Medical Genetics

Uzm. Dr. Özlem Anlaş

Doctor and researcher İzmir Şehir Hastanesi İzmir
Immunologic Deficiency Syndromes
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Person ↔ Disease

Which diseases does this doctor work on?

From source
  • Immunologic Deficiency Syndromes 2 publications
    Source: OpenAlex / PubMed MeSHView publications

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  • SpecialtyMedical Geneticssaglik.gov.trFrom source
  • Institutionİzmir Şehir Hastanesisaglik.gov.trFrom source
  • Area of workImmunologic Deficiency SyndromesExtracted from 2 publications · Model version —From source
  • Publications29 publicationsORCID, Europe PMC, OpenAlexFrom source
  • ORCID0000-0002-2861-1693ORCIDFrom source
  • Last synchronised5 November 2026 09:07https://izmirsehir.saglik.gov.tr/TR-1046642/doktorlarimiz.html#ozlem-anlassaglik.gov.tr

Scientific work

Publications on Immunologic Deficiency Syndromes

29 publications

  1. Characterization of the molecular and clinical features of Multilocus Inherited Neoplasia Allelic Syndrome (MINAS) cases in the Turkish population

    Familial Cancer, 2026

    DOI 10.1007/s10689-026-00577-w PMID 42258060 1 citation (Europe PMC) Source: ORCID

  2. A Case of Carney Complex with Pontine Glioma

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2025.2025-12-22 PMID 40820605 Open-access full textSource: Europe PMC

  3. Assessment of Pediatric Hypertriglyceridemia Etiology: Insights from Next-Generation Sequencing Panels and Identification of Novel Variants

    Biochemical Genetics, 2025

    DOI 10.1007/s10528-025-11209-w PMID 40773003 Source: OpenAlex

  4. Novel EXT1 variants cause divergent symptom severity in multiple cartilaginous exostoses: a family report

    Egyptian Journal of Medical Human Genetics, 2024

    DOI 10.1186/s43042-024-00591-6 Open-access full textSource: ORCID

  5. The Influence of Genetic Polymorphisms on Warfarin Dosage Requirements in Cardiac Valve Surgery Patients

    Cukurova Anestezi ve Cerrahi Bilimler Dergisi, 2024

    DOI 10.36516/jocass.1472877 Open-access full textSource: ORCID

  6. A novel nonsense RPS26 mutation in a patient with Diamond-Blackfan anemia: a case report

    Journal of Medical Case Reports, 2024

    DOI 10.1186/s13256-024-04907-3 PMID 39568018 1 citation (Europe PMC) Open-access full textSource: ORCID

  7. Detecting a Novel NOTCH3 Variant in Patients with Suspected CADASIL: A Single Center Study

    Molecular Syndromology, 2024

    DOI 10.1159/000534243 PMID 38585552 1 citation (Europe PMC) Open-access full textSource: ORCID

  8. Detection of 13 Novel Variants and Investigation of Mutation Distribution by Next Generation Sequencing in Hemoglobinopathies: A Single Center Experience

    Indian Journal of Hematology and Blood Transfusion, 2024

    DOI 10.1007/s12288-023-01694-7 PMID 38708170 Open-access full textSource: ORCID

  9. Distribution of Variants and Identification of Novel Variants in Patients with Obesity Using Next-Generation Sequencing in Genes Associated with Obesity: A Single-Center Experience in Turkey

    Molecular Syndromology, 2024

    DOI 10.1159/000541313 PMID 40475165 Open-access full textSource: OpenAlex

  10. The Genotype-phenotype Correlation of HLA-DQ2 and HLA-DQ8 Haplotypes in Pediatric Celiac Disease: A Single Center Experience

    Meandros Medical and Dental Journal, 2023

    DOI 10.4274/meandros.galenos.2023.90022 Open-access full textSource: ORCID

View all 29 publications