Lipov A, Jurgens SJ, Mazzarotto F, et al. Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies. Nature cardiovascular research. 2023;2(11):1078-1094. doi:10.1038/s44161-023-00346-3
Publications
Weingarten-Gabbay S, Bauer MR, Stanton AC, et al. Pan-viral ORFs discovery using Massively Parallel Ribosome Profiling. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.09.26.559641
Weingarten-Gabbay S, Chen DY, Sarkizova S, et al. The HLA-II immunopeptidome of SARS-CoV-2. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.05.26.542482
Srinivasan S, Chen L, Udler M, et al. Initial Insights into the Genetic Variation Associated with Metformin Treatment Failure in Youth with Type 2 Diabetes. Pediatric diabetes. 2023;2023. doi:10.1155/2023/8883199
Lue NZ, Garcia EM, Ngan K, Lee C, Doench JG, Liau BB. Base editor scanning charts the DNMT3A activity landscape. Nature chemical biology. 2023;19(2):176-186. doi:10.1038/s41589-022-01167-4
Baglaenko Y, Wagner C, Bhoj VG, et al. Making inroads to precision medicine for the treatment of autoimmune diseases: Harnessing genomic studies to better diagnose and treat complex disorders. Cambridge prisms. Precision medicine. 2023;1:e25. doi:10.1017/pcm.2023.14
Huang T, Zhu Y, Shutta KH, et al. A Plasma Metabolite Score Related to Psychological Distress and Diabetes Risk: A Nested Case-control Study in US Women. The Journal of clinical endocrinology and metabolism. 2023. doi:10.1210/clinem/dgad731
GarcÃa-Gavilán JF, Babio N, Toledo E, et al. Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease. Cardiovascular diabetology. 2023;22(1):340. doi:10.1186/s12933-023-02066-1
Wang AS, Lemire G, VanNoy GE, Austin-Tse C, O’Donnell-Luria A, Kilbane C. DNM1L variant presenting as adolescent-onset sensory neuronopathy, spasticity, dystonia, and ataxia. Journal of pediatric neurology : JPN. 2023;21(6):475-478. doi:10.1055/s-0043-1771352
Seddon JM, De D, Casazza W, et al. Risk and protection of different rare protein-coding variants of complement component C4A in age-related macular degeneration. Frontiers in genetics. 2023;14:1274743. doi:10.3389/fgene.2023.1274743