Yayınlar & Eserler

Yayın Ağı
Makaleler 258
Tümü (258)
SCI-E, SSCI, AHCI (171)
SCI-E, SSCI, AHCI, ESCI (208)
ESCI (36)
Scopus (191)
TRDizin (51)
Diğer Yayınlar (30)

1. Vitamin D receptor gene variations and their association with cardiometabolic risk and microvascular complications in metabolic dysfunction-associated steatotic liver disease: evidence from a Turkish cohort.

Guzel Dirim M., Hasanoglu Sayin S., Senkal N., Tuncel F. C., Oyaci Y., Medetalibeyoglu A., et al.
Laboratory medicine , 2025 (SCI-Expanded, Scopus) identifier

2. The role of angiotensinogen, angiotensin II receptor type I and type II receptor polymorphisms (AGTR2 rs11091046, AGT rs699, AGTR1 rs5186, and AGT rs4762) in multiple myeloma

Serin I., Oyaci Y., PEHLİVAN S., Ertas E., Tuncel F. C., Pehlivan M.
Discover Oncology , cilt.16, sa.1, 2025 (SCI-Expanded) identifier identifier identifier

3. Association of Apolipoprotein C-III Gene Polymorphisms (rs2854116 and rs2854117) with Susceptibility to Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) in a Turkish Population

KARAAĞAÇ D., MORKUZU S., ŞENKAL N., BİLGİN E., Oyaci Y., TÜKEK T., et al.
MEDICINA-LITHUANIA , cilt.61, sa.8, 2025 (SCI-Expanded) Creative Commons License identifier identifier identifier

4. Synthesis, in-vitro, in-silico, and global DNA methylation studies of curcumin-benzoquinone analog in triple-negative breast cancer (TNBC) cells

GÜNÇER B., Ozkok F., Aldogan E. H., Oyaci Y., Nazligul E., Edis B., et al.
TOXICOLOGY RESEARCH , cilt.14, sa.4, 2025 (SCI-Expanded) identifier identifier identifier

5. In silico and in vitro investigation of anticancer effect of novel anthraquinone compound on MDA-MB-231 cells

Güler V., Şentürk A. M., Özerman Edis B., Bektaş N., Nazlıgül E., Özkök F., et al.
LETTERS IN DRUG DESIGN & DISCOVERY , cilt.22, sa.5, 2025 (SCI-Expanded) Creative Commons License identifier

6. Metabolic syndrome and effect of gene polymorphisms: ADIPOQ, AGT, AGTR1, AGTR2, ApoC-III, NR3C1 and GNB3 gene polymorphisms.

Pehlivan S., Senkal N., Oyaci Y., Kose M., Pehlivan M., Hasanoglu Sayin S., et al.
Molecular biology reports , cilt.52, sa.1, ss.422, 2025 (SCI-Expanded) identifier

7. Investigation of leukocyte telomere length and hTERT gene MNS16A VNTR variant in microtia patients

Hasanoglu S., Buyukgural B., Tunçel F. C., Oyacı Y., Bekerecioglu M., pehlivan s.
Experimental Biomedical Research , cilt.8, sa.1, ss.8-13, 2025 (Hakemli Dergi) identifier

8. Evaluation of leptin and leptin receptor gene polymorphisms in bipolar disorder: focus on depressive episodes with atypical features

Aytac H. M., Oyaci Y., Aytac E., Pehlivan M., Alptekin F. B., PEHLİVAN S.
Archives of Physiology and Biochemistry , cilt.131, sa.6, ss.918-926, 2025 (SCI-Expanded, Scopus) identifier identifier identifier

9. Investigation of the association between nitric oxide synthase gene variants and NAFLD in adolescents with obesity

Sayın S. H., Kandemir İ., Oyacı Y., Khudiyeva S., Şahin M., Şahin A. Y., et al.
Journal of Pediatric Endocrinology and Metabolism , 2025 (SCI-Expanded) identifier identifier identifier

10. Evaluation of 5-methylcytosine and 5-hydroxymethylcytosine levels in juvenile idiopathic arthritis and its types

Dogantan S., Yücel B. B., Sayin S. H., Taskin S. N., Oyaci Y., PEHLİVAN S.
Revista da Associacao Medica Brasileira (1992) , cilt.71, sa.8, 2025 (SCI-Expanded) identifier identifier identifier

11. Diagnostic and prognostic values of serum Selenoprotein P and soluble St2 levels in pulmonary embolism

Boyracı N., Önür S. T., Kara K., Akyıl F. T., Abalı H., Kocaoğlu A., et al.
American Journal of the Medical Sciences , cilt.368, sa.5, ss.438-445, 2024 (SCI-Expanded) identifier identifier

12. Investigating Leptin Gene Variants and Methylation Status in Relation to Breastfeeding and Preventing Obesity

Kilic A., Pehlivan S., Varkal M. A., Tuncel F. C., Kandemir I., Ozcetin M., et al.
CHILDREN-BASEL , cilt.11, sa.11, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

13. Effect of obesity and NAFLD on leukocyte telomere length and hTERT gene MNS16A VNTR variant.

Kandemir I., Sahin A. Y., Oyaci Y., Khudiyeva S., Sahin M., Aksakal M. Z., et al.
Scientific reports , cilt.14, sa.1, ss.25055, 2024 (SCI-Expanded) identifier identifier

14. The role of immune checkpoint inhibitors: Variable number of tandem repeat (VNTR) polymorphism in the second exon of the P-selectin glycoprotein ligand-1 (PSGL-1) gene polymorphism in multiple myeloma

Oyaci Y., Pehlivan M., PEHLİVAN S., Cinli T. A., Tuncel F. C., Ertas E., et al.
Molecular Carcinogenesis , cilt.63, sa.10, ss.1980-1987, 2024 (SCI-Expanded) identifier identifier

15. The association of HLA-DRB1 alleles and MBL2 gene variant in pediatric acute lymphoblastic leukemia patients.

Oguz R., Ciftci H., Gokce M., Ogret Y., Karadeniz S., Pehlivan S., et al.
Hematology, transfusion and cell therapy , cilt.46, sa.4, ss.327-334, 2024 (ESCI) Creative Commons License identifier identifier

16. LEP rs7799039 and LEPR rs1137101 gene variants are not associated with clinical features in patients with metabolic syndrome in the Turkish population.

Jabbarli M., Senkal N., Tuncel F. C., Oyaci Y., Guzel Dirim M., Kose M., et al.
Laboratory medicine , 2024 (SCI-Expanded) identifier

17. How Effective are leptin Gene Polymorphisms and Methylation during the Course of Multiple Myeloma?

Istemi Serin S., Oyaci Y., Pehlivan M., Demir I., Demir B., Cinli T. A., et al.
Cytology and Genetics , cilt.58, sa.4, ss.319-325, 2024 (SCI-Expanded) identifier identifier

18. The effect of leptin gene polymorphisms (LEP rs7799039 and LEPR rs1137101) on febrile neutropenia.

Uysalol E. P., Uysalol M., Serin I., Pehlivan M., Oyaci Y., Pehlivan S., et al.
Heliyon , cilt.10, sa.7, 2024 (SCI-Expanded) Creative Commons License identifier identifier

19. EXPRESS: The relationship of the methylation status and polymorphism of glucocorticoid receptor gene (NR3C1) with attempted suicide or non-suicidal self-injury patients in schizophrenia.

Oyaci Y., Yildirim Y. E., Aytac H. M., Pehlivan S., Cetinay Aydin P.
Journal of investigative medicine : the official publication of the American Federation for Clinical Research , 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier

20. Relationship of LEP, LEPR Variants, and LEP Methylation with Multiple Myeloma and Prognosis

Oyacı Y., Nursal A. F., Serin İ., Pehlivan S., Pehlivan M.
ISTANBUL MEDICAL JOURNAL , cilt.25, sa.1, ss.6-11, 2024 (ESCI)

21. Evaluation of gene-gene interaction between the interleukin (IL)-2 and IL-2RA gene polymorphisms in schizophrenia patients in the Turkish Population.

Ozdilli K., Mervan Aytac H., Ceren Tuncel F., Oyaci Y., Pehlivan M., Pehlivan S.
Neurosciences (Riyadh, Saudi Arabia) , cilt.29, sa.1, ss.51-56, 2024 (SCI-Expanded) identifier

22. The effect of mesenchymal stem cells administration on DNA repair gene expressions in critically ill COVID-19 patients: prospective controlled study

Işıksaçan N., Adaş G., Kasapoğlu P., Çukurova Z., Yılmaz R., Kurt Yaşar K., et al.
Nucleosides, Nucleotides and Nucleic Acids , cilt.43, sa.12, ss.1431-1446, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

23. Evaluation of the association COMT Val158Met variant and childhood trauma on aggression in Turkish SCZ patients

Çetinay Aydın P., Yıldırım Y. E., Erol A., Nursal A. F., Öngel Atar A., Oyacı Y., et al.
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.43, sa.11, ss.1241-1251, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

24. Effect of interleukin-2 (IL-2) polymorphisms on multiple myeloma: IL-2RA rs2104286, IL-2 rs2069762 and rs2069763 polymorphisms

Serin I., Colak Y., Oyaci Y., Tuncel F. C., Pehlivan M., PEHLİVAN S.
Cytokine , cilt.172, 2023 (SCI-Expanded) identifier identifier

25. IL2RA rs2104286 and IL2 rs2069762 polymorphisms may be associated with bipolar disorder and its clinical findings.

Pehlivan S., Aytac H. M., Nursal A. F., Tuncel F. C., Pehlivan M.
Nucleosides, nucleotides & nucleic acids , ss.1-12, 2023 (SCI-Expanded) identifier

26. Evaluation of the predisposition of serotonin transporter polymorphisms (5-HTTLPR) and complement factor H (CFH) variants to smoking status

Nursal A. F., Sever U., Uysal M. A., Pehlivan M., Pehlivan S.
Experimental Biomedical Research , cilt.6, sa.4, ss.249-256, 2023 (Hakemli Dergi)

27. Evaluation of the methylation status of the MB-COMT, APC2, NR3C1, and DRD2 genes in Turkish patients with microtia

Vagifkızı K., Karataş F., Oyacı Y., İnci F., Pehlivan S.
Kastamonu Medical Journal , cilt.6, ss.257-264, 2023 (Hakemli Dergi)

28. The suppressor of cytokine signaling-1 (SOCS1) gene polymorphism and promoter methylation correlate with the course of COVID-19.

Tukek T., PEHLİVAN S., Medetalibeyoglu A., Serin I., Oyacı Y., Arıcı H., et al.
Pathogens and global health , cilt.117, sa.4, ss.392-400, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

29. Quantitative detection of methylated SOCS-1 in schizophrenia and bipolar disorder considering SOCS-1-1478CA/del polymorphism and clinical parameters

Aytac H. M., Pehlivan S., Pehlivan M., Oyaci Y.
IRISH JOURNAL OF MEDICAL SCIENCE , cilt.192, sa.2, ss.775-783, 2023 (SCI-Expanded) identifier identifier identifier

30. Association of Tumor Necrosis Factor-Alpha (TNF-alpha) and Suppressor of Cytokine Signaling-1 (SOCS-1) Gene Variants in Children with COVID-19

Uysalol M., Serin I., Oyacl Y., Ylldlz R., Uysalol E., PEHLİVAN S.
JOURNAL OF PEDIATRIC INFECTIOUS DISEASES , cilt.18, sa.1, ss.38-45, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

31. Genetic polymorphism of IL-17F rs763780 contributes to the susceptibility to bipolar disorder but not to schizophrenia in the Turkish population

Oyaci Y., Aytac H. M., Pehlivan M., PEHLİVAN S.
Nucleosides, Nucleotides and Nucleic Acids , cilt.42, sa.11, ss.852-866, 2023 (SCI-Expanded) identifier identifier

32. The effect of hereditary thrombotic factors and comorbidities on the severity of COVID-19 disease

Kose M., Senkal N., Konyaoglu H., Emet A., Oyaci Y., PEHLİVAN S., et al.
EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES , cilt.27, sa.1, ss.395-403, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

33. Association of childhood asthma with Gasdermin B (GSDMB) and Oromucoid-like 3 (ORMDL3) genes

Almacioglu M., Keskin O., Ozkars M. Y., Balci S. O., Kucukosmanoglu E., PEHLİVAN S., et al.
Northern Clinics of Istanbul , cilt.10, sa.6, ss.769-777, 2023 (ESCI) Creative Commons License identifier

34. ASSOCIATING eNOS GENE VARIANTS WITH COVID-19 SUSCEPTIBILITY IN THE TURKISH POPULATION

Şenkal N., Oyaci Y., Cebeci T., Konyaoğlu H., Köse M., Önel M., et al.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , cilt.86, sa.1, ss.1-6, 2023 (ESCI, TRDizin) Sürdürülebilir Kalkınma identifier identifier identifier

35. The circadian systems genes and their importance of human health.

Pehlivan S.
Advances in protein chemistry and structural biology , cilt.137, ss.1-15, 2023 (SCI-Expanded) identifier

36. The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course

Senkal N., Serin I., PEHLİVAN S., Pehlivan M., Medetalibeyoglu A., Cebeci T., et al.
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS , cilt.42, sa.8, ss.571-585, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

37. A New Clock is Running for Multiple Myeloma: Circadian Clock Protein-Period 3 (PER-3) Polymorphism

Serin I., Pehlivan S., Demir I., Oyaci Y., Pehlivan M.
BALKAN JOURNAL OF MEDICAL GENETICS , cilt.25, sa.2, ss.37-43, 2022 (SCI-Expanded) Creative Commons License identifier identifier identifier

38. PERIOD3 (PER3) VNTR Variant Associated with Seasonal Pattern and Family History in Bipolar Disorder

Aytac H. M., Pehlivan M., Oyaci Y., PEHLİVAN S.
Psychiatria Danubina , cilt.34, sa.4, ss.695-699, 2022 (SCI-Expanded) Creative Commons License identifier identifier

39. Associations of XRCC4, eNOS, and PER3 VNTR variants with Childhood Acute Lymphoblastic Leukemia in Turkish Patients

Oğuz S. R., Gökçe M., Pehlivan S., Oyacı Y., Şentürk Çiftçi H., Atay A. A., et al.
MEDICAL JOURNAL OF BAKIRKOY , cilt.18, sa.4, ss.463-470, 2022 (ESCI) Creative Commons License

40. Epigenetic and genetic investigation of SOCS-1 gene in patients with multiple myeloma.

Tuncel F. C., Serin I., Pehlivan S., Oyaci Y., Pehlivan M.
Blood research , 2022 (ESCI) Creative Commons License identifier

41. Association of intron 4 VNTR polymorphism in the NOS3 gene with rapid cycling and treatment resistance in bipolar disorder: a case-control study

Aytac H. M., PEHLİVAN M., Oyaci Y., Pehlivan S.
NEUROSCIENCES , cilt.27, sa.4, ss.229-236, 2022 (SCI-Expanded) identifier identifier identifier

42. Interleukin-1 receptor antagonist (IL-1RA) and interleukin-4 (IL-4) variable number of tandem repeat polymorphisms in schizophrenia and bipolar disorder: an association study in Turkish population

Pehlivan S., Oyaci Y., Tuncel F. C., Aytac H. M.
EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS , cilt.23, sa.1, 2022 (ESCI) identifier identifier

43. Mannose-Binding Lectin 2 Gene Polymorphism during Pandemic: COVID-19 Family

Tukek T., Pehlivan S., Oyaci Y., Alkac U. I.
GLOBAL MEDICAL GENETICS , cilt.09, sa.02, ss.185-188, 2022 (ESCI) Creative Commons License Sürdürülebilir Kalkınma identifier identifier

44. Mannose-binding lectin 2 (MBL 2) gene polymorphism during pandemic: COVID-19 family

TÜKEK T., PEHLİVAN S., Oyacı Y., İŞOĞLU Ü.
GLOBAL MEDICAL GENETICS , cilt.9, sa.2, ss.185-188, 2022 (Hakemli Dergi) Sürdürülebilir Kalkınma

45. Association of mannose-binding lectin 2 (MBL2) and suppressor of cytokine signaling-1 (SOCS1) gene variants in children with febrile neutropenia.

Uysalol E. P., Uysalol M., Pehlivan M., Oyaci Y., Pehlivan S., Serin I.
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy , cilt.28, sa.5, ss.657-662, 2022 (SCI-Expanded) identifier identifier identifier

46. Cytokine gene polymorphism frequencies in Turkish population living in Marmara region

Özdilli K., Ögret Y., Oğuz S. R., Sel F. A., Şentürk Çiftçi H., Çınar Ç., et al.
TURKISH JOURNAL OF BIOCHEMISTRY , cilt.47, 2022 (SCI-Expanded) identifier identifier

47. Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (-) patients.

Pehlivan S., Köse M., Mese S., Serin I., Senkal N., Oyacı Y., et al.
Pathogens and global health , cilt.116, sa.3, ss.178-184, 2022 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

48. Role of cytokines in multiple myeloma: IL-1RN and IL-4 VNTR polymorphisms

Serin I., Oyaci Y., Pehlivan M., PEHLİVAN S.
Cytokine , cilt.153, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

49. DNA methylation pattern of gene promoters of MB-COMT, DRD2, and NR3C1 in Turkish patients diagnosed with schizophrenia

Aytac H. M., Oyaci Y., Pehlivan M., PEHLİVAN S.
EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.285, 2022 (SCI-Expanded) identifier

50. GENETIC POLYMORPHISMS IN 15 STR LOCI IN THE TURKISH POPULATION LIVING IN ISTANBUL PROVINCE

Ozdilli K., ÖGRET Y., Oguz R., İŞSEVER H., Yokes M. B., Ciftci H. S., et al.
NOBEL MEDICUS , cilt.18, sa.1, ss.54-61, 2022 (ESCI) identifier identifier

51. Importance of mannose-binding lectin2 polymorphism (rs1800450) in infections in children

Uysalol M., Gumus S., Yildiz R., Pasli Uysalol E., Pehlivan S., Pehlivan M., et al.
BIOMARKERS , cilt.27, sa.1, ss.44-49, 2022 (SCI-Expanded) Creative Commons License identifier identifier identifier

52. Tumor Necrosis Factor-alpha (TNF-alpha)-238 G/A Polymorphism Is Associated with the Treatment Resistance and Attempted Suicide in Schizophrenia

Aytac H. M., Ozdilli K., Tuncel F. C., PEHLİVAN M., Pehlivan S.
IMMUNOLOGICAL INVESTIGATIONS , cilt.51, sa.2, ss.368-380, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

53. Assessment of myeloperoxidase (Mpo) gene polymorphism in cervical cancer

ADALI Y., PEHLİVAN S., OĞUZKAN BALCI S., KOYUNCUOĞLU ÜLGÜN M.
Journal of Surgery and medicine , cilt.6, ss.25-28, 2022 (Hakemli Dergi)

54. COMTVal158Met polymorphism is associated with ecstasy (MDMA)-induced psychotic symptoms in the Turkish population

Aytac H. M., Oyaci Y., Aydin P. C., Pehlivan M., Pehlivan S.
NEUROSCIENCES , cilt.27, sa.1, ss.24-30, 2022 (SCI-Expanded) identifier identifier identifier

55. GENETIC POLYMORPHISMS IN 15 STR LOCI IN THE TURKISH POPULATION LIVING IN ISTANBUL PROVINCE İSTANBUL’DA YAŞAYAN TÜRK NÜFUSUNDA 15 STR LOKUSUNDA GENETİK POLİMORFİZMLER

Ozdilli K., Ogret Y., Oguz R., Issever H., Yokes M. B., Ciftci H. S., et al.
Nobel Medicus , cilt.18, sa.1, ss.54-61, 2022 (ESCI) Sürdürülebilir Kalkınma identifier

56. DNA Methylation Pattern of Gene Promoters of MB-COMT, DRD2, and NR3C1 in Turkish Patients Diagnosed with Schizophrenia

Aytac H. M., Oyaci Y., Pehlivan M., PEHLİVAN S.
CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE , cilt.20, sa.4, ss.685-693, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

57. What are the roles of global DNA and APC 2 gene promotor hypermethylation in multiple myeloma?

Pehlivan S., Serin I., NURSAL A. F., Oyaci Y., GÜNDEŞ İ., Pehlivan M.
MOLECULAR BIOLOGY REPORTS , cilt.48, sa.12, ss.7875-7882, 2021 (SCI-Expanded) identifier identifier identifier

58. Is There a Link between Circadian Clock Protein PERIOD 3 (PER3) (rs57875989) Variant and the Severity of COVID-19 Infection?

Yesil Sayin G., Pehlivan S., Serin I., Medetalibeyoglu A., Kose M., Agacfidan A., et al.
Current medical science , cilt.41, sa.6, ss.1075-1080, 2021 (Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

59. Investigation of inflammation related gene polymorphism of the mannose-binding lectin 2 in schizophrenia and bipolar disorder.

Aytac H. M., Yazar M. S., Erol A., Pehlivan S.
Neurosciences (Riyadh, Saudi Arabia) , cilt.26, sa.4, ss.346-356, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

60. Association of the Uncoupling Protein 2-866 G/A Polymorphism with Family History and Duration of Tobacco Use Disorder in a Turkish Population

Aytac H. M., Pehlivan S., Kurnaz S., PEHLİVAN M., Aydin P. C.
PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY , cilt.31, sa.3, ss.280-285, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

61. Effect of the uncoupling protein-2 (UCP-2) and nuclear receptor subfamily 3 group C member 1 (NR3C1) genes on treatment efficacy and survival in patients with multiple myeloma: a single-center study

Demir I., Pehlivan S., Okan V., ŞAHİN H. H., Durusoy S. S., Serin I., et al.
BMC RESEARCH NOTES , cilt.14, sa.1, 2021 (ESCI) identifier identifier

62. Medication-related osteonecrosis of the jaw (MRONJ) and eNOS Polymorphisms in multiple myeloma patients: a single center experience.

Taş Ozyurtseven B., Serin I., Nursal A. F., Pehlivan S., Pehlivan M.
BMC oral health , cilt.21, ss.272, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

63. Impact of UCP2 -866G/A Variant on Smoking Risk

NURSAL A. F., Uysal M. A., PEHLİVAN M., Sever U., Pehlivan S.
BEZMIALEM SCIENCE , cilt.9, sa.2, ss.185-189, 2021 (ESCI) identifier identifier

64. Mannose binding lectin gene 2 (rs1800450) missense variant may contribute to development and severity of COVID-19 infection.

Medetalibeyoglu A., Bahat G., Senkal N., Kose M., Avcı K., Sayın G., et al.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases , cilt.89, ss.104717, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

65. DNA Repair Genes and Chronic Myeloid Leukemia: ERCC2 (751), XRCC1 (399), XRCC4-Intron 3, XRCC4 (-1394) Gene Polymorphisms

Ozdilli K., Pehlivan M., Serin I., Savran F., Tomatir A. G., PEHLİVAN S.
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES , cilt.13, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

66. A new parameter in multiple myeloma: CYP3A4*1B single nucleotide polymorphism

Serin I., Pehlivan S., GÜNDEŞ İ., Fidan Oyaci Y., PEHLİVAN M.
ANNALS OF HEMATOLOGY , cilt.100, sa.2, ss.421-427, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

67. Global and glucocorticoid receptor gene-specific (NR3C1) DNA methylation analysis in patients with cannabinoid or synthetic cannabinoid use disorder.

Pehlivan S., Aytac H. M., Cetinay Aydin P., Nursal A. F., Pehlivan M.
Psychiatry research , cilt.298, ss.113774, 2021 (SCI-Expanded) identifier identifier identifier

68. Detection of altered methylation of MB-COMT promotor and DRD2 gene in cannabinoid or synthetic cannabinoid use disorder regarding gene variants and clinical parameters.

Oyaci Y., Aytac H. M., Pasin O., Cetinay Aydin P., Pehlivan S.
Journal of addictive diseases , cilt.39, sa.4, ss.526-536, 2021 (SSCI) identifier identifier identifier

69. A relationship between endothelial nitric oxide synthetase gene variants and substance use disorder

Pehlivan S., Aydin P. C., Nursal A. F., Pehlivan M., Oyaci Y., Yazici A. B.
Endocrine, Metabolic and Immune Disorders - Drug Targets , cilt.21, sa.9, ss.1679-1684, 2021 (SCI-Expanded) identifier identifier identifier

70. UCP2 and CFH Gene Variants with Genetic Susceptibility to Schizophre-nia in Turkish Population

NURSAL A. F., Aydin P. C., PEHLİVAN M., Sever U., Pehlivan S.
ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS , cilt.21, sa.11, ss.2084-2089, 2021 (SCI-Expanded) identifier identifier identifier

71. Role of MIF -173G/C and Mbl2 codon 54A/B variants in risk of multiple myeloma: An association study.

Pehlivan M., Nursal A., Gündeş İ., Oyacı Y., Kıvanç D., Pehlivan S.
Endocrine, metabolic & immune disorders drug targets , cilt.21, ss.925-931, 2021 (SCI-Expanded) identifier identifier identifier

72. Macrophage Migration Inhibitory Factor-173 G/C Polymorphism is Associated With The Age of Onset and Insight in Schizophrenia in the Turkish Population

Aytac H. M., Oyaci Y., Yazar M. S., Pehlivan S.
NEUROLOGICAL RESEARCH , cilt.43, sa.12, ss.977-984, 2021 (SCI-Expanded) identifier identifier identifier

73. The miRNA 196a2 rs11614913 variant has prognostic impact on Turkish patients with multiple myeloma.

Kirik M. P., Pehlivan M., Nursal A. F., Oyaci Y., Pehlivan S., Serin I.
BMC research notes , cilt.13, ss.545, 2020 (ESCI) Sürdürülebilir Kalkınma identifier identifier identifier

74. Role of CYP3A4*1B Gene Variant In Substance Use Disorder

Çapar G., Şentürk Çiftçi H., Pehlivan S.
Sağlık Bilimlerinde İleri Araştırmalar Dergisi , cilt.3, sa.3, ss.130-134, 2020 (Hakemli Dergi)

75. TNF-α-308 G/A variant may be associated with bipolar disorder in a Turkish population

Nursal A. F., Aytac H. M., Ciftci H., Yazar M. S., Oyaci Y., Pehlivan M., et al.
ARCHIVES OF CLINICAL PSYCHIATRY , sa.6, ss.176-179, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

76. The role of endothelial nitric oxide synthase gene polymorphisms in patients with lung cancer

Kocer C., Benlier N., Balci S. O., PEHLİVAN S., Sanli M., Nacak M.
CLINICAL RESPIRATORY JOURNAL , cilt.14, sa.10, ss.948-955, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

77. Association of Myeloperoxidase Gene Functional Variant with Schizophrenia and Smoking in a Turkish Population

Pehlivan S., Aydin P. C., Uysal M. A., NURSAL A. F., Kurnaz S., Sever U., et al.
MEDICAL JOURNAL OF BAKIRKOY , cilt.16, sa.3, ss.197-202, 2020 (ESCI) identifier

78. Association of MIF and MBL2 gene polymorphisms with attempted suicide in patients diagnosed with schizophrenia or bipolar disorder

Aytac H. M., Oyaci Y., Yazar M. S., EROL A., PEHLİVAN S.
JOURNAL OF CLINICAL NEUROSCIENCE , cilt.78, ss.264-268, 2020 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

79. Evaluation of COMT (rs4680), CNR2 (rs2501432), CNR2 (rs2229579), UCP2 (rs659366), and IL-17 (rs763780) gene variants in synthetic cannabinoid use disorder patients

PEHLİVAN S., Aytac H. M., Kurnaz S., Pehlivan M., Aydin P. C.
JOURNAL OF ADDICTIVE DISEASES , cilt.38, sa.4, ss.495-505, 2020 (SSCI) Sürdürülebilir Kalkınma identifier identifier identifier

80. The Relationship Between Cd 74 Levels, Macrophage Migration Inhibitory Factor Gene Polymorphism and Clinical Features in Patients with Ankylosing Spondylitis

Akaltun M. S., Pehlivan S., KARSLIGİL T., ALTINDAĞ Ö., AYDENİZ A., GÜR A., et al.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.26, sa.2, ss.97-102, 2020 (ESCI) identifier

81. PER3 VNTR variant and susceptibility to smoking status/substance use disorder in a Turkish population

Nursal A. F., Aydin P. C., Uysal M. A., Pehlivan M., Oyac Y., PEHLİVAN S.
ARCHIVES OF CLINICAL PSYCHIATRY , cilt.47, sa.3, ss.71-74, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

82. Viral Pandemics as Possible Psycho-immunological Causes of Psychiatric Symptoms: From Past to Present

Aytaç H. M., Pehlivan S.
İstanbul Üniversitesi Sağlık Bilimleri Enstitüsü Sağlık Bilimlerinde İleri Araştırmalar Dergisi , cilt.3, sa.1, ss.92-98, 2020 (Hakemli Dergi)

83. THE miR-196a2T/C VARIANT AS A POSSIBLE PREDISPOSING FACTOR FOR ANKYLOSING SPONDYLITIS IN A TURKISH POPULATION2

Pehlivan S., Gursoy S., Nursal A. F., Akaltun M. S., Ozdilli K., Pehlivan M.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , cilt.83, ss.81-85, 2020 (ESCI) identifier

84. Is Complement Factor H Tyr402His Variant a Potential Cause of Ankylosing Spondylitis?

PEHLİVAN S., Akaltun M. S., Pehlivan M., Gursoy S., Nursal A. F.
HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , cilt.58, sa.2, ss.142-147, 2020 (ESCI) Creative Commons License identifier identifier

85. The role of cholesteryl ester transfer protein TaqIB polymorphism in young atheroscleroticmheart disease

Pehlivan S., İlanbey B., Kayıkçıoğlu L. M., Sezer E., Girgin Sağın F., Özkınay F. F., et al.
Int J Med Biochem , cilt.3, sa.1, ss.8-13, 2020 (Hakemli Dergi) Creative Commons License Sürdürülebilir Kalkınma

86. Investigating the eNOS and IFN-γ Gene Variants Susceptible to Bipolar Disorder or Schizophrenia in a Turkish Cohort

PEHLİVAN S., Aytac H. M., ŞENTÜRK ÇİFTÇİ H., Oyaci Y., Pehlivan M., Nursal A. F.
PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY , cilt.30, sa.4, ss.354-361, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

87. The MIF RS755622 variant may increase susceptibility of breast cancer but not gastrointestinal cancer in a Turkish population

Pehlivan S., Işiksaçan N., Pehlivan M., Günaldi M., Oyaci Y., Nursal A. F.
Turk Onkoloji Dergisi , cilt.35, sa.3, ss.283-288, 2020 (ESCI) Sürdürülebilir Kalkınma identifier identifier

88. Investigation of catechol-O-methyltransferase and cannabinoid receptor 2 gene variants in tobacco use disorder or tobacco use disorder and schizophrenia comorbidity Tütün kullanım bozukluğu veya tütün kullanım bozukluğu ve şizofreni komorbiditesinde katekol-o-metiltransferaz ve kannabinoid reseptör 2 gen varyantlarının incelenmesi

Pehlivan S., Çetinay Aydin P., Aytaç H. M., Uysal M. A., Sever Ü., Pehlivan M.
Anadolu Psikiyatri Dergisi , cilt.21, sa.6, ss.572-578, 2020 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier

89. Dopamine D4 Receptor Gene Exon III VNTR Variant Influences Smoking Status in Turkish Population

Uysal M. A., Sever U., NURSAL A. F., Pehlivan S., Bahadir A., Yurt S., et al.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY , cilt.56, sa.4, ss.248-252, 2019 (SCI-Expanded) identifier identifier identifier

90. CNR2 rs2229579 and COMT Val158Met variants, but not CNR2 rs2501432, IL-17 rs763780 and UCP2 rs659366, contribute to susceptibility to substance use disorder in the Turkish population

Kurnaz S., Yazici A. B., NURSAL A. F., Aydin P. C., Atar A. O., Aydin N., et al.
PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY , cilt.29, sa.4, ss.847-853, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

91. Genetic factors associated with the predisposition to late onset Alzheimer's disease

DURMAZ A., Kumral E., Durmaz B., ONAY H., Aslan G. I., Ozkinay F., et al.
GENE , cilt.707, ss.212-215, 2019 (SCI-Expanded) identifier identifier identifier

92. Paraoxonase-1 Polymorphisms (L55M/Q192R) and Activities (PONase/AREase) in Patients with Idiopathic Recurrent Early Pregnancy Loss: A Preliminary Study

Ozturk E., Pehlivan S., Ozcan C., UĞUR M. G., Balat O.
GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.23, sa.7, ss.501-505, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

93. CYP2A6 gene variants may explain smoking status in a Turkish cohort

Pehlivan S., Uysal M. A., Cagatay T., NURSAL A. F., Cinar Ç., Erkan F., et al.
PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY , cilt.29, sa.3, ss.340-345, 2019 (SCI-Expanded) identifier identifier

94. THE ASSOCIATION OF GVHD WITH HLA DR ALLELES, IFN-GAMMA, TGF-BETA, AND MBL2 GENE POLYMORPHISM

Oguz R., Ciftci H., Gokce M., Ogret Y., Karadeniz S., Pehlivan S., et al.
HLA , cilt.93, sa.5, ss.368, 2019 (SCI-Expanded) identifier

95. Association of XRCC1 and XPD functional gene variants with nicotine dependence and/or schizophrenia: a case-control study and in silico analysis

Pehlivan S., Aydin N., Nursal A. F., Uysal M. A., Pehlivan M., Tekcan A., et al.
PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY , cilt.29, sa.1, ss.21-27, 2019 (SCI-Expanded) identifier identifier

96. Effect of monoamine oxidase B A644G variant on nicotine dependence and/or schizophrenia risk

Pehlivan S., Aydin P. C., Uysal M. A., Ciftci H. S., Sever U., Yavuz F. K., et al.
ARCHIVES OF CLINICAL PSYCHIATRY , cilt.46, sa.1, ss.21-24, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

97. Synthesis of New Anthraquinone Derivatives and Anticancer Effects on Breast Cancer Cell Lines

Hacıosmanoğlu E., ÖZKÖK F., Onsu A. K., BEKTAŞ M., VAROL B., PEHLİVAN S.
The Eurasia Proceedings of Science, Technology, Engineering & Mathematics (EPSTEM) , cilt.4, ss.271-276, 2018 (Hakemli Dergi) Sürdürülebilir Kalkınma

98. DNA Repair Gene (XPD, XRCC4, and XRCC1) Polymorphisms in Patients with Endometrial Hyperplasia: A Pilot Study

Orturk E., Pehlivan S., Balat O., UĞUR M. G., ÖZCAN H. Ç., ERKILIÇ S.
MEDICAL SCIENCE MONITOR BASIC RESEARCH , cilt.24, ss.146-150, 2018 (ESCI) identifier identifier identifier

99. SYNTHESIS OF NEW ANTHRAQUINONE DERIVATES AND ANTICANCER EFFECTS ONBREAST CANCER CELL LINES

HACIOSMANOĞLU E., ÖZKÖK F., önsu a., BEKTAŞ M., VAROL B., PEHLİVAN S.
the eurasia proceedings of science technology,engineering,mathematics , 2018 (Hakemli Dergi) Sürdürülebilir Kalkınma

100. Endothelial Nitric Oxide Synthase Gene Variants and Susceptibility to Chronic Myeloid Leukemia (Ph plus )

PEHLİVAN M., Pehlivan S., KAYNAR L., Sever T., YILMAZ M., Eser B., et al.
INTERNATIONAL JOURNAL OF HUMAN GENETICS , cilt.18, sa.3, ss.247-252, 2018 (SCI-Expanded) identifier

101. Is there any Association between the Functional Variants of the NOS3 Gene and Psoriasis?

Pehlivan S., Inaloz H. S., NURSAL A. F., Gulel A., PEHLİVAN M.
ISTANBUL MEDICAL JOURNAL , cilt.19, sa.2, ss.152-157, 2018 (ESCI) identifier

102. XRCC4 rs6869366 polymorphism is associated with susceptibility to both nicotine dependence and/or schizophrenia

Pehlivan S., Uysal M. A., Aydin N., NURSAL A. F., PEHLİVAN M., Yavuzlar H., et al.
ARCHIVES OF CLINICAL PSYCHIATRY , cilt.45, sa.3, ss.53-56, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

103. Effect of the IL-17F rs763780 Variant on Chronic Lymphocytic Leukemia and Multiple Myeloma Risk in a Turkish Cohort

NURSAL A. F., PEHLİVAN M., Kurnaz S., Pehlivan S.
ISTANBUL MEDICAL JOURNAL , cilt.19, sa.1, ss.39-42, 2018 (ESCI) Sürdürülebilir Kalkınma identifier

104. Effect of the IL-17F rs763780 variant on chronic lymphocytic leukemia and multiple myeloma risk in a Turkish cohort.

Nursal A. F., pehlivan M., Kurnaz S., PEHLİVAN S.
Istanbul Med J , cilt.19, ss.39-42, 2018 (Hakemli Dergi)

105. - Are there any association between functional variants of NOS3 gene and Psoriasis?

PEHLİVAN S., INALOZ S., Nursal A. F., Gülel A., pehlivan M.
Istanbul Med J , cilt.19, ss.152-157, 2018 (Hakemli Dergi)

106. Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome

KILIÇ B. D., BÜYÜKÇELİK M., OĞUZKAN BALCI S., Pehlivan S., KUL S., Col N., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.2, ss.295-303, 2018 (SCI-Expanded) identifier identifier identifier

107. Possible association between DNA repair gene variants and cannabis dependence in a Turkish cohort: a pilot study

Pehlivan S., Yazici A. B., Aydin N., NURSAL A. F., Kurnaz S., Atar A. O., et al.
PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY , cilt.28, sa.4, ss.402-407, 2018 (SCI-Expanded) identifier identifier

108. Association of the TNF-alpha, IL-2, and IL-2RB gene variants with susceptibility to psoriasis in a Turkish cohort

Gulel A., Inaloz H. S., NURSAL A. F., Sever T., Pehlivan S.
CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.43, sa.1, ss.50-57, 2018 (SCI-Expanded) identifier identifier identifier

109. Interleukin-1 gene variants and the risk of non-syndromic microtia

Nursal A. F., Bekerecioğlu M., BUYUKGURAL B., PEHLİVAN S.
Pam Med J , cilt.11, sa.2, ss.89-94, 2018 (Hakemli Dergi)

110. Glutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss

Tunc O., Baysal E., OĞUZKAN BALCI S., Mumbuc S., Tunc N. G., Pehlivan S., et al.
ENT UPDATES , cilt.7, sa.3, ss.126-130, 2017 (ESCI) identifier

111. Cytokine gene variants/expressions and non-syndromic microtia - is there a link?

NURSAL A. F., BEKERECİOĞLU M., Pehlivan S., Sever T., Buyukgural B.
ENT UPDATES , cilt.7, sa.2, ss.62-67, 2017 (ESCI) identifier

112. Influence of promoter region of TNF-? gene polymorphisms on anti-TNF treatment in rheumatoid arthritis: Preliminary report

Harunlar T., Aydeniz A., PEHLİVAN S., pehlivan M., Altindag O., gürsoy s.
Pamukkale Medical Journal , cilt.10, sa.3, ss.216-220, 2017 (Hakemli Dergi)

113. The functional variants of endothelial nitric oxide synthase gene associated with rheumatoid arthritis in Turkish adults

Pehlivan S., Aydeniz A., Sever T., Altindag O., Pehlivan M., Gursoy S., et al.
CLINICAL RHEUMATOLOGY , cilt.36, sa.3, ss.537-540, 2017 (SCI-Expanded) identifier identifier identifier

114. MBL2 and MIF gene polymorphisms in cardiovascular patients with atherosclerotic lesions undergoing heart valve replacement

Eksi F., Pehlivan S., Erdogan M. B., Bayram A., Oguzkan-Balci S., YAMAK B., et al.
BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT , cilt.31, sa.6, ss.1173-1177, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

115. Effect of Cytokine Genes in the Pathogenesis and on the Clinical Parameters for the Treatment of Multiple Myeloma

Haydaroglu H., Balci S. O., Pehlivan S., Ozdilli K., Gundogan E., Okan V., et al.
IMMUNOLOGICAL INVESTIGATIONS , cilt.46, sa.1, ss.10-21, 2017 (SCI-Expanded) identifier identifier identifier

116. The Endothelial Nitric Oxide Synthase Gene Variants as a Risk Factor for Chronic Lymphocytic Leukemia

PEHLİVAN M., TOMATIR A. G., Nursal A. F., ŞAHİN H. H., Pehlivan S.
UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.27, sa.2, ss.85-90, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

117. eNOS and XRCC4 VNTR variants contribute to formation of nicotine dependence and/or schizophrenia

Pehlivan S., Uysal M. A., Aydin P. C., Pehlivan M., Nursal A. F., Yavuzlar H., et al.
BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY , cilt.118, sa.8, ss.467-471, 2017 (SCI-Expanded) identifier identifier identifier

118. The roles of endothelial nitric oxide synthase (eNOS) and myeloperoxidase (MPO) genes in microtia

Buyukgural B., Pehlivan S., NURSAL A. F., BEKERECİOĞLU M.
ENT Updates , cilt.6, sa.3, ss.121-125, 2016 (ESCI) identifier

119. The dopamine receptor D4 VNTR 48bp gene variant in nicotine addiction

Uysal M. A., Sever U., PEHLİVAN S.
EUROPEAN RESPIRATORY JOURNAL , cilt.48, 2016 (SCI-Expanded) identifier

120. Relationship between cigarette (nicotine) addiction and dopamine receptor D2 gene variants (TaqlA and-141C Ins/Del)

Sever U., Uysal M. A., PEHLİVAN S.
EUROPEAN RESPIRATORY JOURNAL , cilt.48, 2016 (SCI-Expanded) identifier

121. Analysis of CYP2A6 and CYP2A13 genes using new generation sequencing method in smokers and non-smokers

Pehlivan S., Uysal M. A., Cagatay T., Cinar Ç., Erkan F., Sever U., et al.
EUROPEAN RESPIRATORY JOURNAL , cilt.48, 2016 (SCI-Expanded) identifier

122. The Associations of IL-6, IFN-gamma, TNF-alpha, IL-10, and TGF-beta 1 Functional Variants with Acute Myeloid Leukemia in Turkish Patients

Nursal A. F., PEHLİVAN M., ŞAHİN H. H., Pehlivan S.
GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.20, sa.9, ss.544-551, 2016 (SCI-Expanded) identifier identifier identifier

123. Effects of TNFalpha, NOS3, MDR1 gene polymorphisms on clinical parameters, prognosis and survival of multiple myeloma cases

Basmaci C., Pehlivan M., Tomatir A., Sever T., Okan V., Yilmaz M., et al.
Asian Pacific Journal of Cancer Prevention , cilt.17, sa.3, ss.1009-1014, 2016 (SCI-Expanded) Creative Commons License identifier identifier

124. Cytokine gene polymorphisms and expression in Turkish pediatric cochlear implant patients

BAYSAL E., OĞUZKAN BALCI S., Celenk F., Kahraman M., Deniz M., Tunc O., et al.
ENT UPDATES , cilt.6, sa.1, ss.1-4, 2016 (ESCI) identifier

125. Significance of the T3151, T317L, E255K AND Y253H BCR-ABL gene mutations in Philadelphia positive Chronic Myeloid Leukemia patients

KIS C., PEHLİVAN S., ESER B., YILMAZ M., KAYNAR L., Oğuzkan Balcı S., et al.
Kahramanmaraş Sütçü İmam Üniversitesi Tıp Fakültesi Dergisi , cilt.11, sa.2, ss.9-13, 2016 (Hakemli Dergi)

126. Might there be a link between high expression of interleukine 10 and Netherton Syndrome?.

PEHLİVAN S., Oğuzkan Balcı S., INALOZ S., KESKIN Ö., Küçükosmanoğlu E., Gülel A., et al.
Kahramanmaraş Sütçü İmam Üniversitesi Tıp Fakültesi Dergisi , cilt.11, sa.2, ss.1-5, 2016 (Hakemli Dergi)

127. Genetic contributing factors to substance abuse: an association study between eNOS gene polymorphisms and cannabis addiction in a Turkish population

Isir A. B., Nacak M., Balci S. O., Aynacioglu A. S., Pehlivan S.
AUSTRALIAN JOURNAL OF FORENSIC SCIENCES , cilt.48, sa.6, ss.676-683, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

128. Male Individualization Based on Y-Chromosomal Short Tandem Repeats: A Comparative Information Theoretical Analysis of 16 Y-STR Loci in Central Anatolia and Iraqi Populations

ISIR A. B., Ozkorkmaz A., Baransel C., GÖKALP ÖZKORKMAZ E., Pehlivan S.
INTERNATIONAL JOURNAL OF HUMAN GENETICS , cilt.15, sa.4, ss.157-171, 2015 (SCI-Expanded) identifier identifier

129. Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation

ROSTI R. O., Uyguner Z. O., NAZARENKO I., Bekerecioglu M., CADILLA C. L., Ozgur H., et al.
CLINICAL GENETICS , cilt.88, sa.5, ss.489-493, 2015 (SCI-Expanded) identifier identifier identifier

130. Q192R and L55M Polymorphisms of Paraoxonase 1 Gene in Chronic Myelogenous Leukemia and Chronic Lymphocytic Leukemia

TOMATIR A. G., Pehlivan S., ŞAHİN H. H., OĞUZKAN BALCI S., Budeyri S., PEHLİVAN M.
ANTICANCER RESEARCH , cilt.35, sa.9, ss.4807-4812, 2015 (SCI-Expanded) identifier identifier identifier

131. Investigation of interleukin-12, interleukin-17 and interleukin-23 receptor gene polymorphisms in alopecia areata

AYTEKIN N., Akcali C., Pehlivan S., Kirtak N., Inaloz S.
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , cilt.43, sa.4, ss.526-534, 2015 (SCI-Expanded) identifier identifier identifier

132. Relationship between the 1359 G/A polymorphism of the Central Cannabinoid Receptor 1 (CNR1) gene and susceptibility to cannabis addiction in a Turkish population

ISIR A. B., NACAK M., OĞUZKAN BALCI S., PEHLİVAN S., KUL S., Benlier N., et al.
AUSTRALIAN JOURNAL OF FORENSIC SCIENCES , cilt.47, sa.2, ss.230-238, 2015 (SCI-Expanded) identifier

133. Might There Be a Link Between Intron 3 VNTR Polymorphism in the XRCC4 DNA Repair Gene and the Etiopathogenesis of Rheumatoid Arthritis?

Pehlivan S., Balci S. O., Aydeniz A., Pehlivan M., Sever T., Gursoy S.
GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.19, sa.1, ss.48-51, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

134. Allele frequencies for 13 STRs loci in a Western Anatolia population and their forensic evaluation.

Baransel I., OZKORKMAZ A., Pehlivan S.
Annals of human biology , cilt.42, ss.494-7, 2015 (SCI-Expanded) identifier identifier identifier

135. Gene Polymorphisms and Febrile Neutropenia in Acute Leukemia-No Association with IL-4, CCR-5, IL-1RA, but the MBL-2, ACE, and TLR-4 Are Associated with the Disease in Turkish Patients: A Preliminary Study

Pehlivan M., Sahin H. H., Ozdilli K., ONAY H., ÖZCAN A., Ozkinay F., et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.18, sa.7, ss.474-481, 2014 (SCI-Expanded) identifier identifier identifier

136. Prognostic importance of single-nucleotide polymorphisms in IL-6, IL-10, TGF-β1, IFN-γ, and TNF-α genes in chronic phase chronic myeloid leukemia.

Pehlivan M., Sahin H. H., Pehlivan S., Ozdilli K., KAYNAR L., Oguz F. S., et al.
Genetic testing and molecular biomarkers , cilt.18, sa.6, ss.403-9, 2014 (SCI-Expanded) identifier identifier identifier

137. CYTOKINE GENE POLYMORPHISMS IN TURKISH PATIENTS WITH CHRONIC MYELOID LEUKAEMIA AND IN HEALTHY CONTROLS

Ozdilli K., Pehlivan S., Ogret Y., Sever T., Pehlivan M., Issever H., et al.
NOBEL MEDICUS , cilt.10, sa.1, ss.74-78, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

138. Cytokine Gene Polymorphisms in Childhood Dilated Cardiomyopathy: Interferon- gamma, Tumor Necrosis Factor-alpha and Transforming Growth Factor - beta 1 Genes Are Associated with the Disease in Turkish Patients.

BALCI S., COL-ARAZ N., BASPINAR O., SEVER T., BALAT A., Pehlivan S.
Iranian journal of pediatrics , cilt.23, ss.603-4, 2013 (SCI-Expanded) identifier identifier identifier

139. Association of macrophage migration inhibitory factor and mannose-binding lectin-2 gene polymorphisms in acute rheumatic fever

Col-Araz N., Pehlivan S., Baspinar O., Sever T., Oguzkan-Balci S., Balat A.
CARDIOLOGY IN THE YOUNG , cilt.23, sa.4, ss.486-490, 2013 (SCI-Expanded) identifier identifier identifier

140. Uteroglobin gene polymorphism in childhood nephrotic syndrome

KILIÇ B. D., BÜYÜKÇELİK M., OĞUZKAN BALCI S., PEHLİVAN S., KUL S., Araz N. C., et al.
PEDIATRIC NEPHROLOGY , cilt.28, sa.8, ss.1461-1462, 2013 (SCI-Expanded) identifier

141. The relationship of metalloproteinase gene polymorphisms and lung cancer

ŞANLI M., Akar E., PEHLİVAN S., Bakir K., TUNÇÖZGÜR B., IŞIK A. F., et al.
JOURNAL OF SURGICAL RESEARCH , cilt.183, sa.2, ss.517-523, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma identifier

142. Mitochondrial uncoupling protein 2 (UCP2) gene polymorphisms are associated with childhood obesity and related metabolic disorders

Oguzkan-Balci S., Col-Araz N., Nacak M., Araz M., Sabanci H., Balat A., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.26, ss.277-283, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

143. The polymorphisms of the MBL2 and MIF genes associated with Pediatric Cochlear Implant Patients

Baysal E., Oguzkan-Balci S., Tunc O., Celenk F., Deniz M., Kanlikama M., et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , cilt.77, sa.3, ss.338-340, 2013 (SCI-Expanded) identifier identifier identifier

144. Can mycoplasma contribute to formation of prostate cancer?

erturhan s. m., bayrak ö., PEHLİVAN S., özgül h., seçkiner i., Sever T., et al.
INTERNATIONAL UROLOGY AND NEPHROLOGY , cilt.45, sa.1, ss.33-38, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier identifier

145. Negatif Kronik Myeloproliferatif Hastalıkların Moleküler Patogenezi

PEHLİVAN S., Ozdilli K.
Türkiye Klinikleri J Hematol-Special Topics , cilt.6, sa.2, ss.4-9, 2013 (Hakemli Dergi)

146. Association of an LMP2 Polymorphism with Acute Myeloid Leukemia and Multiple Myeloma

Ozbas-Gerceker F., Bozman N., Kok S., Pehlivan M., Yilmaz M., Pehlivan S., et al.
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION , cilt.14, sa.11, ss.6399-6402, 2013 (SCI-Expanded) identifier identifier identifier

147. Association of TAP1 and TAP2 gene polymorphisms with hematological malignancies.

OZBAS-GERCEKER F., BOZMAN N., GEZICI S., PEHLIVAN M., YILMAZ M., Pehlivan S., et al.
Asian Pacific journal of cancer prevention : APJCP , cilt.14, ss.5213-7, 2013 (SCI-Expanded) identifier identifier identifier

148. Trends in the frequency of HLA DR-DQ haplotypes among children and adolescents with type 1 diabetes mellitus in the Southeast Region of Turkey.

KESKIN M., AYGÜN A., Pehlivan S., KESKIN Ö., KOR Y., BALAT A., et al.
Journal of clinical research in pediatric endocrinology , cilt.4, ss.189-92, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

149. First Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Turkish Silver-Russell Syndrome Patients

KARACA E., Tuysuz B., Pehlivan S., Ozkinay F.
IRANIAN JOURNAL OF PEDIATRICS , cilt.22, sa.4, ss.445-451, 2012 (SCI-Expanded) identifier identifier identifier

150. Childhood obesity and the role of dopamine D2 receptor and cannabinoid receptor-1 gene polymorphisms.

Col A., NACAK M., Oguzkan B., BENLIER N., ARAZ M., Pehlivan S., et al.
Genetic testing and molecular biomarkers , cilt.16, ss.1408-12, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

151. Analysis of Dopamine D2 Receptor (DRD2) Gene Polymorphisms in Cannabinoid Addicts

Nacak M., Isir A. B., Balci S. O., Pehlivan S., Benlier N., Aynacioglu S.
JOURNAL OF FORENSIC SCIENCES , cilt.57, sa.6, ss.1621-1624, 2012 (SCI-Expanded) identifier identifier identifier identifier

152. Research on and clinical importance of duplications in various chromosomal regions in addition to Philadelphia chromosome in chronic myeloid leukemia.

SEVER T., KILICARSLAN C., PEHLIVAN M., KAYNAR L., YILMAZ M., ESER B., et al.
Journal of B.U.ON. : official journal of the Balkan Union of Oncology , cilt.17, ss.490-6, 2012 (SCI-Expanded) identifier identifier identifier

153. Role of cytokine gene (IFN-γ, TNF-α, TGF-β1, IL-6, and IL-10) polymorphisms in pathogenesis of acute rheumatic fever in Turkish children.

COL-ARAZ N., Pehlivan S., BASPINAR O., OGUZKAN-BALCI S., SEVER T., BALAT A.
European journal of pediatrics , cilt.171, ss.1103-8, 2012 (SCI-Expanded) identifier identifier identifier

154. SERUM TOTAL SIALIC ACID LEVELS AND SIALIC ACID ACETYL ESTERASE GENE VARIATION IN PATIENTS WITH PREECLAMPSIA

Gul O., Ozturk E., UĞUR M. G., Cebesoy F. B., Kurtul N., Pence S., et al.
TURKISH JOURNAL OF OBSTETRICS AND GYNECOLOGY , cilt.9, sa.2, ss.99-106, 2012 (ESCI) identifier

155. Pereklamptik Gebelerde Serum Total Sialik Asit Seviyeleri ve Sialik Asit Esteraz Gen Varyasyonu

gül ö., OZTÜRK E., uğur m. g., CEBESOY F., kurtul n., PENÇE S., et al.
TÜRK JİNEKOLOJİ VE OBSTETRİK DERNEĞİ DERGİSİ , cilt.9, ss.99-105, 2012 (Scopus)

156. Mannose binding lectin and macrophage migration inhibitory factor gene polymorphisms in Turkish children with cardiomyopathy: no association with MBL2 codon 54 A/B genotype, but an association between MIF -173 CC genotype.

COL-ARAZ N., OGUZKAN-BALCI S., BASPINAR O., SEVER T., BALAT A., Pehlivan S.
International journal of medical sciences , cilt.9, ss.506-12, 2012 (SCI-Expanded) identifier identifier identifier

157. Association of endothelial nitric oxide synthase gene polymorphisms with endometrial carcinoma: a preliminary study

Ozturk E., Dikensoy E., Balat O., Ugur M. G., Balci S. O., Aydin A., et al.
JOURNAL OF THE TURKISH-GERMAN GYNECOLOGICAL ASSOCIATION , cilt.12, sa.4, ss.229-233, 2011 (ESCI) Sürdürülebilir Kalkınma identifier identifier identifier

158. Endothelial nitric oxide synthase gene polymorphisms in preeclampsia with or without eclampsia in a Turkish population.

OZTÜRK E., BALAT O., Pehlivan S., UGUR M., OZCAN C., SEVER T., et al.
The journal of obstetrics and gynaecology research , cilt.37, ss.1778-83, 2011 (SCI-Expanded) identifier identifier identifier

159. DNA repair genes polymorphisms in multiple myeloma: no association with XRCC1 (Arg399Gln) polymorphism, but the XRCC4 (VNTR in intron 3 and G-1394T) and XPD (Lys751Gln) polymorphisms is associated with the disease in Turkish patients.

CIFCI S., YILMAZ M., PEHLIVAN M., SEVER T., OKAN V., Pehlivan S.
Hematology (Amsterdam, Netherlands) , cilt.16, ss.361-7, 2011 (SCI-Expanded) identifier identifier identifier

160. Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population.

BULUT H., PEHLIVAN M., ALPER S., TOMATIR A., ONAY H., YÜKSEL S., et al.
Genetics and molecular research : GMR , cilt.10, ss.4126-32, 2011 (SCI-Expanded) identifier identifier identifier

161. Nitric oxide levels and endothelial nitric oxide synthase gene polymorphisms in Turkish women with idiopathic recurrent miscarriage.

OZTÜRK E., BALAT O., Pehlivan S., UGUR M., OZKAN Y., SEVER T., et al.
Journal of the Turkish German Gynecological Association , cilt.12, ss.234-8, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

162. No association between DNA repair gene (XPD, XRCC1, and XRCC4) polymorphisms and nonsyndromic microtia in Turkish patients.

SEVER T., BUYUKGURAL B., Pehlivan S., ROSTI R. Ö., BEKERECIOGLU M.
Plastic and reconstructive surgery , cilt.128, 2011 (SCI-Expanded) identifier identifier

163. Polymorphisms of the DNA repair gene XPD (751) and XRCC1 (399) correlates with risk of hematological malignancies in Turkish population

ÖZCAN A., Pehlivan M., Tomatir A. G., KARACA E., Ozkinay C., Ozdemir F., et al.
AFRICAN JOURNAL OF BIOTECHNOLOGY , cilt.10, sa.44, ss.8860-8870, 2011 (SCI-Expanded) identifier identifier

164. A FALSE NEGATIVE QF-PCR AND TRISOMY 18-TRISOMY 9 MOSAICISM

Dikensoy E., Balat O., PEHLİVAN S., Cebesoy F. B., Kutlar A. I., Sever T., et al.
TURKISH JOURNAL OF OBSTETRICS AND GYNECOLOGY , cilt.8, sa.1, ss.67-70, 2011 (ESCI) identifier

165. False negative QF-PCR and trisomy 18-trisomy 9 mosaicism Yanliş negati̇f QF-PCR ve tri̇zomi̇ 18-tri̇zomi̇ 9 mozai̇zma

Dikensoy E., Balat Ö., Pehlivan S., Cebesoy F. B., Kutlar A. I., Sever T., et al.
Turk Jinekoloji ve Obstetrik Dernegi Dergisi , cilt.8, sa.1, ss.67-70, 2011 (Scopus) identifier

166. Yanlış negatif QF-PCR ve Trizomi 18 – Trizomi 9 Mozaizm.

DIKENSOY E., BALAT O., PEHLİVAN S., CEBESOY F., KUTLAR I., Sever T., et al.
J Turk Soc Obstet Gynecol , cilt.8, ss.67-70, 2011 (Hakemli Dergi)

167. Genetic variation of myeloperoxidase gene contributes to preeclampsia: a preliminary association study in Turkish population.

OZTÜRK E., BALAT O., Pehlivan S., UGUR M., SEVER T.
Hypertension in pregnancy , cilt.30, ss.377-83, 2011 (SCI-Expanded) identifier identifier identifier

168. Investigation of TNF-alpha, TGF-beta 1, IL-10, IL-6, IFN-gamma, MBL, GPIA, and IL1A gene polymorphisms in patients with idiopathic thrombocytopenic purpura.

PEHLIVAN M., OKAN V., SEVER T., BALCI S., YILMAZ M., BABACAN T., et al.
Platelets , cilt.22, ss.588-95, 2011 (SCI-Expanded) identifier identifier identifier

169. Investigation of Glucocorticoid Receptor Gene Bcl-1 Polymorphism in Rheumatoid Arthritis

Aydeniz A., Sever T., PEHLİVAN S., Pehlivan M., Altindag O., Budeyri S., et al.
TURKISH JOURNAL OF RHEUMATOLOGY , cilt.26, sa.3, ss.199-203, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

170. Multidrug resistance 1 (MDR1) gene polymorphisms in childhood drug-resistant epilepsy.

ALPMAN A. A., OZKINAY F., TEKGÜL H., GÖKBEN S., Pehlivan S., Schalling M., et al.
Journal of child neurology , cilt.25, ss.1485-90, 2010 (SCI-Expanded) identifier identifier identifier

171. Gene methylation of SFRP2, P16, DAPK1, HIC1, and MGMT and KRAS mutations in sporadic colorectal cancer.

Pehlivan S., ARTAC M., SEVER T., BOZCUK H., KILINÇARSLAN C., PEHLIVAN M.
Cancer genetics and cytogenetics , cilt.201, ss.128-32, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

172. Polymorphism of the NR3C1, a Glucocorticoid Receptor Gene, in Turkish Children with Steroid-Sensitive and Resistant Nephrotic Syndrome

Gundogdu M., Buyukcelik M., PEHLİVAN S., Aydin N., Sever T., KILIÇ B. D., et al.
PEDIATRIC NEPHROLOGY , cilt.25, sa.9, ss.1914, 2010 (SCI-Expanded) identifier

173. Macrophage Migration Inhibitory Factor-173 Polymorphism in Turkish Children with Nephrotic Syndrome: A Preliminary Study

Buyukcelik M., PEHLİVAN S., KILIÇ B. D., Sever T., Balci S., Balat A.
PEDIATRIC NEPHROLOGY , cilt.25, sa.9, ss.1914, 2010 (SCI-Expanded) identifier

174. Association between urotensin II gene polymorphism and pre-eclampsia

Dikensoy E., Balat O., Ugur M. G., Pehlivan S., Balci S. O.
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY , cilt.151, sa.2, ss.140-142, 2010 (SCI-Expanded) identifier identifier identifier identifier

175. MYELOPEROXIDASE GENE PROMOTOR POLYMORPHYSM IN MOTHERS WHO HAVE A CHILD WITH NEURAL TUBE DEFECT

Dikensoy E., Sever T., PEHLİVAN S., Balat O., Cebesoy F. B., Karcin E.
TURKISH JOURNAL OF OBSTETRICS AND GYNECOLOGY , cilt.7, sa.2, ss.102-106, 2010 (ESCI) identifier identifier

176. POLYMORPHISMS OF DNA REPAIR GENES IN MULTIPLE MYELOMA; NO ASSOCIATION WITH XRCC1(399) POLYMORPHISM, BUT THE XRCC4 (VNTR IN INTRON 3 AND 1394) AND XPD (751) POLYMORPHISMS IN ASSOCIATION WITH THE DISEASE IN TURKISH PATIENTS

Ciftci S., Yilmaz M., Pehlivan M., Sever T., Okan V., Pehlivan S.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL , cilt.95, ss.585, 2010 (SCI-Expanded) identifier

177. THE IMPORTANCE OF T315I, T317L, E255K AND Y253H BCR-ABL GENE MUTATIONS IN THE PATIENTS OF CHRONIC MYELOID LEUKEMIA WHO TREATED BY IMATINIB

Kis C., Pehlivan M., Pehlivan S., Eser B., Sever T., Yilmaz M., et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL , cilt.95, ss.546, 2010 (SCI-Expanded) identifier

178. The value of XPD and XRCC1 genotype polymorphisms to predict clinical outcome in metastatic colorectal carcinoma patients with irinotecan-based regimens.

ARTAC M., BOZCUK H., Pehlivan S., AKCAN S., PEHLIVAN M., SEVER T., et al.
Journal of cancer research and clinical oncology , cilt.136, ss.803-9, 2010 (SCI-Expanded) identifier identifier identifier

179. Endothelial nitric oxide synthase gene polymorphisms associated with periodontal diseases in Turkish adults

ERCIYAS K., PEHLİVAN S., Sever T., İĞCİ M., PEHLİVAN M., ARSLAN A., et al.
AFRICAN JOURNAL OF BIOTECHNOLOGY , cilt.9, sa.21, ss.3042-3047, 2010 (SCI-Expanded) identifier identifier

180. 16 yaşıdna bir erkek olguda Pakionişi Konjenita’nın klinik bulguları.

rostı R. O., INALOZ S., ERCIYAS K., PEHLİVAN S.
MERSİN ÜNİVERSİTESİ SAĞLIK BİLİMLERİ DERGİSİ , cilt.3, sa.2, ss.26-29, 2010 (Hakemli Dergi)

181. TNF-alpha promoter polymorphisms in multiple sclerosis: no association with -308 and -238 alleles, but the -857 alleles in associated with the disease in Turkish patients.

AKCALI A., Pehlivan S., PEHLIVAN M., SEVER T., AKGUL P., NEYAL M.
International journal of immunogenetics , cilt.37, ss.91-5, 2010 (SCI-Expanded) identifier identifier identifier

182. Association between TNF-alpha, TGF-beta1, IL-10, IL-6 and IFN-gamma gene polymorphisms and generalized aggressive periodontitis.

ERCIYAS K., Pehlivan S., SEVER T., IGCI M., ARSLAN A., ORBAK R.
Clinical and investigative medicine. Medecine clinique et experimentale , cilt.33, 2010 (SCI-Expanded) identifier identifier identifier

183. Free DNA in Circulation and its Importance

PEHLİVAN S., Avci S., Sever T., Bayram A., OĞUZKAN BALCI S.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.16, sa.2, ss.75-80, 2010 (ESCI) identifier

184. Thalassemia mutations in Gaziantep, Turkey

PEHLİVAN S., Okan V., Guler E., Yilmaz M., Sever T., Dikensoy E., et al.
AFRICAN JOURNAL OF BIOTECHNOLOGY , cilt.9, sa.8, ss.1255-1258, 2010 (SCI-Expanded) identifier identifier

185. Dolaşımdaki serbest DNA ve önemi.

PEHLİVAN S., Avcı S., Sever T., Bayram A., Oğuzkan Balcı S.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.16, sa.2, ss.75-80, 2010 (Hakemli Dergi)

186. Nöral Tüp Defektli Çocuğu Olan Annelerde Myeloperoksidaz Geni Promotor Polimorfizminin Araştırılması

DIKENSOY E., Sever T., PEHLİVAN S., BALAT O., CEBESOY F.
TJOD , cilt.7, ss.251-255, 2010 (Hakemli Dergi)

187. Association of macrophage migration inhibitory factor gene promoter polymorphisms with multiple sclerosis in Turkish patients.

AKCALI A., Pehlivan S., PEHLIVAN M., SEVER T., NEYAL M.
The Journal of international medical research , cilt.38, ss.69-77, 2010 (SCI-Expanded) identifier identifier identifier

188. Genetic variation of myeloperoxidase gene contributes to aggressive periodontitis: a preliminary association study in Turkish population.

ERCIYAS K., Pehlivan S., SEVER T., ORBAK R.
Disease markers , cilt.28, ss.95-9, 2010 (SCI-Expanded) identifier identifier identifier

189. Enzyme levels and G-463A polymorphism of myeloperoxidase in chronic lymphocytic leukemia and multiple myeloma.

SAYGILI E. S., AKSOY N., PEHLIVAN M., SEVER T., YILMAZ M., CIMENCI I., et al.
Leukemia & lymphoma , cilt.50, ss.2030-7, 2009 (SCI-Expanded) identifier identifier identifier

190. Analysis of myeloperoxidase promotor polymorphism and enzyme activity in Turkish patients with vitiligo.

AKSOY S., ERBAGCI Z., SAYGILI E. S., SEVER T., ERBAGCI A., Pehlivan S.
European journal of dermatology : EJD , cilt.19, ss.576-80, 2009 (SCI-Expanded) identifier identifier identifier

191. Evaluation of the SMN and NAIP genes in a family: homozygous deletion of the SMN2 gene in the fetus and outcome of the pregnancy.

COGULU O., DURMAZ B., Pehlivan S., ALPMAN A. A., OZKINAY F.
Genetic testing and molecular biomarkers , cilt.13, ss.287-8, 2009 (SCI-Expanded) identifier identifier identifier

192. TNF-alpha, TGF-beta, IL-10, IL-6 and IFN-gamma gene polymorphisms as risk factors for brucellosis.

KARAOGLAN I., Pehlivan S., NAMIDURU M., PEHLIVAN M., KILINÇARSLAN C., BALKAN Y., et al.
The new microbiologica , cilt.32, ss.173-8, 2009 (SCI-Expanded) identifier identifier identifier

193. Importance Of Polynnorphisms Of The MIF Gene At Acute Leukemia And Its Effect On Febrile Neutropenic Attacks

Guven S., PEHLİVAN M., YILMAZ M. B., Okan V., PEHLİVAN S.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.15, sa.2, ss.5-9, 2009 (ESCI) identifier

194. Late Onset Papillon-Lefevre Syndrome (A Clinical Report)

ERCIYAS K., PEHLİVAN S., Inaloz S., Erciyas A. F., Sever T.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.15, sa.2, ss.44-48, 2009 (ESCI) identifier

195. No association Between Myeloperoxidase Gene G-463A Polymorphism and Rheumatoid Arthritis

PEHLİVAN S., Aydeniz A., Sever T., Altindag O., Oğuzkan Balcı S., Harunlar T.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.15, sa.3, ss.14-16, 2009 (Hakemli Dergi)

196. Association between IL4 (-590), ACE (I)/(D), CCR5 (Delta32), CTLA4 (+49) and IL1-RN (VNTR in intron 2) gene polymorphisms and vitiligo.

Pehlivan S., OZKINAY F., ALPER S., ONAY H., YUKSEL E., PEHLIVAN M., et al.
European journal of dermatology : EJD , cilt.19, ss.126-8, 2009 (SCI-Expanded) identifier identifier identifier

197. ANALYSIS OF CYTOKINE AND HLA DQ GENOTYPING IN TURKISH PATIENTS WITH HAIM-MUNK SYNDROME: A FAMILY STUDY

ERCIYAS K., PEHLİVAN S., Inaloz S., Erciyas A. F., Kilincarslan C., Sever T.
IUBMB LIFE , cilt.61, sa.3, ss.373, 2009 (SCI-Expanded) identifier

198. METHYLATION OF SFRP2, P16, DAPK1, HIC1 AND MGMT GENES AND RELATING K-Ras GENE (CODONS 12-13) MUTATIONS WITH COLORECTAL CANCERS

PEHLİVAN S., Artac M., Kilicarslan C., Bozcuk H., Sever T., Pehlivan M.
IUBMB LIFE , cilt.61, sa.3, ss.372, 2009 (SCI-Expanded) identifier

199. ALLELE FREQUENCIES FOR 14 STRs LOCI IN WESTERN ANATOLIA POPULATION AND THEIR FORENSIC EVALUATION

Baransel-Isir A., Ozkorkmaz A., PEHLİVAN S.
IUBMB LIFE , cilt.61, sa.3, ss.372-373, 2009 (SCI-Expanded) identifier

200. Is pregnancy loss after amniocentesis related to the volume of amniotic fluid obtained?

Cebesoy F. B., Balat O., PEHLİVAN S., Kutlar I., Dikensoy E., UĞUR M. G.
ARCHIVES OF GYNECOLOGY AND OBSTETRICS , cilt.279, sa.3, ss.357-360, 2009 (SCI-Expanded) identifier

201. Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphisms.

SERDAROĞLU G., ALPMAN A. A., TOSUN A., Pehlivan S., OZKINAY F., TEKGÜL H., et al.
Pediatric neurology , cilt.40, ss.113-6, 2009 (SCI-Expanded) identifier identifier identifier

202. Late Onset Papillon-Lefevre Sendromu Olgusu

Erciyas K., PEHLİVAN S., INALOZ S., Erciyas A. F., SEVER T.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.15, sa.2, ss.44-48, 2009 (Hakemli Dergi)

203. Akut Lösemilerde MIF Genindeki Polimorfizmlerin Önemi ve Febril Nötropenik Ataklara Etkisi.

Güven S., PEHLIVAN M., YILMAZ M., OKAN V., PEHLİVAN S.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.15, sa.2, ss.5-9, 2009 (Hakemli Dergi)

204. Türk Toplumundaki Nörofibromatozis Tip 1’li Hastalarda Gen Mutasyonlarının Araştırılması.

PEHLİVAN S., Onay H., ITIRLI G., Erbay A., Koman A., Unal D., et al.
ACTA ONCOLOGİCA TURCİCA , cilt.42, ss.13-16, 2009 (Hakemli Dergi)

205. Eritrosit Membran Hastalıkları ve Enzim Defektlerinin Moleküler Genetiği

PEHLİVAN S., pehlivan M.
Türkiye Klinikleri - Moleküler Hematoloji Özel Sayısı , cilt.2, sa.2, ss.14-21, 2009 (Hakemli Dergi)

206. Multigene methylation analysis of conventional renal cell carcinoma.

ONAY H., Pehlivan S., KOYUNCUOGLU M., KIRKALI Z., OZKINAY F.
Urologia internationalis , cilt.83, ss.107-12, 2009 (SCI-Expanded) identifier identifier identifier

207. FORENSIC VALUE OF TEN SHORT TANDEM REPEAT LOCI IN TURKEY COMPARED TO OTHER ETHNIC GROUPS

Ozkorkmaz A., ISIR A. B., PEHLİVAN S., Ozkorkmaz G. E.
BALKAN JOURNAL OF MEDICAL GENETICS , cilt.12, sa.1, ss.69-72, 2009 (SCI-Expanded) identifier identifier

208. Cytokine (IL-6, IL-10, IFN-gamma, TGF-beta 1, TNF-alpha) genotyping in Turkish children with nephrotic syndrome

Pehlivan S., Balat A., Ozdilli K., Sever T., Duvarci Y., Buyukcelik M., et al.
PEDIATRIC NEPHROLOGY , cilt.23, sa.9, ss.1646, 2008 (SCI-Expanded) identifier

209. Role of angiotensin-converting enzyme gene polymorphisms in children with sepsis and septic shock.

COGULU O., ONAY H., UZUNKAYA D., GUNDUZ C., Pehlivan S., VARDAR F., et al.
Pediatrics international : official journal of the Japan Pediatric Society , cilt.50, ss.477-80, 2008 (SCI-Expanded) identifier identifier identifier

210. Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: a preliminary study.

AYLIN A., CENGIZ T., EMIN E., NERIMAN A., Sacide P.
Neurology India , cilt.56, ss.156-60, 2008 (SCI-Expanded) identifier identifier identifier

211. The role of microsatellite instability to predict clinical benefit from irinotecan-based regimens in metastatic colorectal cancer

Artaç M., Pehlivan S., Akcan S., Pehlivan M., Gelen T., Itirli G., et al.
Turkish Journal of Cancer , cilt.38, sa.2, ss.49-56, 2008 (Scopus) Sürdürülebilir Kalkınma identifier

212. Angiotensin Converting Enzyme Gene Polymorphisms In Male Infertility

PEHLİVAN S., Onay H., TAVMERGEN E., Goker N. T., ÇOĞULU M. Ö., ÖZKINAY F. F.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.14, sa.2, ss.15-17, 2008 (ESCI) identifier

213. The role of microsatellite instability to predict from irinotekan-based regimens in metastatic colorectal cancer

ARTAC M., PEHLİVAN S., PEHLIVAN M., Gelen T., AKCAN S.
TURKISH JOURNAL OF CANCER , cilt.38, ss.49-56, 2008 (Hakemli Dergi) Sürdürülebilir Kalkınma

214. Y CHROMOSOMAL STR LOCUS DYS385 IN AZOOSPERMIC AND FERTILE MEN FROM THE AEGEAN REGION OF TURKEY: IS THERE ANY FORENSIC RELEVANCE?

Unuvar D., Isir B. A., Cankus G., Pehlivan S.
BALKAN JOURNAL OF MEDICAL GENETICS , cilt.11, sa.2, ss.39-44, 2008 (SCI-Expanded) identifier identifier

215. Biyobankalar ve Biyobankalamada Etik Konular

OZBAS-GERCEKER F., OGUZKAN-BALCI S., PEHLİVAN S.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.14, ss.35-40, 2008 (Hakemli Dergi)

216. Erkek İnfertilitesinde Anjiotensin Konverting Enzim Polimorfizmleri.

PEHLİVAN S., ONAY H., Tavmergen E., Tavmergen E. N., COGULU O., OZKINAY F.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.14, ss.15-17, 2008 (Hakemli Dergi)

217. Biobanks and Ethical Issues in Biobanking

Ozbas Gerceker F., OĞUZKAN BALCI S., PEHLİVAN S.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.14, sa.1, ss.35-40, 2008 (ESCI) identifier

218. Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.

ONAY H., UGURLU T., AYKUT A., Pehlivan S., INAL M., TINAR S., et al.
Gynecologic and obstetric investigation , cilt.66, ss.104-10, 2008 (SCI-Expanded) identifier identifier identifier

219. Pregnancy in patients with chronic myeloid leukemia treated with imatinib.

YILMAZ M., DEMIRHAN O., KUÇUKOSMANOGLU E., PEHLIVAN M., OKAN V., BALAT O., et al.
Leukemia & lymphoma , cilt.48, ss.2454-6, 2007 (SCI-Expanded) identifier identifier identifier

220. Interleukin 1 receptor antagonist gene polymorphism in childhood nephrotic syndrome

Balat A., Sever T., Kilicarslan C., Buyukcelik M., Araz N., PEHLİVAN S.
PEDIATRIC NEPHROLOGY , cilt.22, sa.9, ss.1506, 2007 (SCI-Expanded) identifier

221. Evidence of an association between mannose binding lectin codon 54 polymorphism and adenoidectomy and/or tonsillectomy in children.

KOTUROGLU G., ONAY H., MIDILLI R., Pehlivan S., EREN E., ITIRLI G., et al.
International journal of pediatric otorhinolaryngology , cilt.71, ss.1157-61, 2007 (SCI-Expanded) identifier identifier identifier

222. Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis.

VARDAR F., Pehlivan S., ONAY H., ATLIHAN F., GÜLIZ N., OZKINAY C., et al.
The Turkish journal of pediatrics , cilt.49, ss.270-3, 2007 (SCI-Expanded) identifier identifier identifier

223. Purine nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections

OZKINAY F., PEHLİVAN S., Onay H., van den Berg P., Vardar F., Koturoğlu G., et al.
JOURNAL OF CHILD NEUROLOGY , cilt.22, sa.6, ss.741-743, 2007 (SCI-Expanded) identifier identifier identifier identifier

224. Factor VIII-intron 1 inversion of Hemophilia A patients in West Anatolia

Pehlivan M., PEHLİVAN S., Büyükkeçeci F., Çağırgan S., Yılmaz M., Omay B. S., et al.
BALKAN JOURNAL OF MEDICAL GENETICS , cilt.10, sa.1, ss.49-50, 2007 (SCI-Expanded) identifier identifier

225. Might there be a link between mannose binding lectin and vitiligo?

Onay H., Pehlivan M., Alper S., Özkınay F., PEHLİVAN S.
EUROPEAN JOURNAL OF DERMATOLOGY , cilt.17, sa.2, ss.146-148, 2007 (SCI-Expanded) identifier identifier identifier identifier

226. Molecular genetic diagnosis and clinical applications in medicine

PEHLİVAN S.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.13, sa.1, ss.17-21, 2007 (ESCI) Sürdürülebilir Kalkınma identifier

227. Sağlıklı Türk Populasyonunda XRCC1 DNA Tamir Geninindeki A399G Polimorfizm Sıklığının Araştırılması.

SEVER T., PEHLİVAN S.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.13, ss.22-24, 2007 (Hakemli Dergi)

228. Türk Populasyonunda Kolesterol Ester Transfer Protein Genindeki TaqIB Polimorfizm Sıklığının Araştırılması.

KILICARSLAN C., PEHLİVAN S.
Çukurova Tıp Dergisi , cilt.31, ss.73-76, 2007 (Hakemli Dergi)

229. Tıpta Moleküler Genetik Tanı ve Klinik Uygulamaları

PEHLİVAN S.
Gaziantep Üniversitesi Tıp Fakültesi Dergisi , cilt.13, ss.17-21, 2007 (Hakemli Dergi)

230. The Frequency of XRCC1 DNA Repair Gene A399G Polymorphism In The Western Anatolia

Sever T., PEHLİVAN S.
EUROPEAN JOURNAL OF THERAPEUTICS , cilt.13, sa.1, ss.22-25, 2007 (ESCI) Sürdürülebilir Kalkınma identifier

231. Effects of β-carotene and porphyridium cruentum polysaccharide extract on mitomycin c sensitivity of blood lymphocyte chromosomes of radiology technicians

ŞENOL S. G., Pehlivan M., ÖZDEMİR G., Conk-Dalay M., Kucuk O., Pehlivan S.
Balkan Journal of Medical Genetics , cilt.9, sa.1-2, ss.63-66, 2006 (SCI-Expanded) identifier

232. Küçük RNA’ların etki mekanizmaları ve önemi

PEHLİVAN S., DURMAZ B., AYKUT A., OZKINAY F.
ARŞİV KAYNAK TARAMA DERGİSİ , cilt.15, ss.320-330, 2006 (Hakemli Dergi)

233. Exon-3 polymorphism of CTLA-4 gene in Turkish patients with vitiligo

Itirli G., Pehlivan M., Alper S., Yuksel S., Onay H., Ozkinay F., et al.
JOURNAL OF DERMATOLOGICAL SCIENCE , cilt.38, sa.3, ss.225-227, 2005 (SCI-Expanded) identifier identifier identifier

234. Might there be a link between mannose-binding lectin polymorphism and dental caries?

Pehlivan S., Koturoglu G., Ozkinay F., Alpoz A., Sipahi M., Pehlivan M.
MOLECULAR IMMUNOLOGY , cilt.42, sa.9, ss.1125-1127, 2005 (SCI-Expanded) identifier

235. Can mycoplasma-mediated oncogenesis be responsible for formation of conventional renal cell carcinoma?

Pehlivan M., PEHLİVAN S., ONAY H., Koyuncuoğlu M., Kırkali Z.
UROLOGY , cilt.65, sa.2, ss.411-414, 2005 (SCI-Expanded) identifier identifier identifier identifier

236. İzmir körfezinde gelişen bir kahverengi alg olan Cystoseria mediterranea Sauvageau’dan DNA İzolasyonu.

Sukatar İ., Sukatar A., PEHLİVAN S.
Türk sucul yaşam dergisi , cilt.13, ss.100-103, 2005 (Hakemli Dergi)

237. Does Mycoplasma sp play role in small cell lung cancer?

Pehlivan M., Itirli G., Onay H., Bulut H., Koyuncuoglu M., Pehlivan S.
LUNG CANCER , cilt.45, sa.1, ss.129-130, 2004 (SCI-Expanded) Sürdürülebilir Kalkınma identifier

238. Premalignant lesions of the kidney share the same genetics changes as conventional renal cell carcinoma

Pehlivan S., Koyuncuoglu M., Pehlivan M., Izzetoglu S., Mater Y., Cabuk M., et al.
WORLD JOURNAL OF UROLOGY , cilt.22, sa.2, ss.120-123, 2004 (SCI-Expanded) identifier

239. DNA mikroarraylerinin tıpta kullanımı ve önemi

PEHLIVAN M., ONAY H., PEHLİVAN S.
ARŞİV KAYNAK TARAMA DERGİSİ , cilt.13, ss.439-447, 2004 (Hakemli Dergi)

240. RNA polimerazların görevleri ve önemi

PEHLİVAN S., ONAY H., BULUT H., ITIRLI G., Ekmekçi A., UNUVAR D., et al.
ARŞİV KAYNAK TARAMA DERGİSİ , cilt.13, ss.575-592, 2004 (Hakemli Dergi)

241. DNA replikasyonu ve tamirinde görevli DNA polimerazlar.

PEHLİVAN S., ONAY H., ekmekçi a., UNUVAR D., BULUT H., OZKINAY F.
ARŞİV KAYNAK TARAMA DERGİSİ , cilt.13, ss.256-278, 2004 (Hakemli Dergi)

242. Kronik X ışınına maruz kalan bireylerin kromozomları üzerine beta-karoten etkisinin araştırılması

şenol s., PEHLIVAN M., bal f., PEHLİVAN S.
İZMİR ATATÜRK EĞİTİM HASTANESİ TIP DERGİSİ , cilt.41, ss.173-177, 2004 (Hakemli Dergi)

243. Screening of Y chromosome microdeletion which contains AZF regions in 71 Turkish azoospermic men

Okutman-Emonts O., PEHLİVAN S., Tavmergen E., Tavmergen-Goker E., Ozkinay F.
GENETIC COUNSELING , cilt.15, sa.2, ss.199-205, 2004 (SCI-Expanded) identifier identifier

244. Detection of achondroplasia G380R mutation from PCR amplicons by using inosine modified carbon electrodes based on electrochemical DNA chip technology

Kara P., Ozkan D., ERDEM GÜRSAN K. A., Kerman K., Pehlivan S., Ozkinay F., et al.
CLINICA CHIMICA ACTA , cilt.336, sa.1-2, ss.57-64, 2003 (SCI-Expanded) identifier identifier identifier

245. Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene

PEHLİVAN S., Ozkinay F., Okutman O., Cogulu O., Ozcan A., Cankaya T., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.45, sa.2, ss.99-101, 2003 (SCI-Expanded) identifier identifier

246. Revers Transkriptaz Polimeraz Zincir Reaksiyonu ve Uygulama Alanları

okutucu b., PEHLİVAN S.
ARŞİV KAYNAK TARAMA DERGİSİ , cilt.12, ss.138-148, 2003 (Hakemli Dergi)

247. Centromeric SMN deletions in Various Congenital Muscular Dystrophies.

Erdem H., dayangaç d., PEHLİVAN S., talim b., topaloğlu h.
TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.32, ss.145-148, 2002 (Scopus)

248. Spinal Müsküler Atrofi’de Moleküler Tanı: Ege Bölgesinde bir referans merkezindeki uygulamalar.

PEHLİVAN S., OZKINAY F., izzetoğlu s., COGULU O., kunt a., çankaya t.
EGE TIP DERGİSİ , cilt.41, ss.7-10, 2002 (Hakemli Dergi)

249. Böbreğin Renal Hücreli Kanserlerinde Prognostik Faktörlerden Cathepsin D1 Ekspresyonu ve Genetik Heterojenitenin Önemi

KOYUNCUOGLU M., PEHLIVAN M., PEHLİVAN S., Kırkalı Z.
EGE TIP DERGİSİ , cilt.40, ss.151-157, 2001 (Hakemli Dergi) Sürdürülebilir Kalkınma

250. Apoptozisin Morfolojik, Biyokimyasal ve Moleküler İşaretleri

Göncü E., PEHLİVAN S.
ARŞİV KAYNAK TARAMA DERGİSİ , cilt.10, ss.292-306, 2001 (Hakemli Dergi)

251. Hücre Siklüsü ve Moleküler Kontrolu

Okutman Ö., PEHLİVAN S.
ARŞİV KAYNAK TARAMA DERGİSİ , cilt.10, ss.277-291, 2001 (Hakemli Dergi)

252. Adhesion of hemocytes to desialylated prothoracic glands of Galleria mellonella (Lepidoptera) in the larval stage

Karacali S., Deveci R., Pehlivan S., Ozcan A.
INVERTEBRATE REPRODUCTION & DEVELOPMENT , cilt.37, sa.2, ss.167-170, 2000 (SCI-Expanded) identifier identifier

253. Deletion analysis in Turkish patients with spinal muscular atrophy

Erdem H., PEHLİVAN S., Topaloglu H., Ozguc M.
BRAIN & DEVELOPMENT , cilt.21, sa.2, ss.86-89, 1999 (SCI-Expanded) identifier

254. Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy families

Erdem H., PEHLİVAN S., Topaloglu H., Togan I., Ozguc M.
TURKISH JOURNAL OF PEDIATRICS , cilt.39, sa.4, ss.447-452, 1997 (SCI-Expanded) identifier identifier

255. Spinal müsküler atrofide prenatal tanı.

Erdem H., PEHLİVAN S., topaloğlu h.
katkı pediatri dergisi , cilt.18, ss.425-430, 1997 (Hakemli Dergi)

256. Lenfoblastoid hücre hattı oluşturulması

Erdem H., PEHLİVAN S., Özgüç M.
ÇOCUK SAĞLIĞI VE HASTALIKLARI DERGİSİ , cilt.39, ss.197-198, 1996 (Scopus)

257. DNA-PLOIDY, PROLIFERATIVE ACTIVITY, AND CONCANAVALIN-A REACTIVITY IN BREAST-CANCER

Paydaş S., Sarpel S., GILMANSACHS A., Tuncer I., PEHLİVAN S., Tunalı N., et al.
JOURNAL OF SURGICAL ONCOLOGY , cilt.56, sa.1, ss.21-24, 1994 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier identifier

258. Escherichia coli suşlarında beta-laktam antibiyotik dirençliliği ve beta-laktamaz inhibitörlerinin etkisinin in vitro üretim sisteminde izlenmesi.

Terzioğlu O., PEHLİVAN S.
ANKEM Dergisi , cilt.19, ss.176-181, 1989 (Hakemli Dergi)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 100

1. Is LCP1 rs7324845 Gene Variant Related to Obesity or NAFLD in Adolescents?

Yetim Şahin A., Hasanoğlu Sayın S., Kandemir I., Oyacı Y., Kılıç A., Pehlivan S.
European Human Genetics Conference (ESHG), Milan, İtalya, 24 - 27 Mayıs 2025, ss.1-2, (Özet Bildiri)

2. Non-alkolik karaciğer yağlanması (NAFLD) Olan Ergenlerde, VDR Gen Varyantlarının Araştırılması.

Hasanoğlu Sayın S., Kandemir İ., Tuncel F. C., Şahin M., Oyacı Y., Yetim Şahin A., et al.
47. Pediatri Günleri , İstanbul, Türkiye, 9 - 11 Nisan 2025, ss.101, (Özet Bildiri)

3. Obez Ergenlerde Nitrik Oksit Sentaz Gen Varyantları ile NAFLD Arasındaki İlişkinin Araştırılması.

Hasanoğlu Sayın S., Kandemir İ., Oyacı Y., Khudiyeva S., Şahin M., Yetim Şahin A., et al.
47. Pediatri Günleri , İstanbul, Türkiye, 9 - 11 Nisan 2025, ss.98-99, (Özet Bildiri)

4. Exploring apoptotic responses and oxidative stress regulation by curcumin and a novel curcumin analogue (B3) in glioblastoma: Insights for therapeutic strategies

quler V., Ozkok F., GÜNÇER B., PEHLİVAN S.
57th Conference of the European-Society-of-Human-Genetics (ESHG), Berlin, Almanya, 1 - 04 Haziran 2024, cilt.32, ss.915, (Özet Bildiri) identifier

5. Analysis of lncrna expression in patients with metabolic syndrome: an investigation based on RNA- sequencing data

Oyacı Y., Şenkal N., Medetalibeyoğlu A., Tuncel F. C., Köse M., Tükek T., et al.
European Human Genetics Conference, Berlin, Almanya, 1 - 04 Haziran 2024, ss.100-101, (Özet Bildiri)

6. Is there a relationship between global 5-methylcytosine and 5-hydroxymethylcytosine levels and metabolic syndrome and its clinical findings?

Pehlivan S., Şenkal N., Oyacı Y., Teberik Kama E., Pehlivan M., Tükek T., et al.
European Human Genetics Conference, Berlin, Almanya, 1 - 04 Haziran 2024, ss.100-101, (Özet Bildiri)

7. PNPLA3-rs738409 and TM6SF2-rs58542926 missense variants are associated with laboratory parameters in obese adolescents.

KHUDİYEVA S., OYACI Y., YETİM ŞAHİN A., BAŞ F., SAYIN S., KANDEMİR İ., et al.
European Human Genetics Conference, Berlin, Almanya, 01 Haziran 2024, (Tam Metin Bildiri)

8. Investigation of leukocyte telomere length and hTERT gene (MNS16A-VNTR) variant in obese adolescents.

YETİM ŞAHİN A., OYACI Y., KHUDİYEVA S., PEHLİVAN M., TUĞRUL AKSAKAL M., PEHLİVAN S.
European Human Genetics Conference, Berlin, Almanya, 01 Haziran 2024, (Özet Bildiri)

9. Unveiling novel antitumor properties of an anthraquinone derivative: In vitro and in silico investigations

Günçer B., Güler V., Pehlivan S., Şentürk A. M., Özerman Edis B.
European Human Genetics Conference, Berlin, Almanya, 01 Haziran 2024, (Özet Bildiri)

10. Differentiating Pefld type 3 from MAFLD: Is it about genetics?

KHUDİYEVA S., OYACI Y., YETİM ŞAHİN A., BAŞ F., SAYIN S., KANDEMİR İ., et al.
ESPGHAN 56th Annual Meeting, İtalya, 15 Mayıs 2024, (Tam Metin Bildiri)

11. Analysis Of Small Non Coding RNA (sncRNA) Expression In Patients with Metabolic Syndrome: An Investigation Based On Small RNA-Sequencing Data

Şenkal N., Oyacı Y., Medetalibeyoğlu A., Sayın S., Pehlivan S.
4th International Conference On Health, Engineerıng and Applied Sciences, Paris, Fransa, 12 - 14 Nisan 2024, ss.56-58, (Tam Metin Bildiri)

12. Obez Ergenlerde Alkolik Olmayan Karaciğer Yağlanmasında Genetik ve Epigenetik Değişikliklerin Araştırılması

Khudiyeva S., oYACI Y., YETİM ŞAHİN A., BAŞ F., Sayın S., KANDEMİR İ., et al.
46. Pediatri Günleri Geçmişten geleceğe hep birlikte el ele, Türkiye, 16 - 18 Nisan 2024, (Özet Bildiri)

13. Obez ergenlerde adiponektin (rs266729 ve rs17300539) gen varyantlarının değerlendirilmesi: Ön çalışma.

Oyacı Y., Yetim Şahin A., Hasanoğlu Sayın S., Khudiyeva S., Pehlivan S.
2. ADSAD Ergen Sağlığı Kongresi, İstanbul, Türkiye, 12 - 14 Ocak 2024, ss.1-2, (Özet Bildiri)

14. EVALUATION OF ADIPONECTIN (rs266729 and rs17300539) GENE VARIANTS IN OBESE ADOLESCENTS: A PRELIMINARY STUDY

OYACI Y., YETİM ŞAHİN A., sayın s., KHUDİYEVA S., PEHLİVAN S.
AVRASYA 9th INTERNATIONAL CONFERENCE ON APPLIED SCIENCES, Tiflis, Gürcistan, 24 Kasım 2023, ss.141-149, (Tam Metin Bildiri)

15. Metabolik Sendrom Hastalarında Adiponektin Gen Varyantlarının (rs17300539, rs266729 ve rs2241766) Araştırılması: Ön Çalışma

Pehlivan S., Şenkal N., Oyacı Y., Köse M., Medetalibeyoğlu A., Tükek T.
25. Ulusal İç Hastalıkları Kongresi, Antalya, Türkiye, 8 - 12 Kasım 2023, ss.26-27, (Özet Bildiri)

16. Could Telomere Length Be a Biomarker in Metabolic Syndrome?

Şenkal N., Tuncel F. C., Tükek T., Oyacı Y., Pehlivan M., Pehlivan S.
2nd Internatıonal Cankaya Congress, Ankara, Türkiye, 28 - 29 Eylül 2023, ss.20-22, (Tam Metin Bildiri)

17. Meme ve Gastroı̇ntestı̇nal Kanserler Hastalarında Il-2 Ra (Rs2104286) Fonksı̇yonel Varyantının Araştırılması

Tunçel F. C., Günaldı M., Hasanoğlu S., Işıksaçan N., Pehlivan S.
The 15th International Scientific Research Congress, Ankara, Türkiye, 17 - 18 Aralık 2022, ss.11-16, (Tam Metin Bildiri)

18. Mikrotialı Türk Hastalarda Leptin ve Leptin Reseptör Genlerine Ait Fonksiyonel Varyantlarının Araştırılması

Tunçel F. C., Bekerecioğlu M., Pehlivan S.
The 15th International Scientific Research Congress, Ankara, Türkiye, 17 - 18 Aralık 2022, ss.17-22, (Tam Metin Bildiri)

19. CAN LEP AND LEPR FUNCTIONAL GENE VARIANTS (rs1137101 AND rs7799039) CONTRIBUTE TO FORMATION OF BREAST AND GASTROINTESTINAL CANCERS?

Pehlivan S., Işıksaçan N., Oyacı Y., Günaldı M., Tunçel F. C., Pehlivan M.
BURSA 3rd INTERNATIONAL SCIENTIFIC RESEARCH CONFERENCE, Bursa, Türkiye, 22 - 23 Ekim 2022, ss.153-161, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

20. HOMEODİNAMİK ALAN, YAŞLANMA SÜRECİ VE MÜDAHALELER

Oyacı Y., Pehlivan S.
BURSA 3rd INTERNATIONAL SCIENTIFIC RESEARCH CONFERENCE, Bursa, Türkiye, 22 - 23 Ekim 2022, ss.162-170, (Tam Metin Bildiri)

21. EPIGENETIC AND GENETIC INVESTIGATION OF SOCS-1 GENE IN PATIENTS WITH MULTIPLE MYELOMA

Tunçel F. C., Serin İ., Pehlivan S., Oyacı Y., Pehlivan M.
European Hematology Association (EHA) Congress 2022, Vienna, Avusturya, 15 - 17 Haziran 2022, ss.1-2, (Özet Bildiri)

22. INVESTIGATING THE rs33989964 VARIANT AND THE PROMOTER REGION METHYLATION STATUS OF SOCS-1 GENE IN TURKISH PATIENTS WITH MICROTIA

Oyacı Y., Bekerecioğlu M., Pehlivan S.
8th INTERNATIONAL BLACK SEA COASTLINE COUNTRIES SCIENTIFIC RESEARCH CONFERENCE, Sofija, Bulgaristan, 29 - 30 Ağustos 2022, ss.372-379, (Tam Metin Bildiri)

23. INVESTIGATED THE IL-1 RECEPTOR ANTAGONIST (IL-1RN) AND INTERLEUKIN-4 (IL-4) VNTR PROFILES IN PULMONARY EMBOLISM PATIENTS

Pehlivan S., Tural Önür S., Oyacı Y., Boyracı N., Pehlivan M.
8th INTERNATIONAL BLACK SEA COASTLINE COUNTRIES SCIENTIFIC RESEARCH CONFERENCE, Sofija, Bulgaristan, 29 - 30 Ağustos 2022, ss.386-391, (Tam Metin Bildiri)

24. Gen-Çevre İlişkisi Ve Travmada Epigenetiğin Rolü

Çıkrıkçı A., Karimov E., Varkal M. A., Özçetin M., Pehlivan S.
SOCRATES 5TH INTERNATIONAL CONFERENCE ON ENGINEERING, HEALTH AND APPLIED SCIENCES, Tunis, Tunus, 6 - 07 Ağustos 2022, ss.26-35, (Tam Metin Bildiri)

25. IN SILICO ANALYSIS OF LEPTIN AND LEPTIN RECEPTOR GENES AND THEIR RELATIONSHIP WITH DISEASES

Pehlivan S., Oyacı Y.
INTERNATIONAL ASIAN CONGRESS ON CONTEMPORARY SCIENCES-VI, Van, Türkiye, 27 - 29 Mayıs 2022, ss.68-73, (Tam Metin Bildiri)

26. SYNAPTONEMAL COMPLEX AND ITS RELATIONSHIP WITH DISEASES

Oyacı Y., Pehlivan S.
INTERNATIONAL ASIAN CONGRESS ON CONTEMPORARY SCIENCES-VI, Van, Türkiye, 27 - 29 Mayıs 2022, ss.74-78, (Tam Metin Bildiri)

27. COVID-19 İMMÜNOLOJİSİ İÇİN YENİ FİKİRLER: SİTOKİN SİNYALLEME BASKILAYICISI-1 (SOCS-1) GENİ rs33989964 POLİMORFİZMİ, GLOBAL DNA VE SOCS-1 GEN PROMOTÖRÜ METİLASYONU

Tükek T., Pehlivan S., Medetalibeyoğlu A., Serin İ., Oyacı Y., Arıcı H., et al.
7. ULUSLARARASI ERCİYES BİLİMSEL ARAŞTIRMALAR KONGRESİ, Kayseri, Türkiye, 9 - 10 Mart 2022, ss.159-168, (Tam Metin Bildiri)

28. COVID‐19 VE AŞILAR

Hasanoğlu S., Pehlivan S., Bektaş M.
7. ULUSLARARASI ERCİYES BİLİMSEL ARAŞTIRMALAR KONGRESİ, Kayseri, Türkiye, 9 - 10 Mart 2022, ss.154-158, (Tam Metin Bildiri)

29. Er stress in central nervous system cells and its role in neurodegenerative diseases

Oyacı Y., Pehlivan S.
INTERNATIONAL CONFERENCE ON GLOBAL PRACTICE OF MULTIDISCIPLINARY SCIENTIFIC STUDIES, Girne, Kıbrıs (Kktc), 6 - 08 Mart 2022, ss.727-742, (Tam Metin Bildiri)

30. Il-1 receptor antagonist (il-1rn) and interleukin-4 (il-4) vntr polymorphisms in schizophrenia and bipolar disorder: an association study in turkish population

Pehlivan S., Oyacı Y., Tunçel F. C., Aytaç H. M.
INTERNATIONAL CONFERENCE ON GLOBAL PRACTICE OF MULTIDISCIPLINARY SCIENTIFIC STUDIES, Girne, Kıbrıs (Kktc), 6 - 08 Mart 2022, ss.743-755, (Tam Metin Bildiri)

31. Global Hipometilasyon Ve APC2, DRD2 VE NR3C1 Hipermetilasyonunun Türk Popülasyonunda Sigara İçme Riskine Etkisi

Uysal M. A., Çınarka H., Nursal A. F., Oyacı Y., Pehlivan S.
AEGEAN SUMMIT 4th INTERNATIONAL APPLIED SCIENCES CONGRESS, Muğla, Türkiye, 12 - 13 Şubat 2022, ss.62-72, (Tam Metin Bildiri)

32. Sentetik Biyoloji Ve Biyosensörler

Oyacı Y., Pehlivan S., Bektaş M.
AEGEAN SUMMIT 4th INTERNATIONAL APPLIED SCIENCES CONGRESS, Muğla, Türkiye, 12 - 13 Şubat 2022, ss.48-61, (Tam Metin Bildiri)

33. Laboratory And In Sılıco Analysıs Of The Pathogenic Variant Of Interleukin-17 (Rs763780) In Patients Diagnosed Wıth Covid-19

Oyacı Y., Şenkal N., MEDETALİBEYOĞLU A., YEŞİL SAYIN G., KÖSE M., PEHLİVAN M., et al.
Vııı.International Congress Of Molecular Medicine, Türkiye, 9 - 12 Kasım 2021, ss.13-17, (Tam Metin Bildiri)

34. Covid-19 Tanısı Konulan Hastalarda İnterlökin-17'nin Patojenik Varyantının (Rs763780) Laboratuvar Ve Siliko Analizi

Oyacı Y., Şenkal N., Medetalibeyoğlu A., Yeşil Sayın G., Köse M., Pehlivan M., et al.
VIII.International Congress Of Molecular Medicine, İstanbul, Türkiye, 9 - 12 Kasım 2021, ss.10, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

35. MB-COMT ve DRD2 Geninin Gen Varyantları ve Metilasyon Durumuna İlişkin Madde Kullanım Bozukluklarının Eğilimini Öngörmede Bilgi Kazanım Sınıflandırması

Oyacı Y., Aytaç H. M., Zaim Gökbay İ., Çetinay Aydın P., Pehlivan S.
Tıbbi Biyoloji ve Genetik Kongresi, İstanbul, Türkiye, 28 - 31 Ekim 2021, ss.104, (Özet Bildiri)

36. COVID-19 PCR (-) Hastalarda Mbl2 Ve Nos3 Fonksiyonel Gen Varyantlarının Araştırılması

Pehlivan S., Köse M., Meşe S., Serin I., Şenkal N., Oyacı Y., et al.
Tıbbi Biyoloji ve Genetik Kongresi, İstanbul, Türkiye, 28 - 31 Ekim 2021, ss.105, (Özet Bildiri) Sürdürülebilir Kalkınma

37. İLK TANI PCR (-) COVİD-19 HASTALARINDA MBL2 VE NOS3 FONKSİYONEL GEN VARYANTLARININ ARAŞTIRILMASI

SERİN İ., PEHLİVAN S., KÖSE M., MEŞE S., ŞENKAL N., OYACI Y., et al.
47. Ulusal Hematoloji Kongresi, Antalya, Türkiye, 4 - 07 Kasım 2021, ss.357, (Tam Metin Bildiri)

38. DNA ONARIM GEN VARYANTLARI (XRCC4 VE XRCC1) İLE COVİD-19 ENFEKSİYONU ARASINDA BİR BAĞLANTI OLABİLİR Mİ?

SERİN İ., KÖSE M., PEHLİVAN S., ŞENKAL N., PEHLİVAN M., MEDETALİBEYOĞLU A., et al.
47. Ulusal Hematoloji Kongresi, Türkiye, 4 - 07 Kasım 2021, ss.358, (Tam Metin Bildiri)

39. PERIOD 3 (PER3) (RS57875989) VARYANTI İLE COVİD-19 ENFEKSİYONUNUN ŞİDDETİ ARASINDA BİR BAĞLANTI OLABİLİR Mİ?

SERİN İ., PEHLİVAN S., KÖSE M., ŞENKAL N., OYACI Y., MEDETALİBEYOĞLU A., et al.
47. Ulusal Hematoloji Kongresi, Türkiye, 4 - 07 Kasım 2021, ss.379, (Tam Metin Bildiri)

40. A Novel Molecule For Lung Cancer Treatment: Curcumın-Quınone Derıvatıve

Özkök F., Hacıosmanoğlu E., Oyacı Y., Varol B., Onul N., Pehlivan S.
III. International Cancer And Ion Channels Congress, İstanbul, Türkiye, 16 - 18 Eylül 2021, ss.60, (Özet Bildiri) Sürdürülebilir Kalkınma

41. Hücresel Yaşlanmanın Nörodejeneratif Hastalıkların Patogenezindeki Rolü Ve Tedavi Yaklaşımları

Pehlivan S., Oyacı Y.
Euroasıa Summıt 4th Internatıonal Applıed Scıence Congress, Odessa, Ukrayna, 11 - 12 Eylül 2021, ss.134-143, (Tam Metin Bildiri)

42. Dna Onarım Gen Varyantları (Xrcc4 Ve Xrcc1) İle Covıd-19 Enfeksiyonu Arasında Bir Bağlantı Olabilir Mi?

Köse M., Serin I., Pehlivan S., Şenkal N., Pehlivan M., Medetalibeyoğlu A., et al.
Euroasıa Summıt 4th Internatıonal Applıed Scıence Congress, Odessa, Ukrayna, 10 - 11 Eylül 2021, cilt.1, sa.1, ss.125-132, (Tam Metin Bildiri)

43. A NOVEL MOLECULE FOR LUNG CANCER TREATMENT: CURCUMIN-QUINONE DERIVATIVE

ÖZKÖK F., HACIOSMANOĞLU E., oyacı y., VAROL B., ONUL N., PEHLİVAN S.
3rd international cancer and ion channels congress, İstanbul, Türkiye, 16 - 18 Eylül 2021, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

44. DNA methylation pattern of gene promoters of MB-COMT, DRD2, and NR3C1 in Turkish patients diagnosed with schizophrenia

Aytaç H. M., Oyacı Y., Pehlivan M., Pehlivan S.
European Human Genetics Conference, Vienna, Avusturya, 28 - 31 Ağustos 2021, ss.1, (Özet Bildiri)

45. Assesment Of Gini Index and Information Gain Classification On Predicting Substance Use Disorders Tendency Related to NOS3 (intron 4 A/B VNTR and rs1799983) and PER3 (rs57875989) Gene Variants.

ZAİM GÖKBAY İ., Oyacı Y., PEHLİVAN S.
4th International Conference on Data Science and Applications (ICONDATA'21), 4 - 06 Haziran 2021, ss.669-679, (Tam Metin Bildiri)

46. NOS3 (intron 4 A / B VNTR ve rs1799983) ve PER3 (rs57875989) Gen Varyantlarına İlişkin Madde Kullanım Bozukluklarının Öngörülmesine İlişkin Gini İndeksinin Değerlendirilmesi ve Bilgi Kazanımı Sınıflandırması

Zaim Gökbay İ., Oyacı Y., Pehlivan S.
IV International Conference on Data Science and Applications (ICONDATA’21), Muğla, Türkiye, 4 Haziran - 06 Kasım 2021, cilt.1, sa.1, ss.669-679, (Tam Metin Bildiri) Creative Commons License

47. Information Gain Classification On Predicting Substance Use Disorders Tendency Related to Gene Variants and Methylation Status of MB-COMT and DRD2 Gene.

Zaim Gökbay İ., Oyacı Y., Pehlivan S.
4th International Conference on Data Science and Applications (ICONDATA'21), Muğla, Türkiye, 4 - 06 Haziran 2021, ss.663-668, (Tam Metin Bildiri)

48. Evaluation Of Methylation Status Of MB-COMT, APC2, NR3C1 And DRD2 Genes In Turkish Patients With Microtia

Pehlivan S., Nursal A. F., Oyacı Y., Pehlivan M., Bekerecioğlu M.
4th International Health Sciences And Innovation Congress, Baku, Azerbaycan, 5 - 06 Temmuz 2021, ss.694-703, (Tam Metin Bildiri)

49. Mannose-Binding Lectin 2 (MBL2) Gene Polymorphism During Pandemic: Covid-19 Family.

Tükek T., Pehlivan S., Oyacı Y., İşoğlu Ü.
4th International Health Sciences And Innovation Congress, Baku, Azerbaycan, 5 - 06 Temmuz 2021, cilt.1, sa.1, ss.704-712, (Tam Metin Bildiri)

50. Molecular Genetics Of Multiple System Atrophy (Msa)

Hasanoğlu S., Pehlivan S.
Anatolian Congresses, 6th Internatıonal Applied Scıence Congress, Van, Türkiye, 21 - 23 Mayıs 2021, ss.1-8, (Tam Metin Bildiri)

51. The Importance Of Mannose Binding Lectin 2 Gene And Their Relationship Wıth Neurological, Autoimmune, Periodental, Infectious, Psychiatric Diseases And Cancer

Pehlivan S.
Anatolian Congress, 6th Internatıonal Applıed Scıence Congress, Van, Türkiye, 21 - 23 Mayıs 2021, ss.9-17, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

52. Telomeres And Telomer-Related Diseases In Humans: Telomerapathies

Pehlivan S., Tunçel F. C., Oyacı Y.
International Black Sea Coastline Countries Symposium-VI, Giresun, Türkiye, 28 - 30 Nisan 2021, ss.839-847, (Tam Metin Bildiri)

53. Cell Culture And Methods Used In The Study Of Molecular Mechanisms In Cells

Oyacı Y., Güler V., Pehlivan S.
International Black Sea Coastline Countries Symposium VI, Giresun, Türkiye, 28 - 30 Nisan 2021, ss.695-706, (Tam Metin Bildiri)

54. The Effect of Childhood Trauma And COMT Val158Met Polymorphism On Agression in Schizophrenia

Çetinay Aydın P., Erol A., Yıldırım Y. E., Oyacı Y., Öngel Atar A., Pehlivan S., et al.
Turkish Association for Psychopharmacology International Update Symposium 2021, 10 - 11 Nisan 2021, ss.167-168, (Özet Bildiri)

55. COVID-19 Hastalarında Endotel Nitrik Oksit Sentetaz Geninin (rs1799983 ve Intron 4a/b VNTR) Fonksiyonel Varyantlarının Araştırılması

Şenkal N., Oyacı Y., Köse M., Medetalibeyoğlu A., Önel M., Yeşil Sayın G., et al.
International Symposium On Global Pandemics And Multidisciplinary Covid-19 Studies , Ankara, Türkiye, 19 - 20 Mart 2021, ss.1-7, (Tam Metin Bildiri)

56. Investigation of Functional Variants of the Endothelital Nitric Oxide Synthetase Gene (rs1799983 and Intron 4a / b VNTR) in COVID-19 Patients

Şenkal N., Oyacı Y., KÖSE M., MEDETALİBEYOĞLU A., YEŞİL SAYIN G., PEHLİVAN M., et al.
International Symposium On Global Pandemics And Multidisciplinary Covid-19 Studies, 19 - 20 Mart 2021, ss.1-7, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

57. Psikiyatrik Belirtilerin Olası Psikoimmünolojik Nedenleri Olarak Geçmişten Günümüze Viral Pandemiler)

Aytaç H. M., Pehlivan S.
International Symposium On Global Pandemics And Multidisciplinary Covid-19 Studies, Ankara, Türkiye, 19 - 20 Mart 2021, ss.27-32, (Tam Metin Bildiri)

58. Bipolar Bozukluk ve Şizofreni Hastalarında Interleukin-17 (7488A / G = rs763780) Patojenik Varyantının Laboratuvar ve In Silico Analizi

Oyacı Y., Aytaç H. M., Pehlivan M., Tunçel F. C., Pehlivan S.
Euro Asia 8th. International Congress On Applied Sciences Congress, Toskent, Özbekistan, 15 - 16 Mart 2021, ss.875-886, (Tam Metin Bildiri)

59. VNTR Polimorfizmlerinin Önemi ve Nörolojik, Otoimmün Hastalıklar ve Kanserle İlişkisi

Oyacı Y., Pehlivan S.
Euro Asia 8th. International Congress On Applied Sciences Congress , Toskent, Özbekistan, 15 - 16 Mart 2021, ss.887-898, (Tam Metin Bildiri)

60. The Relationship Of Problematic Gaming With Smoking And Impulsivity In University Students

Çayır S., Kervancıoğlu E., Bozkurt M., Meral R., Eker E. B., Bozdağ F. Z., et al.
Euro Asia 8th. International Congress On Applied Sciences, Toskent, Özbekistan, 15 - 16 Mart 2021, ss.933-941, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

61. INVESTIGATION OF FUNCTIONAL VARIANTS OF THE ENDOTHELITAL NITRIC OXIDE SYNTHETASE GENE (rs1799983 AND INTRON 4a/b VNTR-27 BP) IN COVID-19 PATIENTS

ŞENKAL N., OYACI Y., KÖSE M., MEDETALİBEYOĞLU A., ÖNEL M., YEŞİL SAYIN G., et al.
International Symposium on Global Pandemics and Multidisciplinary Covid-19 Studies, Ankara, Türkiye, 19 Mart 2021, (Tam Metin Bildiri)

62. The Asssociations of XRCC4, eNOS and Per3 VNTR Variants with Chilhood Acute Lymphoblastic Leukemia in Turkish Patients

GÖKÇE M., OĞUZ S. R., Oyacı Y., ŞENTÜRK ÇİFTÇİ H., ATAY A. A., öğret Y., et al.
8. Multidisciplinary Cancer Research Congress, İstanbul, Türkiye, 15 - 18 Ocak 2021, (Tam Metin Bildiri)

63. Türk Hastalarında XRCC4, eNOS ve Per3 VNTR Varyantlarının Çocukluk Çağı Akut Lenfoblastik Lösemi ile İlişkisi

Gökçe M., Oğuz S. R., Oyacı Y., Atay A. A., Öğret Y., Pehlivan S., et al.
8. Multidisciplinary Cancer Research Congress, İstanbul, Türkiye, 16 Ocak 2021 - 17 Ocak 2022, ss.79, (Özet Bildiri)

64. The Asssocıatıons of XRCC4, ENOS and HPER3 VNTR Varıants wıth Chılhood Acute Lymphoblastıc Leukemıa ın Turkısh Patıents

Gökçe M., Oğuz R., Oyacı Y., Şentürk Çiftçi H., Atay A., Öğret Y., et al.
8. Multidisciplinary Cancer Research Congress., İstanbul, Türkiye, 16 - 17 Ocak 2021, ss.79, (Özet Bildiri)

65. The effect of the originally synhesized curcumin analogue (JWB1) on triple breat cancer

VAROL B., ÖZKÖK F., HACIOSMANOĞLU E., oyacı y., ONUL N., PEHLİVAN S.
BioTechBioChem 2020, Ankara, Türkiye, 16 - 18 Aralık 2020, cilt.1, ss.206, (Özet Bildiri)

66. INVESTIGATION OF MBL2 AND NOS3 FUNCTIONAL GENE VARIANTS IN SUSPECTED COVID-19 PCR (-) PATIENTS:

PEHLİVAN S., KÖSE M., MEŞE S., serin i., Şenkal N., oyacı y., et al.
Eurosia Summit, Congress on Scientific Researches and Recent Trends-7, Baku, Azerbaycan, 6 - 09 Aralık 2020, ss.21-26, (Tam Metin Bildiri)

67. INVESTIGATION OF MBL2 AND NOS3 FUNCTIONAL GENE VARIANTS IN SUSPECTED COVID-19 PCR (-) PATIENTS

PEHLİVAN S., KÖSE M., MEŞE S., SERİN İ., Şenkal N., Oyacı Y., et al.
EUROASIA Congress on Scientific Researches and Recent Trends-VII, Baku, Azerbaycan, 6 - 08 Aralık 2020, cilt.1, (Özet Bildiri)

68. Evaluation of the relationship between antioxidant gene polymorphisms and breast cancer

Topcu T. O., Isiksacan N., Kilic Z. A., Pehlivan S., Gunaldi M.
San Antonio Breast Cancer Symposium, San-Antonio, Kuzey Mariana Adaları, 10 - 14 Aralık 2019, cilt.80, (Özet Bildiri) Sürdürülebilir Kalkınma identifier

69. TNF-alpha 308 G/A variany may be associated with bipolar disorder in a Turkish Population

Nursal A. F., Aytaç H. M., ŞENTÜRK ÇİFTÇİ H., Oyacı Y., Yazar M. S., PEHLİVAN M., et al.
3. Uluslararası GAP Matematik Mühendislik Fen ve Sağlık Bilimleri Kongresi Tam Metin Kitabı, 29 Kasım - 01 Aralık 2019, (Tam Metin Bildiri)

70. Investigation of MiR-21, MiR-32 and MiR-181a/b in terms of Treatment Response in Multiple Myeloma

Alsaadoni H., Pençe S., Pehlivan S., Pehlivan M.
VII. International Congress of Molecular Medicine, İstanbul, Türkiye, 5 - 07 Eylül 2019, ss.24-25, (Özet Bildiri) Creative Commons License Sürdürülebilir Kalkınma

71. İnvestigation of the eNOS (rs1799983) and IFN- (rs6255944) gene variants with susceptibility to Schizophrenia and Bipolar Disorders in a Turkish Cohort.

PEHLİVAN S., Aytaç H. M., ŞENTÜRK ÇİFTÇİ H., Yazar M. S., Oyacı Y., PEHLİVAN M., et al.
7.Uluslararası Moleküler Tıp Kongresi, 5 - 07 Eylül 2019, (Özet Bildiri)

72. Might there be a link between VNTR Variants in the eNOS, HPER and XRCC4 Genes and the etiopathogenesis of Bipolar Disorders.

Yasemin O., ŞENTÜRK ÇİFTÇİ H., Aytaç H. M., Yazar M. S., PEHLİVAN M., Tunçel F. C., et al.
7. Uluslararası Moleküler Tıp Kongresi, 5 - 07 Eylül 2019, (Özet Bildiri)

73. Role of CYP3A41B gene variant in substance use disorder

Gazi Ç., ŞENTÜRK ÇİFTÇİ H., PEHLİVAN S.
7. Uluslararsı Moelküler Tıp Kongresi, 5 - 07 Eylül 2019, (Özet Bildiri)

74. The Association of GVHD With HLA-DR Alleles, IFN-Gamma, TGF-Beta, and MBL2 Gene Polymorphism

Oğuz R., Şentürk Çiftçi H., Gökçe M., Ögret Y., Karadeniz S., Pehlivan S., et al.
33rd European Immunogenetics and Histocompatibility Conference,, Lisbon, Portekiz, 8 - 11 Mayıs 2019, ss.104, (Özet Bildiri)

75. INVESTIGATION OF THE ROLE OF HLA-DR ALLELES AND MBL2 GENE VARIANT IN THE ETIOPATOGENESIS OF CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA

OĞUZ S. R., ŞENTÜRK ÇİFTÇİ H., öğret Y., karadeniz s., PEHLİVAN S., gökçe m., et al.
13. east-West Immunogenetic Conference, 14 - 16 Mart 2019, (Özet Bildiri)

76. Cyp2A13 Polimorfizmleri ve Nikotin Bağımlılığına Duyarlılığı: Genetik Bir İlişkilendirmeBir Silico Analizi.

PEHLİVAN S., UYSAL M. A., ÇAĞATAY T., ŞENTÜRK ÇİFTÇİ H., PEHLİVAN M., PENÇE S.
International Academic research Symposium, İzmir, Türkiye, 5 - 06 Nisan 2019, ss.15, (Özet Bildiri)

77. Cytokine Gene Polymorphism Frequency in Turkish Population with Comparisons to Other populations: A meta-analysis.

Pehlivan S., Özdilli K., Ögret Y., Oğuz R., Şentürk Çiftçi H., Savran Oguz F.
International Participated Erciyes Medical Gnetics days (Uluslararası Katılımlı Erciyees Tıp Genetik Günleri, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.38, (Özet Bildiri)

78. DO FUNCTIONAL VARIANTS OF MIF AND MBL GENES INFLUENCE OUTCOME IN PATIENTS UNDERWENT AUTOLOGOUS STEM CELL TRANSPLANTATION FOR MULTIPLE MYELOMA?

PEHLİVAN M., NURSAL A. F., GÜNDEŞ İ., OYACI Y., KIVANÇ D., PEHLİVAN S.
Uluslararası Katılımlı Erciyes Tıp Genetik Günleri 2019, Kayseri, Türkiye, 21 Şubat 2019, (Tam Metin Bildiri)

79. E-Cigarette Vaping/Aerosols: Safe Go-To Alternative to Cigarettes?

Grunig G., Durmus N., PEHLİVAN S., Zelikoff J.
International Conference of the American-Thoracic-Society, Texas, Amerika Birleşik Devletleri, 17 - 22 Mayıs 2019, cilt.199, (Özet Bildiri) identifier

80. Association between COMT CNR2 and MPO genes and healthy smokers or heavy smoker schizophrenia patients in Turkish population

Pehlivan S., Cetinay P. A., Uysal M. A., Kurnaz S., Sever U., Aydin A., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.946, (Özet Bildiri) identifier

81. Association and in silico analysis of (Diseases) Genetic Merkers Affecting CYPA6 Gene and Smoking Status Risk.

PEHLİVAN S., ŞENTÜRK ÇİFTÇİ H.
Uluslararsı Bilimsel Araştırmalar Kongresi, Nevşehir, Türkiye, 9 - 12 Eylül 2018, cilt.1, ss.15, (Özet Bildiri)

82. Can VNTR Variants in eNOS and XRCC4 genes contibute to formation of Bİpolar disorder

Oyacı Y., Aytaç H. M., ŞENTÜRK ÇİFTÇİ H., Yazar M. S., PEHLİVAN S.
Uluslararsı Bilimsel Araştırmalar Kongresi, Nevşehir, Türkiye, 9 - 12 Eylül 2018, cilt.1, ss.81, (Özet Bildiri)

83. In Silico Analysis of the TNF-alpha Effect on Cancer (Multple Myeloma) and Autoimmune Diseases (Psoriasis and Rheumatiod Arthritisis

ŞENTÜRK ÇİFTÇİ H., PEHLİVAN S.
Uluslararsı Bilimsel Araştırmalar Kongresi, Nevşehir, Türkiye, 9 - 12 Eylül 2018, cilt.1, ss.67, (Özet Bildiri) Sürdürülebilir Kalkınma

84. Nikotin bağımlısı bireylerin sosyal davranışların lineer stokastik matematiksel model ile analizi: ön çalışma

ZAİM GÖKBAY İ., Yüksel C., PEHLİVAN S., YARMAN B. S. B.
2. Uluslararası Bilimsel Araştırmalar Kongresi, Mardin, Türkiye, 9 - 13 Mayıs 2018, cilt.1, ss.20-24, (Özet Bildiri)

85. mi196a2 T/C variant as possible predisposal factor for ankylosing spondylitis in a Turkish population

Pehlivan S., Gursoy S., NURSAL A. F., Akaltun M. S., Ozdilli K., PEHLİVAN M.
European Biotechnology Congress, Athens, Yunanistan, 26 - 28 Nisan 2018, cilt.280, (Özet Bildiri) identifier

86. Do UCP2, IL-17, mi196a2, and NR3C1 gene variants contribute to the risk of microtia? A preliminary study in Turkish population

Ozdilli K., BEKERECİOĞLU M., NURSAL A. F., PEHLİVAN M., Sever U., Buyukgural B., et al.
European Biotechnology Congress, Athens, Yunanistan, 26 - 28 Nisan 2018, cilt.280, (Özet Bildiri) identifier

87. Nikotin bağımlısı bireylerin sosyal davranıGların lineer stokastik matematiksel model ile analizi: ön çalıGma

ZAİM GÖKBAY İ., Yüksel C., PEHLİVAN S., YARMAN B. S. B.
Uluslararası Bilimsel Araştırmalar Kongresi (UBAK), Mardin, Türkiye, 9 - 13 Mayıs 2018, cilt.1, sa.1, ss.262-263, (Tam Metin Bildiri)

88. Lack of association of Monoamine oxidase-B gene A644G variant with Schizophrenia and/or nicotine dependence.

PEHLİVAN S., Çetinay Aydın P., Uysal A. m., ŞENTÜRK ÇİFTÇİ H., Sevaen Ü., Yavuz F. K., et al.
International Molecular Biology and Biotechnology Congress, 25 - 27 Nisan 2018, (Özet Bildiri)

89. THE ROLE OF DAT, 5-HTT, MAOA AND MAOB OF NICOTINE DEPENDENCE IN A TURKISH POPULATION

Sever Ü., Uysal M. A., PASİN Ö., cessation polyclinic working group Y. s., Pehlivan S.
VI International Congress of Molecular Medicine, İstanbul, Türkiye, 22 - 25 Mayıs 2017, ss.88, (Özet Bildiri)

90. The effect of catechol-oomethyltransferase (comt) polymorphism on acute postoperative morphine requirement: A clinical pilot study.

Karadeniz Savran M., ŞENTÜRK ÇİFTÇİ H., Oğuz R., Karadeniz S. T., AYGÜN E., PEHLİVAN S., et al.
Erciyes Medical Genetics Days, Türkiye, 11 - 13 Mayıs 2017, (Özet Bildiri)

91. The effect of Catechol-O-Methyltransferase (COMT) Variants on Acute Postoperative Morphhine Requirements: A Clinical Pilot Study

ŞENTÜRK ÇİFTÇİ H., SAVRAN KARADENİZ M., TUĞRUL K. M., Oğuz R., KARADENİZ S. T., PEHLİVAN S.
International DNA DAY and GENOME congress, Kırşehir, Türkiye, 24 - 27 Nisan 2017, ss.45, (Özet Bildiri)

92. A preliminary association study in Turkish population: Do IL-17 and UCP2 Gene variants Contributes to The Ethiology of Microtia?

Ozdilli K., Bekerecioglu M., Pehlivan S., Buyukgural B.
Annual Joint Meeting of the American-Society-for-Cell-Biology and the European-Molecular-Biology-Organization (ASCB/EMBO), Pennsylvania, Amerika Birleşik Devletleri, 2 - 06 Aralık 2017, cilt.28, (Özet Bildiri) identifier

93. Association Between Thr241met Variant Of Xrcc3 Homologous Recombination Repair Gene And Smokers Or Heavy Smoker Schizophrenia Patients In Turkish Population

Uysal M. A., Aydin P. C., Pehlivan M., Kurnaz S., Yavuzlar H., Sever U., et al.
International Conference of the American-Thoracic-Society (ATS), Washington, Kiribati, 19 - 24 Mayıs 2017, cilt.195, (Özet Bildiri) identifier

94. The role of endothelial nitric oxide synthase gene polymorphisms in patients with lung cancer

Kocer C., Benlier N., Balci S. O., Pehlivan S., Nacak I., Sanli M., et al.
41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Türkiye, 3 - 08 Eylül 2016, cilt.283, ss.262-263, (Özet Bildiri) identifier

95. Sıgara bağımlılarında ve sıgara içmeyenlerde CYP2A6 ve CYP2A13 genlerine ait varyantların yeni nesil dizileme (YND) ile belirlenmesi.

Çınar Ç., Pehlivan S.
Türk Toraks Derneği 19. Yıllık Kongresi, Antalya, Türkiye, 6 - 10 Nisan 2016, ss.1, (Özet Bildiri)

96. TNF-alpha, TGF-beta1, IL-10, IL-1A, IL-1alpha, IL-6 and IFN-gamma gene polymorphisms contribute to non-syndromic microtia: a preliminary association study in Turkish population

PEHLİVAN S., Rosti R. O., Bekerecioglu M., Sever T., Buyukgural B.
European Biotechnology Congress, İstanbul, Türkiye, 28 Eylül - 01 Ekim 2011, cilt.22, (Özet Bildiri) identifier

97. MDR1 POLYMORPHISMS IN CHILDHOOD DRUG RESISTANCE EPILEPSY

Alpman A., Ozkinay F., Tekgul H., Gokben S., PEHLİVAN S., Schalling M., et al.
9th European Congress on Epileptology, Rhodes, Yunanistan, 27 Haziran - 01 Temmuz 2010, cilt.51, ss.105, (Özet Bildiri) identifier

98. POLYMORPHISMS OF THE DNA REPAIR GENE XRCC1 (399) AND XPD (751) CORRELATES WITH RISK OF ACUTE MYELOID LEUKEMIA IN TURKISH POPULATION

Ozcan A., Pehlivan M., Karaca E., Ozkinay C., Ozdemir F., Pehlivan S.
13th Congress of the European-Hematology-Association, Copenhagen, Danimarka, 12 - 15 Haziran 2008, cilt.93, ss.205-206, (Özet Bildiri) identifier

99. ADAM33, TLR-4 and CCR5 Delta 32 polymorphisms in children sensitized to same antigen displaying different phenotype

Yuksel H., Onay H., Yilmaz O., Sogut A., PEHLİVAN S., Kirmaz C., et al.
26th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology, Goteborg, İsveç, 9 - 13 Haziran 2007, cilt.62, ss.124, (Özet Bildiri) identifier

100. False negative results in non-invasive down syndrome screening tests

Pehlivan P., Acarsoz D., Azakli Z., Kayserili H., Basaran S.
6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.249, (Özet Bildiri) identifier
Kitaplar 12

1. The Analysis on the Effects of COMT, DRD2, PER3, eNOS, NR3C1 Functional Gene Variants and Methylation Differences on Behavoiral Inclinations in Addicts through the Decision Tree Algorythm

ZAİM GÖKBAY İ., Oyacı Y., PEHLİVAN S.
Numerical Simulation [Working Title], Ali Soofastaei, Editör, IntechOpen, Londrina, ss.1-17, 2022

2. Matrix Metalloproteinazlar ve İnsan Hastalıklarındaki Rolleri

PEHLİVAN S., OYACI Y.
Sağlık bilimlerinde güncel araştırmalar-IV, Işık Bülent, KÖSE Fulya, KÜÇÇÜKTÜRK Serkan, Editör, Duvar Kitabevi, İzmir, ss.205-238, 2022

3. HÜCRESEL YAŞLANMA VE NÖRODEJENERATİF HASTALIKLAR

PEHLİVAN S., Oyacı Y.
Sağlık Bilimlerinde Araştırma ve Değerlendirmeler- III, cem evereklioğlu, Editör, gece kitaplığı, ss.363-390, 2021

4. Bölüm 2 - Hücre İskeletinin Fonksiyonları ve Hastalıklarla İlişkisi

oyacı y., PEHLİVAN S.
Sağlık Bilimlerinde Teori ve Araştırmalar II, Cem Evereklioğlu, Editör, GECE Yayınevi, ss.35-59, 2020

5. Bölüm 1 - Farklılık Sebebimiz: Mayoz Bölünmede Crossing - Over

YÜRÜK YILDIRIM Z. N., Zanjani B. N., PEHLİVAN S.
Sağlık Bilimlerinde Teori ve Araştırmalar II (Cilt 1), Cem Evereklioğlu, Editör, GECE yayınevi, ss.9-34, 2020

6. CYP2A13 Polimorfizmleri ve Nikotin Bağımlılığına Duyarlılığı: Genetik Bir İlişkilendirme ve Bir Siliko Analizi

PEHLİVAN S., UYSAL M. A., ÇAĞATAY T., ŞENTÜRK ÇİFTÇİ H., PEHLİVAN M., PENÇE S.
Sağlık Bilimleri Alanında Araştırma ve Derlemeler, Doç. Dr. Meriç ERASLAN, Editör, Gece Akademisi, Ankara, ss.233-242, 2019

7. Mitochondrial MIRNAS (MITOMIRS) in Breast Cancer

tokgün E. P., TOMATIR A. G., TOKGÜN O., PEHLİVAN S.
Research Reviews in Health Sciences, 2019, Everekoglu Cem, Goncagul Gulsen, Dikmetas Cesarettin, Editör, GECE AKADEMI, ss.16-26, 2019

8. Epigenetikte histon modifikasyonları ve analiz yöntemleri

GÜLER V., PEHLİVAN S.
Sağlık Bilimleri Alanında Araştırma ve Derlemeler, Atilla Atik, Editör, Gece Akademi, ss.121-131, 2019

9. CYP2A13 polimorfizmleri ve nikotin bağımlılığına duyarlılığı: Genetik bir ilişkilendirme ve in silico analizi

Pehlivan S., Uysal M. A., Çağatay T., Şentürk Çiftçi H., Pehlivan M., Pençe S.
Sağlık Bilimleri Alanınsa Araştırma ve Derlemeler, Atilla Atik, Editör, Gece Yayınevi, Ankara, ss.231-242, 2019

10. Molecular pathogenesis of rheumatoid arthritis

PEHLİVAN S., TOMATIR A. G.
International Researches in Health Sciences, Dalkılıc Mehmet, Editör, GECE AKADEMİ, ss.88-98, 2019

11. DNA Tamir Genlerinin (XPD, XRCC1 ve XRCC4) Siliko Ekspresyon ve Hastalık İlişkili Analizleri

ŞENTÜRK ÇİFTÇİ H., NURSAL A. F., PEHLİVAN S.
Tıpta İnovasyon ve Renovasyon Mozaiği, Sibel AKYOL, Editör, Berikan Elektronik Basım Yayın, Ankara, ss.545-555, 2018

12. Nikotin Bağımlısı Bireylerin Sosyal Davranışların Lineer Stokastik Matematiksel Model ile Analizi: Ön Çalışma

ZAİM GÖKBAY İ., YÜKSEL C., PEHLİVAN S., YARMAN B. S. B.
Modern DönemdeEdebiyat, Eğitim,İktisat ve Mühendislik, Prof. Dr. Handan Asude BAŞAL, Dr. Mine Nazan Kerimak ÖNER, Dr. Yasemin ULUTÜRK, Editör, BERİKAN YAYINEVİ, Ankara, ss.713-727, 2018
Metrikler

Yayın

370

Yayın (WoS)

222

Yayın (Scopus)

191

Atıf (WoS)

1314

H-İndeks (WoS)

20

Atıf (Scopus)

1374

H-İndeks (Scopus)

21

Atıf (Scholar)

45

H-İndeks (Scholar)

3

Atıf (TrDizin)

1

H-İndeks (TrDizin)

1

Atıf (Sobiad)

172

H-İndeks (Sobiad)

3

Atıf (Diğer Toplam)

4

Proje

34

Fikri Mülkiyet

1

Tez Danışmanlığı

7

Açık Erişim

20
BM Sürdürülebilir Kalkınma Amaçları