<?xml version="1.0" encoding="UTF-8"?>
<xml>
 <records>
  <record>
   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors/>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2020</year>
    <pub-dates>
     <date>2020-12-04</date>
    </pub-dates>
   </dates>
   <doi>10.1002/gepi.22288</doi>
   <abstract>Previous transcriptome-wide association studies (TWAS) have identified breast cancer risk genes by integrating data from expression quantitative loci and genome-wide association studies (GWAS), but analyses of breast cancer subtype-specific associations have been limited. In this study, we conducted a TWAS using gene expression data from GTEx and summary statistics from the hitherto largest GWAS meta-analysis conducted for breast cancer overall, and by estrogen receptor subtypes (ER+ and ER−). We further compared associations with ER+ and ER− subtypes, using a case-only TWAS approach. We also conducted multigene conditional analyses in regions with multiple TWAS associations. Two genes, STXBP4 and HIST2H2BA, were specifically associated with ER+ but not with ER– breast cancer. We further identified 30 TWAS-significant genes associated with overall breast cancer risk, including four that were not identified in previous studies. Conditional analyses identified single independent breast-cancer gene in three of six regions harboring multiple TWAS-significant genes. Our study provides new information on breast cancer genetics and biology, particularly about genomic differences between ER+ and ER− breast cancer.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/886</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/1009</url>
    </pdf-urls>
   </urls>
  </record>
 </records>
</xml>
