ALDEMİR-ENGİN, R., SADİ-YILMAZ, S. (2023) "Matematik Öğretmeni Adaylarının Artırılmış Gerçeklik Uygulamasıyla Oluşturdukları Materyallerin Revize Edilmiş Bloom Taksonomisine Göre İncelenmesi ve Öğretmen Adaylarının AR Uygulamasına Yönelik Görüşleri", 6. Uluslararası Türk Bilgisayar ve Matematik Eğitimi (TÜRKBİLMAT-6) Sempozyumu , (pp. 152-153), Ankara, Türkiye, (Ekim 2023)
Djurovic, J., Stojkovıc, O., Akurut, C., Sılan, F., Todorovıc, J., Stamenkovıc, G., ÖZDEMİR, Ö. () "Association between vitamin D receptor gene polymorphisms and Hashimoto s thyroiditis in Serbian population a pilot study based on FokI ApaI and TaqI RFLP technique", European Human Genetics Conference (ESHG) 31 May- 3 June 2014, Milan/ITALY. J07.07.
Fidan, M., ALDEMİR-ENGİN, R. (2023) "Matematikte GeoGebra Kullanılarak Yapılan Lisansüstü Tezlerin İncelenmesi", 6. Uluslararası Türk Bilgisayar ve Matematik Eğitimi (TÜRKBİLMAT-6) Sempozyumu , (pp. 228-229), Ankara, Türkiye, (Ekim 2023)
Oguz, S., Sılan, F., Akurut, Ç., Topaloğlu, N., Isık, S., Sık, E., Uludağ, A., ÖZDEMİR, Ö. () "Correlation between vitamin D receptor gene polymorphisms and atopic dermatitis in Canakkale population a study based on FokI and TaqI RFLP technique", European Human Genetics Conference (ESHG
Kurtulgan, H.K., Bagcı, G., Yıldırım, M., ÖZDEMİR, Ö. () "A novel Q97R MEFV gene mutation in a Turkish FMF patient", European Human Genetics Conference (ESHG)
Sılan, F., Uludağ, A., Akurut, C., Kankaya, D., Gencer, M., Urfalı, M., Yalcıntepe, S., ÖZDEMİR, Ö. () "Parental idendification of aborted materials for chimerism and other molecular etiological parameters by microsatellite STR profilling", European Human Genetics Conference (ESHG)
Yalcıntepe, S., Hacıvelioğlu, O., Sılan, C., Akurut, C., Koç, E., Sılan, F., Coşar, E., Coşar, E., Uludağ, A., ÖZDEMİR, Ö. () "Is apolipoprotien E polymorphisms associated with spontaneous pregnancy loss", European Human Genetics Conference (ESHG)
Sılan, F., Has, H., Urfalı, M., Uludağ, A., Arı, E., Gencer, M., ÖZDEMİR, Ö. () "Premature chromatid separation in a woman with unexplained recurrent pregnancy loss A case report", European Human Genetics Conference
Yalcıntepe, S., ÖZDEMİR, Ö., Hacıvelioğlu, O., Akurut, C., Kumcular, T., Uysal, D., Yucesoy, K., Uludağ, A., Cosar, E., Sılan, F. () "The association between endothelial nitric oxide synthase gene Glu298Asp polymorphism and spontaneous pregnancy loss", European Human Genetics Conference (ESHG)
ÖZDEMİR, Ö., Urfalı, M., Sılan, F., Uludağ, A., Arı, E., Kayatas, M. () "Variable R Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677Tgene polymorphism from genetics to epigenetics", European Human Genetics Conference (ESHG)
Sılan, F., Yalcıntepe, S., Uysal, D., Urfalı, M., Uludağ, A., ÖZDEMİR, Ö., Sık, E., Cosar, E., Cakır, A. () "High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey", European Human Genetics Conference (ESHG)
Sılan, F., Yalcıntepe, S., Uysal, D., Urfalı, M., Uludağ, A., ÖZDEMİR, Ö., Sık, E., Cosar, E., Cakır, A. () "High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey", European Human Genetics Conference (ESHG)
Urfalı, M., ÖZDEMİR, Ö., Kankaya, D., Uludağ, A., Yalçıntepe, S., Sılan, F. () "Deleterious mutations in mitochondrial NADH dehydrogenase subunit 4 and ATPase subunit 6 in two siblings of Leigh Syndrome with progressive motor retardation and loss of visual function", European Human Genetics Conference (ESHG)
Ozen, F., Sen, M., Ozcırak, S., Çolak, A., ÖZDEMİR, Ö. () "Functional gene mediated oncogenesis by germ line MTHFR polymorphism in colorectal carcinoma", 9th European Cytogenetics Conference
Atik, S., Ozen, F., Gur, S., Uludağ, A., Sılan, C., Sılan, F., ÖZDEMİR, Ö. () "Polymorphism in gene encoding drugs and xenobiotic metabolizing enzyme CYP2D6 as a risk factor for drug response in colchicine unresponsive FMF patients", European Human Genetics Conference
Arslan, S., Doğan, T., Koksal, B., Yıldırım, M., Gumus, C., Elagoz, C., Akkurt, I., ÖZDEMİR, Ö. (2009) "Tumoral tissue specific promoter hypermethylation of tumor supressor genes SFRp2 p16 DAPK1 HIC and MGMT in a case with non small cell carcinoma A case report", 7th European Cytogenetics Conference , (Temmuz 2009)
Sezgin, İ., Çolak, A., Cakar, E., Ozen, F., Kocak, N., Ejder, M., ÖZDEMİR, Ö. () "Chromosome 7 duplication in a young girl with congenital heart disease unusual behaviours and low IQ level clinical and cytogenetical characterisation", European Human Genetics Conference
O., O., A., C., G., B., M, A., R, G., E, G. () "Homeobox gene Pax9 variation in a family with Hypohidrotic Ectodermal Dysplasia", European Human Genetics conference Amsterdam, The Netherlands
H., E., E., G., T., E., C, G., O, O.S.A.O. () "In Vivo Evaluation Of Micronuclei In Rat Reticulocytes For The Relative Efficacy Of Genomic Instability In Medical Radiation Exposure", 5.th Euoropean Cytogenetics Conference
ÖZDEMİR, Ö., Özdemir, A., Doruk, C., Gül, E., Yılmaz, S., Coskun, A., Bolayır, G., Kılıc, B., Ozdemir, D., Kılıc, B. () "The SSCP profiles of mutated homeobox PAX9 gene in orofacial clefts in human Two cases report", 5.th Euoropean Cytogenetics Conference
