Xun-lun Sheng

1228-437, Guangzhou Road Qilihe District
Lanzhou, 730050, China

Last Updated: 09/26/2026

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Found 13 publications

Genotype-phenotype correlations in Chinese patients with congenital stationary night blindness and early-onset high myopia: evidence from electrophysiology and whole-exome sequencing.

Genotype-phenotype correlations in Chinese patients with congenital stationary night blindness and early-onset high myopia: evidence from electrophysiology and whole-exome sequencing.

Journal: International journal of ophthalmology

Published: February 04, 2026

Early Onset High Myopia and Severe Anisometropia Associated With Familial Exudative Vitreoretinopathy of Irregular Dominant Inheritance in 11 Chinese Families: Analysis of Refraction Features and Pathogenic Variations.

Early Onset High Myopia and Severe Anisometropia Associated With Familial Exudative Vitreoretinopathy of Irregular Dominant Inheritance in 11 Chinese Families: Analysis of Refraction Features and Pathogenic Variations.

Journal: Genetics research

Published: March 31, 2025

De novo variant in GUCY2D gene causing atypical cone-rod dystrophy in a consanguineous family and literature review.

De novo variant in GUCY2D gene causing atypical cone-rod dystrophy in a consanguineous family and literature review.

Journal: International journal of ophthalmology

Published: May 11, 2024

De novel heterozygous copy number deletion on 7q31.31-7q31.32 involving TSPAN12 gene with familial exudative vitreoretinopathy in a Chinese family.

De novel heterozygous copy number deletion on 7q31.31-7q31.32 involving TSPAN12 gene with familial exudative vitreoretinopathy in a Chinese family.

Journal: International journal of ophthalmology

Published: July 28, 2023

Identification of genetic variants in five chinese families with keratoconus: Pathogenicity analysis and characteristics of parental corneal topography.

Identification of genetic variants in five chinese families with keratoconus: Pathogenicity analysis and characteristics of parental corneal topography.

Journal: Frontiers in genetics

Published: June 26, 2022

Identification of Four Novel Variants and Determination of Genotype-Phenotype Correlations for ABCA4 Variants Associated With Inherited Retinal Degenerations.

Identification of Four Novel Variants and Determination of Genotype-Phenotype Correlations for ABCA4 Variants Associated With Inherited Retinal Degenerations.

Journal: Frontiers in cell and developmental biology

Published: November 29, 2020

Identification of a novel FOXL2 mutation in a fourth-generation Chinese family with blepharophimosis-ptosis-epicanthus inversus syndrome.

Identification of a novel FOXL2 mutation in a fourth-generation Chinese family with blepharophimosis-ptosis-epicanthus inversus syndrome.

Journal: International journal of ophthalmology

Published: November 01, 2020

Myopia with X-linked retinitis pigmentosa results from a novel gross deletion of RPGR gene.

Myopia with X-linked retinitis pigmentosa results from a novel gross deletion of RPGR gene.

Journal: International journal of ophthalmology

Published: April 10, 2020

FGFR2 mutation in a Chinese family with unusual Crouzon syndrome.

FGFR2 mutation in a Chinese family with unusual Crouzon syndrome.

Journal: International journal of ophthalmology

Published: January 10, 2016

Prevalence and associated factors of corneal blindness in Ningxia in northwest China.

Prevalence and associated factors of corneal blindness in Ningxia in northwest China.

Journal: International journal of ophthalmology

Published: January 04, 2014

Identification of a novel p.R1443W mutation in RP1 gene associated with retinitis pigmentosa sine pigmento.

Identification of a novel p.R1443W mutation in RP1 gene associated with retinitis pigmentosa sine pigmento.

Journal: International journal of ophthalmology

Published: January 30, 2013

Analysis of clinical phenotype and mode of inheritance in retinitis pigmentosa patients with consanguineous marriage

Analysis of clinical phenotype and mode of inheritance in retinitis pigmentosa patients with consanguineous marriage

Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology

Published: January 11, 2013

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Last Updated: 09/26/2026