<?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>2026-04-27T07:54:48Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18140" metadataPrefix="mets">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18140</identifier><datestamp>2024-02-12T19:47:43Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_20.500.12105-18140" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:20.500.12105/18140">
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                  <mods:namePart>Cismaru, Anca Liliana</mods:namePart>
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                  <mods:namePart>Hallberg, Pär</mods:namePart>
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                  <mods:namePart>Wadelius, Mia</mods:namePart>
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                  <mods:namePart>Amstutz, Ursula</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-02-12T19:47:43Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2020-10-29</mods:dateIssued>
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               <mods:identifier type="other">http://hdl.handle.net/10668/16529</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/18140</mods:identifier>
               <mods:identifier type="pubmedID">33138277</mods:identifier>
               <mods:identifier type="doi">10.3390/genes11111275</mods:identifier>
               <mods:identifier type="e-issn">2073-4425</mods:identifier>
               <mods:identifier type="journal">Genes</mods:identifier>
               <mods:abstract>Agranulocytosis is a rare yet severe idiosyncratic adverse drug reaction to metamizole, an analgesic widely used in countries such as Switzerland and Germany. Notably, an underlying mechanism has not yet been fully elucidated and no predictive factors are known to identify at-risk patients. With the aim to identify genetic susceptibility variants to metamizole-induced agranulocytosis (MIA) and neutropenia (MIN), we conducted a retrospective multi-center collaboration including cases and controls from three European populations. Association analyses were performed using genome-wide genotyping data from a Swiss cohort (45 cases, 191 controls) followed by replication in two independent European cohorts (41 cases, 273 controls) and a joint discovery meta-analysis. No genome-wide significant associations (p</mods:abstract>
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               <mods:subject>
                  <mods:topic>Dipyrone</mods:topic>
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                  <mods:topic>Drug-induced agranulocytosis</mods:topic>
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               <mods:subject>
                  <mods:topic>Genome-wide association study</mods:topic>
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                  <mods:topic>Metamizole</mods:topic>
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                  <mods:title>Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations.</mods:title>
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