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ACS Applied Materials & Interfaces|January 26, 2021
MAX Phase Ceramics/Composites with Complex ShapesJianning Zhang, Ke Chen, Xun Sun, et al.
Human Genetics|July 3, 2007
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 geneQingjiong Zhang, Fareeha Zulfiqar, Xueshan Xiao, et al.
Frontiers in Cell and Developmental Biology|December 20, 2021
Novel BMP4 Truncations Resulted in Opposite Ocular Anomalies: Pathologic Myopia Rather Than MicrophthalmiaYi Jiang, Jiamin Ouyang, Xueqing Li, et al.
Investigative Ophthalmology & Visual Science|January 30, 2025
ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder PhenotypeYingwei Wang, Pangfeng Wang, Zhen Yi, et al.
Progress in Retinal and Eye Research|May 31, 2025
Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomesDongwei Guo, Yi Jiang, Yuxi Zheng, et al.
Human Genetics|September 29, 2005
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4Qingjiong Zhang, Fareeha Zulfiqar, Xueshan Xiao, et al.
International Journal of Molecular Medicine|June 11, 2014
Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosaShiqiang Li, Liping Guan, Shaohua Fang, et al.
Molecular Vision|May 23, 2015
Mutation analysis in 129 genes associated with other forms of retinal dystrophy in 157 families with retinitis pigmentosa based on exome sequencingYan Xu, Liping Guan, Xueshan Xiao, et al.
International Journal of Molecular Sciences|April 13, 2023
New Insight into the Genotype-Phenotype Correlation of PRPH2-Related Diseases Based on a Large Chinese Cohort and Literature ReviewYingwei Wang, Junwen Wang, Yi Jiang, et al.
Molecular Vision|December 2, 2005
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 geneQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
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