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)

Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain development - Bo Chen; Chenyang Zhang; Huanwen Rui; Dan Shen; Zhuxi Huang; Weijun Feng (Human Genetics, 2025)

Leveraging molecular quantitative trait loci to comprehend complex diseases/traits from the omics perspective - Zijun Zhu; Xinyu Chen; Sainan Zhang; Rui Yu; Changlu Qi; Liang Cheng; Xue Zhang (Human Genetics, 2023)

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)

Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial - Nicola G. Ghazi; Emad B. Abboud; Sawsan R. Nowilaty; Hisham Alkuraya; Abdulrahman Alhommadi; Huimin Cai; Rui Hou; Wen-Tao Deng; Sanford L. Boye; Abdulrahman Almaghamsi; Fahad Al Saikhan; Hassan Al-Dhibi; et al. (Human Genetics, 2016)

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)

Ascertainment adjustment in genetic studies of ordinal traits - Rui Feng; Heping Zhang (Human Genetics, 2006)

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)