Sotabase

Career

· Research Scientist, Meta AI

Publications (27)

Exome Sequencing Identifies ZNF644 Mutations in High Myopia
PLoS Genetics · 2011
193
cited
Genetic and Functional Dissection of HTRA1 and LOC387715 in Age-Related Macular Degeneration
PLoS Genetics · 2010
127
cited
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.
American Journal of Human Genetics · 2011
119
cited
Supramolecular Photothermal Cascade Nano‐Reactor Enables Photothermal Effect, Cascade Reaction, and In Situ Hydrogelation for Biofilm‐Associated Tooth‐Extraction Wound Healing
Advances in Materials · 2023
96
cited
Metal‐Phenolic Network with Pd Nanoparticle Nodes Synergizes Oxidase‐Like and Photothermal Properties to Eradicate Oral Polymicrobial Biofilm‐Associated Infections
Advances in Materials · 2023
78
cited
A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy
Nature Genetics · 2016
75
cited
Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese Families
Scientific Reports · 2017
41
cited
Neighboring Carboxylic Acid Boosts Peroxidase-Like Property of Metal-Phenolic Nano-Networks in Eradicating Streptococcus mutans Biofilms.
Small · 2022
40
cited
Targeted Adjusting Molecular Arrangement in Organic Solar Cells via a Universal Solid Additive
Advanced Functional Materials · 2022
29
cited
Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population
Scientific Reports · 2016
28
cited
Evaluation of the Association Between Common Genetic Variants Near the ABCA1 Gene and Primary Angle Closure Glaucoma in a Han Chinese Population.
Investigative Ophthalmology and Visual Science · 2015
19
cited
Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Genetics in Medicine · 2019
19
cited
Bacterial membrane nanovesicles encapsulating prodrug assemblies combine chemical and immunological therapies for chronic bacterial infection
Nature Communications · 2025
18
cited
Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese population
Eye · 2018
17
cited
Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy
Genetic Testing and Molecular Biomarkers · 2016
15
cited
Novel Compound Heterozygous CBS Mutations Cause Homocystinuria in a Han Chinese Family
Scientific Reports · 2015
11
cited
Association of IGF1 and IGF1R gene polymorphisms with high myopia in a Han Chinese population
Ophthalmic Genetics · 2017
9
cited
Association of MCP‐1 promoter polymorphism with susceptibility to nasopharyngeal carcinoma
Journal of Cellular Biochemistry · 2018
9
cited
Association study of candidate genes for susceptibility to Kashin-Beck disease in a Tibetan population
BMC Medical Genetics · 2017
9
cited
A novel deleterious mutation in the COMP gene that causes pseudoachondroplasia
Human Genome Variation · 2016
5
cited
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