Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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) identifier

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 , 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

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 , 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

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

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

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

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) Sürdürülebilir Kalkınma identifier identifier identifier

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

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

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

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

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

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) identifier identifier identifier

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

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

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

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

Investigation of <i><u>MBL2</u></i> and <i><u>NOS3</u></i> 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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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

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

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

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

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

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

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

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

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

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

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

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) Sürdürülebilir Kalkınma identifier identifier identifier

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Nursal A. F., Aytac H. M., Ciftci H. S., Yazar M. S., Oyaci Y., Pehlivan M., et al.
Revista de Psiquiatria Clinica , cilt.47, sa.6, ss.176-179, 2020 (SCI-Expanded) identifier identifier

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

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

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

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

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

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

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

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

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

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

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

XRCC4 rs6869366 polymorphism is associated with suspectibility to nicotine dependence and/or schizophrenia

PEHLİVAN S., Uysal M. A., Aydın N., NURSAL A., PEHLIVAN M., Yavuzlar H., et al.
SAO PAULO MEDICAL JOURNAL , cilt.45, sa.3, ss.53-56, 2018 (SCI-Expanded)

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

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

Can VNTR variants in eNOS and XRCC4 genes contribute to formation of nicotine dependence and/or schizophrenia?

PEHLİVAN S., Uysal M. A., Aydın P., pehlivan M., Nursal A. F., Yavuzlar H., et al.
BRATİSLAVA MEDİCAL JOURNAL-BRATİSLAVSKE LEKARSKE LİSTY , cilt.118, sa.8, ss.467-471, 2017 (SCI-Expanded)

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

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

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

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

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

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

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

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

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

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

Effects of TNF?, NOS3, MDR1 Gene Polymorphisms on Clinical Parameters, Prognosis and Survival of Multiple Myeloma Cases

PEHLİVAN S., TOMATIR A. G., PEHLIVAN M., OGUZKAN-BALCI S.
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION , cilt.17, sa.3, ss.1009-1014, 2016 (SCI-Expanded)

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

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

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

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

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

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

Baransel Isir A, Nacak M, Oguzkan Balci S, Pehlivan S, Kul K, Benlier N, Aynacioglu AS. Relationship between the 1359 G/A polymorphism of the Central Cannabinoid Receptor 1 (CNR1) gene and susceptibility to cannabis addiction in a Turkish population. Australian Journal of Forensic Sciences, 2015: 47(2); 230-238.

PEHLİVAN S.
AUSTRALIAN JOURNAL OF FORENSIC SCIENCES , sa.47, ss.230-238, 2015 (SCI-Expanded)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Nitric Oxide Levels and Endothelial Nitric Oxide Synthase Gene Polymorphisms in Turkish Women with Idiopathic Recurrent Miscarriage

OZTÜRK E., BALAT O., PEHLİVAN S., uğur m. g., OZKAN Y., Sever T., et al.
Journal of the Turkish-German Gynecological Association , cilt.12, ss.234-238, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

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

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

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

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

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

Erciyas K, Pehlivan S, Sever T, İğci M, Pehlivan M, Arslan A, Orbak R. Endothelial nitric oxide synthase gene polymorphisms associated with periodontol diseases in Turkish adults. African J Biotechnology. 9, 3042-3047, (2010).

PEHLİVAN S.
AFRICAN JOURNAL OF BIOTECHNOLOGY , sa.9, ss.3042-3047, 2010 (SCI-Expanded)

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

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

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

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

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

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

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

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

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

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

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

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

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 &amp; lymphoma , cilt.50, ss.2030-7, 2009 (SCI-Expanded) identifier identifier identifier

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 &amp; lymphoma , cilt.48, ss.2454-6, 2007 (SCI-Expanded) identifier identifier identifier

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

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

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

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

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

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

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

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

Might There be a link between MBL and dental caries?

PEHLİVAN S., Sipahi M., Özkınay F., Pehlivan M., Koturoğlu G., Alpoz A. R.
MOLECULAR IMMUNOLOGY , cilt.42, ss.1125-1127, 2005 (SCI-Expanded)

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

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

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

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

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

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

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

Genetik Olarak Modifiye Edilmiş Gıdalar, Genetik Modifikasyonları Oluşturma Yöntemleri ve Toplumsal Önemi.

Özatay Ş., PEHLİVAN S., Sükan S.
ANADOLU UNIVERSITY JOURNAL OF SCIENCE AND TECHNOLOGY –A Applied Sciences and Engineering , cilt.4, ss.111-122, 2003 (SSCI)

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

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

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

Spinal müsküler atrofinin moleküler genetiği.

PEHLİVAN S., Erdem H., topaloğlu h.
ÇOCUK SAĞLIĞI VE HASTALIKLARI DERGİSİ , cilt.40, ss.467-474, 1997 (SCI-Expanded)

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

Diğer Dergilerde Yayınlanan Makaleler

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)

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)

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)

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

Oguz R., Ciftci H. S., Gokce M., Ogret Y., Karadeniz S., Pehlivan S., et al.
Hematology, transfusion and cell therapy , 2023 (ESCI) Creative Commons License identifier identifier

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.
İstanbul Tıp Fakültesi Dergisi , cilt.86, sa.1, ss.1-6, 2023 (ESCI) Sürdürülebilir Kalkınma identifier identifier identifier

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

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

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

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

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

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

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)

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

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

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

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

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

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)

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

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

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)

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

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

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

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

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

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

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

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

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)

- 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)

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)

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

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

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)

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

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

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)

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)

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)

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

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)

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

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

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

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)

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

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)

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

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)

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)

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

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

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)

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)

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)

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)

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)

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

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

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

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)

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

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)

Tıpta Moleküler Genetik Tanı ve Klinik Uygulamaları

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

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

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)

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

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)

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)

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)

DNA mikroarraylerinin tıpta kullanımı ve önemi

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

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)

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)

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)

Revers Transkriptaz Polimeraz Zincir Reaksiyonu ve Uygulama Alanları

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

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)

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)

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

Apoptozisin Morfolojik, Biyokimyasal ve Moleküler İşaretleri

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

Hücre Siklüsü ve Moleküler Kontrolu

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

Spinal müsküler atrofide prenatal tanı.

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

Mitokondrial DNA.

PEHLİVAN S.
ÇUKUROVA ÜNİVERSİTESİ EĞİTİM FAKÜLTESİ DERGİSİ , cilt.22, ss.64-68, 1997 (ESCI)

Lenfoblastoid hücre hattı oluşturulması

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

Myeloid ve lenfoid neoplazilerde sitogenetik değişiklikler. Çukurova Üniversitesi Tıp Fakültesi Dergisi

şahin b., paydaş s., PEHLİVAN S., seyrek e.
ÇUKUROVA ÜNİVERSİTESİ EĞİTİM FAKÜLTESİ DERGİSİ , cilt.19, ss.176-181, 1994 (ESCI)

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 Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 Sürdürülebilir Kalkınma

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 Sürdürülebilir Kalkınma

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

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

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

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

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

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 Creative Commons License

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

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

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 Sürdürülebilir Kalkınma

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

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

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

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

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

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

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

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

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 Sürdürülebilir Kalkınma

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

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

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

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 Sürdürülebilir Kalkınma identifier

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 Creative Commons License Sürdürülebilir Kalkınma

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

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

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

ŞENTÜRK ÇİFTÇİ H., SAVRAN OGUZ F., OĞUZ R., ÖGRET Y., Özdilli K., PEHLİVAN S.
International Participated Erciyes Medical Gnetics days (Uluslararası Katılımlı Erciyees Tıp Genetik Günleri, Kayseri, Türkiye, 21 - 23 Şubat 2019, ss.38

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 identifier

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 identifier

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

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

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 Sürdürülebilir Kalkınma

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 identifier

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 identifier

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

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

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

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 identifier

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 identifier

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 identifier

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

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 identifier

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 identifier

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 identifier

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 identifier

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 identifier

Kitap & Kitap Bölümleri

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

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

HÜCRESEL YAŞLANMA VE NÖRODEJENERATİF HASTALIKLAR

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

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

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

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

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

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

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

PEHLİVAN S., UYSAL M. A., ÇAĞATAY T., ŞENTÜRK ÇİFTÇİ H., PEHLİVAN M., PENÇE S.
Sağlık Bilimleri Alanınsa Araştırma ve Derlemeler, Atilla Atik, Editör, Gece Yayınevi, ss.231-242, 2019

Molecular pathogenesis of rheumatoid arthritis

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

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

Metrikler

Yayın

325

Atıf (WoS)

1177

H-İndeks (WoS)

19

Atıf (Scopus)

1189

H-İndeks (Scopus)

20

Proje

26

Fikri Mülkiyet

1

Tez Danışmanlığı

7

Açık Erişim

18
BM Sürdürülebilir Kalkınma Amaçları