Liping Yang

发表

Application of Whole Exome and Targeted Panel Sequencing in the Clinical Molecular Diagnosis of 319 Chinese Families with Inherited Retinal Dystrophy and Comparison Study

Zhi-zhong Ma, Likun Wang, Jinlu Zhang, 2018, Genes.

Molecular diagnosis based on comprehensive genetic testing in 800 Chinese families with non‐syndromic inherited retinal dystrophies

Genlin Li, Liping Yang, Xiaozhen Liu, 2020, Clinical & experimental ophthalmology.

Retinal degeneration in humanized mice expressing mutant rhodopsin under the control of the endogenous murine promoter.

Y. Li, Liping Yang, Xiaozhen Liu, 2021, Experimental eye research.

Simultaneous expression of two pathogenic genes in four Chinese patients affected with inherited retinal dystrophy.

Zhi-zhong Ma, N. Chen, Liping Yang, 2020, International journal of ophthalmology.

Correlation between Genotype and Phenotype in 69 Chinese Patients with USH2A Mutations: A comparative study of the patients with Usher Syndrome and Nonsyndromic Retinitis Pigmentosa

Y. Li, Liping Yang, Xiaozhen Liu, 2020, Acta ophthalmologica.

Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa

J. Xu, Lei Wang, Genlin Li, 2019, BMC Ophthalmology.

Dependable and Efficient Clinical Molecular Diagnosis of Chinese RP Patient with Targeted Exon Sequencing

Lin Zhao, D. Sharon, H. Dou, 2015, PloS one.

Characteristics of genotype and phenotype in Chinese patients with Bardet–Biedl syndrome

Lei Wang, Genlin Li, Liping Yang, 2020, International Ophthalmology.

Novel mutations of CRB1 in Chinese families presenting with retinal dystrophies

Zhi-zhong Ma, N. Chen, Genlin Li, 2014, Molecular vision.

Single amino acid variation in MAB21L1 is dominantly associated with congenital eye defects

Likun Wang, Jinlu Zhang, Liping Yang, 2022, Journal of Medical Genetics.

Clinical, cytogenetic, and molecular analysis with 46,XX male sex reversal syndrome: case reports

Liping Yang, Jing Huang, Yanling Wei, 2013, Journal of Assisted Reproduction and Genetics.

A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa

Zhi-zhong Ma, Likun Wang, Jinlu Zhang, 2016, Human Genetics.

Identification of a Novel NHS Mutation in a Chinese Family with Nance-Horan Syndrome

Zhi-zhong Ma, N. Chen, Liping Yang, 2015, Current eye research.

Analysis of RPGR gene mutations in 41 Chinese families affected by X-linked inherited retinal dystrophy

Likun Wang, Liping Yang, Xiaozhen Liu, 2022, Frontiers in Genetics.

Novel Mutations of RPGR in Chinese Retinitis Pigmentosa Patients and the Genotype-Phenotype Correlation

Zhi-zhong Ma, N. Chen, Genlin Li, 2014, PloS one.

Analysis of germplasm genetic diversity and construction of a core collection in Camellia oleifera C.Abel by integrating novel simple sequence repeat markers

Yuansong Chen, Liping Yang, Naiming Chen, 2023, Genetic Resources and Crop Evolution.

In Vivo CRISPR/Cas9-Mediated Genome Editing Mitigates Photoreceptor Degeneration in a Mouse Model of X-Linked Retinitis Pigmentosa

Jinlu Zhang, N. Chen, Liping Yang, 2020, Investigative ophthalmology & visual science.

Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy.

Lin Zhao, Zhi-zhong Ma, N. Chen, 2016, Experimental eye research.

Allele-specific gene-editing approach for vision loss restoration in RHO-associated retinitis pigmentosa

Fan Zhang, Yang Li, Liping Yang, 2022, bioRxiv.

Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families

N. Chen, Genlin Li, Liping Yang, 2013, BMJ Open.

In vivo genome editing via CRISPR/Cas9-mediated homology-independent targeted integration for Bietti crystalline corneoretinal dystrophy treatment

Jinlu Zhang, Liping Yang, Xiaozhen Liu, 2024, Nature communications.

Gene replacement therapy in Bietti crystalline corneoretinal dystrophy: an open-label, single-arm, exploratory trial

Likun Wang, Jinlu Zhang, Liping Yang, 2024, Signal transduction and targeted therapy.