Powell G, Simon MM, Pulit S, Mallon AM, Lindgren CM. Genic constraint against nonsynonymous variation across the mouse genome. BMC genomics. 2023;24(1):562. doi:10.1186/s12864-023-09637-2
Publications
Estabrooks T, Gurinovich A, Pietruska J, et al. Identification of genomic alterations with clinical impact in canine splenic hemangiosarcoma. Veterinary and comparative oncology. 2023. doi:10.1111/vco.12925
Mangalhara KC, Varanasi SK, Johnson MA, et al. Manipulating mitochondrial electron flow enhances tumor immunogenicity. Science (New York, N.Y.). 2023;381(6664):1316-1323. doi:10.1126/science.abq1053
Ahmad N, Fazeli W, Schließke S, et al. De Novo Variants in RAB11B Cause Various Degrees of Global Developmental Delay and Intellectual Disability in Children. Pediatric neurology. 2023;148:164-171. doi:10.1016/j.pediatrneurol.2023.08.023
Marchel D, Trachtman H, Larkina M, et al. The Significance of Hematuria in Podocytopathies. Clinical journal of the American Society of Nephrology : CJASN. 2023. doi:10.2215/CJN.0000000000000309
Williams CM, Poore H, Tanksley PT, et al. Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.21.533641
Schmied C, Nelson M, Avilov S, et al. Community-developed checklists for publishing images and image analysis. ArXiv. 2023.
Lizano P, Pong S, Santarriaga S, Bannai D, Karmacharya R. Brain microvascular endothelial cells and blood-brain barrier dysfunction in psychotic disorders. Molecular psychiatry. 2023. doi:10.1038/s41380-023-02255-0
Yuan F, Gasser GN, Lemire E, et al. Transgenic ferret models define pulmonary ionocyte diversity and function. Nature. 2023. doi:10.1038/s41586-023-06549-9
Perry AS, Zhao S, Gajjar P, et al. Proteomic architecture of frailty across the spectrum of cardiovascular disease. Aging cell. 2023. doi:10.1111/acel.13978