Kılınç, D., ÖZDEMİR, Ö., Özdemir, S., Korgalı, E., Köksal, B., Uslu, A., Gültekin, E.Y. (2012) "Alterations in Promoter Methylation Status of Tumor Suppressor HIC1, SFRP2, and DAPK1 Genes in Prostate Carcinomas , iSFRP2/i , and iDAPK1/i Genes in Prostate Carcinomas/title", DNA and Cell Biology, 31 (5) pp. 826-832 [SCI] Link DOI " data-bs-content-id="YazarBilgi-21416">
Kılınç, D., ÖZDEMİR, Ö., Özdemir, S., Korgalı, E., Köksal, B., Uslu, A., Gültekin, E.Y. (2012) "Alterations in Promoter Methylation Status of Tumor Suppressor HIC1, SFRP2, and DAPK1 Genes in Prostate Carcinomas , iSFRP2/i , and iDAPK1/i Genes in Prostate Carcinomas/title", DNA and Cell Biology, 31 (5) pp. 826-832 [SCI] Link DOI Kılınç, D., ÖZDEMİR, Ö., Özdemir, S., Korgalı, E., Köksal, B., Uslu, A., Gültekin, E.Y. (2012) "Alterations in Promoter Methylation Status of Tumor Suppressor HIC1, SFRP2, and DAPK1 Genes in Prostate Carcinomas , iSFRP2/i , and iDAPK1/i Genes in Prostate Carcinomas/title", DNA and Cell Biology, 31 (5) pp. 826-832 [SCI] Link DOI
ÖZDEMİR, Ö., Kayataş, M., Çetinkaya, S., Yıldırım, M.E., Sılan, F., Kurtulgan, H.K., Urfalı, M., Candan, F. (2015) "Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis", RENAL FAILURE, 37 (2) pp. 292-296 [SSCI] Link DOI " data-bs-content-id="YazarBilgi-21417">
ÖZDEMİR, Ö., Kayataş, M., Çetinkaya, S., Yıldırım, M.E., Sılan, F., Kurtulgan, H.K., Urfalı, M., Candan, F. (2015) "Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis", RENAL FAILURE, 37 (2) pp. 292-296 [SSCI] Link DOI ÖZDEMİR, Ö., Kayataş, M., Çetinkaya, S., Yıldırım, M.E., Sılan, F., Kurtulgan, H.K., Urfalı, M., Candan, F. (2015) "Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis", RENAL FAILURE, 37 (2) pp. 292-296 [SSCI] Link DOI
Bağcı, B., Bağcı, G., Candan, F., ÖZDEMİR, Ö., Sezgin, İ. (2015) "The protective effect of MCP 1 2518 A G promoter polymorphism in Turkish chronic renal failure patients requiring long term hemodialysis", INTERNATIONAL UROLOGY AND NEPHROLOGY, 47 (3) pp. 551-556 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-21418">
Bağcı, B., Bağcı, G., Candan, F., ÖZDEMİR, Ö., Sezgin, İ. (2015) "The protective effect of MCP 1 2518 A G promoter polymorphism in Turkish chronic renal failure patients requiring long term hemodialysis", INTERNATIONAL UROLOGY AND NEPHROLOGY, 47 (3) pp. 551-556 [SCI Expanded] Link DOI Bağcı, B., Bağcı, G., Candan, F., ÖZDEMİR, Ö., Sezgin, İ. (2015) "The protective effect of MCP 1 2518 A G promoter polymorphism in Turkish chronic renal failure patients requiring long term hemodialysis", INTERNATIONAL UROLOGY AND NEPHROLOGY, 47 (3) pp. 551-556 [SCI Expanded] Link DOI
Çitli, Ş., Köksal, B., Kurtulgan, H.K., Akkuş, N., ÖZDEMİR, Ö., Sezgin, İ. (2011) "Prenatal dönemde multiplex kantitatif fluoresan PCR QF PCR tekniği ile yaygın kromozomal anoploidilerin tespiti Cumhuriyet Üniversitesi Tıp Fakültesi deneyimi", Cumhuriyet Medical Journal, 33 (4) pp. 389-395 [TR Dizin] " data-bs-content-id="YazarBilgi-21419">
Çitli, Ş., Köksal, B., Kurtulgan, H.K., Akkuş, N., ÖZDEMİR, Ö., Sezgin, İ. (2011) "Prenatal dönemde multiplex kantitatif fluoresan PCR QF PCR tekniği ile yaygın kromozomal anoploidilerin tespiti Cumhuriyet Üniversitesi Tıp Fakültesi deneyimi", Cumhuriyet Medical Journal, 33 (4) pp. 389-395 [TR Dizin] Çitli, Ş., Köksal, B., Kurtulgan, H.K., Akkuş, N., ÖZDEMİR, Ö., Sezgin, İ. (2011) "Prenatal dönemde multiplex kantitatif fluoresan PCR QF PCR tekniği ile yaygın kromozomal anoploidilerin tespiti Cumhuriyet Üniversitesi Tıp Fakültesi deneyimi", Cumhuriyet Medical Journal, 33 (4) pp. 389-395 [TR Dizin]
Şen, M., ÖZDEMİR, Ö., Turan, M., Arıcı, S., Yıldız, F., Köksal, B., Göze, Ö.F. (2010) "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, 49 (15) pp. 1637-1640 [SCI Expanded]
Altuntaş, E.E., ÖZDEMİR, Ö., Bora, A., Köksal, B., Kurtulgan, H.K., Müderris, S. (2011) "Heterozygous Deletion of Exon 8 in WFS1 Gene in Two Wolfram Syndrome Probands with Hearing Loss Case Report", Turkiye Klinikleri Journal of Medical Sciences, 31 (1) pp. 245-250 Link DOI " data-bs-content-id="YazarBilgi-21421">
Altuntaş, E.E., ÖZDEMİR, Ö., Bora, A., Köksal, B., Kurtulgan, H.K., Müderris, S. (2011) "Heterozygous Deletion of Exon 8 in WFS1 Gene in Two Wolfram Syndrome Probands with Hearing Loss Case Report", Turkiye Klinikleri Journal of Medical Sciences, 31 (1) pp. 245-250 Link DOI Altuntaş, E.E., ÖZDEMİR, Ö., Bora, A., Köksal, B., Kurtulgan, H.K., Müderris, S. (2011) "Heterozygous Deletion of Exon 8 in WFS1 Gene in Two Wolfram Syndrome Probands with Hearing Loss Case Report", Turkiye Klinikleri Journal of Medical Sciences, 31 (1) pp. 245-250 Link DOI
Polat, F., Turaçlar, N., Gül, E., ÖZDEMİR, Ö., Bingöl, G. (2008) "Mutation analiysis of the proto-oncogenes Ki-ras and C-Myc in the Soft Tissue Tumors of the rats that were formed by 3-methylcholanthrene in vivo", Dumlupinar Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 17 (0) pp. 11-18
Paksoy, B., Sılan, F., Yıldız, O., ÖZDEMİR, Ö., Tas, Y. (2016) "MEIRER GORLIN SYNDROME A PRIMORDIAL DWARFIC RARE CASE WITH GROWTH AND MENTAL RETARDATION IN NORMAL KARYOTYPE", GENETIC COUNSELING, (0) [SCI Expanded]
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 Biomarkers, 17 (2) pp. 133-143 [SCI Expanded] DOI " data-bs-content-id="YazarBilgi-21424">
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 Biomarkers, 17 (2) pp. 133-143 [SCI Expanded] DOI 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 Biomarkers, 17 (2) pp. 133-143 [SCI Expanded] DOI
Yenicesu, A.G., Çetin, M., ÖZDEMİR, Ö., Çetin, A., Özen, F., Yenicesu, C., Ce, Y., Koçak, N. (2010) "A prospective case control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss", American Journal of Reproductive Immunology, 63 (2) pp. 126-136 [SCI]
Güngörçakır, A., Sılan, F., Gencer, M., Uludağ, A., Coşar, E., Koç, E., ÖZDEMİR, Ö. (2016) "GÜNGÖR ANC SILAN F KILINC N GENCER M ULUDAĞ A COŞAR E KOC E OZDEMIR O Is 9qh Positivity A Risk Factor For Molar Pregnancy 2016 14 15", Jinekoloji - Obstetrik ve Neonatoloji Tıp Dergisi, (0) pp. 14-15 [TR Dizin]
Katrancıoğlu, N., Manduz, Ş., Özen, F., Yılmaz, M.B., Karahan, O., ÖZDEMİR, Ö., Berkan, Ö. (2010) "Type I Plasminogen Activator Inhibitor4G Allele Frequency is Associated withChronic Venous Insufficiency", The Journal of International Medical Research, 38 (0) pp. 1513-1518 [SCI Expanded]
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]
