Medical Genetics

Prof. Dr. Gülay Güleç Ceylan

Doctor and researcher Ankara Bilkent Şehir Hastanesi Ankara
Familial Mediterranean FeverCOVID-19AmyloidosisUrinary Bladder Neoplasms
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Person ↔ Disease

Which diseases does this doctor work on?

From source
  • Familial Mediterranean Fever 7 publications
    Source: OpenAlex / PubMed MeSHView publications
  • COVID-19 2 publications
  • Amyloidosis 2 publications
  • Urinary Bladder Neoplasms 2 publications

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Where does this information come from?

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  • SpecialtyMedical Geneticssaglik.gov.trFrom source
  • InstitutionAnkara Bilkent Şehir Hastanesisaglik.gov.trFrom source
  • Area of workFamilial Mediterranean FeverExtracted from 7 publications · Model version —From source
  • Publications57 publicationsOpenAlex, Europe PMCFrom source
  • ORCID0000-0002-7825-8808ORCIDFrom source
  • Last synchronised5 November 2026 07:22https://ankarasehir.saglik.gov.tr/TR-435798/tibbi-genetik-klinigi-doktorlarimiz.html#gulay-gulec-ceylansaglik.gov.tr

Scientific work

Publications on Familial Mediterranean Fever

57 publications

  1. PTCH1-Related Gorlin Syndrome: Expanding the Clinical and Molecular Spectrum in a Cohort of 11 Patients

    Klinische Pädiatrie, 2026

    DOI 10.1055/a-2896-4106 PMID 42462758 Source: OpenAlex

  2. Genotype and pulmonary function in children with primary ciliary dyskinesia: a cross-sectional cohort study

    European Journal of Pediatrics, 2026

    DOI 10.1007/s00431-026-07574-2 PMID 42975723 Source: OpenAlex

  3. Effect of Hereditary Thrombophilia on the Clinical Severity of Covid-19 Pneumonia

    Research Square, 2024

    DOI 10.21203/rs.3.rs-4343534/v1 1 citation (OpenAlex) Open-access full textSource: OpenAlex

  4. Determination of homeodomain interacting protein kinase 2 polymorphisms rs2058265, rs6464214, and rs7456421 in patients with kidney stone

    Cirugía y Cirujanos (English Edition), 2024

    DOI 10.24875/cirue.m22000624 Open-access full textSource: OpenAlex

  5. Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy

    Molecular Syndromology, 2024

    DOI 10.1159/000540925 PMID 40176833 Open-access full textSource: OpenAlex

  6. Impact of Inflammation-Related Genes on COVID-19: Prospective Study at Turkish Cohort

    The Tohoku Journal of Experimental Medicine, 2023

    DOI 10.1620/tjem.2023.j071 PMID 37635061 2 citations (OpenAlex) Open-access full textSource: OpenAlex

  7. High diagnostic yield with algorithmic molecular approach on hereditary neuropathies

    Revista da Associacao Medica Brasileira (1992), 2023

    DOI 10.1590/1806-9282.20220929 PMID 36790232 3 citations (Europe PMC) Open-access full textSource: Europe PMC

  8. Relationship between asthma and IL-17 gene polymorphism in a Turkish population

    Irish journal of medical science, 2023

    DOI 10.1007/s11845-022-02956-5 PMID 35325374 5 citations (Europe PMC) Open-access full textSource: Europe PMC

  9. Neuromuscular disease genetics in under-represented populations: increasing data diversity

    Brain : a journal of neurology, 2023

    DOI 10.1093/brain/awad254 PMID 37516995 25 citations (Europe PMC) Open-access full textSource: Europe PMC

  10. Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency

    European Journal of Pediatrics, 2023

    DOI 10.1007/s00431-023-05376-4 PMID 38141137 14 citations (OpenAlex) Source: OpenAlex

View all 57 publications