Gazı, E., Barutcu, A., Altun, B., Temız, A., Bekler, A., Urfalı, M., Sılan, F., Colkesen, Y., ÖZDEMİR, Ö. (2014) "Intercellular Adhesion Molecule 1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow", Medical Principle and Practise, (0) [SSCI]
Bağcı, B., Sarı, M., Karadayı, K., Turan, M., ÖZDEMİR, Ö., Bağcı, G. (2016) "KRAS BRAF oncogene mutations and tissue specific promoter hypermethylation of tumor suppressor SFRP2 DAPK1 MGMT HIC1 and p16 genes in colorectal cancer patients", Cancer Biomark., (0) [SSCI]
ÖZDEMİR, Ö., Paksoy, B., Gürgen, A., Oruç, M., Yıldız, O., Diğdem, U., 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 Tıp Dergisi, 38 (4) pp. 355-360 [TR Dizin] Link " data-bs-content-id="YazarBilgi-21430">
ÖZDEMİR, Ö., Paksoy, B., Gürgen, A., Oruç, M., Yıldız, O., Diğdem, U., 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 Tıp Dergisi, 38 (4) pp. 355-360 [TR Dizin] Link ÖZDEMİR, Ö., Paksoy, B., Gürgen, A., Oruç, M., Yıldız, O., Diğdem, U., 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 Tıp Dergisi, 38 (4) pp. 355-360 [TR Dizin] Link
S, O., A, U., F, S., SY, A., B, T., O, O. (2013) "Possible roles of the xenobiotic transporter P glycoproteins encoded by the MDR1 3435 C T gene polymorphism in differentiated thyroid cancers", Asian Pac J Cancer Prev, 14 (5) pp. 3213-3217 [SSCI]
Sılan, F., Paksoy, B., ÖZDEMİR, Ö., Tas, Z. (2016) "Meirer Gorlin Syndrome A primordial dwarfic rare case with growth and mental retardation in normal karyotype", Genetic Caunseling, 27 (2) pp. 149-157 [SCI]
Yalçıntepe, S., ÖZDEMİR, Ö., Silan, C., Filiz, Ö., Uludağ, A., Candan, F., Silan, F. (2016) "The CYP4502D6 4 and 6 alleles are the molecular genetic markers for drug response implications in colchicine non responder FMF patients", European Journal of Drug Metabolism and Pharmacokinetics, 41 (3) pp. 281-286 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-21433">
Yalçıntepe, S., ÖZDEMİR, Ö., Silan, C., Filiz, Ö., Uludağ, A., Candan, F., Silan, F. (2016) "The CYP4502D6 4 and 6 alleles are the molecular genetic markers for drug response implications in colchicine non responder FMF patients", European Journal of Drug Metabolism and Pharmacokinetics, 41 (3) pp. 281-286 [SCI Expanded] Link DOI Yalçıntepe, S., ÖZDEMİR, Ö., Silan, C., Filiz, Ö., Uludağ, A., Candan, F., Silan, F. (2016) "The CYP4502D6 4 and 6 alleles are the molecular genetic markers for drug response implications in colchicine non responder FMF patients", European Journal of Drug Metabolism and Pharmacokinetics, 41 (3) pp. 281-286 [SCI Expanded] Link DOI
Işık, S., Sılan, F., Kılıç, S., Hız, M.M., Öğretmen, Z., ÖZDEMİR, Ö. (2016) "308G A and 238G A polymorphisms in the TNF gene may not contribute to the risk of arthritis among Turkish psoriatic patients", The Egyptian Rheumatologist, 38 (0) pp. 313-317 [SCI] Link DOI " data-bs-content-id="YazarBilgi-21435">
Işık, S., Sılan, F., Kılıç, S., Hız, M.M., Öğretmen, Z., ÖZDEMİR, Ö. (2016) "308G A and 238G A polymorphisms in the TNF gene may not contribute to the risk of arthritis among Turkish psoriatic patients", The Egyptian Rheumatologist, 38 (0) pp. 313-317 [SCI] Link DOI Işık, S., Sılan, F., Kılıç, S., Hız, M.M., Öğretmen, Z., ÖZDEMİR, Ö. (2016) "308G A and 238G A polymorphisms in the TNF gene may not contribute to the risk of arthritis among Turkish psoriatic patients", The Egyptian Rheumatologist, 38 (0) pp. 313-317 [SCI] Link DOI
Sık, E., ÖZDEMİR, Ö., Kurtulgan, H.K., Urfalı, M., Şen, M., Sılan, F. (2016) "Hypermethylated promoter profiles for tumour suppressor APC p53 MSH6 and MGMT genes in CRC tumours", journal of biomedical research, 2 (6) pp. 41-47 [TR Dizin]
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
