Abstract Vogt–Koyanagi–Harada (VKH) disease is a leading cause of blindness in young
and middle-aged people. However, the etiology of VKH disease remains unclear. Here, we …

Abstract Vogt‒Koyanagi‒Harada (VKH) disease is a severe autoimmune disease. Herein,
whole‐exome sequencing (WES) study are performed on 2,573 controls and 229 VKH …

Abstract Vogt-Koyanagi-Harada (VKH) disease, a major blinding eye disease, is
characterized by an autoimmune response against melanocytes in multiple organs …

Objective: The aim of this study was to evaluate the association of human leukocyte antigen
(HLA)-DQ and HLA-DQA1/DQB1 alleles with Vogt–Koyanagi–Harada (VKH), providing …

Vogt–Koyanagi–Harada (VKH) disease is a systemic autoimmune disorder affecting multiple
organs, including eyes, skin, and central nervous system. It is known that monocytes …

Abstract Vogt-Koyanagi-Harada (VKH) disease is a systemic autoimmune disorder against
melanocytes. Recent studies have identified multiple genetic factors that might be …

Vogt-Koyanagi-Harada (VKH) disease is a systemic inflammatory disorder that affects
pigment cell-containing organs such as the eye (eg, chronic and/or recurrent granulomatous …

Background Polymorphisms of genes related to the immune response have been reported
to confer susceptibility to Vogt-Koyanagi-Harada (VKH) disease. This study was carried out …

The barrier to curing Vogt–Koyanagi–Harada disease (VKH) is thought to reside in a lack of
understanding in the roles and regulations of peripheral inflammatory immune cells. Here …

Purpose: This study was aimed at investigating the association of long noncoding RNA
(lncRNA)–related single nucleotide polymorphisms (SNPs) with Vogt-Koyanagi-Harada …