Qiuxia Yu

Analysis of human upstream open reading frames and impact on gene expression

Lingling Hu, Zhenhai Zhang, Haoli Li, 2015, Human Genetics.

A Double Heterozygous Mutation of TNNI3 Causes Hypertrophic Cardiomyopathy in a Han Chinese Family

Fan Shen, Qiuxia Yu, Huajie Huang, 2015, Cardiology.

Analysis of human upstream open reading frames and impact on gene expression

Zhenhai Zhang, Haoli Li, Yuhua Ye, 2015, Human Genetics.

Mutation in SSUH2 Causes Autosomal‐Dominant Dentin Dysplasia Type I

Qiuxia Yu, Lingling Hu, Xiangmin Xu, 2017, Human mutation.

Anti-Hyperuricemic and Nephroprotective Effects of Dihydroberberine in Potassium Oxonate- and Hypoxanthine-Induced Hyperuricemic Mice

Guoshu Lin, Ziren Su, Jianhui Xie, 2021, Frontiers in Pharmacology.

Abnormal Expression of Dysferlin in Blood Monocytes Supports Primary Dysferlinopathy in Patients Confirmed by Genetic Analyses

Qiuxia Yu, Ya⁃qin Li, Hui-li Zhang, 2021, Frontiers in Neurology.

Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population

Qiuxia Yu, Chengcong Chen, Yue Su, 2021, Frontiers in Endocrinology.

A splicing mutation in VPS4B causes dentin dysplasia I

Wanjun Zhou, Jinzhong Liu, Yuhua Ye, 2016, Journal of Medical Genetics.

A novel splicing mutation in F8 causes various aberrant transcripts in a hemophilia A patient and identifies a new transcript from healthy individuals

Qiuxia Yu, Qinle Zhang, Mengting Li, 2020, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.