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Molecular and Cellular Endocrinology|January 19, 2016
Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidismXuyun Hu, Rongyu Chen, Chunyun Fu, et al.
Oncotarget|September 15, 2017
Association between the functional polymorphism Ile31Phe in the AURKA gene and susceptibility of hepatocellular carcinoma in chronic hepatitis B virus carriersZhiyu Bao, Lei Lu, Xinyi Liu, et al.
Scientific Reports|April 22, 2017
Comprehensive assessment showed no associations of variants at the SLC10A1 locus with susceptibility to persistent HBV infection among Southern ChineseYing Zhang, Yuanfeng Li, Miantao Wu, et al.
Frontiers in Cell and Developmental Biology|May 3, 2021
Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short StatureBaoheng Gui, Chenxi Yu, Xiaoxin Li, et al.
Gastroenterology|April 28, 2018
Germline Duplication of SNORA18L5 Increases Risk for HBV-related Hepatocellular Carcinoma by Altering Localization of Ribosomal Proteins and Decreasing Levels of p53Pengbo Cao, Aiqing Yang, Rui Wang, et al.
Frontiers in Endocrinology|September 30, 2021
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency PatientsChenxi Yu, Bobo Xie, Zhengye Zhao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 6, 2021
CNV profiles of Chinese pediatric patients with developmental disordersHaiming Yuan, Shaofang Shangguan, Zhengchang Li, et al.
Nature Communications|June 1, 2016
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among ChineseYuanfeng Li, Lanlan Si, Yun Zhai, et al.
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