Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China - Shuyi Li; Yuchun Wang; Qu Shen; Jinguo Zan; Mengying Han; Zishuai Huang; Rui Wang; Xinyi Wang; Haifeng He; Le Tao; Hao Ma; Kongyang Zhu; et al. (Human Genetics, 2026)

Identification of novel loci regulating circulating melatonin and its causal relationship with hypertension - Lin Yan; Yang Qiu; Zhiwen Mo; Mingli Li; Xueran Huang; Yongfen Gao; Boteng Yan; Qiantu Hu; Haiying Zhang; Zengnan Mo; Rui Lin (Human Genetics, 2026)

Creation of miniature pig model of human Waardenburg syndrome type 2A by ENU mutagenesis - Tang Hai; Weiwei Guo; Jing Yao; Chunwei Cao; Ailing Luo; Meng Qi; Xianlong Wang; Xiao Wang; Jiaojiao Huang; Ying Zhang; Hongyong Zhang; Dayu Wang; et al. (Human Genetics, 2017)

Mutations in human IFT140 cause non-syndromic retinal degeneration - Mingchu Xu; Lizhu Yang; Feng Wang; Huajin Li; Xia Wang; Weichen Wang; Zhongqi Ge; Keqing Wang; Li Zhao; Hui Li; Yumei Li; Ruifang Sui; et al. (Human Genetics, 2015)

Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland - Li Zhao; Feng Wang; Hui Wang; Yumei Li; Sharon Alexander; Keqing Wang; Colin E. Willoughby; Jacques E. Zaneveld; Lichun Jiang; Zachry T. Soens; Philip Earle; David Simpson; et al. (Human Genetics, 2015)

Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements - Feng Wang; Hui Wang; Han-Fang Tuan; Duy H. Nguyen; Vincent Sun; Vafa Keser; Sara J. Bowne; Lori S. Sullivan; Hongrong Luo; Ling Zhao; Xia Wang; Jacques E. Zaneveld; et al. (Human Genetics, 2014)

A miR-570 binding site polymorphism in the B7-H1 gene is associated with the risk of gastric adenocarcinoma - Weipeng Wang; Fang Li; Yong Mao; Huan Zhou; Jing Sun; Rui Li; Cuiping Liu; Weichang Chen; Dong Hua; Xueguang Zhang (Human Genetics, 2013)

Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations - Jing He; Li-Xin Qiu; Meng-Yun Wang; Rui-Xi Hua; Ruo-Xin Zhang; Hong-Ping Yu; Ya-Nong Wang; Meng-Hong Sun; Xiao-Yan Zhou; Ya-Jun Yang; Jiu-Cun Wang; Li Jin; et al. (Human Genetics, 2012)

A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophy - Laura Lucarini; Betti Giusti; Rui-Zhu Zhang; Te-Cheng Pan; Cecilia Jimenez-Mallebrera; Eugenio Mercuri; Francesco Muntoni; Guglielmina Pepe; Mon-Li Chu (Human Genetics, 2005)