, Yuki K. IQGAP1 Influences Neutrophil Maturation and Its Effector Functions. European journal of immunology. 2025;55(2):e202451349. doi:10.1002/eji.202451349
Smith JD, Stillerová VT, Dračinský M, et al. Discovery and isolation of novel capsaicinoids and their TRPV1-related activity. European journal of pharmacology. 2025;999:177700. doi:10.1016/j.ejphar.2025.177700
Khoury R, Longobardi G, Barnatan TT, et al. Radiation-guided nanoparticles enhance the efficacy of PARP inhibitors in primary and metastatic BRCA1-deficient tumors via immunotherapy. Journal of controlled release : official journal of the Controlled Release Society. 2025;383:113812. doi:10.1016/j.jconrel.2025.113812
Parantainen J, Barreto G, Strandberg TE, Mars N, Nurmi K, Eklund KK. Increased intestinal mucosal permeability and metabolic endotoxemia predict the risk of cardiovascular mortality. Atherosclerosis. 2025;405:119220. doi:10.1016/j.atherosclerosis.2025.119220
Rämö JT, Gorman BR, Weng LC, et al. Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma. Nature communications. 2025;16(1):4127. doi:10.1038/s41467-025-58686-6