<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Sornsamdang G</submitter><funding>Chulabhorn Royal Academy</funding><pubmed_abstract>Behçet's disease (BD) manifests as an autoimmune disorder featuring recurrent ulcers and multi-organ involvement, influenced by genetic factors associated with both HLA and non-HLA genes, including TNF-α and ERAP1. The study investigated the susceptible alleles of both Class I and II molecules of the HLA gene in 56 Thai BD patients and 192 healthy controls through next-generation sequencing using a PacBio kit. The study assessed 56 BD patients, primarily females (58.9%), revealing diverse manifestations including ocular (41.1%), vascular (35.7%), skin (55.4%), CNS (5.4%), and GI system (10.7%) involvement. This study found associations between BD and HLA-A*26:01:01 (OR 3.285, 95% CI 1.135-9.504, P-value 0.028), HLA-B*39:01:01 (OR 6.176, 95% CI 1.428-26.712, P-value 0.015), HLA-B*51:01:01 (</pubmed_abstract><journal>Scientific reports</journal><pagination>7967</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10995258</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Novel genetic variants of HLA gene associated with Thai Behcet's disease (BD) patients using next generation sequencing technology.</pubmed_title><pmcid>PMC10995258</pmcid><pubmed_authors>Limtong P</pubmed_authors><pubmed_authors>Shobana J</pubmed_authors><pubmed_authors>Chanprapaph K</pubmed_authors><pubmed_authors>Sukasem C</pubmed_authors><pubmed_authors>Sornsamdang G</pubmed_authors><pubmed_authors>Chantratita W</pubmed_authors><pubmed_authors>O-Charoen P</pubmed_authors><pubmed_authors>Chotewutmontri S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Novel genetic variants of HLA gene associated with Thai Behcet's disease (BD) patients using next generation sequencing technology.</name><description>Behçet's disease (BD) manifests as an autoimmune disorder featuring recurrent ulcers and multi-organ involvement, influenced by genetic factors associated with both HLA and non-HLA genes, including TNF-α and ERAP1. The study investigated the susceptible alleles of both Class I and II molecules of the HLA gene in 56 Thai BD patients and 192 healthy controls through next-generation sequencing using a PacBio kit. The study assessed 56 BD patients, primarily females (58.9%), revealing diverse manifestations including ocular (41.1%), vascular (35.7%), skin (55.4%), CNS (5.4%), and GI system (10.7%) involvement. This study found associations between BD and HLA-A*26:01:01 (OR 3.285, 95% CI 1.135-9.504, P-value 0.028), HLA-B*39:01:01 (OR 6.176, 95% CI 1.428-26.712, P-value 0.015), HLA-B*51:01:01 (</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-04-18T20:13:33.04Z</modification><creation>2025-04-07T08:04:53.656Z</creation></dates><accession>S-EPMC10995258</accession><cross_references><pubmed>38575661</pubmed><doi>10.1038/s41598-024-58254-w</doi></cross_references></HashMap>