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Lee AA, Mokhtari DA, Egan ED, Blacklow SC, Herschlag D, Fordyce PM. High-throughput biochemical phenotyping of SHP2 variants reveals the molecular basis of diseases and allosteric drug inhibition. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.30.715055

Garcia-Urena M, Toh PJY, Martinez RS, et al. Genome-Wide Discovery Reveals Adipose-Specific and Systemic Regulators of Insulin Resistance. medRxiv : the preprint server for health sciences. 2026. doi:10.64898/2026.03.31.26349822

Cobuccio L, Avellí MP, Webel H, et al. Deep learning-based stratification of Schizophrenia Spectrum Disorder from real-world data reveals distinct profiles of common and rare variant genetic signal. medRxiv : the preprint server for health sciences. 2026. doi:10.64898/2026.03.30.26349393

Liedtke D, Rak K, Schrode KM, et al. , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss. medRxiv : the preprint server for health sciences. 2026. doi:10.64898/2026.03.27.26349271

Goonewardena SN, Yao S, Jurga T, et al. Lipoprotein(a)-Associated Proteomic Signature Predicts Cardiovascular Disease in Young Adults. The Journal of clinical investigation. 2026. doi:10.1172/JCI204287

Gao C, Cai R, Zheng X, et al. Objectively Measured Daytime Napping Patterns and All-Cause Mortality in Older Adults. JAMA network open. 2026;9(4):e267938. doi:10.1001/jamanetworkopen.2026.7938

Smith EA, Jeshvaghane MA, Pilz DA, et al. Community-led standards for global wastewater-based infectious disease surveillance. PLOS global public health. 2026;6(4):e0006266. doi:10.1371/journal.pgph.0006266

Zhao C, Hatzikotoulas K, Balasubramanian R, et al. Associations of Combined Genetic and Lifestyle Risks With Incident Type 2 Diabetes in the UK Biobank. Diabetes. 2026;75(5):860-866. doi:10.2337/db25-0672