Xulin Zhang

发表

The Metabolic Reprogramming of Frem2 Mutant Mice Embryos in Cryptophthalmos Development

Wangting Li, Xiaohang Wu, Dongni Wang, 2021, Frontiers in Cell and Developmental Biology.

Deep learning for automated glaucomatous optic neuropathy detection from ultra-widefield fundus images

C. Jin, Dongni Wang, Jinghui Wang, 2020, British Journal of Ophthalmology.

Extracellular vesicles promote epithelial-to-mesenchymal transition of lens epithelial cells under oxidative stress.

Zhenzhen Liu, Xiaohang Wu, Dongni Wang, 2020, Experimental cell research.

Automated detection of retinal exudates and drusen in ultra-widefield fundus images based on deep learning

C. Jin, Dongni Wang, Haotian Lin, 2021, Eye.

Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the LIM2 gene in four Chinese families with congenital cataracts

Zhuoling Lin, J. Li, Dongni Wang, 2021, Annals of translational medicine.

Development and effects of tacrolimus-loaded nanoparticles on the inhibition of corneal allograft rejection

Dongni Wang, Haotian Lin, Duoru Lin, 2019, Drug delivery.

Artificial intelligence manages congenital cataract with individualized prediction and telehealth computing

Chuan Chen, Xin Liu, Min Li, 2020, npj Digital Medicine.

Anterior Umbilication of Lens in a Family with Congenital Cataracts Associated with a Missense Mutation of MIP Gene

Dongni Wang, Haotian Lin, Xulin Zhang, 2022, Genes.

Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome

Zhuoling Lin, Xiaoyan Li, J. Li, 2022, Genes.

Novel mutation in OCRL leading to a severe form of Lowe syndrome.

Zhenzhen Liu, Dongni Wang, Haotian Lin, 2019, International journal of ophthalmology.

Broadening the Mutation Spectrum in GJA8 and CHMP4B: Novel Missense Variants and the Associated Phenotypes in Six Chinese Han Congenital Cataracts Families

Zhuoling Lin, Xiaoyan Li, J. Li, 2021, Frontiers in Medicine.

Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases

Hao Tan, Zhuoling Lin, J. Li, 2022, Genes.

Novel compound heterozygous variants of the SEC23A gene in a Chinese family with cranio-lenticulo-sutural dysplasia based on data from a large cohort of congenital cataract patients

Zhuoling Lin, Xiaoyan Li, Haotian Lin, 2023, BMC Medical Genomics.

EE-Explorer: A Multimodal Artificial Intelligence System for Eye Emergency Triage and Primary Diagnosis.

Xiaohang Wu, Dongni Wang, Haotian Lin, 2023, American journal of ophthalmology.

LensAge index as a deep learning-based biological age for self-monitoring the risks of age-related diseases and mortality

Xiaohang Wu, Dongni Wang, Haotian Lin, 2023, Nature communications.

Digital ray: enhancing cataractous fundus images using style transfer generative adversarial networks to improve retinopathy detection

Xiaohang Wu, Dongni Wang, Duoru Lin, 2024, The British journal of ophthalmology.