- Whole exome sequencing: Uncovering causal genetic variants for ocular diseases
Shashank Gupta et al, 2017, Experimental Eye Research CrossRef - USH2A variants in Chinese patients with Usher syndrome type II and non-syndromic retinitis pigmentosa
Tian Zhu et al, 2021, British Journal of Ophthalmology CrossRef - Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing
Ling-hui Qu et al, 2020, Bioscience Reports CrossRef - Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation
Mee Hyun Song et al, 2019, Ear & Hearing CrossRef - Usher Syndrome in Chinese and Japanese Population
Shi-Ying Li et al, 2017, Advances in Vision Research, Volume I CrossRef - Genomic Approaches to Eye Diseases: An Asian Perspective
Bharanidharan Devarajan et al, 2019, Advances in Vision Research, Volume II CrossRef - Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants
María González-del Pozo et al, 2020, Journal of Translational Medicine CrossRef