S., O., F., S., T., E., A, U., F, U., A, C., S, A., O, O. () "Increased T allele frequency in MTHFR C677T gene in thyroid carcinme", 8th European Cytogenetic Conference
O., O., H., A., M., T., S, O., M, K., B, K., F, O. () "The endemic RTL80V I and RTM204V I YMDD mutation profiles in a case of chronic hepatitis B", 8th European Cytogenetic Conference
D., K., O., O., E., K., S, O., B, K., EY, G. () "Epigenetic silencing of the tumor supressor HIC1 and SFRP2 genes in prostate carcinomas", European Cytogenetic Conference
S., A., F., O., C., S., A, U., F, C., F, S., S, O., O, O. () "Increased T allele frequency in multidrug transporter ABCB1 MDR1 gene in FMF patients of colchicine unresponsiveness", European Human Genetics Conference
O., O., Gİ., Y., F., S., M, Ç., B, K., S, A., F, Ö., M, G., A, Ç. () "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", European Human Genetics Conference
A., U., Y., D., AS., G., C, S., S, A., F, S., Ö, Ö. () "Combine effect of Factor V Leiden MTHFR and Angiotensin converting enzyme insertion deletion gene mutations in hypertensive adult individuals a population based study from Sivas and Canakkale TURKEY", European Human Genetics Conference
F., S., O., G., LE., K., C, S., S, A., A, U., A, D., FS, D., Ö, Ö. () "GJB2 35delG and Mitochondrial A1555G mutations and etiology of deafness at the Gelibolu School for the Deaf in Turkey", European Human Genetics Conference
E., E., O, O. () "Genome based transcriptome profile of some etiological parameters in breast cancer", Abstracts of the 2011 MASCC\ISOO Symposium
Silan., C., Dogan., O., Silan., F., Kukulguven, F., Asgun, H., Ozdemir, S., Uludag, A., SAtik, , Gungor, B., Akdur, S., Aksulu, H., Ozdemir, O. () "The prevalence of VKORC1 1639 G A and CYP2C9 2 3 genotypes in patients that requiring anticoagulant therapy in Turkish population", European Human GeneticsConference
Ozdemir., O., Alagozlu., H., Timucin, M. () "Strong association between ABCB1 gene MDR1 3435 C T polymorphism and multiple drug nonresponder patients of chronic hepatitis C", European Human Genetics Conference
Ozdemir., S., Uludag., A., Silan., F., Atik, S., Turgut, B., Ozdemir, O. () "The possible role of the xenobiotic transporter P glycoproteinpolymorphism that encoded by the MDR1 3435 C T gene in the susceptibility of differentiated thyroid cancer", European Human Genetics Conference
Uludag., A., Ozdemir., S., Silan., C., Uludag, A., Atik, S., Silan, F., Ozdemir, O. () "Evaluation of CYP2C9 CYP2C19 and CYP2D6 gene polymorphisms in thyroid cancer", European Human Genetics Conference
Uudag., A., Silan., F., Uludag., A., Silan, C., Atik, S., Sahin, E., Ozdemir, O. () "What about the relatives who have MTHFR C677T polymorphism", European Human GeneticsConference
Ozen., F., Kocak., N., Ulasoglu., C., Sezgin, , Colak, A., Ozdemir, O. (2012) "KRAS mutation genotypes and prometer methylation of tumor suppressor genes in cancer tissue and peripheral blood in colorectal cancer patients", European Human GeneticsConference , (Haziran 2012)
Silan., F., Atik., S., Gultekin., Y., Kılınc, D., Alan, C., Uludag, A., Colak, A., Ozdemir, O. (2012) "Combined point mutations in codon 12 and 13 of KRAS oncogene in prostate carcinomas with high gleason score", European Human GeneticsConference , (Haziran 2012)
Z., O., F., S., MM., H., AS, Y., B, K., O, O. (2013) "The relatinship between psoriasis and TNF alpha G308A and G238A Polymorphisms", 4th Congress of the psoriasis international network , (Temmuz 2013)
O., O., S., C., M., K., F, S., ME, Y., HK, K., B, K., SA, Y., E, A., F, C. (2013) "The MEFV mutation profiles and SAA1 gene BcII polymorphism in chronic renal failure patients that requiring long term haemodialysis in Turkish population", ESHG Conference European Journal of Human Genetics , (Kasım 2013)
F., S., SA., Y., D., U., U, U., E, C., AN, C., O, O. (2013) "High Incidence of Chromosomal Aberrations in Couples with Reproductive Failure in Canakkale", ESHG Conference, European Journal of Human Genetics, , (Kasım 2013)
G., B., HK., K., OT., D., O, O. (2013) "The association between Factor V G1691A mutation and obstructive sleep apnoea syndrome Preliminary results from Turkey", ESHG Conference, European Journal of Human Genetics , (Kasım 2013)
A., U., C., S., SA., Y., C, A., A, U., F, S., O, O. (2013) "Relationship between response to colchicine treatment and MDR1 polymorphism in FMF patients", ESHG Conference, European Journal of Human Genetics , (Kasım 2013)
