<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen Y</submitter><funding>Fundamental Research Funds for the Central Universities</funding><pagination>9490639</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6589239</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2019</volume><pubmed_abstract>A genome-wide association study (GWAS) identified that &lt;i>BET1L&lt;/i> rs2280543 at chromosome 11p15.5 was a susceptibility loci of intracranial aneurysm (IA). Long noncoding RNA &lt;i>H19&lt;/i>, located in this region, was reported to play a crucial role in the formation of IA. In this study, we aimed to examine whether &lt;i>BET1L&lt;/i> rs2280543 and potentially functional polymorphisms in &lt;i>H19&lt;/i> influence the risk of IA. A hospital-based case-control study was performed involving 542 IA patients and 588 age- and gender-matched controls. The &lt;i>BET1L&lt;/i> rs2280543 and &lt;i>H19&lt;/i> polymorphisms were genotyped using the TaqMan assay. The &lt;i>BET1L&lt;/i> rs2280543 CT, CT/TT genotypes, and T allele were associated with an increased risk of IA (CT vs. CC, adjusted OR = 1.43, 95% CI: 1.08-1.90, &lt;i>P&lt;/i> = </pubmed_abstract><journal>Disease markers</journal><pubmed_title>Replication of GWAS Loci Revealed an Increased Risk of &lt;i>BET1L&lt;/i> and &lt;i>H19&lt;/i> Polymorphisms with Intracranial Aneurysm.</pubmed_title><pmcid>PMC6589239</pmcid><funding_grant_id>2017scu11038</funding_grant_id><funding_grant_id>2018SZ0216</funding_grant_id><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Sima X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Replication of GWAS Loci Revealed an Increased Risk of &lt;i>BET1L&lt;/i> and &lt;i>H19&lt;/i> Polymorphisms with Intracranial Aneurysm.</name><description>A genome-wide association study (GWAS) identified that &lt;i>BET1L&lt;/i> rs2280543 at chromosome 11p15.5 was a susceptibility loci of intracranial aneurysm (IA). Long noncoding RNA &lt;i>H19&lt;/i>, located in this region, was reported to play a crucial role in the formation of IA. In this study, we aimed to examine whether &lt;i>BET1L&lt;/i> rs2280543 and potentially functional polymorphisms in &lt;i>H19&lt;/i> influence the risk of IA. A hospital-based case-control study was performed involving 542 IA patients and 588 age- and gender-matched controls. The &lt;i>BET1L&lt;/i> rs2280543 and &lt;i>H19&lt;/i> polymorphisms were genotyped using the TaqMan assay. The &lt;i>BET1L&lt;/i> rs2280543 CT, CT/TT genotypes, and T allele were associated with an increased risk of IA (CT vs. CC, adjusted OR = 1.43, 95% CI: 1.08-1.90, &lt;i>P&lt;/i> = </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2025-04-05T16:24:04.841Z</modification><creation>2019-07-24T07:26:36Z</creation></dates><accession>S-EPMC6589239</accession><cross_references><pubmed>31275455</pubmed><doi>10.1155/2019/9490639</doi></cross_references></HashMap>