Xiaoyun Z. Jia

State Key Laboratory Of Ophthalmology
Guangzhou, China

Last Updated: 09/26/2026

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Found 90 publications

Clinical and Genetic Characteristics of a Chinese Occult Maculopathy Cohort.

Clinical and Genetic Characteristics of a Chinese Occult Maculopathy Cohort.

Journal: Translational vision science & technology

Published: March 27, 2026

Pigmentation Pattern of Iris and Fundus in 75 Chinese Families With GPR143-Associated Ocular Albinism.

Pigmentation Pattern of Iris and Fundus in 75 Chinese Families With GPR143-Associated Ocular Albinism.

Journal: Investigative ophthalmology & visual science

Published: September 30, 2025

Effects of Social Media Consumption on Loneliness and Depression During the Pandemic: A Quantitative Online Survey With the Asian Community of New Zealand.

Effects of Social Media Consumption on Loneliness and Depression During the Pandemic: A Quantitative Online Survey With the Asian Community of New Zealand.

Journal: Journal of the Royal Society of New Zealand

Published: September 06, 2025

Retinitis Pigmentosa-Associated Gene TRIM49 Regulates ULK1-Mediated Autophagy and Photoreceptor Phagocytosis by the Retinal Pigment Epithelium.

Retinitis Pigmentosa-Associated Gene TRIM49 Regulates ULK1-Mediated Autophagy and Photoreceptor Phagocytosis by the Retinal Pigment Epithelium.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: July 02, 2025

Genetic and Clinical Features of FOXL2-Associated Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Based on 11 Chinese Families and Literature Review.

Genetic and Clinical Features of FOXL2-Associated Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Based on 11 Chinese Families and Literature Review.

Journal: American journal of medical genetics. Part A

Published: June 20, 2025

Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndrome.

Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndrome.

Journal: Molecular vision

Published: June 20, 2025

Case report: refractory atelectasis after infection of adenovirus and Mycoplasma Pneumoniae in an immunocompetent patient.

Case report: refractory atelectasis after infection of adenovirus and Mycoplasma Pneumoniae in an immunocompetent patient.

Journal: BMC pulmonary medicine

Published: February 24, 2025

ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype.

ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype.

Journal: Investigative ophthalmology & visual science

Published: January 30, 2025

Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomes.

Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomes.

Journal: Progress in retinal and eye research

Published: January 06, 2025

Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes.

Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes.

Journal: Brain : a journal of neurology

Published: July 11, 2024

MSC-mediated mitochondrial transfer restores mitochondrial DNA and function in neural progenitor cells of Leber's hereditary optic neuropathy.

MSC-mediated mitochondrial transfer restores mitochondrial DNA and function in neural progenitor cells of Leber's hereditary optic neuropathy.

Journal: Science China. Life sciences

Published: May 16, 2024

Datasets-Based IMPDH1 Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-Pathogenic.

Datasets-Based IMPDH1 Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-Pathogenic.

Journal: Current eye research

Published: April 11, 2024

Showing 1-12 of 90

Last Updated: 09/26/2026