Wells MF, Nemesh J, Ghosh S, et al. Natural variation in gene expression and viral susceptibility revealed by neural progenitor cell villages. Cell stem cell. 2023;30(3):312-332.e13. doi:10.1016/j.stem.2023.01.010
Publications
Bhattacharya R, Libby P. Clonal Hematopoiesis and Cardiac Transplantation: the intersection of inflammation and arteriopathy. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons. 2023. doi:10.1016/j.ajt.2023.02.017
Reichart D, Newby GA, Wakimoto H, et al. Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice. Nature medicine. 2023;29(2):412-421. doi:10.1038/s41591-022-02190-7
Mages S, Moriel N, Avraham-Davidi I, et al. TACCO unifies annotation transfer and decomposition of cell identities for single-cell and spatial omics. Nature biotechnology. 2023. doi:10.1038/s41587-023-01657-3
Zanovello M, Ibáñez K, Brown AL, et al. Unexpected frequency of the pathogenic AR CAG repeat expansion in the general population. Brain : a journal of neurology. 2023. doi:10.1093/brain/awad050
Myserlis EP, Georgakis MK, Demel SL, et al. A Genomic Risk Score Identifies Individuals at High Risk for Intracerebral Hemorrhage. Stroke. 2023;54(4):973-982. doi:10.1161/STROKEAHA.122.041701
Renall N, Lawley B, Vatanen T, et al. The fecal microbiotas of women of Pacific and New Zealand European ethnicities are characterized by distinctive enterotypes that reflect dietary intakes and fecal water content. Gut microbes. 2023;15(1):2178801. doi:10.1080/19490976.2023.2178801
Nascimento A, Bruels CC, Donkervoort S, et al. Variants in DTNA cause a mild, dominantly inherited muscular dystrophy. Acta neuropathologica. 2023;145(4):479-496. doi:10.1007/s00401-023-02551-7
de Prisco N, Ford C, Elrod ND, et al. Alternative polyadenylation alters protein dosage by switching between intronic and 3’UTR sites. Science advances. 2023;9(7):eade4814. doi:10.1126/sciadv.ade4814
Li C, Georgakopoulou A, Newby GA, et al. In vivo HSC prime editing rescues sickle cell disease in a mouse model. Blood. 2023;141(17):2085-2099. doi:10.1182/blood.2022018252