Bağcı, B., Bağcı, G., Hüzmeli, C., Sezgin, İ., ÖZDEMİR, Ö. (2016) "Associations of fractalkine receptor CX3CR1 and CCR5 gene variants with hypertension diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis", International Urology and Nephrology, 48 (7) pp. 1163-1170 [SCI] Link DOI " data-bs-content-id="YazarBilgi-21437">
Bağcı, B., Bağcı, G., Hüzmeli, C., Sezgin, İ., ÖZDEMİR, Ö. (2016) "Associations of fractalkine receptor CX3CR1 and CCR5 gene variants with hypertension diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis", International Urology and Nephrology, 48 (7) pp. 1163-1170 [SCI] Link DOI Bağcı, B., Bağcı, G., Hüzmeli, C., Sezgin, İ., ÖZDEMİR, Ö. (2016) "Associations of fractalkine receptor CX3CR1 and CCR5 gene variants with hypertension diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis", International Urology and Nephrology, 48 (7) pp. 1163-1170 [SCI] Link DOI
Akbal, A., Reşorlu, H., Gökmen, F., Savaş, Y., Zateri, C., Sılan, F., ÖZDEMİR, Ö. (2015) "The relationship between C reactive protein rs3091244 polymorphism and ankylosing spondylitis", International Journal of Rheumatic Diseases, (0) [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-21438">
Akbal, A., Reşorlu, H., Gökmen, F., Savaş, Y., Zateri, C., Sılan, F., ÖZDEMİR, Ö. (2015) "The relationship between C reactive protein rs3091244 polymorphism and ankylosing spondylitis", International Journal of Rheumatic Diseases, (0) [SCI Expanded] Link DOI Akbal, A., Reşorlu, H., Gökmen, F., Savaş, Y., Zateri, C., Sılan, F., ÖZDEMİR, Ö. (2015) "The relationship between C reactive protein rs3091244 polymorphism and ankylosing spondylitis", International Journal of Rheumatic Diseases, (0) [SCI Expanded] Link DOI
Uludağ, A., Uysal, A., Ertekin, Y.H., Tekin, M., Kütük, B., Sılan, F., ÖZDEMİR, Ö. (2016) "Prevalence and mutations of thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province Turkey", Balkan Journal of Medical Genetics, 19 (1) pp. 29-33 [SCI] Link DOI " data-bs-content-id="YazarBilgi-21440">
Uludağ, A., Uysal, A., Ertekin, Y.H., Tekin, M., Kütük, B., Sılan, F., ÖZDEMİR, Ö. (2016) "Prevalence and mutations of thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province Turkey", Balkan Journal of Medical Genetics, 19 (1) pp. 29-33 [SCI] Link DOI Uludağ, A., Uysal, A., Ertekin, Y.H., Tekin, M., Kütük, B., Sılan, F., ÖZDEMİR, Ö. (2016) "Prevalence and mutations of thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province Turkey", Balkan Journal of Medical Genetics, 19 (1) pp. 29-33 [SCI] Link DOI
Sılan, F., Mosse, İ., Gonchar, A., Sedlyar, N., Kilchevsky, A.V., Yıldız, O., Kuru, B., ÖZDEMİR, Ö. (2016) "Comparison of the thrombophilic gene polymorphisms and recurrent pregnancy loss Results on combined gene effect of FVLeiden FVR2 FXIII MTHFR A1298C and C677T PAI 1 4G 5G and ACE I D genes in RPL Women from Misk Belarus and Canakkale Sivas Turkey", Biomedical Genetics and Genomics, 1 (4) [SCI] Link DOI " data-bs-content-id="YazarBilgi-21441">
Sılan, F., Mosse, İ., Gonchar, A., Sedlyar, N., Kilchevsky, A.V., Yıldız, O., Kuru, B., ÖZDEMİR, Ö. (2016) "Comparison of the thrombophilic gene polymorphisms and recurrent pregnancy loss Results on combined gene effect of FVLeiden FVR2 FXIII MTHFR A1298C and C677T PAI 1 4G 5G and ACE I D genes in RPL Women from Misk Belarus and Canakkale Sivas Turkey", Biomedical Genetics and Genomics, 1 (4) [SCI] Link DOI Sılan, F., Mosse, İ., Gonchar, A., Sedlyar, N., Kilchevsky, A.V., Yıldız, O., Kuru, B., ÖZDEMİR, Ö. (2016) "Comparison of the thrombophilic gene polymorphisms and recurrent pregnancy loss Results on combined gene effect of FVLeiden FVR2 FXIII MTHFR A1298C and C677T PAI 1 4G 5G and ACE I D genes in RPL Women from Misk Belarus and Canakkale Sivas Turkey", Biomedical Genetics and Genomics, 1 (4) [SCI] Link DOI
Sılan, F., Yıldız, O., Urfalı, M., Güler, Z., ÖZDEMİR, Ö. (2016) "A mental and motor retarded dysmorphic case with heterozygous 1p36 deletion Comparable results from cytogenetic MicroArray CGH FISH and MLPA techniques", Merit Research Journal of Medicine and Medical Sciences, 4 (12) pp. 490-494
ÖZDEMİR, Ö., Paksoy, B., Gürgen, A., Oruç, M., Yıldız, O., Uysa, D., Uludağ, A., Sılan, F. (2016) "An infertile case of 47 XYY syndrome without autistic spectrum Cost effective well define of extra Y chromosome by GTG C bandings QF PCR and FISH analyses", Cumhuriyet Medical Journal, 38 (4) pp. 355-360 [TR Dizin]
Özdal, A., Erselcan, T., ÖZDEMİR, Ö., Silov, G., Erdoğan, Z., Turhal, Ö. (2016) "Micronucleus frequencies in groups receiving external or internal radiation", Indian Journal of Nuclear Medicine, 31 (3) p. 179 [SCI] Link DOI " data-bs-content-id="YazarBilgi-21444">
Özdal, A., Erselcan, T., ÖZDEMİR, Ö., Silov, G., Erdoğan, Z., Turhal, Ö. (2016) "Micronucleus frequencies in groups receiving external or internal radiation", Indian Journal of Nuclear Medicine, 31 (3) p. 179 [SCI] Link DOI Özdal, A., Erselcan, T., ÖZDEMİR, Ö., Silov, G., Erdoğan, Z., Turhal, Ö. (2016) "Micronucleus frequencies in groups receiving external or internal radiation", Indian Journal of Nuclear Medicine, 31 (3) p. 179 [SCI] Link DOI
Paksoy, B., Sılan, F., Yıldız, O., ÖZDEMİR, Ö., Tas, Z.T. (2016) "Microtia micrognati facial dysmorphism short stature and mental retardation A rare case with Meirer Gorlin syndrome", genetic counseling, 27 (2) pp. 149-157 [SCI]
Doğan, A.S., Yenicesu, C., Sucaklı, M.H., ÖZDEMİR, Ö., Demirel, Y. (2014) "Hipertansif hastaların ailelerinde Apo E gen polimorfizmleri ve kan lipit profillerinin değerlendirilmesi", Cumhuriyet Tıp Dergisi, (36) pp. 459-465 [TR Dizin] DOI " data-bs-content-id="YazarBilgi-21446">
Doğan, A.S., Yenicesu, C., Sucaklı, M.H., ÖZDEMİR, Ö., Demirel, Y. (2014) "Hipertansif hastaların ailelerinde Apo E gen polimorfizmleri ve kan lipit profillerinin değerlendirilmesi", Cumhuriyet Tıp Dergisi, (36) pp. 459-465 [TR Dizin] DOI Doğan, A.S., Yenicesu, C., Sucaklı, M.H., ÖZDEMİR, Ö., Demirel, Y. (2014) "Hipertansif hastaların ailelerinde Apo E gen polimorfizmleri ve kan lipit profillerinin değerlendirilmesi", Cumhuriyet Tıp Dergisi, (36) pp. 459-465 [TR Dizin] DOI
Doğan, Ö.T., Özşahin, S.L., Gül, E., Binnur, K., Berk, S., ÖZDEMİR, Ö., Akkurt, İ. (2010) "A Frame shift Mutation in the SLC34A2 Gene in Three Patients with Pulmonary Alveolar Microlithiasis in an Inbred Family", INTERNAL MEDICINE, 49 (1) pp. 45-49 [SCI Expanded]
Kılıç, S., ÖZDEMİR, Ö., Sılan, F., Işık, S., Yıldız, O., Damla, K., Sılan, C., Öğretmen, Z. (1900) "The possible association between germ line Methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in Turkish population Accepted 2015", Clinical and Experimental Dermatology, (0) [SCI]
Öğretmen, Z., Hız, M.M., Sılan, F., Koşar, Ş., ÖZDEMİR, Ö. (2014) "Is the HLA B27 genotype a risc faktor for psoriatic arthritis and psoriasis vulgaris", TURKDERM, 48 (3) pp. 131-134 [ESCI] Link DOI " data-bs-content-id="YazarBilgi-21451">
Öğretmen, Z., Hız, M.M., Sılan, F., Koşar, Ş., ÖZDEMİR, Ö. (2014) "Is the HLA B27 genotype a risc faktor for psoriatic arthritis and psoriasis vulgaris", TURKDERM, 48 (3) pp. 131-134 [ESCI] Link DOI Öğretmen, Z., Hız, M.M., Sılan, F., Koşar, Ş., ÖZDEMİR, Ö. (2014) "Is the HLA B27 genotype a risc faktor for psoriatic arthritis and psoriasis vulgaris", TURKDERM, 48 (3) pp. 131-134 [ESCI] Link DOI
Koksal, B., Nur, N., Sari, M., Candan, F., Acemoglu, M., Kocak, N., Ozen, F., Ozdemir, O. (2009) "Clinical and molecular analysis of common MEFV gene mutations in familial Mediterranean fever in Sivas population", Biologia, 64 (2) pp. 388-393 [SSCI]
Uludağ, A., Sılan, C., Sinem, A., Çisem, A., Uludağ, A., Sılan, F., ÖZDEMİR, Ö. (2013) "Relationship Between Response to Colchicine Treatment and MDR1 Polymorphism in Familial Mediterranean Fever Patients", Genet Test Mol Biomarkers, 17 (2) pp. 135-139 [SSCI]
Erselcan, T., Süngü, S., Özdemir, S., Turgut, B., Dogan, D., ÖZDEMİR, Ö. (2004) "Iodine 131 treatment and chromosomal damage in vivo dose effect relationship", EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 31 (5) pp. 676-684 [SCI Expanded]
Sılan, F., Güngör, A.N.Ç., Urfalı, M., Uludağ, A., ÖZDEMİR, Ö. (2015) "Triploidy Diploidy Mosaisizm Diandry and Uniparental Isodisomy Fetus withOmphalocele and Contracted Finger", Family Medicine & Medical ScienceResearch, (0) DOI " data-bs-content-id="YazarBilgi-21455">
Sılan, F., Güngör, A.N.Ç., Urfalı, M., Uludağ, A., ÖZDEMİR, Ö. (2015) "Triploidy Diploidy Mosaisizm Diandry and Uniparental Isodisomy Fetus withOmphalocele and Contracted Finger", Family Medicine & Medical ScienceResearch, (0) DOI Sılan, F., Güngör, A.N.Ç., Urfalı, M., Uludağ, A., ÖZDEMİR, Ö. (2015) "Triploidy Diploidy Mosaisizm Diandry and Uniparental Isodisomy Fetus withOmphalocele and Contracted Finger", Family Medicine & Medical ScienceResearch, (0) DOI
Ozcan, L., Polat, E.C., KOCAASLAN, R., Önen, E., Beşiroğlu, H., Çakır, S.S., Erkoç, M., Otunctemur, A., Ozbek, E. (2016) "Metabolik Sendromlu Benign Prostat Hiperplazili Hastalarda Alfa Reseptör Antagonisti ve 5 Alfa Redüktaz İnhibisyonu Kombinasyonu Çok Etkilidir", 25. Ulusal Üroloji Kongresi , (pp. 1), Girne, Kuzey Kıbrıs Türk Cumhuriyeti, (Ekim 2016)
Bağcıoğlu, M., KOCAASLAN, R., USLU, M., Güvendi, G.F. (2017) "TP-11 Böbrekte iskemi-reperfüzyon hasarında Ticagrelor un etkisi:Pleyiotropik etki geçerli bir faktör mü?", 26. ULUSAL ÜROLOJİ KONGRESİ , Girne, Kuzey Kıbrıs Türk Cumhuriyeti, (Ekim 2017)
Şen, M., ÖZDEMİR, Ö., Turan, M., Arıcı, D.S., Yıldız, F., Binnur, K., Göze, Ö.F. (2009) "Epigenetic inactivation of tumor suppressor SFRP2 and point mutation in KRAS proto oncogene in fistula associated mucinous type anal adenocarcinoma report of two cases", Internal medicine (Tokyo, Japan), 49 (15) pp. 1637-1640 [SSCI]
Bağcıoğlu, M., KOCAASLAN, R., USLU, M., Güvendi, G.F. (2017) "Böbrekte İskemi-Reperfüzyon Hasarında Ticagrelor’un Etkisi: Pleyiotropik Etki Geçerli bir Faktör mü?", 26.ulusal üroloji kongresi , Girne, (Ekim 2017)
