Jinlu Zhang

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.

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

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

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

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

A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa

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

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.

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.