Genetic associations of high myopia
This study identified 22 SNPs in 13 genes (<i>ACAN</i>, <i>COL1A1</i>, <i>CRYBA4</i>, <i>FGF10</i>, <i>HIVEP3</i>, <i>LUM</i>, <i>MIPEP</i>, <i>MMP2</i>, <i>PAX6</i>, <i>RASGRF1</i>, <i>SNTB1</i>, <i>TGFβ1</i> and <i>ZMAT4</i>) as potential genetic biomarkers for HM. Future research should conduct large-scale genome-wide association studies across diverse populations to yield more robust evidence.
Authors
- Bin Mao (ORCID: https://orcid.org/0000-0002-5332-7002)
- Qiao Fan (ORCID: https://orcid.org/0000-0002-2762-8346)
- Chen‐Wei Pan (ORCID: https://orcid.org/0000-0003-3362-4613)
- Dan‐Lin Li (ORCID: https://orcid.org/0000-0003-0800-4308)
- Xing‐Xuan Dong (ORCID: https://orcid.org/0000-0001-6791-4833)
- Shan Gong
Institutions
- Soochow University (CN)
- Duke-NUS Medical School (SG)
Publication Details
- Journal
- British Journal of Ophthalmology
- Published
- 2025-10-28
- DOI
- https://doi.org/10.1136/bjo-2025-327791
- Citations
- 1
- Primary Topic
- Ophthalmology and Visual Impairment Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.35