Xunlun L. Sheng

Lanzhou, 730000, China

Last Updated: 09/26/2026

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Found 54 publications

Clinical outcomes of a monocular bi-aspheric ablation profile for the correction of refractive errors associated with presbyopia

Clinical outcomes of a monocular bi-aspheric ablation profile for the correction of refractive errors associated with presbyopia

Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology
Published: August 04, 2026

Novel variant in PNPLA6 gene causes Oliver-McFarlane syndrome in a Chinese family: 13 years follow-up.

Novel variant in PNPLA6 gene causes Oliver-McFarlane syndrome in a Chinese family: 13 years follow-up.

Journal: Frontiers in genetics
Published: August 27, 2025

A novel homozygous ADAMTS10 frameshift variant in Weill-Marchesani syndrome in a Chinese family.

A novel homozygous ADAMTS10 frameshift variant in Weill-Marchesani syndrome in a Chinese family.

Journal: BMC medical genomics
Published: August 13, 2025

Clinical characteristics and risk factors for readmission after deep anterior lamellar keratoplasty: a nationwide, cross-sectional, multicenter study.

Clinical characteristics and risk factors for readmission after deep anterior lamellar keratoplasty: a nationwide, cross-sectional, multicenter study.

Journal: BMC ophthalmology
Published: January 28, 2025

Identification of pathogenic variants in six Chinese families with keratoconus of autosomal dominant inheritance: pathogenicity analysis and variable phenotype.

Identification of pathogenic variants in six Chinese families with keratoconus of autosomal dominant inheritance: pathogenicity analysis and variable phenotype.

Journal: International ophthalmology
Published: January 11, 2025

Whole-exome sequencing screening for candidate genes and potential pathogenic variants associated with early-onset high myopia in 47 Chinese families.

Whole-exome sequencing screening for candidate genes and potential pathogenic variants associated with early-onset high myopia in 47 Chinese families.

Journal: Scientific reports
Published: January 04, 2025

Genotype-phenotype correlations for 17 Chinese families with inherited retinal dystrophies due to homozygous variants.

Genotype-phenotype correlations for 17 Chinese families with inherited retinal dystrophies due to homozygous variants.

Journal: Scientific reports
Published: July 21, 2024

Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family.

Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family.

Journal: Frontiers in genetics
Published: April 15, 2024

A Novel Compound Heterozygous Variant in the ABHD12 Gene Cause PHARC Syndrome in a Chinese Family: The Proband Presenting New Genotype and Phenotype.

A Novel Compound Heterozygous Variant in the ABHD12 Gene Cause PHARC Syndrome in a Chinese Family: The Proband Presenting New Genotype and Phenotype.

Journal: Molecular genetics & genomic medicine
Published: April 05, 2024

MFRP variations cause nanophthalmos in five Chinese families with distinct phenotypic diversity.

MFRP variations cause nanophthalmos in five Chinese families with distinct phenotypic diversity.

Journal: Frontiers in genetics
Published: March 26, 2024

De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia.

De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia.

Journal: BMC medical genomics
Published: January 06, 2024

Xp21 DNA microdeletion syndrome in a Chinese family: clinical features show retinitis pigmentosa and chronic granuloma.

Xp21 DNA microdeletion syndrome in a Chinese family: clinical features show retinitis pigmentosa and chronic granuloma.

Journal: Frontiers in genetics
Published: August 11, 2023
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Last Updated: 09/26/2026