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Pharmacogenomics|June 9, 2012
UGT2B7 genetic polymorphisms are associated with the withdrawal symptoms in methadone maintenance patientsJia-Ni Tian, Ing-Kang Ho, Hsiao-Hui Tsou, et al.Zhonghua Yi Xue Za Zhi|January 6, 2005
[Pathology and molecular pathogenesis of spondyloepiphyseal dysplasia tarda with progressive arthropathy caused by compound CCN6 heterogeneous gene mutations]Yi-qun Peng, Er-yuan Liao, Hui-min Gu, et al.Yi Chuan = Hereditas|March 11, 2025
Expert consensus on clinical genome sequencing interpretation and reportingYulan Lu, Guozhuang Li, Yaqiong Wang, et al.Human Mutation|August 27, 2019
Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndromeHadia Hijazi, Fernanda S Coelho, Claudia Gonzaga-Jauregui, et al.Annals of Translational Medicine|November 9, 2019
Evaluation of manual and electronic healthcare-associated infections surveillance: a multi-center study with 21 tertiary general hospitals in ChinaWen-Sen Chen, Wei-Hong Zhang, Zhan-Jie Li, et al.Nature|January 28, 2026
Prethermalization by random multipolar driving on a 78-qubit processorZheng-He Liu, Yu Liu, Gui-Han Liang, et al.Pageof 83