<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-14T03:56:07Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/13823" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/13823</identifier><datestamp>2024-11-29T12:30:35Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_15322</setSpec><setSpec>col_20.500.12105_19609</setSpec><setSpec>col_20.500.12105_16988</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Martínez-Sanz, Javier</subfield>
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      <subfield code="a">Jiménez, Daniel</subfield>
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      <subfield code="a">Martínez-Campelo, Laura</subfield>
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      <subfield code="a">Cruz, Raquel</subfield>
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      <subfield code="a">Vizcarra, Pilar</subfield>
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      <subfield code="a">Sánchez-Conde, Matilde</subfield>
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      <subfield code="a">Ron, Raquel</subfield>
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      <subfield code="a">Rodríguez, Mario</subfield>
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      <subfield code="a">Herrera, Sabina</subfield>
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      <subfield code="a">Moreno, Santiago</subfield>
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      <subfield code="a">Serrano-Villar, Sergio</subfield>
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      <subfield code="c">2021-12</subfield>
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      <subfield code="a">We aim to evaluate the role of single-nucleotide polymorphisms of the angiotensin-converting enzyme 2 in susceptibility to SARS-CoV-2 infection. We included 28 uninfected but highly exposed healthcare workers and 39 hospitalized patients with COVID-19. Thirty-five SNPs were rationally selected. Two variants were associated with increased risk of being susceptible to SARS-CoV-2: the minor A allele in the rs2106806 variant (OR 3.75 [95% CI 1.23-11.43]) and the minor T allele in the rs6629110 variant (OR 3.39 [95% CI 1.09-10.56]). Evaluating the role of genetic variants in susceptibility to SARS-CoV-2 infection could help identify more vulnerable individuals and suggest potential drug targets for COVID-19 patients.</subfield>
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      <subfield code="a">Emerg Microbes Infect. 2021 Dec;10(1):493-496.</subfield>
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      <subfield code="a">10.1080/22221751.2021.1902755</subfield>
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      <subfield code="a">2222-1751</subfield>
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      <subfield code="a">Emerging Microbes &amp; Infections</subfield>
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      <subfield code="a">33704002</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/13823</subfield>
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      <subfield code="a">COVID-19</subfield>
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      <subfield code="a">SARS-CoV-2</subfield>
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      <subfield code="a">Genetic variants</subfield>
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      <subfield code="a">Single-nucleotide polymorphism</subfield>
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      <subfield code="a">Susceptibility</subfield>
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      <subfield code="a">Role of ACE2 genetic polymorphisms in susceptibility to SARS-CoV-2 among highly exposed but non infected healthcare workers</subfield>
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