Bilimsel çalışmalar

Prof. Dr. Gülay Güleç Ceylan

57 yayın. Her yayının yanında bilginin kaynağı yazar.

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  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 Kaynak: 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 Kaynak: 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 atıf (OpenAlex) Açık erişimli tam metinKaynak: 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 Açık erişimli tam metinKaynak: OpenAlex

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

    Molecular Syndromology, 2024

    DOI 10.1159/000540925 PMID 40176833 Açık erişimli tam metinKaynak: 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 atıf (OpenAlex) Açık erişimli tam metinKaynak: 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 atıf (Europe PMC) Açık erişimli tam metinKaynak: 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 atıf (Europe PMC) Açık erişimli tam metinKaynak: 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 atıf (Europe PMC) Açık erişimli tam metinKaynak: 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 atıf (OpenAlex) Kaynak: OpenAlex

  11. P293 Clinical and genetic spectrum of sarcoglycanopathies in a cohort of Turkish patients with a possible founder variation

    Neuromuscular Disorders, 2023

    DOI 10.1016/j.nmd.2023.07.203 1 atıf (OpenAlex) Kaynak: OpenAlex

  12. Determinación de los polimorfismos rs2058265, rs6464214 y rs7456421 de la proteína cinasa 2 que interactúan con el homeodominio en pacientes con cálculos renales

    Cirugía y Cirujanos, 2023

    DOI 10.24875/ciru.22000472 PMID 37677956 Açık erişimli tam metinKaynak: OpenAlex

  13. The effectiveness of anti-interleukin-1 therapy on subclinical inflammation parameters during the attack-free period in familial Mediterranean fever patients: A case-control study

    Turkish journal of medical sciences, 2022

    DOI 10.3906/sag-2106-324 PMID 38812979 Açık erişimli tam metinKaynak: Europe PMC

  14. Contribution of Inherited Variants to Hereditary Cancer Syndrome Predisposition

    The Tohoku Journal of Experimental Medicine, 2022

    DOI 10.1620/tjem.2022.j087 PMID 36288950 2 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  15. The Mediterranean Fever Gene Mutations and Its Association with HRQoL, Depression and Fatigue in Patients with Familial Mediterranean Fever Associated Spondyloarthropathies

    Turkish Journal of Osteoporosis, 2022

    DOI 10.4274/tod.galenos.2022.37132 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  16. Are angiotensin converting enzyme (ACE1/ACE2) gene variants associated with the clinical severity of COVID-19 pneumonia? A singlecenter cohort study

    The Anatolian Journal of Cardiology, 2021

    DOI 10.5152/anatoljcardiol.2021.502 PMID 35190362 9 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  17. APPLICATION OF NEXT GENERATION TECHNOLOGIES

    Neuromuscular Disorders, 2021

    DOI 10.1016/j.nmd.2021.07.342 Kaynak: OpenAlex

  18. Association Between Plasminogen Activator Inhibitor type-1 Gene (PAI-1) Polymorphism and Pulmonary Embolism

    Journal of İzmir Chest Hospital, 2020

    DOI 10.5222/igh.2020.1746 1 atıf (OpenAlex) Kaynak: OpenAlex

  19. APC gene analysis in familial adenomatosis polyposis: 3 new mutations in Turkish population

    Acta Oncologica Turcica, 2020

    DOI 10.5505/aot.2020.08931 Açık erişimli tam metinKaynak: OpenAlex

  20. Gastrointestinal Sistem İnflamatuar Hastalıklarının Genetiği

    Turkiye Klinikleri Medical Genetics - Special Topics, 2019

    Kaynak: OpenAlex

  21. The Association Between Blood Homocystein-Paraoxonase Levels and the Polymorphisms of Methylenetetrahydrofolate Reductase and Paraoxonase 1 Genes in Alzheimer Disease Patients

    DergiPark (Istanbul University), 2018

    1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  22. The increased expression of Piezo1 and Piezo2 ion channels in human and mouse bladder carcinoma

    Advances in Clinical and Experimental Medicine, 2018

    DOI 10.17219/acem/71080 PMID 30010255 60 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  23. Vitamin D reseptör gen polimorfizmi ile primer biliyer siroz ilişkisi

    Akademik Gastroenteroloji Dergisi, 2017

    DOI 10.17941/agd.351668 2 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  24. Türkiye'de çölyak hastalığı ile ICAM-1 gen polimorfizminin ilişkisi

    AYBU AVESIS, 2017

    DOI 10.17941/agd.315845 Kaynak: OpenAlex

  25. Türkiyede Çölyak hastalığı ile ICAM 1 gen polimorfizmi ilişkisi

    AYBU AVESIS, 2017

    Kaynak: OpenAlex

  26. Potential role of melastatin-related transient receptor potential cation channel subfamily M gene expression in the pathogenesis of urinary bladder cancer

    Oncology Letters, 2016

    DOI 10.3892/ol.2016.5359 PMID 28101241 22 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  27. Polymorphisms of eNOS, catalase, and myeloperoxidase genes in prostate cancer in Turkish men: preliminary results

    Genetics and Molecular Research, 2016

    DOI 10.4238/gmr.15038543 PMID 27706591 5 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  28. THE EFFICACY OF TISSUE FACTOR −603A/G AND +5466A>G POLIMORPHISMS AT THE DEVELOPMENT OF VENOUS THROMBOEMBOLISM IN CANCER PATIENTS

    Experimental Oncology, 2016

    DOI 10.31768/2312-8852.2016.38(3):187-190 PMID 27685527 7 atıf (OpenAlex) Kaynak: OpenAlex

  29. Clinical characteristics and HLA alleles of a family with simultaneously occurring alopecia areata.

    PubMed, 2016

    PMID 27416096 3 atıf (OpenAlex) Kaynak: OpenAlex

  30. The Importance of Molecular Diagnosis in Alpha 1 Antitrypsin Deficiency: Case Report

    Van Medical Journal, 2016

    DOI 10.5505/vtd.2016.75271 Açık erişimli tam metinKaynak: OpenAlex

  31. Clinical and Radiological Diagnosis of Rarely Seen OSMED Syndrome

    Journal of Medical Cases, 2016

    DOI 10.14740/jmc2431w Açık erişimli tam metinKaynak: OpenAlex

  32. Genetics and male infertility

    World Journal of Clinical Urology, 2015

    DOI 10.5410/wjcu.v4.i1.38 3 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  33. Undifferentiated spondyloarthritis is more frequently seen in women than in men

    The Egyptian Journal of Internal Medicine, 2015

    DOI 10.4103/1110-7782.158000 Açık erişimli tam metinKaynak: OpenAlex

  34. Methylenetetrahydrofolate Reductase Polymorphisms at Familial Bladder Cancer: Case Report

    The Annals of Clinical and Analytical Medicine, 2015

    DOI 10.4328/jcam.3753 Açık erişimli tam metinKaynak: OpenAlex

  35. İnsan mesane kanserlerinde transient reseptör potansiyel melastatin (TRPM)iyon kanalı genlerinin ekspresyonlarının araştırılması / Investigation of transient receptor potential melastatin (TRPM)ion channels genes expressions in human bladder carcinomas

    DSpace - FIRAT (Fırat University), 2015

    Açık erişimli tam metinKaynak: OpenAlex

  36. HLA-B51 subtypes in Turkish patients with Behcet's disease and their correlation with clinical manifestations

    Genetics and Molecular Research, 2014

    DOI 10.4238/2014.july.2.8 PMID 25062414 21 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  37. Focal epithelial hyperplasia associated with human papillomavirus 13 and common human leukocyte antigen alleles in a Turkish family

    International Journal of Dermatology, 2014

    DOI 10.1111/ijd.12538 PMID 24738569 14 atıf (OpenAlex) Kaynak: OpenAlex

  38. The effect of Glutathione-S-transferases in the susceptibility to bladder cancer

    Irish Journal of Medical Science (1971 -), 2014

    DOI 10.1007/s11845-014-1200-6 PMID 25284638 7 atıf (OpenAlex) Kaynak: OpenAlex

  39. Co-existence of familial Mediterranean fever and multiple sclerosis in two patients.

    PubMed, 2014

    PMID 25005448 5 atıf (OpenAlex) Kaynak: OpenAlex

  40. Venöz Tromboemboli Hastalarında Gen Mutasyonları ve Risk Faktörlerinin Değerlendirilmesi

    AYBU AVESIS, 2013

    Kaynak: OpenAlex

  41. Phenotype 2 Familial Mediterranean Fever: Evaluation of 22 Case Series and Review of the Literature on Phenotype 2 FMF

    Renal Failure, 2012

    DOI 10.3109/0886022x.2012.745115 PMID 23228227 20 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  42. Frequency of alterations in the MEFV gene and clinical signs in familial Mediterranean fever in Central Anatolia, Turkey

    Genetics and Molecular Research, 2012

    DOI 10.4238/2012.may.7.4 PMID 22614345 15 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  43. Concomitance of Gitelman Syndrome and Familial Mediterranean Fever: A Rare Case Presentation

    Renal Failure, 2012

    DOI 10.3109/0886022x.2012.718950 PMID 23009175 7 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  44. Increased frequency of MEFV gene mutations in patients with primary dysmenorrhea

    Modern Rheumatology, 2012

    DOI 10.1007/s10165-012-0779-6 PMID 23053724 6 atıf (OpenAlex) Kaynak: OpenAlex

  45. Low plasma vitamin D levels in patients with familial Mediterranean fever

    Rheumatology International, 2011

    DOI 10.1007/s00296-011-2281-4 PMID 22193220 24 atıf (OpenAlex) Kaynak: OpenAlex

  46. MEFV Gene Mutations in a Sample of Turkish Population: A Retrospective Study

    Turkiye Klinikleri Journal of Medical Sciences, 2011

    DOI 10.5336/medsci.2009-15868 3 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  47. The azoospermia factor locus-c region was found to be related to Klinefelter syndrome in Turkish patients

    Genetics and Molecular Research, 2010

    DOI 10.4238/vol9-2gmr826 PMID 20603808 10 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  48. Genetic anomalies in patients with severe oligozoospermia and azoospermia in eastern Turkey: a prospective study

    Genetics and Molecular Research, 2009

    DOI 10.4238/vol8-3gmr616 PMID 19731213 43 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  49. CYTOGENETIC ANALYSIS IN INFERTILE MALES WITH SPERM ANOMALIES

    Dspace Repository (Marmara Üniversitesi), 2009

    14 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  50. Cytogenetic Evaluation of Infertile Men: A Retrospective Study

    DSpace - FIRAT (Fırat University), 2009

    4 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex