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Li D, Viñado AC, Garcia-Olloqui P, et al. Clonal Hematopoiesis Instructs Maladaptive Tissue Repair to Promote Fibrosis. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.24.710438

Belmont-Rausch DM, Kapel BS, Tomlinson AJ, et al. A uniquely leptin sensitive hypothalamic neuron population limits hyperphagia and weight gain in diet-induced obesity. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.26.714161

Yuan Y, Guan Y, Feng Y, et al. Rare coding and noncoding variants map 1,342 diseases and biomarkers in 490,549 whole genomes. medRxiv : the preprint server for health sciences. 2026. doi:10.64898/2026.03.24.26349148

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

Guez J, Goodrich JK, Moldovan MA, et al. Integrating 730,947 exome sequences with clinical literature improves gene discovery. medRxiv : the preprint server for health sciences. 2026. doi:10.64898/2026.03.23.26349081

Ardissino M, Morley AP, Richards EMF, et al. Effects of Genetically-Proxied Antihypertensive Drug Targets on Preeclampsia and Birth Weight. medRxiv : the preprint server for health sciences. 2026. doi:10.64898/2026.03.17.26346752

Burger S, Yoo O, Nemesh J, et al. Inter-individual variation of cellular and gene-expression properties of the human striatum. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.20.713160

Ye T, Xu W, Barrachina MN, et al. Epigenome editing of human hematopoietic stem cells enables sustained and reversible thrombosis prevention. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.27.714536

Steele L, Foster AR, Roberts K, et al. Hidden immune memory niches in inflammatory skin diseases. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.20.713219

Kim K, Lin Z, Simmons SK, et al. Integrating Long-Read Structural Variant Analysis with single-nucleus RNA-seq to Elucidate Gene Expression Effects in Disease. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.20.713192