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    <Journal>
      <PublisherName>journal-jmsr</PublisherName>
      <JournalTitle>Journal of Medical and Surgical Research</JournalTitle>
      <PISSN>I</PISSN>
      <EISSN>S</EISSN>
      <Volume-Issue>Vol. XII, n 3</Volume-Issue>
      <PartNumber/>
      <IssueTopic>Multidisciplinary</IssueTopic>
      <IssueLanguage>English</IssueLanguage>
      <Season>March 2026</Season>
      <SpecialIssue>N</SpecialIssue>
      <SupplementaryIssue>N</SupplementaryIssue>
      <IssueOA>Y</IssueOA>
      <PubDate>
        <Year>2026</Year>
        <Month>03</Month>
        <Day>31</Day>
      </PubDate>
      <ArticleType>JMSR Oncology</ArticleType>
      <ArticleTitle>Molecular Profiling of Colorectal Cancer in a Moroccan Cohort Using Targeted Next-Generation Sequencing</ArticleTitle>
      <SubTitle/>
      <ArticleLanguage>English</ArticleLanguage>
      <ArticleOA>Y</ArticleOA>
      <FirstPage>1517</FirstPage>
      <LastPage>1522</LastPage>
      <AuthorList>
        <Author>
          <FirstName>Soufiane</FirstName>
          <LastName>Yassara</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>N</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Ismail</FirstName>
          <LastName>Boujida</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Youssef</FirstName>
          <LastName>Mahdi</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Soumaya</FirstName>
          <LastName>Ech-charif</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Chaimae</FirstName>
          <LastName>Moujahid</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Fatima-Zahra</FirstName>
          <LastName>Bakhtaoui</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Douae</FirstName>
          <LastName>Cherqui</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Najlaa</FirstName>
          <LastName>Lehmissi</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Chaimaa</FirstName>
          <LastName>Mounjid</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Basma El</FirstName>
          <LastName>Khannoussi</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
        </Author>
      </AuthorList>
      <DOI/>
      <Abstract>Objective: To determine the mutational spectrum and microsatellite instability (MSI) status in colorectal cancer (CRC) patients in Morocco, and to examine associations between the clinical characteristics.Methodology: This prospective study was conducted on 55 patients diagnosed with colorectal adenocarcinoma at the National Institute of Oncology in Rabat. DNA was extracted from FFPE tumor tissues and sequenced using the Oncomine__ampersandsigntrade; Colorectal and Pancreatic Cancer Research Panel. Immunohistochemistry was performed to assess MSI status. Statistical analyses, including correlations between mutations and clinicopathological parameters, were conducted. Results: The study found that APC (45.5%), TP53 (43.6%), KRAS (21.8%), ARID1A (20%), PIK3CA (14.5%) and BRAF (12.7%) were the most common mutations. MSI-high status was found in 9.1% of patients, all of whom were __ampersandsignle;60 years old. Statistical analysis revealed a significant correlation between MSI-high status and age (p = 0.023), with no correlation found between mutations and other clinicopathological parameters. Conclusion: This study provides one of the first comprehensive insight into the mutational landscape of colorectal cancer (CRC) in Morocco, demonstrating a significant associations.The findings highlight the importance of next-generation sequencing (NGS) in guiding personalized treatment strategies for CRC and underscore the need to improve access to molecular diagnostics in Morocco.</Abstract>
      <AbstractLanguage>English</AbstractLanguage>
      <Keywords>Colorectal Cancer, Next-Generation Sequencing, Somatic Mutations, Molecular Diagnostics, Microsatellite Instability, Morocco</Keywords>
      <URLs>
        <Abstract>https://www.journal-jmsr.net/ubijournal-v1copy/journals/abstract.php?article_id=16205&amp;title=Molecular Profiling of Colorectal Cancer in a Moroccan Cohort Using Targeted Next-Generation Sequencing</Abstract>
      </URLs>
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        <ReferenceslastPage>19</ReferenceslastPage>
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