Tengyang Sun

发表

Comprehensive Molecular Screening in Chinese Usher Syndrome Patients.

Xiao-hui Zhang, Yue Xie, Yang Li, 2018, Investigative ophthalmology & visual science.

Genetic and clinical findings in a Chinese cohort with Leber congenital amaurosis and early onset severe retinal dystrophy

Xiao-hui Zhang, Yue Xie, Yang Li, 2019, British Journal of Ophthalmology.

Phenotypic differences in the inner ears of CBA/CaJ and C57BL/6J mice carrying missense and single base pair deletion mutations in the Cdh23 gene

Ruishuang Geng, Jing Yuan, Q. Zheng, 2021, Journal of neuroscience research.

Clinical findings and RS1 genotype in 90 Chinese families with X-linked retinoschisis

Xiao-hui Zhang, Yue Xie, Yang Li, 2020, Molecular vision.

Clinical and genetic findings in a Chinese cohort with choroideremia

Yue Xie, Yang Li, Chunjie Chen, 2022, Eye.

Screening of BEST1 Gene in a Chinese Cohort With Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy.

Yang Li, Xiao-hui Zhang, Xiaoyan Peng, 2017, Investigative ophthalmology & visual science.

Variants of BEST1 and CRYBB2 cause a complex ocular phenotype comprising microphthalmia, microcornea, cataract, and vitelliform macular dystrophy: case report

Xin Zhang, Jie-Feng Shi, Yang Li, 2023, BMC Ophthalmology.

Phenotypic diversity observed in a Chinese patient cohort with biallelic variants in Bardet-Biedl syndrome genes

Xiao-hui Zhang, Yue Xie, Yang Li, 2023, Eye.

Comprehensive Genetic Analysis Unraveled the Missing Heritability and a Founder Variant of BEST1 in a Chinese Cohort With Autosomal Recessive Bestrophinopathy

Xiao Zhang, Yue Xie, Jie-Feng Shi, 2023, Investigative ophthalmology & visual science.