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Molecular Vision|October 22, 2020
A large deletion spanning <i>PITX2</i> and <i>PANCR</i> in a Chinese family with Axenfeld-Rieger syndromeYayun Qin, Pang Gao, Shanshan Yu, et al.
BMC Medical Genomics|October 25, 2023
Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese casesYayun Qin, Yanyi Yao, Nian Liu, et al.
Developmental Neuroscience|October 24, 2025
Genetic Characterization of 128 Chinese Individuals with Neurodevelopmental Disorders via Whole-Exome SequencingYayun Qin, Huang Cao, Lijun Liu, et al.
Frontiers in Genetics|November 17, 2022
A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese familyYayun Qin, Hui Xu, Jingmin Yang, et al.
Frontiers in Cell and Developmental Biology|June 23, 2023
Retinal degeneration in <i>rpgra</i> mutant zebrafishXiliang Liu, Shanshan Han, Fei Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
Genetic insights and clinical outcomes in fetal ventriculomegaly: A retrospective analysisLing Zeng, Meiqi Yi, Ting Wang, et al.
Clinical Biochemistry|January 7, 2023
Identification of a novel 10.3 kb deletion causing α<sup>0</sup>-thalassemia by third-generation sequencing: Pedigree analysis and genetic diagnosisRunhong Xu, Hui Li, Song Yi, et al.
Human Molecular Genetics|June 3, 2015
Knockout of RP2 decreases GRK1 and rod transducin subunits and leads to photoreceptor degeneration in zebrafishFei Liu, Jiaxiang Chen, Shanshan Yu, et al.
Scientific Reports|April 6, 2017
Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophyZhaojing Lu, Xuebin Hu, Fei Liu, et al.
The Journal of Biological Chemistry|February 18, 2017
Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafishFei Liu, Yayun Qin, Shanshan Yu, et al.
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