İstanbul Üniversitesi
Akademik Veri Yönetim Sistemi
Yayınlar & Eserler
SCI,SSCI,AHCI İNDEKSLERİNE GİREN DERGİLERDE YAYINLANAN MAKALELER
Durmaz A., Kumral E., Durmaz B., Onay H., Itırlı G., Ozkinay F., et al., "Genetic factors associated with the predisposition to late onset Alzheimer's disease", GENE, vol.19, pp.30493-30497, 2019
Pehlivan S., "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 ", PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY, vol.1, pp.1-7, 2019 (Link)
Pehlivan S., Aydın P., Uysal M.A., Şentürk Çiftçi H., Sever U., Yavuz F.K., et al., "Effect of monoamine oxidase B A644G variant on nicotine dependence and/or schizophrenia risk", REVISTA DE PSIQUIATRIA CLINICA, vol.46, no.1, pp.21-24, 2019
Kurnaz S., Yazıcı A.B., Nursal A.F., Aydın P., Öngel Atar A., Aydın N., et al., "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 ", REVISTA DE PSIQUIATRIA CLINICA, vol.1, no.1, pp.1-7, 2019 (Link)
Oztürk E., Pehlivan S., Ozcan C., Uğur M.G., Balat O., "Paraoxonase-1 Polymorphisms (L55M/Q192R) and Activities (PONase/AREase) in Patients with Idiopathic Recurrent Early Pregnancy Loss: A Preliminary Study.", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.23, pp.501-505, 2019
Pehlivan S., Aydın N., Nursal A., Pehlivan M., Tekcan A., Yavuz F.K., et al., "Association of XRCC1 and XPD functional gene variants with nicotine dependence and/or schizophrenia: A case-control study and in silico analysis ", REVISTA DE PSIQUIATRIA CLINICA, vol.1, pp.1-7, 2019 (Link)
Pehlivan S., Uysal M.A., Aydın N., Nursal A., Pehlivan M., Yavuzlar H., et al., "XRCC4 rs6869366 polymorphism is associated with suspectibility to nicotine dependence and/or schizophrenia", SAO PAULO MEDICAL JOURNAL, vol.45, pp.53-56, 2018
Oztürk E., Pehlivan S., Balat O., Ugur M., Ozcan C., Erkılıç S., "DNA Repair Gene (XPD, XRCC4 and XRCC1) Polymorphisms in Patients with Endometrial Hyperplasia: A Pilot Study", MEDICAL SCIENCE MONITOR BASIC RESEARCH, vol.24, pp.146-150, 2018
Demircioğlu B., Büyükçelik M., Oğuzkan Balcı S., Kul S., Pehlivan S., Çöl N., et al., "Demircioglu Kılıc B, Buyukcelik M, Oguzkan Balcı S, Pehlivan S, Kul S, Col N, Balat A. Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome. Pediatr Nephrol (2018) 33:295–303", PEDIATRIC NEPHROLOGY, vol.33, pp.295-303, 2018
Gülel A., Pehlivan S., Inaloz S., Nursal A.F., Pehlivan M., "Gulel A, Pehlivan S, Inaloz, S, Nursal AF, Pehlivan M. Association of the TNF-?, IL-2, and IL-2RB gene variants with suspectibility to psoriasis in a Turkish cohort. Centr Eur Immunol 2018; 43 (1): 50-57", CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY, pp.50-57, 2018
Pehlivan M., Pehlivan S., Kaynar L., Sever T., Yilmaz M., Eser B., et al., "Endothelial Nitric Oxide Synthase Gene Variants and Susceptibility to Chronic Myeloid Leukemia (Ph+).", INTERNATIONAL JOURNAL OF HUMAN GENETICS, vol.18, pp.247-252, 2018
Pehlivan S., Uysal M.A., Çağatay T., Nursal A., Krause F.E., Sever U., et al., "CYP2A6 gene variants may explain smoking status in a Turkish cohort", PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY, no.1, pp.1-6, 2018
Pehlivan S., Aydın N., Nursal A., Yavuzlar H., Pehlivan M., "Possible association between DNA repair gene variants and cannabis dependence in a Turkish cohort: A pilot study ", PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY, vol.1, pp.13-20, 2018
Eksi F., Pehlivan S., Erdogan M.B., Bayram A., Oguzkan-Balci S., Yamak B., et al., "MBL2 and MIF gene polymorphisms in cardiovascular patients with atherosclerotic lesions undergoing heart valve replacement", BİOTECHNOLOGY & BİOTECHNOLOGİCAL EQUİPMENT, vol.31, pp.1173-1177, 2017
Pehlivan M., Tomatir A., Nursal A., Haydaroğlu Şahin H., Pehlivan S., "The endothelial nitric oxide synthetase gene variants as a risk factor for chronic lymphocytic leukemia. ", UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI, vol.27, pp.85-90, 2017
Pehlivan M., Tomatır A.G., Nursal A.F., Haydaroğlu Şahin H., Pehlivan S., "The endothelial nitric oxide synthetase gene variants as a risk factor for chronic lymphocytic leukemia", UHOD-ULUSLARARASİ HEMATOLOJİ-ONKOLOJİ DERGİSİ, vol.27, pp.85-90, 2017
Haydaroğlu H., Oguzkan-Balci S., Pehlivan S., Özdilli K., Gündoğan E. , Okan V., et al., "Effect of Cytokine Genes in the Pathogenesis and on the Clinical Parameters for the Treatment of Multiple Myeloma", IMMUNOLOGİCAL INVESTİGATİONS, vol.46, pp.10-21, 2017
Pehlivan S., Aydeniz A., Sever T., Altindag O., Pehlivan M., Gursoy S., et al., "The functional variants of endothelial nitric oxide synthase gene associated with rheumatoid arthritis in Turkish adults", CLİNİCAL RHEUMATOLOGY, vol.36, pp.537-540, 2017
Pehlivan S., Uysal M.A., Aydın P., Pehlivan M., Nursal A.F., Yavuzlar H., et al., "Can VNTR variants in eNOS and XRCC4 genes contribute to formation of nicotine dependence and/or schizophrenia? ", BRATİSLAVA MEDİCAL JOURNAL-BRATİSLAVSKE LEKARSKE LİSTY, vol.118, pp.467-471, 2017
Isir A.B., Nacak M., Balci S.O., Aynacioglu A.S., Pehlivan S., "Genetic contributing factors to substance abuse: an association study between eNOS gene polymorphisms and cannabis addiction in a Turkish population", AUSTRALIAN JOURNAL OF FORENSIC SCIENCES, vol.48, pp.676-683, 2016
Pehlivan S., Tomatir A.G., Pehlivan M., Oguzkan-Balci S., "Effects of TNF?, NOS3, MDR1 Gene Polymorphisms on Clinical Parameters, Prognosis and Survival of Multiple Myeloma Cases", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.17, pp.1009-1014, 2016
Pehlivan S., "Nursal AF, Pehlivan M, Sahin HH, Pehlivan S. The Associations of IL-6, IFN-?, TNF-?, IL-10, and TGF-ß1 Functional Variants with Acute Myeloid Leukemia in Turkish Patients. Genet Test Mol Biomarkers. 2016 Aug 3.", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.20, pp.544-551, 2016
Pehlivan S., Balci S.O., Aydeniz A., Pehlivan M., Sever T., Gursoy S., "Might There Be a Link Between Intron 3 VNTR Polymorphism in the XRCC4 DNA Repair Gene and the Etiopathogenesis of Rheumatoid Arthritis?", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.19, pp.48-51, 2015
Pehlivan S., "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.", AUSTRALIAN JOURNAL OF FORENSIC SCIENCES, pp.230-238, 2015
Tomatir A.G., Pehlivan S., Sahin H.H., Balci S.O., Budeyri S., Pehlivan M., "Q192R and L55M Polymorphisms of Paraoxonase 1 Gene in Chronic Myelogenous Leukemia and Chronic Lymphocytic Leukemia", ANTICANCER RESEARCH, vol.35, pp.4807-4812, 2015
Baransel I.A., Ozkorkmaz A., Pehlivan S., "Allele frequencies for 13 STRs loci in a Western Anatolia population and their forensic evaluation.", ANNALS OF HUMAN BIOLOGY, vol.42, pp.494-7, 2015
Isir A.B., Ozkorkmaz A., Baransel C., Ozkorkmaz E.G., Pehlivan S., "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", INTERNATIONAL JOURNAL OF HUMAN GENETICS, vol.15, pp.157-171, 2015
Rostı R.O., Uyguner Z.O., Nazarenko A., Bekerecioglu M., Cadilla C.L., Ozgur H., et al., "Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation", CLINICAL GENETICS, vol.88, pp.489-493, 2015
Aytekin N., Akcali C., Pehlivan S., Kirtak N., Inaloz S., "Investigation of interleukin-12, interleukin-17 and interleukin-23 receptor gene polymorphisms in alopecia areata", JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, vol.43, pp.526-534, 2015
Pehlivan S., "Gene polymorphisms and Febrile Neutropenia in Acute leukemia: no association with IL4, ACE, CCR5, IL-1RA, but the MBL2 and TLR4 in associated with the disease in Turkish patients (A Preliminary Study).", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.18, pp.474-481, 2014
Pehlivan M., Sahin H.H., Pehlivan S., Özdilli K., Kaynar L., Oğuz F., et al., "Prognostic Importance of Single-Nucleotide Polymorphisms in IL-6, IL-10, TGF-beta 1, IFN-gamma, and TNF-alpha Genes in Chronic Phase Chronic Myeloid Leukemia", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.18, pp.403-409, 2014
Özdilli K., Pehlivan S., Ogret Y.D., Sever T., Pehlivan M., İşsever H., et al., "CYTOKINE GENE POLYMORPHISMS IN TURKISH PATIENTS WITH CHRONIC MYELOID LEUKAEMIA AND IN HEALTHY CONTROLS", NOBEL MEDICUS, vol.10, pp.74-78, 2014
Pehlivan M., Sahin H.H., Ozdilli K., Onay H., Ozcan A., Ozkinay F., et al., "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", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.18, pp.474-481, 2014
Pehlivan S., "Mitochondrial uncoupling protein 2 (UCP2) gene polymorphisms are associated with childhood obesity and related metabolic disorders", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.26, pp.277-283, 2013
Pehlivan S., "Can mycoplasma contribute to formation of prostate cancer?", INTERNATIONAL UROLOGY AND NEPHROLOGY, vol.45, pp.33-38, 2013
Pehlivan S., "Association of TAP1 and TAP2 Gene Polymorphisms with Hematological Malignancies.", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.14, pp.5213-5217, 2013
Baysal E., Oğuzkan Balcı S., Tunc O., Celenk F., Deniz M., Kanlikama M., et al., "The polymorphisms of the MBL2 anf MIF genes associated with Pediatric Cochlear Implant Patients", INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, vol.77, pp.338-340, 2013
Balci S., Col-Araz N., Baspinar O., Sever T., Balat A., Pehlivan S., "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.", IRANIAN JOURNAL OF PEDIATRICS, vol.23, pp.603-4, 2013
Sanli M., Akar E., Pehlivan S., Bakır K., Tuncozgur B., Isik A., et al., "The relationship of metalloproteinase gene polymorphisms and lung cancer.", JOURNAL OF SURGICAL RESEARCH, vol.183, pp.517-23, 2013
Ozbas-Gerceker F., Bozman N., Gezici S., Pehlivan M., Yilmaz M., Pehlivan S., et al., "Association of TAP1 and TAP2 gene polymorphisms with hematological malignancies.", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.14, pp.5213-7, 2013
Ozbas-Gerceker F., Bozman N., Kök S., Pehlivan M., Yilmaz M., Pehlivan S., et al., "Association of an LMP2 Polymorphism with Acute Myeloid Leukemia and Multiple Myeloma ", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.14, pp.6399-6402, 2013
Col-Araz N., Pehlivan S., Baspinar O., Sever T., Oğuzkan Balcı S., Balat A., "Association of macrophage migration inhibitory factor and mannose-binding lectin-2 gene polymorphisms in acute rheumatic fever", CARDIOLOGY IN THE YOUNG, vol.23, pp.486-490, 2013
Erturhan S.M., Bayrak Ö., Pehlivan S., Özgül H., Seçkiner I., Sever T., et al., "Can mycoplasma contribute to formation of prostate cancer?", INTERNATIONAL UROLOGY AND NEPHROLOGY, vol.45, pp.33-38, 2013
Oguzkan-Balci S., Col-Araz N., Nacak M., Araz M., Sabancı H., Balat A., et al., " Mitochondrial uncoupling protein 2 (UCP2) gene polymorphisms are associated with childhood obesity and related metabolic disorders ", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.26, pp.277-283, 2013
Pehlivan S., "Trends in the frequency of HLA DR-DQ haplotypes among children and adolescents with type 1 diabetes mellitus in the Southeast Region of Turkey. ", JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.4, pp.189-192, 2012
Sever T., Kilicarslan C., Pehlivan M., Kaynar L., Yilmaz M., Eser B., et al., "Research on and clinical importance of duplications in various chromosomal regions in addition to Philadelphia chromosome in chronic myeloid leukemia.", JOURNAL OF BUON, vol.17, pp.490-6, 2012
Pehlivan S., "Role of cytokine gene (IFN-?, TNF-?, TGF-ß1, IL-6, and IL-10) polymorphisms in pathogenesis of acute rheumatic fever in Turkish children", EUROPEAN JOURNAL OF PEDIATRICS, vol.171, pp.1103-1108, 2012
Pehlivan S., "Childhood obesity and the role of dopamine d2 receptor and cannabinoid receptor-1 gene polymorphisms", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.16, pp.1408-1412, 2012
Pehlivan S., "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", INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, vol.9, pp.506-512, 2012
Col-Araz N., Pehlivan S., Baspinar O., Oguzkan-Balci S., Sever T., Balat A., "Role of cytokine gene (IFN-?, TNF-?, TGF-ß1, IL-6, and IL-10) polymorphisms in pathogenesis of acute rheumatic fever in Turkish children.", EUROPEAN JOURNAL OF PEDIATRICS, vol.171, pp.1103-8, 2012
Col A.N., Nacak M., Oguzkan B.S., Benlier N., Araz M., Pehlivan S., et al., "Childhood obesity and the role of dopamine D2 receptor and cannabinoid receptor-1 gene polymorphisms.", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.16, pp.1408-12, 2012
Karaca E., Tuysuz B., Pehlivan S., Ozkinay F., "First genetic screening for maternal uniparental disomy of chromosome 7 in Turkish silver-russell syndrome patients.", IRANIAN JOURNAL OF PEDIATRICS, vol.22, pp.445-51, 2012
Karaca E., Tüysüz B., Pehlivan S., Ozkinay F., "First Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Turkish Silver-Russell Syndrome Patients", IRANIAN JOURNAL OF PEDIATRICS, vol.22, pp.445-451, 2012
Pehlivan S., "Analysis of Dopamine D2 Receptor (DRD2) Gene Polymorphisms in Cannabinoid", JOURNAL OF FORENSIC SCIENCES, vol.57, pp.1621-1624, 2012
Karaca E., Tüysüz B., Pehlivan S., Ozkinay F., "First Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Turkish Silver-Russell Syndrome Patients", IRANIAN JOURNAL OF PEDIATRICS, vol.22, pp.445-451, 2012
Keskin M., Aygün A., Pehlivan S., Keskin Ö., Kor Y., Balat A., et al., "Trends in the frequency of HLA DR-DQ haplotypes among children and adolescents with type 1 diabetes mellitus in the Southeast Region of Turkey.", JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.4, pp.189-92, 2012
Col-Araz N., Oguzkan-Balci S., Baspinar O., Sever T., Balat A., Pehlivan S., "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.", INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, vol.9, pp.506-12, 2012
Oztürk E., Balat O., Pehlivan S., Ugur M., Ozcan C., Sever T., et al., "Endothelial nitric oxide synthase gene polymorphisms in preeclampsia with or without eclampsia in a Turkish population.", JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, vol.37, pp.1778-83, 2011
Oztürk E., Balat O., Pehlivan S., Ugur M., Ozkan Y., Sever T., et al., "Nitric oxide levels and endothelial nitric oxide synthase gene polymorphisms in Turkish women with idiopathic recurrent miscarriage.", JOURNAL OF THE TURKISH-GERMAN GYNECOLOGICAL ASSOCIATION, vol.12, pp.234-8, 2011
Pehlivan S., "Genetic variation of myeloperoxidase gene contributes to Preeclampsia: A preliminary association study in Turkish population. ", HYPERTENSION IN PREGNANCY, vol.30, pp.377-383, 2011
Pehlivan S., "DNA repear genes polymorphisims in multiple myeloma: no assaciation with XRCC4 (Arg399Gln) polymorphisim, but the XRCC4 (VNTR in intron 3 and G-1394T) and XPD (Lys751Gln) polymorphisms is associated with the disease in Turkish patients", HEMATOLOGY, vol.16, pp.361-367, 2011
Pehlivan S., "Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population", GENETICS AND MOLECULAR RESEARCH, vol.10, pp.4126-4132, 2011
Pehlivan S., "No association between DNA repair gene (XPD, XRCC1 and XRCC4) polymorphisms and Nonsydromic Microtia in Turkish patients. ", PLASTIC AND RECONSTRUCTIVE SURGERY, vol.128, pp.75-76, 2011
Pehlivan S., "Polymorphisms of the DNA repair gene XPD (751) and XRCC1 (399) correlates with risk of hematological malignancies in Turkish population", AFRICAN JOURNAL OF BIOTECHNOLOGY, vol.10, pp.8860-8870, 2011
Pehlivan S., "Endothelial nitric oxide synthetase gene polymorphisms in preeclampsia with or without eclampsia in a Turkish population", JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, vol.37, pp.1778-1783, 2011
Pehlivan S., "Investigation of Glucocorticoid Receptor Gene Bcl-1 Polymorphism in Rheumatoid Arthritis", TURKISH JOURNAL OF RHEUMATOLOGY-TURK ROMATOLOJI DERGISI, vol.26, pp.199-203, 2011
Pehlivan S., "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", PLATELETS, vol.22, pp.588-595, 2011
Oztürk E., Balat O., Pehlivan S., Ugur M., Sever T., "Genetic variation of myeloperoxidase gene contributes to preeclampsia: a preliminary association study in Turkish population.", HYPERTENSION IN PREGNANCY, vol.30, pp.377-83, 2011
Cifci S., Yilmaz M., Pehlivan M., Sever T., Okan V., Pehlivan S., "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.", HEMATOLOGY, vol.16, pp.361-7, 2011
Pehlivan M., Okan V., Sever T., Balci S., Yilmaz M., Babacan T., et al., "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.", PLATELETS, vol.22, pp.588-95, 2011
Sever T., Buyukgural B., Pehlivan S., Rosti R., Bekerecioglu M., "No association between DNA repair gene (XPD, XRCC1, and XRCC4) polymorphisms and nonsyndromic microtia in Turkish patients.", PLASTIC AND RECONSTRUCTIVE SURGERY, vol.128, pp.75e-76e, 2011
Bulut H., Pehlivan M., Alper S., Tomatir A., Onay H., Yüksel S., et al., "Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population.", GENETICS AND MOLECULAR RESEARCH, vol.10, pp.4126-32, 2011
Alpman A., Ozkinay F., Tekgül H., Gökben S., Pehlivan S., Schalling M., et al., "Multidrug resistance 1 (MDR1) gene polymorphisms in childhood drug-resistant epilepsy.", JOURNAL OF CHILD NEUROLOGY, vol.25, pp.1485-90, 2010
Akcali A., Pehlivan S., Pehlivan M., Sever T., Akgul P., Neyal M., "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.", INTERNATIONAL JOURNAL OF IMMUNOGENETICS, vol.37, pp.91-5, 2010
Pehlivan S., "Multidrug Resistance 1 (MDR1) Gene Polymorphisms in Childhood Drug-Resistant Epilepsy", JOURNAL OF CHILD NEUROLOGY, vol.151, pp.1485-1490, 2010
Pehlivan S., "The value of XPD and XRCC1 genotype polymorphisms to predict clinical outcome in metastatic colorectal carcinoma patients with irinotecan-based regimens", JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, vol.136, pp.803-809, 2010
Pehlivan S., "Association between urotensin II gene polymorphism and pre-eclampsia.", EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, vol.151, pp.140-142, 2010
Pehlivan S., "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).", AFRICAN JOURNAL OF BIOTECHNOLOGY, pp.3042-3047, 2010
Pehlivan S., "Gene methylation of SFRP2, P16, DAPK1, HIC1, and MGMT and KRAS mutations in sporadic colorectal cancer", CANCER GENETICS AND CYTOGENETICS, vol.201, pp.128-132, 2010
Pehlivan S., "Thalassemia mutations in Gaziantep,Turkey", AFRICAN JOURNAL OF BIOTECHNOLOGY, pp.1255-1259, 2010
Artac M., Bozcuk H., Pehlivan S., Akcan S., Pehlivan M., Sever T., et al., "The value of XPD and XRCC1 genotype polymorphisms to predict clinical outcome in metastatic colorectal carcinoma patients with irinotecan-based regimens.", JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, vol.136, pp.803-9, 2010
Dikensoy E., Balat O., Ugur M., Pehlivan S., Balci S., "Association between urotensin II gene polymorphism and pre-eclampsia.", EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, vol.151, pp.140-2, 2010
Erciyas K., Pehlivan S., Sever T., Igci M., Arslan A., Orbak R., "Association between TNF-alpha, TGF-beta1, IL-10, IL-6 and IFN-gamma gene polymorphisms and generalized aggressive periodontitis.", CLINICAL AND INVESTIGATIVE MEDICINE, vol.33, pp.E85-E85, 2010
Erciyas K., Pehlivan S., Sever T., Orbak R., "Genetic variation of myeloperoxidase gene contributes to aggressive periodontitis: a preliminary association study in Turkish population.", DISEASE MARKERS, vol.28, pp.95-9, 2010
Pehlivan S., Artac M., Sever T., Bozcuk H., Kilinçarslan C., Pehlivan M., "Gene methylation of SFRP2, P16, DAPK1, HIC1, and MGMT and KRAS mutations in sporadic colorectal cancer.", CANCER GENETICS AND CYTOGENETICS, vol.201, pp.128-32, 2010
Akcali A., Pehlivan S., Pehlivan M., Sever T., Neyal M., "Association of macrophage migration inhibitory factor gene promoter polymorphisms with multiple sclerosis in Turkish patients.", JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, vol.38, pp.69-77, 2010
Pehlivan S., Ozkinay F., Alper S., Onay H., Yuksel E., Pehlivan M., et al., "Association between IL4 (-590), ACE (I)/(D), CCR5 (Delta32), CTLA4 (+49) and IL1-RN (VNTR in intron 2) gene polymorphisms and vitiligo.", EUROPEAN JOURNAL OF DERMATOLOGY, vol.19, pp.126-8, 2009
Karaoglan I., Pehlivan S., Namiduru M., Pehlivan M., Kilinçarslan C., Balkan Y., et al., "TNF-alpha, TGF-beta, IL-10, IL-6 and IFN-gamma gene polymorphisms as risk factors for brucellosis.", NEW MICROBIOLOGICA, vol.32, pp.173-8, 2009
Cebesoy F., Balat O., Pehlivan S., Kutlar I., Dikensoy E., Ugur M., "Is pregnancy loss after amniocentesis related to the volume of amniotic fluid obtained?", ARCHIVES OF GYNECOLOGY AND OBSTETRICS, vol.279, pp.357-60, 2009
Onay H., Pehlivan S., Koyuncuoglu M., Kirkali Z., Ozkinay F., "Multigene methylation analysis of conventional renal cell carcinoma.", UROLOGIA INTERNATIONALIS, vol.83, pp.107-12, 2009
Serdaroğlu G., Alpman A., Tosun A., Pehlivan S., Ozkinay F., Tekgül H., et al., "Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphisms.", PEDIATRIC NEUROLOGY, vol.40, pp.113-6, 2009
Saygili E., Aksoy N., Pehlivan M., Sever T., Yilmaz M., Cimenci I., et al., "Enzyme levels and G-463A polymorphism of myeloperoxidase in chronic lymphocytic leukemia and multiple myeloma.", LEUKEMIA, vol.50, pp.2030-7, 2009
Aksoy S., Erbagci Z., Saygili E., Sever T., Erbagci A., Pehlivan S., "Analysis of myeloperoxidase promotor polymorphism and enzyme activity in Turkish patients with vitiligo.", EUROPEAN JOURNAL OF DERMATOLOGY, vol.19, pp.576-80, 2009
Cogulu O., Durmaz B., Pehlivan S., Alpman A., Ozkinay F., "Evaluation of the SMN and NAIP genes in a family: homozygous deletion of the SMN2 gene in the fetus and outcome of the pregnancy.", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.13, pp.287-8, 2009
Unuvar D., Isir B.A., Cankus G., Pehlivan S., "Y CHROMOSOMAL STR LOCUS DYS385 IN AZOOSPERMIC AND FERTILE MEN FROM THE AEGEAN REGION OF TURKEY: IS THERE ANY FORENSIC RELEVANCE?", BALKAN JOURNAL OF MEDICAL GENETICS, vol.11, pp.39-44, 2008
Aylin A., Cengiz T., Emin E., Neriman A., Pehlivan S., "Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: a preliminary study.", NEUROLOGY INDIA, vol.56, pp.156-60, 2008
Onay H., Ugurlu T., Aykut A., Pehlivan S., Inal M., Tinar S., et al., "Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.", GYNECOLOGIC AND OBSTETRIC INVESTIGATION, vol.66, pp.104-10, 2008
Cogulu O., Onay H., Uzunkaya D., Gunduz C., Pehlivan S., Vardar F., et al., "Role of angiotensin-converting enzyme gene polymorphisms in children with sepsis and septic shock.", PEDIATRICS INTERNATIONAL, vol.50, pp.477-80, 2008
Onay H. , Pehlivan M., Alper S., Özkınay F., Pehlivan S., "Might there be a link between mannose binding lectin and vitiligo?", EUROPEAN JOURNAL OF DERMATOLOGY, vol.17, pp.146-148, 2007
Ozkinay F., Pehlivan S., Onay H. , Van Den Berg P., Vardar F., Koturoğlu G., et al., "Purine nucleoside phosphorylase deficiency in a patient with Spastic Paraplegia and Recurrent infections", JOURNAL OF CHILD NEUROLOGY, vol.22, pp.741-743, 2007
Yilmaz M., Demirhan O., Kuçukosmanoglu E., Pehlivan M., Okan V., Balat O., et al., "Pregnancy in patients with chronic myeloid leukemia treated with imatinib.", LEUKEMIA, vol.48, pp.2454-6, 2007
Pehlivan M., Pehlivan S., Büyükkeçeci F., Çağırgan S., Yılmaz M., Omay B.S., et al., "Factor VIII-intron 1 inversion of Hemophilia A patients in West Anatolia ", BALKAN JOURNAL OF MEDICAL GENETICS, vol.10, pp.49-50, 2007
Koturoglu G., Onay H., Midilli R., Pehlivan S., Eren E., Itirli G., et al., "Evidence of an association between mannose binding lectin codon 54 polymorphism and adenoidectomy and/or tonsillectomy in children.", INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, vol.71, pp.1157-61, 2007
Vardar F., Pehlivan S., Onay H., Atlihan F., Güliz N., Ozkinay C., et al., "Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis.", TURKISH JOURNAL OF PEDIATRICS, vol.49, pp.270-3, 2007
Pehlivan M., Pehlivan S., Onay H., Koyuncuoğlu M., Kırkali Z., "Can mycoplasma-mediated oncogenesis be responsible for formation of conventional renal cell carcinoma? ", UROLOGY, vol.65, pp.411-414, 2005
Itırlı G., Pehlivan M., Alper S., Onay H. , Yüksel E. , Özkınay F., et al., "Exon-3 Polymorphism of CTLA-4 gene in Turkish Patients with Vitiligo.", JOURNAL OF DERMATOLOGICAL SCIENCE, vol.38, pp.225-227, 2005
Pehlivan S., Sipahi M., Özkınay F., Pehlivan M., Koturoğlu G., Alpoz A.R., "Might There be a link between MBL and dental caries?", MOLECULAR IMMUNOLOGY, vol.42, pp.1125-1127, 2005
Paydaş S., Sarpel S., Gilman-Sachs A., Tuncer I., Pehlivan S., Tunalı N., et al., "DNA ploidy, proliferative activity, and Concanavalin A Reactivity in breast cancer. ", JOURNAL OF SURGICAL ONCOLOGY, vol.56, pp.21-24, 1994
DİĞER DERGİLERDE YAYINLANAN MAKALELER
Nursal A.F., Pehlivan M., Kurnaz S., Pehlivan S., "Effect of the IL-17F rs763780 variant on chronic lymphocytic leukemia and multiple myeloma risk in a Turkish cohort. ", Istanbul Med J, cilt.19, ss.39-42, 2018
Nursal A.F., Bekerecioğlu M., Buyukgural B., Pehlivan S., "Interleukin-1 gene variants and the risk of non-syndromic microtia", Pam Med J, cilt.11, ss.89-94, 2018
Hacıosmanoğlu E., Özkök F., Onsu A.K., Bektaş M., Varol B., Pehlivan S., "Synthesis of New Anthraquinone Derivatives and Anticancer Effects on Breast Cancer Cell Lines", The Eurasia Proceedings of Science, Technology, Engineering & Mathematics (EPSTEM) , vol.4, pp.271-276, 2018 (Link)
Pehlivan S., "Interleukin-1 gene variants and the risk of non-syndromic microtia", Pam Med J, cilt.11, ss.89-94, 2018
Pehlivan S., Inaloz S., Nursal A.F., Gülel A., Pehlivan M., "- Are there any association between functional variants of NOS3 gene and Psoriasis? ", Istanbul Med J, cilt.19, ss.152-157, 2018
Tunc O., Baysal E., Oğuzkan Balcı S., Mumbuç S., Güngör Tunç N., Pehlivan S., et al., "Glutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss", ENT Updates, vol.7, pp.126-130, 2017
Nursal A.F., Bekerecioğlu M., Pehlivan S., Sever T., Buyukgural B., "Cytokine gene variants/expressions and non-syndromic microtia- is there a link?", ENT Updates, vol.7, pp.62-67, 2017
Harunlar T., Aydeniz A., Pehlivan S., Pehlivan M., Altindag O., Gürsoy S., "Influence of promoter region of TNF-? gene polymorphisms on anti-TNF treatment in rheumatoid arthritis: Preliminary report", Pamukkale Medical Journal, cilt.10, ss.216-220, 2017
Pehlivan S., Oğuzkan Balcı S., Inaloz S., Keskin Ö., Küçükosmanoğlu E., Gülel A., et al., "Might there be a link between high expression of interleukine 10 and Netherton Syndrome?. ", Kahramanmaraş Sütçü İmam Üniversitesi Tıp Fakültesi Dergisi , cilt.11, ss.1-5, 2016
Kis C., Pehlivan S., Eser B., Yilmaz M., Kaynar L., Oğuzkan Balcı S., et al., "Significance of the T3151, T317L, E255K AND Y253H BCR-ABL gene mutations in Philadelphia positive Chronic Myeloid Leukemia patients", Kahramanmaraş Sütçü İmam Üniversitesi Tıp Fakültesi Dergisi , cilt.11, ss.9-13, 2016
Büyükgüral B., Pehlivan S., Nursal A.F., Bekerecioğlu M., "The roles of endothelial nitric oxide synthase (eNOS) and myeloperoxidase (MPO) genes in microtia ", ENT Updates, vol.6, no.1, pp.121-125, 2016
Baysal E., Oğuzkan Balcı S., Celenk F., Kahraman M., Deniz M., Tunc O., et al., "Cytokine gene polymorphisms and expression in Turkish pediatric cochlear implant patients.", ENT Updates, vol.6, pp.1-4, 2016
Pehlivan S., Ozdilli K., "Negatif Kronik Myeloproliferatif Hastalıkların Moleküler Patogenezi", Türkiye Klinikleri J Hematol-Special Topics, cilt.6, ss.4-9, 2013
Gül Ö., Oztürk E., Uğur M.G., Cebesoy F., Kurtul N., Pençe S., et al., "Pereklamptik Gebelerde Serum Total Sialik Asit Seviyeleri ve Sialik Asit Esteraz Gen Varyasyonu", Türk Jinekoloji ve Obstetrik Derneği Dergisi, cilt.9, ss.99-105, 2012
Oztürk E., Dikensoy E., Balat O., Uğur M.G., Oğuzkan Balcı S., Aydın A., et al., "Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms with Endometrial Carcinoma: A Preliminary Study", Journal of the Turkish-German Gynecological Association, cilt.12, ss.229-233, 2011
Aydeniz A., Sever T., Pehlivan S., Pehlivan M., Altındağ Ö., Büdeyri S., et al., "Investigation of Glucocorticoid Receptor Gene Bcl-1 Polymorphism in Rheumatoid Arthritis.", Turkish Journal of Rheumatology, cilt.26, ss.199-203, 2011
Dikensoy E., Balat O., Pehlivan S., Cebesoy F., Kutlar I., Sever T., et al., "Yanlış negatif QF-PCR ve Trizomi 18 – Trizomi 9 Mozaizm. ", J Turk Soc Obstet Gynecol, cilt.8, ss.67-70, 2011
Oztürk E., Balat O., Pehlivan S., Uğur M.G., Ozkan Y., Sever T., et al., "Nitric Oxide Levels and Endothelial Nitric Oxide Synthase Gene Polymorphisms in Turkish Women with Idiopathic Recurrent Miscarriage", Journal of the Turkish-German Gynecological Association, cilt.12, ss.234-238, 2011
Pehlivan S., Avcı S., Sever T., Bayram A., Oğuzkan Balcı S., "Dolaşımdaki serbest DNA ve önemi. ", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.16, ss.75-80, 2010
Rostı R.O., Inaloz S., Erciyas K., Pehlivan S., "16 yaşıdna bir erkek olguda Pakionişi Konjenita’nın klinik bulguları. ", Mersin Üniversitesi Sağlık Bilimleri Degisi, cilt.3, ss.26-29, 2010
Dikensoy E., Sever T., Pehlivan S., Balat O., Cebesoy F., "Nöral Tüp Defektli Çocuğu Olan Annelerde Myeloperoksidaz Geni Promotor Polimorfizminin Araştırılması", TJOD, cilt.7, ss.251-255, 2010
Erciyas K., Pehlivan S., Inaloz S., Erciyas A.F., Sever T., "Late Onset Papillon-Lefevre Sendromu Olgusu", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.15, ss.44-48, 2009
Pehlivan S., Pehlivan M., "Eritrosit Membran Hastalıkları ve Enzim Defektlerinin Moleküler Genetiği", Türkiye Klinikleri - Moleküler Hematoloji Özel Sayısı, cilt.2, ss.14-21, 2009
Güven S., Pehlivan M., Yilmaz M., Okan V., Pehlivan S., "Akut Lösemilerde MIF Genindeki Polimorfizmlerin Önemi ve Febril Nötropenik Ataklara Etkisi. ", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.15, ss.5-9, 2009
Pehlivan S., Onay H. , Itirli G., Erbay A., Koman A., Unal D., et al., "Türk Toplumundaki Nörofibromatozis Tip 1’li Hastalarda Gen Mutasyonlarının Araştırılması.", Acta Oncologica Turcica, cilt.42, ss.13-16, 2009
Pehlivan S., Aydeniz A., Sever T., Altindag O., Oğuzkan Balcı S., Harunlar T., "No association Between Myeloperoxidase Gene G-463A Polymorphism and Rheumatoid Arthritis ", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.15, ss.14-16, 2009
Pehlivan S., Onay H., Tavmergen E., Tavmergen E.N., Cogulu O., Ozkinay F., "Erkek İnfertilitesinde Anjiotensin Konverting Enzim Polimorfizmleri. ", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.14, ss.15-17, 2008
Ozbas-Gerceker F., Oguzkan-Balci S., Pehlivan S., "Biyobankalar ve Biyobankalamada Etik Konular", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.14, ss.35-40, 2008
Artac M., Pehlivan S., Pehlivan M., Gelen T., Akcan S., "The role of microsatellite instability to predict from irinotekan-based regimens in metastatic colorectal cancer", Turkish Journal of Cancer, cilt.38, ss.49-56, 2008
Kilicarslan C., Pehlivan S., "Türk Populasyonunda Kolesterol Ester Transfer Protein Genindeki TaqIB Polimorfizm Sıklığının Araştırılması. ", Çukurova Tıp Dergisi, cilt.31, ss.73-76, 2007
Pehlivan S., "Tıpta Moleküler Genetik Tanı ve Klinik Uygulamaları", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.13, ss.17-21, 2007
Sever T., Pehlivan S., "Sağlıklı Türk Populasyonunda XRCC1 DNA Tamir Geninindeki A399G Polimorfizm Sıklığının Araştırılması.", Gaziantep Üniversitesi Tıp Fakültesi Dergisi, cilt.13, ss.22-24, 2007
Pehlivan S., Durmaz B., Aykut A., Ozkinay F., "Küçük RNA’ların etki mekanizmaları ve önemi", Arşiv kaynak tarama dergisi, cilt.15, ss.320-330, 2006
Sukatar İ., Sukatar A. , Pehlivan S., "İzmir körfezinde gelişen bir kahverengi alg olan Cystoseria mediterranea Sauvageau’dan DNA İzolasyonu.", Türk sucul yaşam dergisi, cilt.13, ss.100-103, 2005
Pehlivan S., Onay H., Bulut H., Itirli G., Ekmekçi A., Unuvar D., et al., "RNA polimerazların görevleri ve önemi", Arşiv kaynak tarama dergisi, cilt.13, ss.575-592, 2004
Pehlivan S., Onay H., Ekmekçi A., Unuvar D., Bulut H., Ozkinay F., "DNA replikasyonu ve tamirinde görevli DNA polimerazlar. ", Arşiv kaynak tarama dergisi, cilt.13, ss.256-278, 2004
Şenol S., Pehlivan M., Bal F., Pehlivan S., "Kronik X ışınına maruz kalan bireylerin kromozomları üzerine beta-karoten etkisinin araştırılması", İzmir Atatürk Eğitim Hastanesi Tıp Dergisi, cilt.41, ss.173-177, 2004
Pehlivan M., Onay H., Pehlivan S., "DNA mikroarraylerinin tıpta kullanımı ve önemi", Arşiv kaynak tarama dergisi, cilt.13, ss.439-447, 2004
Okutucu B., Pehlivan S., "Revers Transkriptaz Polimeraz Zincir Reaksiyonu ve Uygulama Alanları", Arşiv Kaynak Tarama Dergisi, cilt.12, ss.138-148, 2003
Özatay Ş., Pehlivan S., Sükan S., "Genetik Olarak Modifiye Edilmiş Gıdalar, Genetik Modifikasyonları Oluşturma Yöntemleri ve Toplumsal Önemi.", ANADOLU UNIVERSITY JOURNAL OF SCIENCE AND TECHNOLOGY –A Applied Sciences and Engineering, cilt.4, ss.111-122, 2003
Pehlivan S., Ozkinay F., Izzetoğlu S., Cogulu O., Kunt A., Çankaya T., "Spinal Müsküler Atrofi’de Moleküler Tanı: Ege Bölgesinde bir referans merkezindeki uygulamalar. ", Ege Tıp Dergisi, cilt.41, ss.7-10, 2002
Erdem H., Dayangaç D., Pehlivan S., Talim B., Topaloğlu H., "Centromeric SMN deletions in Various Congenital Muscular Dystrophies.", Turkish Journal of Medical Sciences, vol.32, pp.145-148, 2002
Koyuncuoglu M., Pehlivan M., Pehlivan S., Kırkalı Z., "Böbreğin Renal Hücreli Kanserlerinde Prognostik Faktörlerden Cathepsin D1 Ekspresyonu ve Genetik Heterojenitenin Önemi", Ege Tıp Dergisi, cilt.40, ss.151-157, 2001
Göncü E., Pehlivan S., "Apoptozisin Morfolojik, Biyokimyasal ve Moleküler İşaretleri", arşiv kaynak tarama dergisi, cilt.10, ss.292-306, 2001
Okutman Ö., Pehlivan S., "Hücre Siklüsü ve Moleküler Kontrolu", arşiv kaynak tarama dergisi, cilt.10, ss.277-291, 2001
Pehlivan S., Erdem H., Topaloğlu H., "Spinal müsküler atrofinin moleküler genetiği. ", ÇOCUK SAĞLIĞI VE HASTALIKLARI DERGİSİ, cilt.40, ss.467-474, 1997
Erdem H., Pehlivan S., Topaloğlu H., "Spinal müsküler atrofide prenatal tanı. ", katkı pediatri dergisi, cilt.18, ss.425-430, 1997
Pehlivan S., "Mitokondrial DNA. ", Çukurova Üniversitesi Tıp Fakültesi Dergisi, cilt.22, ss.64-68, 1997
Erdem H., Pehlivan S., Özgüç M., "Lenfoblastoid hücre hattı oluşturulması", ÇOCUK SAĞLIĞI VE HASTALIKLARI DERGİSİ, cilt.39, ss.197-198, 1996
Şahin B., Paydaş S. , Pehlivan S., Seyrek E., "Myeloid ve lenfoid neoplazilerde sitogenetik değişiklikler. Çukurova Üniversitesi Tıp Fakültesi Dergisi", Çukurova Üniversitesi Tıp Fakültesi Dergisi, cilt.19, ss.176-181, 1994
Terzioğlu O., Pehlivan S., "Escherichia coli suşlarında beta-laktam antibiyotik dirençliliği ve beta-laktamaz inhibitörlerinin etkisinin in vitro üretim sisteminde izlenmesi.", ANKEM Dergisi, cilt.19, ss.176-181, 1989
HAKEMLİ KONGRE / SEMPOZYUMLARIN BİLDİRİ KİTAPLARINDA YER ALAN YAYINLAR
Pehlivan S., Uysal M.A., Çağatay T., Şentürk Çiftçi H., Pehlivan M., Pençe S., "Cyp2A13 Polimorfizmleri ve Nikotin Bağımlılığına Duyarlılığı: Genetik Bir İlişkilendirmeBir Silico Analizi.", International Academic research Symposium, İZMİR, TÜRKIYE, 5-6 Nisan 2019, pp.15-15
Şentürk Çiftçi H., Savran Oguz F., Oğuz R., Ögret Y., Özdilli K., Pehlivan S., "Cytokine Gene Polymorphism Frequency in Turkish Population with Comparisons to Other populations: A meta-analysis. ", International Participated Erciyes Medical Gnetics days (Uluslararası Katılımlı Erciyees Tıp Genetik Günleri, KAYSERİ, TÜRKIYE, 21-23 Şubat 2019, ss.38-38
Şentürk Çiftçi H., Pehlivan S., "In Silico Analysis of the TNF-alpha Effect on Cancer (Multple Myeloma) and Autoimmune Diseases (Psoriasis and Rheumatiod Arthritisis", Uluslararsı Bilimsel Araştırmalar Kongresi , NEVŞEHİR, TÜRKIYE, 9-12 Eylül 2018, vol.1, pp.67-67
Pehlivan S., Şentürk Çiftçi H., "Association and in silico analysis of (Diseases) Genetic Merkers Affecting CYPA6 Gene and Smoking Status Risk.", Uluslararsı Bilimsel Araştırmalar Kongresi , NEVŞEHİR, TÜRKIYE, 9-12 Eylül 2018, vol.1, pp.15-15
Oyacı Y., Aytaç H.M., Şentürk Çiftçi H., Yazar M.S., Pehlivan S., "Can VNTR Variants in eNOS and XRCC4 genes contibute to formation of Bİpolar disorder", Uluslararsı Bilimsel Araştırmalar Kongresi , NEVŞEHİR, TÜRKIYE, 9-12 Eylül 2018, vol.1, pp.81-81
Şentürk Çiftçi H., Savran Karadeniz M., Oğuz R., Aygün S., Aygün E., Pehlivan S., et al.,"THE EFFECT OF CATECHOL-O-METHYLTRANSFERASE (COMT) VARIANTS ON ACUTE POSTOPERATIVE MORPHINE REQUIREMENTS: A CLINICAL PILOT STUDY", Erciyes Medikal Genetik Days, KAYSERİ, TÜRKIYE, 11-13 Mayıs 2017, pp.50-50
KİTAP ve KİTAP BÖLÜMLERİ
Pehlivan S., Uysal M.A., Çağatay T., Şentürk Çiftçi H., Pehlivan M., Pençe S., "CYP2A13 Polimorfizmleri ve Nikotin Bağımlılığına Duyarlılığı: Genetik Bir İlişkilendirme ve Bir Siliko Analizi", Sağlık Bilimleri Alanında Araştırma ve Derlemeler, Doç. Dr. Meriç ERASLAN, Ed., Gece Akademisi, Ankara, ss.233-242, 2019
Şentürk Çiftçi H., Nursal A.F., Pehlivan S., "DNA Tamir Genlerinin (XPD, XRCC1 ve XRCC4) Siliko Ekspresyon ve Hastalık İlişkili Analizleri", Tıpta İnovasyon ve Renovasyon Mozaiği, Sibel AKYOL, Ed., Berikan Elektronik Basım Yayın, Ankara, ss.545-555, 2018
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