Sanidas I, Lawrence MS, Dyson NJ. Patterns in the tapestry of chromatin-bound RB. Trends in cell biology. 2023. doi:10.1016/j.tcb.2023.07.012
Publications
Wang H, Fu T, Du Y, et al. Publisher Correction: Scientific discovery in the age of artificial intelligence. Nature. 2023. doi:10.1038/s41586-023-06559-7
Stefanski A, Pérez-Palma E, Brünger T, et al. SLC6A1 variant pathogenicity, molecular function, and phenotype: a genetic and clinical analysis. Brain : a journal of neurology. 2023. doi:10.1093/brain/awad292
Rodin RE, Dou Y, Kwon M, et al. Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nature neuroscience. 2023. doi:10.1038/s41593-023-01437-x
Ralvenius WT, Mungenast AE, Woolf H, et al. A novel molecular class that recruits HDAC/MECP2 complexes to PU.1 motifs reduces neuroinflammation. The Journal of experimental medicine. 2023;220(11). doi:10.1084/jem.20222105
Nowbandegani PS, Wohns AW, Ballard JL, et al. Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies. Nature genetics. 2023. doi:10.1038/s41588-023-01487-8
Soffer MD, James KE, Thaweethai T, Callahan M, Barth WH, Powe CE. Glycated Albumin and Glycemia in Pregnancy and Postpartum: A Pilot Study. American journal of perinatology. 2023. doi:10.1055/s-0043-1772746
Bouras E, Kim AE, Lin Y, et al. Genome-wide interaction analysis of folate for colorectal cancer risk. The American journal of clinical nutrition. 2023. doi:10.1016/j.ajcnut.2023.08.010
Pergu R, Shoba VM, Chaudhary SK, et al. Development and Applications of Chimera Platforms for Tyrosine Phosphorylation. ACS central science. 2023;9(8):1558-1566. doi:10.1021/acscentsci.3c00200
Ross JP, Akçimen F, Liao C, et al. Rare variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome. Genetics in medicine : official journal of the American College of Medical Genetics. 2023:100967. doi:10.1016/j.gim.2023.100967