Battal, F., Sılan, F., Aylanç, H., Yıldırım, Ş., Binnetoğlu, F.K., Tekin, M., Kaymaz, N., ÖZDEMİR, Ö. (2016) "The MEFV gene pathogenic variants and phenotype-genotype correlation in children with familial Mediterranean fever in the Çanakkale population", Balkan Journal of Medical Genetics, 19 (2) pp. 23-28 [SCI]
Albuz, B., Sılan, F., Öztürk, M., Yıldız, O., ÖZDEMİR, Ö. (2019) "BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q", Balkan Journal of Medical Genetics, 22 (0) pp. 156-156 [SCI Expanded] Link " data-bs-content-id="YazarBilgi-21386">
Albuz, B., Sılan, F., Öztürk, M., Yıldız, O., ÖZDEMİR, Ö. (2019) "BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q", Balkan Journal of Medical Genetics, 22 (0) pp. 156-156 [SCI Expanded] Link Albuz, B., Sılan, F., Öztürk, M., Yıldız, O., ÖZDEMİR, Ö. (2019) "BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q", Balkan Journal of Medical Genetics, 22 (0) pp. 156-156 [SCI Expanded] Link
Manduz, Ş., Katrancıoğlu, N., Karahan, O., ÖZDEMİR, Ö. (2010) "Association of the plasminogen activator inhibitor-1(PAI-1) gene 4G/5G promoter polymorphism in Buerger’xxs disease (Tromboangiitis obliterans)", Health, 2 (5) pp. 454-457 Link DOI " data-bs-content-id="YazarBilgi-21387">
Manduz, Ş., Katrancıoğlu, N., Karahan, O., ÖZDEMİR, Ö. (2010) "Association of the plasminogen activator inhibitor-1(PAI-1) gene 4G/5G promoter polymorphism in Buerger’xxs disease (Tromboangiitis obliterans)", Health, 2 (5) pp. 454-457 Link DOI Manduz, Ş., Katrancıoğlu, N., Karahan, O., ÖZDEMİR, Ö. (2010) "Association of the plasminogen activator inhibitor-1(PAI-1) gene 4G/5G promoter polymorphism in Buerger’xxs disease (Tromboangiitis obliterans)", Health, 2 (5) pp. 454-457 Link DOI
Katrancıoğlu, N., Manduz, Ş., Ozen, F., Yılmaz, M.B., Atahan, E., ÖZDEMİR, Ö., Berkan, O. (2011) "Association Between ApoE4 Allele and Deep Venous Thrombosis: A Pilot Study", CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 17 (2) pp. 225-228 [SCI] DOI " data-bs-content-id="YazarBilgi-21388">
Katrancıoğlu, N., Manduz, Ş., Ozen, F., Yılmaz, M.B., Atahan, E., ÖZDEMİR, Ö., Berkan, O. (2011) "Association Between ApoE4 Allele and Deep Venous Thrombosis: A Pilot Study", CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 17 (2) pp. 225-228 [SCI] DOI Katrancıoğlu, N., Manduz, Ş., Ozen, F., Yılmaz, M.B., Atahan, E., ÖZDEMİR, Ö., Berkan, O. (2011) "Association Between ApoE4 Allele and Deep Venous Thrombosis: A Pilot Study", CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 17 (2) pp. 225-228 [SCI] DOI
Arslan, S., Karadayı, Ş., Yıldırım, M.E., ÖZDEMİR, Ö., Akkurt, İ. (2011) "The association between methylene tetrahydrofolate reductase gene polymorphism and lung cancer risk", Molecular Biology Reports, (0) [SCI Expanded]
Özdal, A., Erselcan, T., ÖZDEMİR, Ö., Özgüven, Y., Silov, G., Erdoğan, Z. (2018) "Evaluation of the physical and biological dosimetry methods in iodine-131-treated patients", World Journal of Nuclear Medicine, 17 (4) pp. 253-260 Link DOI " data-bs-content-id="YazarBilgi-21390">
Özdal, A., Erselcan, T., ÖZDEMİR, Ö., Özgüven, Y., Silov, G., Erdoğan, Z. (2018) "Evaluation of the physical and biological dosimetry methods in iodine-131-treated patients", World Journal of Nuclear Medicine, 17 (4) pp. 253-260 Link DOI Özdal, A., Erselcan, T., ÖZDEMİR, Ö., Özgüven, Y., Silov, G., Erdoğan, Z. (2018) "Evaluation of the physical and biological dosimetry methods in iodine-131-treated patients", World Journal of Nuclear Medicine, 17 (4) pp. 253-260 Link DOI
Altınbaş, K., Yeşilbaş, D., İnce, B., Cansız, A., Sılan, F., ÖZDEMİR, Ö., Guloksuz, S. (2018) "Evaluation of The Association Between Lithium Treatment and GSK3ß Polymorphism in Bipolar Disorder Patients", Turkish Journal of Psychiatry, (0) [SSCI] Link DOI " data-bs-content-id="YazarBilgi-21392">
Altınbaş, K., Yeşilbaş, D., İnce, B., Cansız, A., Sılan, F., ÖZDEMİR, Ö., Guloksuz, S. (2018) "Evaluation of The Association Between Lithium Treatment and GSK3ß Polymorphism in Bipolar Disorder Patients", Turkish Journal of Psychiatry, (0) [SSCI] Link DOI Altınbaş, K., Yeşilbaş, D., İnce, B., Cansız, A., Sılan, F., ÖZDEMİR, Ö., Guloksuz, S. (2018) "Evaluation of The Association Between Lithium Treatment and GSK3ß Polymorphism in Bipolar Disorder Patients", Turkish Journal of Psychiatry, (0) [SSCI] Link DOI
Sılan, F., Bourouba, R., Karakaya, T., Yıldız, O., Paksoy, B., Urfalı, M., ÖZDEMİR, Ö. (2018) "The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report", Egyptian Journal of Medical Human Genetics, 19 (4) pp. 437-441 Link DOI " data-bs-content-id="YazarBilgi-21393">
Sılan, F., Bourouba, R., Karakaya, T., Yıldız, O., Paksoy, B., Urfalı, M., ÖZDEMİR, Ö. (2018) "The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report", Egyptian Journal of Medical Human Genetics, 19 (4) pp. 437-441 Link DOI Sılan, F., Bourouba, R., Karakaya, T., Yıldız, O., Paksoy, B., Urfalı, M., ÖZDEMİR, Ö. (2018) "The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report", Egyptian Journal of Medical Human Genetics, 19 (4) pp. 437-441 Link DOI
Ari, E., ÖZDEMİR, Ö., Djurovic, J., Sılan, F. (2018) "Prenatal diagnosis of aneuploidies and microdelation/duplication in amniotic fluid and fetal aborted material by QF-PCR and MLPA analysis.", Biomed Genet Genomics, 3 (1) pp. 1-6 DOI " data-bs-content-id="YazarBilgi-21395">
Ari, E., ÖZDEMİR, Ö., Djurovic, J., Sılan, F. (2018) "Prenatal diagnosis of aneuploidies and microdelation/duplication in amniotic fluid and fetal aborted material by QF-PCR and MLPA analysis.", Biomed Genet Genomics, 3 (1) pp. 1-6 DOI Ari, E., ÖZDEMİR, Ö., Djurovic, J., Sılan, F. (2018) "Prenatal diagnosis of aneuploidies and microdelation/duplication in amniotic fluid and fetal aborted material by QF-PCR and MLPA analysis.", Biomed Genet Genomics, 3 (1) pp. 1-6 DOI
Yenicesu, G.I., Çetin, M., ÖZDEMİR, Ö., Çetin, A., Ozen, F., Yıldız, Ç., Kocak, 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 Expanded] Link DOI " data-bs-content-id="YazarBilgi-21396">
Yenicesu, G.I., Çetin, M., ÖZDEMİR, Ö., Çetin, A., Ozen, F., Yıldız, Ç., Kocak, 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 Expanded] Link DOI Yenicesu, G.I., Çetin, M., ÖZDEMİR, Ö., Çetin, A., Ozen, F., Yıldız, Ç., Kocak, 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 Expanded] Link DOI
Özen, F., Koçak, N., Kelekçi, S., Yıldırım, İ.H., Hacimuto, G., ÖZDEMİR, Ö. (2014) "The prevalence of Familial Mediterranean Fever common gene mutations in patients with simple febrile seizures.", European review for medical and pharmacological sciences, 18 (5) pp. 657-60 [SCI Expanded] Link " data-bs-content-id="YazarBilgi-21397">
Özen, F., Koçak, N., Kelekçi, S., Yıldırım, İ.H., Hacimuto, G., ÖZDEMİR, Ö. (2014) "The prevalence of Familial Mediterranean Fever common gene mutations in patients with simple febrile seizures.", European review for medical and pharmacological sciences, 18 (5) pp. 657-60 [SCI Expanded] Link Özen, F., Koçak, N., Kelekçi, S., Yıldırım, İ.H., Hacimuto, G., ÖZDEMİR, Ö. (2014) "The prevalence of Familial Mediterranean Fever common gene mutations in patients with simple febrile seizures.", European review for medical and pharmacological sciences, 18 (5) pp. 657-60 [SCI Expanded] Link
ÖZDEMİR, Ö., Paksoy, B., Sılan, F. (2017) "A mosaic infertile case of isodicentric Y-chromosome with duplicated SRY, SHOX and deleted AZF locus", Biomedical Genetics and Genomics, 2 (1) pp. 1-3
Sılan, F., Kankaya, D., Karakaya, T., Paksoy, B., Turunz, V., ÖZDEMİR, Ö. (2017) "Fatma Sılan, Duygu Kankaya, Taner Karakaya, Baris Paksoy, Volkan Turunz and Ozturk Ozdemir.The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale.", Biomedical Genetics and Genomics, 2 (2) pp. 1-5
Sargin, B., Akbal, A., Reşorlu, H., Savaş, Y., Zateri, C., Sılan, F., ÖZDEMİR, Ö. (2017) "The frequency of toll-like receptor 4 gene polymorphism in ankylosing spondylitis and its relationship between disease activity.", The European Research Journal, (0)
ÖZDEMİR, Ö. (2017) "Çok Parametreli ve Çoklu Bilinmeyenli Kanser", Türkiye Klinikleri Journal of Medical Genetics-Special Topics, 2 (2) pp. 60-68
Yalcintepe, S., ÖZDEMİR, Ö., Guler, Z., Sılan, F. (2017) "Günümüzde Kanser Tanısında Kullanılan Geçerli ve Güvenilir Moleküler Tetkikler", Turkiye Klinikleri Journal of Medical Genetics-Special Topics, 2 (2) pp. 113-122
ÖZDEMİR, Ö., Kuru, B., Paksoy, B., Sılan, F. (2017) "Kanser Etyolojisinde Tetikleyici Moleküler Mekanizmalar", Turkiye Klinikleri Journal of Medical Genetics-Special Topics, 2 (2) pp. 74-87
Kılıç, S., ÖZDEMİR, Ö., Sılan, F., Işık, S., Yıldız, O., Karaağaçlı, D., Sılan, C., Öğretmen, Z. (2017) "Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population.", Clin Exp Dermatol., 42 (1) pp. 8-13 [SCI]
Öğretmen, Z., Hız, M.M., Sılan, F., Uludağ, A., ÖZDEMİR, Ö. (2014) "Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension", ANNALS OF SAUDI MEDICINE, 34 (4) pp. 340-345 [SCI Expanded] DOI " data-bs-content-id="YazarBilgi-21406">
Öğretmen, Z., Hız, M.M., Sılan, F., Uludağ, A., ÖZDEMİR, Ö. (2014) "Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension", ANNALS OF SAUDI MEDICINE, 34 (4) pp. 340-345 [SCI Expanded] DOI Öğretmen, Z., Hız, M.M., Sılan, F., Uludağ, A., ÖZDEMİR, Ö. (2014) "Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension", ANNALS OF SAUDI MEDICINE, 34 (4) pp. 340-345 [SCI Expanded] DOI
Özen, F., Şen, M., ÖZDEMİR, Ö. (2014) "Methylenetetrahydrofolate reductase gene germ-line C677T and A1298C SNPs are associated with colorectal cancer risk in the Turkish population", Asian Pac J Cancer Prev, 15 (18) pp. 7731-7735 [SCI]
