Li P, Hu K. Circadian Disturbances and Age-Related Disorders. Advanced biology. 2023;7(11):e2300405. doi:10.1002/adbi.202300405
Publications
Kim SN, Viswanadham V V, Doan RN, et al. Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.11.06.565899
Urbut SM, Yeung MW, Khurshid S, et al. MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.11.08.23298229
St Fleur RG, Tanofsky-Kraff M, Yanovski JA, Horton NJ, Hirschhorn JN, Field AE. Phenotyping children and adolescents with obesity using behavioral, psychological, and familial data. Obesity (Silver Spring, Md.). 2023;31(12):3016-3024. doi:10.1002/oby.23893
Liuska PJ, Rämö JT, Lemmelä S, et al. Association of APOE Haplotypes With Common Age-Related Ocular Diseases in 412,171 Individuals. Investigative ophthalmology & visual science. 2023;64(14):33. doi:10.1167/iovs.64.14.33
Pichavaram P, Jablonowski CM, Fang J, et al. Oncogenic cells of renal embryonic lineage sensitive to the small molecule inhibitor QC6352 display depletion of KDM4 levels and disruption of ribosome biogenesis. Molecular cancer therapeutics. 2023. doi:10.1158/1535-7163.MCT-23-0312
Jin L, Sullivan HA, Zhu M, et al. Third-generation rabies viral vectors allow nontoxic retrograde targeting of projection neurons with greatly increased efficiency. Cell reports methods. 2023;3(11):100644. doi:10.1016/j.crmeth.2023.100644
Hudson L, Mason JW, Westphal M V, et al. Author Correction: Diversity-oriented synthesis encoded by deoxyoligonucleotides. Nature communications. 2023;14(1):7589. doi:10.1038/s41467-023-43518-2
Infante T, Pepin ME, Ruocco A, Trama U, Mauro C, Napoli C. CDK5R1, GSE1, HSPG2 and WDFY3 as indirect epigenetic-sensitive genes in atrial fibrillation. European journal of clinical investigation. 2023:e14135. doi:10.1111/eci.14135
Greenberg ABW, Mehta NH, Allington G, Jin SC, Moreno-De-Luca A, Kahle KT. Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus: A Systematic Review and Meta-Analysis. JAMA network open. 2023;6(11):e2343384. doi:10.1001/jamanetworkopen.2023.43384