Yuqian Zheng

发表

Whole exome sequencing analysis identifies novel Stargardt disease-related gene mutations in Chinese Stargardt disease and retinitis pigmentosa patients

T. Ng, H. Chen, Yingjie Cao, 2021, Eye.

Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing

C. Pang, Mingzhi Zhang, Chukai Huang, 2018, Scientific Reports.

Substituted zinc phthalocyanine as an antimicrobial photosensitizer for periodontitis treatment

Mingdong Huang, Fuhua Yan, Zhuo Chen, 2011 .

Association of single nucleotide polymorphisms at 20q12 with nonsyndromic cleft lip with or without cleft palate in a Southern Chinese Han cohort

Shijie Tang, Y. He, Yuqian Zheng, 2019, Molecular genetics & genomic medicine.

Evaluation of Canine Bone Marrow-derived Mesenchymal Stem Cells After Long-term Cryopreservation

Xiaofeng Zhu, Fuhua Yan, Yin Xiao, 2013, Zoological science.

Endophenotyping reveals differential phenotype-genotype correlations between myopia-associated polymorphisms and eye biometric parameters

C. Pang, H. Chen, Mingzhi Zhang, 2012, Molecular vision.

COL2A1 protective variant reduces sporadic rhegmatogenous retinal detachment severity.

C. Pang, T. Ng, H. Chen, 2019, Experimental eye research.

Association analysis of cigarette smoking with onset of primary open-angle glaucoma and glaucoma-related biometric parameters

Y. Liang, Yi Peng, Mingzhi Zhang, 2012, BMC Ophthalmology.

Comparative transcriptomic analysis of the gene expression and underlying molecular mechanism of submergence stress response in orchardgrass roots

B. Zeng, Xiaoli Zhou, Minghao Qu, 2023, Frontiers in Plant Science.

LncRNA BBOX1-AS1 promotes pituitary adenoma progression via sponging miR-361-3p/E2F1 axis

Xinjun Wang, Zheng Pan, Yuqian Zheng, 2022, Anti-cancer drugs.

Evaluation of NTF4 as a causative gene for primary open-angle glaucoma

X. Y. Liang, C. Pang, Ningli Wang, 2012, Molecular vision.

Reduction of Laser-Induced Choroidal Neovascularization in Mice With Erythropoietin RNA Interference

T. Ng, H. Chen, Jiajian Liang, 2022, Translational vision science & technology.

Interactive effects of ATOH7 and RFTN1 in association with adult-onset primary open-angle glaucoma.

C. Pang, H. Chen, Mingzhi Zhang, 2012, Investigative ophthalmology & visual science.

Integrated Transcriptomic and Metabolomics Analysis of the Root Responses of Orchardgrass to Submergence Stress

Yiwei Jiang, B. Zeng, Minghao Qu, 2023, International journal of molecular sciences.

Novel Mutations in PRPF31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing.

C. Pang, H. Chen, L. J. Chen, 2017, Investigative ophthalmology & visual science.

Novel Mutations in PRPF 31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing

C. Pang, H. Chen, L. J. Chen, 2017 .

Whole exome sequencing identifies novel USH2A mutations and confirms Usher syndrome 2 diagnosis in Chinese retinitis pigmentosa patients

T. Ng, H. Chen, Xiaoqiang Xiao, 2019, Scientific reports.

No association of age-related maculopathy susceptibility protein 2/HtrA serine peptidase 1 or complement factor H polymorphisms with early age-related maculopathy in a Chinese cohort

C. Pang, H. Chen, Mingzhi Zhang, 2013, Molecular vision.

Genotype–phenotype correlation and interaction of 4q25, 15q14 and MIPEP variants with myopia in southern Chinese population

C. Pang, T. Ng, Mingzhi Zhang, 2019, British Journal of Ophthalmology.

Whole exome sequencing reveals novel EYS mutations in Chinese patients with autosomal recessive retinitis pigmentosa

T. Ng, H. Chen, Xiaoqiang Xiao, 2019, Molecular vision.

Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing

C. Pang, Mingzhi Zhang, Chukai Huang, 2018, Scientific Reports.

Corneal curvature-associated MTOR variant differentiates mild myopia from high myopia in Han Chinese population

T. Ng, K. Qiu, Lixia Sun, 2021, Ophthalmic genetics.

Primary open-angle glaucoma risk prediction with ABCA1 and LOC102723944 variants and their genotype–phenotype correlations in southern Chinese population

C. Pang, T. Ng, L. J. Chen, 2023, Molecular Genetics and Genomics.

Association of body mass index and PXDNL gene variants with acute primary angle closure in southern Chinese population

T. Ng, Chukai Huang, Shaowan Chen, 2023, Heliyon.

Whole exome sequencing identifies novel USH2A mutations and confirms Usher syndrome 2 diagnosis in Chinese retinitis pigmentosa patients

T. Ng, H. Chen, Xiaoqiang Xiao, 2019, Scientific Reports.