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ABSTRACT: Purpose
Alopecia areata (AA) is one of the most prevalent autoimmune diseases affecting humans. Given that hair follicles are immune-privileged, autoimmunity can result in disfiguring hair loss. However, the genetic basis for AA in the Taiwanese population remains unknown.Materials and methods
A genome-wide association study was conducted using a cohort of 408 AA cases and 8167 controls. To link variants to gene relationships, we used 882 SNPs (P<1E-05) within 74 genes that were associated with AA group to build the biological networks by IPA software. HLA diplotypes and haplotypes were analyzed using Attribute Bagging (HIBAG)-R package and chi-square analysis.Results
Seven single nucleotide polymorphisms (SNPs) including LINC02006 (rs531166736, rs187306735), APC (r
SUBMITTER: Yang JS
PROVIDER: S-EPMC10519225 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature