Oh J, Lee M, Lee H, et al. Hand and Oral Hygiene Practices of South Korean Adolescents Before and During the COVID-19 Pandemic. JAMA network open. 2023;6(12):e2349249. doi:10.1001/jamanetworkopen.2023.49249
Publications
Brooks IR, Alrokh Y, Kazemizadeh A, et al. Highly efficient bi-allelic correction of homozygous COL7A1 mutation using ABE8e adenine base editor. The British journal of dermatology. 2023. doi:10.1093/bjd/ljad522
Weber B, Honigberg MC. Lessons From Genetics About the Interleukin 1 Gene and Treatment of Recurrent Pericarditis. JAMA cardiology. 2023. doi:10.1001/jamacardio.2023.4831
Payton M, Belmontes B, Hanestad K, et al. Small-molecule inhibition of kinesin KIF18A reveals a mitotic vulnerability enriched in chromosomally unstable cancers. Nature cancer. 2023. doi:10.1038/s43018-023-00699-5
Prapiadou S, Živković L, Thorand B, et al. Proteogenomic Data Integration Reveals CXCL10 as a Potentially Downstream Causal Mediator for IL-6 Signaling on Atherosclerosis. Circulation. 2023. doi:10.1161/CIRCULATIONAHA.123.064974
Hills S, Li Q, Madden JA, et al. High number of candidate gene variants are identified as disease-causing in a period of 4 years. American journal of medical genetics. Part A. 2023. doi:10.1002/ajmg.a.63509
He Y, Martin AR. We need more-diverse biobanks to improve behavioural genetics. Nature human behaviour. 2023. doi:10.1038/s41562-023-01795-3
Dedeilia A, Lwin T, Li S, et al. Factors Affecting Recurrence and Survival for Patients with High-Risk Stage II Melanoma. Annals of surgical oncology. 2023. doi:10.1245/s10434-023-14724-5
Scala M, Khan K, Beneteau C, et al. Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities. Genetics in medicine : official journal of the American College of Medical Genetics. 2023:101057. doi:10.1016/j.gim.2023.101057
Kany S, Khurshid S. Keeping to the Rhythm of Cardiovascular Health. European journal of preventive cardiology. 2023. doi:10.1093/eurjpc/zwad410