专题:Ocular Disorders and Treatments

This cluster of papers focuses on genetic and clinical studies related to ocular development, particularly microphthalmia, anophthalmia, and associated syndromes such as Fraser syndrome. It explores the genetic mutations in genes like SOX2 and BCOR, as well as the use of orbital implants in surgical management of eye malformations. The research also delves into epidermal adhesion and its role in ocular development.
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Sebaceous Carcinomas of the Ocular Adnexa: A Clinicopathologic Study of 104 Cases, with Five-Year Follow-up Data

book-chapter Full Text OpenAlex 334 FWCI4.3487

Current concepts regarding Graves’ orbitopathy

article Full Text OpenAlex 197 FWCI21.8212

Persistent hyperplastic primary vitreous

reference-entry Full Text OpenAlex 185 FWCI0

The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries

article Full Text OpenAlex 167 FWCI24.8373

Cell atlas of the human ocular anterior segment: Tissue-specific and shared cell types

article Full Text OpenAlex 161 FWCI9.1782

Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci

article Full Text OpenAlex 145 FWCI29.8172

Augmentation of scleral glycolysis promotes myopia through histone lactylation

article Full Text OpenAlex 143 FWCI37.0465

Amblyopia Preferred Practice Pattern

article Full Text OpenAlex 134 FWCI11.1349

Candidate pathways for retina to scleral signaling in refractive eye growth

article Full Text OpenAlex 130 FWCI15.574

The uveal effusion syndrome

article Full Text OpenAlex 122 FWCI0.1348