Veiga SI, Porter RL, Aldikacti B, et al. Cell Culture Substrate Variation Alters Extracellular Vesicle Biogenesis Without Affecting Non-Coding Repeat RNA Profile. Small (Weinheim an der Bergstrasse, Germany). 2026:e10233. doi:10.1002/smll.202510233
Publications
Jachim SK, Venkatasubramanian D, Senevirathne G, et al. Leveraging single cell multiomic analyses to identify gene regulatory networks that drive human articular cartilage cell fate. Osteoarthritis and cartilage. 2026. doi:10.1016/j.joca.2025.12.025
Lee S, Miller CL, Bentley AR, et al. A Large-Scale Genome-wide Association Study of Blood Pressure Accounting for Gene-Depressive Symptomatology Interactions in 564,680 Individuals from Diverse Populations. HGG advances. 2026:100566. doi:10.1016/j.xhgg.2026.100566
Broberg M, Gen F, Kalso E, Ollila HM. Genome-wide meta-analysis identifies genetic risk loci for mono- and polyneuropathies in 983 477 individuals. Human molecular genetics. 2026. doi:10.1093/hmg/ddaf200
Ashenberg O, Xavier RJ. Bridging AI and biology: Foundation models meet human physiology and disease. Med (New York, N.Y.). 2026;7(1):100971. doi:10.1016/j.medj.2025.100971
Nicholas JC, Alkis T, Bis JC, et al. Fibrinogen-Associated Plasma Metabolites and Implications for Coagulation, Inflammation, and Vascular Diseases. Journal of thrombosis and haemostasis : JTH. 2026. doi:10.1016/j.jtha.2025.12.016
Rahimi RA, Smith NP, Selle A, et al. Distinct phenotypes and repertoires of bronchoalveolar and airway mucosal T cells in health and allergic asthma. Mucosal immunology. 2026. doi:10.1016/j.mucimm.2026.01.001
Knight E, Li J, Jensen M, Yolou I, Kockan C, Gerstein M. Homomorphic encryption enables privacy preserving polygenic risk scores. Cell reports methods. 2026:101271. doi:10.1016/j.crmeth.2025.101271
Pilcher WC, Yao L, Gonzalez-Kozlova E, et al. A single-cell atlas characterizes dysregulation of the bone marrow immune microenvironment associated with outcomes in multiple myeloma. Nature cancer. 2026. doi:10.1038/s43018-025-01072-4
Owrang D, Rad A, Alerasool M, et al. Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window. Molecular neurobiology. 2026;63(1):354. doi:10.1007/s12035-025-05615-9