Xin Jin

发表

Detecting genetic variations in hereditary retinal dystrophies with next-generation sequencing technology

Xin Jin, Ling-hui Qu, Xiaohong Meng, 2014, Molecular vision.

Identification of two novel insertion abnormal transcripts in two Chinese families affected with Dystrophinopathy

Yingqi Zhang, Xin Jin, Ying Xu, 2019, Journal of clinical laboratory analysis.

Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing

Yong Liu, Xin Jin, Ling-hui Qu, 2020, Bioscience reports.

A Novel Missense SNRNP200 Mutation Associated with Autosomal Dominant Retinitis Pigmentosa in a Chinese Family

G. Tian, Mao‐nian Zhang, Xin Jin, 2012, PloS one.

[A review of gene therapy for Duchenne muscular dystrophy].

Xin Jin, Hui Chen, Qichao Dong, 2018, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Novel compound heterozygous mutation in the POC1B gene underlie peripheral cone dystrophy in a Chinese family

Dajiang Wang, Houbin Huang, Xin Jin, 2018, Ophthalmic genetics.

Molecular Diagnosis and Prenatal Phenotype Analysis of Eight Fetuses With Ciliopathies

Q. Shao, Hui Wang, Xin Jin, 2021, Frontiers in Genetics.

Correction: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Xin Jin, Ling-hui Qu, Liang-mao Li, 2014, Lipids in Health and Disease.

A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Xin Jin, Ling-hui Qu, Shi-Ying Li, 2014, Lipids in Health and Disease.

Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti’s crystalline corneoretinal dystrophy

Yun Bai, Xin Jin, Xiaohong Meng, 2014, Molecular vision.

Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family

C. Pang, Xin Jin, Ling-hui Qu, 2016, Bioscience reports.

Correction: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Xin Jin, Ling-hui Qu, Z. Yin, 2014, Lipids in Health and Disease.

Detecting novel genetic mutations in Chinese Usher syndrome families using next-generation sequencing technology

Xin Jin, Ling-hui Qu, Haiwei Xu, 2015, Molecular Genetics and Genomics.

A novel variant in PAX6 as the cause of aniridia in a Chinese family

W. Liu, Xin Jin, 2020 .

Familial and genetic association with neurodevelopmental disorders caused by a heterozygous variant in the SRRM2 gene

Jinlong Ding, Yuyi Ying, Xin Jin, 2023, Frontiers in endocrinology.