Medical Genetics

Uzm. Dr. Taner Karakaya

Doctor and researcher Isparta Şehir Hastanesi Isparta
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  • SpecialtyMedical Geneticssaglik.gov.trFrom source
  • InstitutionIsparta Şehir Hastanesisaglik.gov.trFrom source
  • Publications40 publicationsOpenAlex, Europe PMCFrom source
  • ORCID0000-0002-3437-5324ORCIDFrom source
  • Last synchronised7 November 2026 00:04https://ispartasehir.saglik.gov.tr/TR-1547056/genetik-hastaliklari-tani-merkezi-doktorlarimiz.html#taner-karakayasaglik.gov.tr

Scientific work

Publications

40 publications

  1. Targeted gene panel testing in pediatric epilepsy: Diagnostic outcomes and expanding genetic insights

    Brain and Development, 2026

    DOI 10.1016/j.braindev.2025.104498 PMID 41518736 2 citations (OpenAlex) Source: OpenAlex

  2. Kisspeptin levels in infertile and miscarried women: a cross-sectional study on the relationship with methylenetetrahydrofolate reductase gene polymorphisms and biochemical parameters

    Revista da Associacao Medica Brasileira (1992), 2025

    DOI 10.1590/1806-9282.20250716 PMID 41124561 Open-access full textSource: Europe PMC

  3. Utility of Optical Genome Mapping in Repeat Disorders

    Clinical genetics, 2025

    DOI 10.1111/cge.14633 PMID 39435674 4 citations (Europe PMC) Source: Europe PMC

  4. Evaluation of Full Blood Count–Derived Inflammatory Indices (SII, SIRI, PIV, NLR) in Behçet’s Disease Patients and Healthy Controls

    OBM Genetics, 2025

    DOI 10.21926/obm.genet.2504318 6 citations (OpenAlex) Open-access full textSource: OpenAlex

  5. The Distribution of Hereditary Risk Factors in Patients with Pulmonary Thromboembolism without Identifiable Acquired Risk Factors

    Düzce Tıp Fakültesi Dergisi, 2025

    DOI 10.18678/dtfd.1583292 2 citations (OpenAlex) Open-access full textSource: OpenAlex

  6. The frequency of JAK2 V617F mutation and its association with low EPO levels in polycythemia vera patients

    Scandinavian Journal of Clinical and Laboratory Investigation, 2025

    DOI 10.1080/00365513.2025.2502945 PMID 40337844 1 citation (OpenAlex) Source: OpenAlex

  7. Featured Cover

    Clinical Genetics, 2025

    DOI 10.1111/cge.14700 Open-access full textSource: OpenAlex

  8. Ligneous periodontitis: A molecularly confirmed case of type I plasminogen deficiency

    Journal of Clinical and Experimental Dentistry, 2025

    DOI 10.4317/jced.62773 PMID 40621135 Open-access full textSource: OpenAlex

  9. Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis

    European Journal Of Haematology, 2024

    DOI 10.1111/ejh.14194 PMID 38556258 3 citations (Europe PMC) Open-access full textSource: OpenAlex

  10. SYSTEMIC IMMUNE INFLAMMATION INDEX AND PAN-IMMUNE INFLAMMATION VALUE IN PREDICTING HUMAN LEUKOCYTE ANTIGEN-B27 POSITIVITY: A STUDY ON ANKYLOSING SPONDYLITIS PATIENTS

    Meandros Medical And Dental Journal, 2024

    DOI 10.69601/meandrosmdj.1542434 2 citations (OpenAlex) Open-access full textSource: OpenAlex

View all 40 publications