Arslan, S., Karadayı, Ş., Yıldırım, M.E., Özdemir, Ö., Akkurt, İ. (2011) "The association between methylene tetrahydrofolate reductase gene polymorphism and lung cancer risk", Molecular Biology Reports, 38 (2) pp. 991-996 [SCI] Link DOI " data-bs-content-id="YazarBilgi-31247">
Arslan, S., Karadayı, Ş., Yıldırım, M.E., Özdemir, Ö., Akkurt, İ. (2011) "The association between methylene tetrahydrofolate reductase gene polymorphism and lung cancer risk", Molecular Biology Reports, 38 (2) pp. 991-996 [SCI] Link DOI Arslan, S., Karadayı, Ş., Yıldırım, M.E., Özdemir, Ö., Akkurt, İ. (2011) "The association between methylene tetrahydrofolate reductase gene polymorphism and lung cancer risk", Molecular Biology Reports, 38 (2) pp. 991-996 [SCI] Link DOI
Öğretmen, Z., Hız, M.M., Sılan, F., Uludağ, A., Özdemir, Ö. (2014) "Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension", Annals of Saudi medicine, 34 (4) p. 340 [SCI]
Özen, F., Karahan, O., Manduz, Ş., Katrancıoğlu, N., Köksal, B., Özdemir, Ö. (2009) "Role of prothrombotic gene polymorphism in patients with thromboangiitis obliterans", Türkiye Klinikleri Cardiovascular Sciences, 21 (2) pp. 160-164
Arslan, S., Akkurt, İ., Köksal, B., Karadayı, Ş., Özdemir, Ö. (2010) "Predictive significance of KRAS point mutation in patients with non small cell lung carcinoma relation to smoking and asbestos exposure in middle Anatolia population", Healthmed, 4 (4) pp. 715-719 [SCI Expanded]
Gazi, E., Barutçu, A., Altun, B., Temiz, A., Bekler, A., Urfalı, M., Sılan, F., Çölkesen, A.Y., Özdemir, Ö., Çavuş, E. (2014) "Intercellular Adhesion Molecule 1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow", MEDICAL PRINCIPLES AND PRACTICE, 23 (4) pp. 346-350 [SSCI] Link DOI " data-bs-content-id="YazarBilgi-31254">
Gazi, E., Barutçu, A., Altun, B., Temiz, A., Bekler, A., Urfalı, M., Sılan, F., Çölkesen, A.Y., Özdemir, Ö., Çavuş, E. (2014) "Intercellular Adhesion Molecule 1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow", MEDICAL PRINCIPLES AND PRACTICE, 23 (4) pp. 346-350 [SSCI] Link DOI Gazi, E., Barutçu, A., Altun, B., Temiz, A., Bekler, A., Urfalı, M., Sılan, F., Çölkesen, A.Y., Özdemir, Ö., Çavuş, E. (2014) "Intercellular Adhesion Molecule 1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow", MEDICAL PRINCIPLES AND PRACTICE, 23 (4) pp. 346-350 [SSCI] Link DOI
Köksal, B., Nur, N., Sari, M., Candan, F., Acemoğlu, M., Koçak, N., Özen, F., Özdemir, Ö. (2009) "Clinical and molecular analysis of common MEFV gene mutations in familial Mediterranean fever in Sivas population", Biologia, (0) [SCI Expanded]
Binnur, K., Nur, N., Sari, M., Candan, F., Mürşit, A., Koçak, N., Filiz, Ö., Özdemir, Ö. (2009) "Clinical and molecular analysis of common MEFV gene mutations in familial Mediterranean fever in Sivas population", Biologia, 64 (2) pp. 388-393 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-31259">
Binnur, K., Nur, N., Sari, M., Candan, F., Mürşit, A., Koçak, N., Filiz, Ö., Özdemir, Ö. (2009) "Clinical and molecular analysis of common MEFV gene mutations in familial Mediterranean fever in Sivas population", Biologia, 64 (2) pp. 388-393 [SCI Expanded] Link DOI Binnur, K., Nur, N., Sari, M., Candan, F., Mürşit, A., Koçak, N., Filiz, Ö., Özdemir, Ö. (2009) "Clinical and molecular analysis of common MEFV gene mutations in familial Mediterranean fever in Sivas population", Biologia, 64 (2) pp. 388-393 [SCI Expanded] Link DOI
Sılan, F., Gültekin, E.Y., Sinem, A., Devran, K., Alan, C., Yıldız, F., Uludağ, A., Özdemir, Ö. (2012) "Combined point mutations in codon 12 and 13 of KRAS oncogene in prostate carcinomas", Mol Biol Rep, 39 (2) pp. 1595-1599 [SSCI]
Özdemir, S., Silan, F., Hasbek, Z., Uludağ, A., Atik, S., Erselcan, T., Özdemir, Ö. (2012) "Increased T Allele Frequency of 677 C T Polymorphism in the Methylenetetrahydrofolate Reductase Gene in Differentiated Thyroid Carcinoma", Genet Test Mol Biomarkers, 16 (0) pp. 780-784 [SCI Expanded]
Yalçıntepe, S., Özdemir, Ö., Hacıvelioğlu, S., Mail, C., Kumcular, T. (2013) "Maternal Fetal eNOS Genotipleri ile Spontan Abortus İlişkisi", Erişkin Yaşta Görülen Genetik Hastalıklar Sempozyumu , Türkiye, (Aralık 2013)
Öztürk, M., Demir, B., Arayici, S., Demir, S., Özdemir, Ö., Sılan, F. (2019) "Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism", 13th Balcan Human Genetic Congress , Edirne, Türkiye, (Nisan 2019)
Öztürk, M., Demir, B., Arayici, S., Demir, S., Özdemir, Ö., Sılan, F. (2019) "Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism", 13th Balcan Human Genetic Congress , Edirne, Türkiye, (Nisan 2019)
Öztürk, M., Demir, B., Arayici, S., Demir, S., Özdemir, Ö., Sılan, F. (2019) "Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism", 13th Balcan Human Genetic Congress , Edirne, Türkiye, (Nisan 2019)
Öztürk, M., Demir, B., Arayici, S., Demir, S., Özdemir, Ö., Sılan, F. (2019) "Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism", 13th Balcan Human Genetic Congress. 17-20 April 2019 , Edirne, Türkiye, (Nisan 2019)
Öztürk, M., Demir, B., Arayici, S., Demir, S., Özdemir, Ö., Sılan, F. (2019) "Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism", 13th Balcan Human Genetic Congress. 17-20 April 2019, Edirne/Turkey. , (Nisan 2019)
Öztürk, M., Demir, B., Arayici, S., Demir, S., Özdemir, Ö., Sılan, F. (2019) "Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism", 13th Balcan Human Genetic Congress. 17-20 April 2019, Edirne/Turkey. , (Nisan 2019)
Öztürk, M., Demir, B., Arayici, S., Demir, S., Özdemir, Ö., Sılan, F. (2019) "Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism", 13th Balcan Human Genetic Congress. 17-20 April 2019, Edirne/Turkey. , (Nisan 2019)
Albuz, B., Sılan, F., Öztürk, M., Yıldız, O., Özdemir, Ö. (2019) "BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q", 13th Balkan Congress of Human Genetics , (pp. 156-1156), Edirne, Türkiye, (Haziran 2019)
Sılan, F., Jelena, D., Bir, F.D., Sılan, C., Özdemir, Ö. (2018) "Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale", European Biotechnology Congress , (pp. 65), Atina, Yunanistan, (Ekim 2018)
