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                  <mods:namePart>National Institutes of Health (Estados Unidos)</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>NIH - National Heart, Lung, and Blood Institute (NHLBI) (Estados Unidos)</mods:namePart>
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               <mods:name>
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                  <mods:dateAccessioned encoding="iso8601">2019-04-25T12:21:32Z</mods:dateAccessioned>
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               <mods:identifier type="citation">Front Genet. 2019; 10:158</mods:identifier>
               <mods:identifier type="doi">10.3389/fgene.2019.00158</mods:identifier>
               <mods:identifier type="issn">1664-8021</mods:identifier>
               <mods:identifier type="journal">Frontiers in genetics</mods:identifier>
               <mods:identifier type="pubmedID">30863429</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/7512</mods:identifier>
               <mods:abstract>Background: Associations of both common and rare genetic variants with fasting blood lipids have been extensively studied. However, most of the rare coding variants associated with lipids are population-specific, and exploration of genetic data from diverse population samples may enhance the identification of novel associations with rare variants. Results: We searched for novel coding genetic variants associated with fasting lipid levels in 894 samples from the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) with exome-wide sequencing-based genotype data. In single variant tests, one variant (rs11171663 in ITGA7) was associated with fasting triglyceride levels (P = 7.66E-08), explaining approximately 3.2% of the total trait variance. In gene-based tests, we found statistically significant associations between ITGA7 (P = 1.77E-07) and SLCO2A1 (P = 7.18E-07) and triglycerides, as well as between POT1 (P = 3.00E-07) and low-density lipoprotein cholesterol. In another independent replication cohort consisting of 3,183 African American samples from Hypertension Genetic Epidemiology Network (HyperGEN) and the Genetic Epidemiology Network of Arteriopathy (GENOA), the top genes achieved P-values of 0.04 (ITGA7), 0.08 (SLCO2A1), and 0.02 (POT1). In GOLDN, gene transcript levels of ITGA7 and SLCO2A1 were associated with fasting triglycerides (P = 0.07 and P = 0.02), highlighting functional relevance of our findings. Conclusion: In this study, we present preliminary evidence of novel rare variant determinants of fasting lipids, and reveal potential underlying molecular mechanisms. Moreover, these results were replicated in an independent cohort. Our findings may inform novel biomarkers of disease risk and treatment targets.</mods:abstract>
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                  <mods:topic>HDL</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>LDL</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Cholesterol</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Epidemiology</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Genetics</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Rare variant</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Triglyceride</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Whole exome sequencing</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>An Exome-Wide Sequencing Study of the GOLDN Cohort Reveals Novel Associations of Coding Variants and Fasting Plasma Lipids</mods:title>
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         <file ID="BITSTREAM_TEXT_20.500.12105_7512_8" MIMETYPE="text/plain" SEQ="8" SIZE="828" CHECKSUM="c46007d15a26a8ef59f1881513fb7a2e" CHECKSUMTYPE="MD5" ADMID="FT_20.500.12105_7512_8" GROUPID="GROUP_BITSTREAM_20.500.12105_7512_8">
            <FLocat LOCTYPE="URL" xlink:type="simple" xlink:href="https://repisalud.isciii.es/bitstreams/c6d41495-9ada-4e66-b9bc-f9c04130da17/download"/>
         </file>
      </fileGrp>
   </fileSec>
   <structMap LABEL="DSpace Object" TYPE="LOGICAL">
      <div TYPE="DSpace Object Contents" ADMID="DMD_20.500.12105_7512">
         <div TYPE="DSpace BITSTREAM">
            <fptr FILEID="BITSTREAM_ORIGINAL_20.500.12105_7512_1"/>
         </div>
         <div TYPE="DSpace BITSTREAM">
            <fptr FILEID="BITSTREAM_ORIGINAL_20.500.12105_7512_9"/>
         </div>
      </div>
   </structMap>
</mets></metadata></record></GetRecord></OAI-PMH>