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                  <mods:namePart>Fundació ACE</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>Centro de Investigación Biomédica en Red - CIBERNED (Enfermedades Neurodegenerativas)</mods:namePart>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>Fundación Reina Sofía</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2022-04-20T09:48:19Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2021-12-07</mods:dateIssued>
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               <mods:identifier type="citation">J Pers Med. 2021 Dec 7;11(12):1318.</mods:identifier>
               <mods:identifier type="doi">10.3390/jpm11121318</mods:identifier>
               <mods:identifier type="issn">2075-4426</mods:identifier>
               <mods:identifier type="journal">Journal of Personalized Medicine</mods:identifier>
               <mods:identifier type="pubmedID">34945790</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/14128</mods:identifier>
               <mods:abstract>Emerging studies have suggested several chromosomal regions as potential host genetic factors involved in the susceptibility to SARS-CoV-2 infection and disease outcome. We nested a COVID-19 genome-wide association study using the GR@ACE/DEGESCO study, searching for susceptibility factors associated with COVID-19 disease. To this end, we compared 221 COVID-19 confirmed cases with 17,035 individuals in whom the COVID-19 disease status was unknown. Then, we performed a meta-analysis with the publicly available data from the COVID-19 Host Genetics Initiative. Because the APOE locus has been suggested as a potential modifier of COVID-19 disease, we added sensitivity analyses stratifying by dementia status or by disease severity. We confirmed the existence of the 3p21.31 region (LZTFL1, SLC6A20) implicated in the susceptibility to SARS-CoV-2 infection and TYK2 gene might be involved in COVID-19 severity. Nevertheless, no statistically significant association was observed in the COVID-19 fatal outcome or in the stratified analyses (dementia-only and non-dementia strata) for the APOE locus not supporting its involvement in SARS-CoV-2 pathobiology or COVID-19 prognosis.</mods:abstract>
               <mods:language>
                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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               <mods:accessCondition type="useAndReproduction"/>
               <mods:subject>
                  <mods:topic>APOE</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>COVID-19</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>GR@ACE/DEGESCO</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>GWAS</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>SARS-CoV-2</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>dementia</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Genomic Characterization of Host Factors Related to SARS-CoV-2 Infection in People with Dementia and Control Populations: The GR@ACE/DEGESCO Study</mods:title>
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