Richmond RC, Howe LJ, Heilbron K, et al. Correlations in sleeping patterns and circadian preference between spouses. Communications biology. 2023;6(1):1156. doi:10.1038/s42003-023-05521-7
Publications
Aguado J, Amarilla AA, Fard AT, et al. Senolytic therapy alleviates physiological human brain aging and COVID-19 neuropathology. Nature aging. 2023;3(12):1561-1575. doi:10.1038/s43587-023-00519-6
Pignolo RJ, Mukaddam MA, Baujat G, et al. Study methodology and insights from the palovarotene clinical development program in fibrodysplasia ossificans progressiva. BMC medical research methodology. 2023;23(1):269. doi:10.1186/s12874-023-02080-7
Bustos FJ, Pandian S, Haensgen H, et al. Removal of a partial genomic duplication restores synaptic transmission and behavior in the MyosinVA mutant mouse Flailer. BMC biology. 2023;21(1):232. doi:10.1186/s12915-023-01714-y
van der Voorn SM, van Drie E, Proost V, et al. Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies. International journal of molecular sciences. 2023;24(21). doi:10.3390/ijms242115931
Koyama S, Wang Y, Paruchuri K, et al. Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.10.24.23297096
Parres-Gold J, Levine M, Emert B, Stuart A, Elowitz MB. Principles of Computation by Competitive Protein Dimerization Networks. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.10.30.564854
Wong Y, Ignatieva A, Koskela J, Gorjanc G, Wohns AW, Kelleher J. A general and efficient representation of ancestral recombination graphs. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.11.03.565466
Strober BJ, Zhang MJ, Amariuta T, Rossen J, Price AL. Fine-mapping causal tissues and genes at disease-associated loci. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.11.01.23297909
Li X, Chen H, Selvaraj MS, et al. A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.10.30.564764