<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(64)</volume><submitter>Wang P</submitter><pubmed_abstract>Stroke is one of the most common causes of death worldwide. Genetic risk factors have been found to play important roles in the pathology of ischemic stroke. In a previous genome-wide association study, a functional variant (rs9943582, -154G/A) in the 5' flanking region of the apelin receptor gene (&lt;i>APLNR&lt;/i>) was shown to be significantly associated with stroke in the Japanese population. However, the association required validation in other ethnicities. To validate the genetic relationship between &lt;i>APLNR&lt;/i> and ischemic stroke in the Chinese Han population, we genotyped rs9943582 in a case-control population containing 1,158 ischemic stroke patients and 1,265 common controls enrolled from the GeneID database, and performed a genetic association study. We detected no allelic or genot</pubmed_abstract><journal>Oncotarget</journal><pagination>107678-107684</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5746099</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lack of association between the &lt;i>APLNR&lt;/i> variant rs9943582 with ischemic stroke in the Chinese Han GeneID population.</pubmed_title><pmcid>PMC5746099</pmcid><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Xiong L</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Wang QK</pubmed_authors><pubmed_authors>Xu CQ</pubmed_authors><pubmed_authors>Tu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lack of association between the &lt;i>APLNR&lt;/i> variant rs9943582 with ischemic stroke in the Chinese Han GeneID population.</name><description>Stroke is one of the most common causes of death worldwide. Genetic risk factors have been found to play important roles in the pathology of ischemic stroke. In a previous genome-wide association study, a functional variant (rs9943582, -154G/A) in the 5' flanking region of the apelin receptor gene (&lt;i>APLNR&lt;/i>) was shown to be significantly associated with stroke in the Japanese population. However, the association required validation in other ethnicities. To validate the genetic relationship between &lt;i>APLNR&lt;/i> and ischemic stroke in the Chinese Han population, we genotyped rs9943582 in a case-control population containing 1,158 ischemic stroke patients and 1,265 common controls enrolled from the GeneID database, and performed a genetic association study. We detected no allelic or genot</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Dec</publication><modification>2025-04-27T03:03:58.855Z</modification><creation>2019-03-27T03:05:55Z</creation></dates><accession>S-EPMC5746099</accession><cross_references><pubmed>29296197</pubmed><doi>10.18632/oncotarget.22588</doi></cross_references></HashMap>