Link DOI   ÖZDEMİR, Ö., Sezgin, İ., Kurtulgan, H.K., Candan, F., Binnur, K., Sümer, E.H., İçağasıoğlu, D.F., Uslu, A., Yıldız, F., Arslan, S., Öztemur, Z., Çetinkaya, S., Kayataş, M. (2011) "Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers", Molecular Biology Reports, 38 (5) pp. 3195-3200 [SSCI] Link DOI  " data-bs-content-id="YazarBilgi-21371"> ÖZDEMİR, Ö., Sezgin, İ., Kurtulgan, H.K., Candan, F., Binnur, K., Sümer, E.H., İçağasıoğlu, D.F., Uslu, A., Yıldız, F., Arslan, S., Öztemur, Z., Çetinkaya, S., Kayataş, M. (2011) "Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers", Molecular Biology Reports, 38 (5) pp. 3195-3200 [SSCI] Link DOI   ÖZDEMİR, Ö., Sezgin, İ., Kurtulgan, H.K., Candan, F., Binnur, K., Sümer, E.H., İçağasıoğlu, D.F., Uslu, A., Yıldız, F., Arslan, S., Öztemur, Z., Çetinkaya, S., Kayataş, M. (2011) "Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers", Molecular Biology Reports, 38 (5) pp. 3195-3200 [SSCI] Link DOI  

2011 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

Link DOI    Akurut, Ç., Sılan, F., Yalçıntepe, S., ÖZDEMİR, Ö. (2019) "The Diagnostic Accuracy of Non-invasive Fetal RhD Genotyping by Using Cell-free Fetal DNA in Maternal Plasma", Family Practice and Palliative Care, 4 (1) pp. 1-6 [TR Dizin] Link DOI   " data-bs-content-id="YazarBilgi-21372"> Akurut, Ç., Sılan, F., Yalçıntepe, S., ÖZDEMİR, Ö. (2019) "The Diagnostic Accuracy of Non-invasive Fetal RhD Genotyping by Using Cell-free Fetal DNA in Maternal Plasma", Family Practice and Palliative Care, 4 (1) pp. 1-6 [TR Dizin] Link DOI    Akurut, Ç., Sılan, F., Yalçıntepe, S., ÖZDEMİR, Ö. (2019) "The Diagnostic Accuracy of Non-invasive Fetal RhD Genotyping by Using Cell-free Fetal DNA in Maternal Plasma", Family Practice and Palliative Care, 4 (1) pp. 1-6 [TR Dizin] Link DOI   

2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

Karakaya, T., Sılan, F., ÖZDEMİR, Ö. (2020) "Tedaviyi Etkileyen Tarama Testleri", Türkiye Klinikleri Sağlık Bilimleri Dergisi, (0) pp. 16-24 [TR Dizin]   Karakaya, T., Sılan, F., ÖZDEMİR, Ö. (2020) "Tedaviyi Etkileyen Tarama Testleri", Türkiye Klinikleri Sağlık Bilimleri Dergisi, (0) pp. 16-24 [TR Dizin]  

2020 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

DOI   Paksoy, B., Sılan, F., ÖZDEMİR, Ö. (2020) "Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma", Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, 17 (4) pp. 599-609 [TR Dizin] DOI  " data-bs-content-id="YazarBilgi-21374"> Paksoy, B., Sılan, F., ÖZDEMİR, Ö. (2020) "Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma", Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, 17 (4) pp. 599-609 [TR Dizin] DOI   Paksoy, B., Sılan, F., ÖZDEMİR, Ö. (2020) "Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma", Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, 17 (4) pp. 599-609 [TR Dizin] DOI  

2020 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

DOI   Gençer, E.G., Özdemir, L., ÖZDEMİR, Ö. (2020) "Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay", Cumhuriyet Medical Journal, 42 (1) pp. 79-85 [TR Dizin] DOI  " data-bs-content-id="YazarBilgi-21375"> Gençer, E.G., Özdemir, L., ÖZDEMİR, Ö. (2020) "Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay", Cumhuriyet Medical Journal, 42 (1) pp. 79-85 [TR Dizin] DOI   Gençer, E.G., Özdemir, L., ÖZDEMİR, Ö. (2020) "Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay", Cumhuriyet Medical Journal, 42 (1) pp. 79-85 [TR Dizin] DOI  

2020 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

DOI   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", Clinical and Experimental Dermatology, 42 (1) pp. 8-13 [SCI Expanded] DOI  " data-bs-content-id="YazarBilgi-21376"> 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", Clinical and Experimental Dermatology, 42 (1) pp. 8-13 [SCI Expanded] DOI   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", Clinical and Experimental Dermatology, 42 (1) pp. 8-13 [SCI Expanded] DOI  

2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

Link DOI   ÖZDEMİR, Ö., Yenicesu, G.İ., Sılan, F., Köksal, B., Atik, S., Özen, F., Göl, M., Çetin, A. (2012) "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", Genetic Testing and Molecular Biomarkers, 16 (4) pp. 279-286 [SCI Expanded] Link DOI  " data-bs-content-id="YazarBilgi-21378"> ÖZDEMİR, Ö., Yenicesu, G.İ., Sılan, F., Köksal, B., Atik, S., Özen, F., Göl, M., Çetin, A. (2012) "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", Genetic Testing and Molecular Biomarkers, 16 (4) pp. 279-286 [SCI Expanded] Link DOI   ÖZDEMİR, Ö., Yenicesu, G.İ., Sılan, F., Köksal, B., Atik, S., Özen, F., Göl, M., Çetin, A. (2012) "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", Genetic Testing and Molecular Biomarkers, 16 (4) pp. 279-286 [SCI Expanded] Link DOI  

2012 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

ERDİŞ, E., KARAHAN, O., MANDUZ, Ş., ÖZDEMİR, Ö. (2010) "Akciğer Kanserli Derin Ven Trombozu Olgularında Protrombotik Gen Polimorfizmi Farklılıkları", Turkiye Klinikleri Cardiovascular Sciences, 22 (1) pp. 54-60 [SSCI]   ERDİŞ, E., KARAHAN, O., MANDUZ, Ş., ÖZDEMİR, Ö. (2010) "Akciğer Kanserli Derin Ven Trombozu Olgularında Protrombotik Gen Polimorfizmi Farklılıkları", Turkiye Klinikleri Cardiovascular Sciences, 22 (1) pp. 54-60 [SSCI]  

2010 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

Link DOI   Özen, F., Erdiş, E., Şık, E., Silan, F., Uludağ, A., ÖZDEMİR, Ö. (2013) "Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma", Asian Pacific Journal of Cancer Prevention, 14 (5) pp. 2903-2908 [SCI Expanded] Link DOI  " data-bs-content-id="YazarBilgi-21380"> Özen, F., Erdiş, E., Şık, E., Silan, F., Uludağ, A., ÖZDEMİR, Ö. (2013) "Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma", Asian Pacific Journal of Cancer Prevention, 14 (5) pp. 2903-2908 [SCI Expanded] Link DOI   Özen, F., Erdiş, E., Şık, E., Silan, F., Uludağ, A., ÖZDEMİR, Ö. (2013) "Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma", Asian Pacific Journal of Cancer Prevention, 14 (5) pp. 2903-2908 [SCI Expanded] Link DOI  

2013 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

DOI    Gönlügür, U., Gönlügür, T., ÖZDEMİR, Ö., Sılan, F. (2019) "Warfarin Resistance: A Case Report", EURASIAN JOURNAL OF EMERGENCY MEDICINE, 18 (1) pp. 61-63 [SSCI] DOI   " data-bs-content-id="YazarBilgi-21381"> Gönlügür, U., Gönlügür, T., ÖZDEMİR, Ö., Sılan, F. (2019) "Warfarin Resistance: A Case Report", EURASIAN JOURNAL OF EMERGENCY MEDICINE, 18 (1) pp. 61-63 [SSCI] DOI    Gönlügür, U., Gönlügür, T., ÖZDEMİR, Ö., Sılan, F. (2019) "Warfarin Resistance: A Case Report", EURASIAN JOURNAL OF EMERGENCY MEDICINE, 18 (1) pp. 61-63 [SSCI] DOI   

2019 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus

DOI    Erdiş, E., Yücel, B., ÖZDEMİR, Ö. (2019) "MEME KANSERLİ HASTALAR VE BİRİNCİ DERECEYAKINLARINDA PERİFERAL TRANSKRİPTOMPROFİLLERİNİN ARAŞTIRILMASI", Bozok Tıp Derg, 9 (4) pp. 27-31 [TR Dizin] DOI   " data-bs-content-id="YazarBilgi-21382"> Erdiş, E., Yücel, B., ÖZDEMİR, Ö. (2019) "MEME KANSERLİ HASTALAR VE BİRİNCİ DERECEYAKINLARINDA PERİFERAL TRANSKRİPTOMPROFİLLERİNİN ARAŞTIRILMASI", Bozok Tıp Derg, 9 (4) pp. 27-31 [TR Dizin] DOI    Erdiş, E., Yücel, B., ÖZDEMİR, Ö. (2019) "MEME KANSERLİ HASTALAR VE BİRİNCİ DERECEYAKINLARINDA PERİFERAL TRANSKRİPTOMPROFİLLERİNİN ARAŞTIRILMASI", Bozok Tıp Derg, 9 (4) pp. 27-31 [TR Dizin] DOI   

2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

Link DOI   Battal, F., Aylanç, H., Yıldırım, Ş., Yeliz, E., Sılan, F., ÖZDEMİR, Ö. (2017) "Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation", Family Practice and Palliative Care, (0) pp. 23-28 Link DOI  " data-bs-content-id="YazarBilgi-21384"> Battal, F., Aylanç, H., Yıldırım, Ş., Yeliz, E., Sılan, F., ÖZDEMİR, Ö. (2017) "Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation", Family Practice and Palliative Care, (0) pp. 23-28 Link DOI   Battal, F., Aylanç, H., Yıldırım, Ş., Yeliz, E., Sılan, F., ÖZDEMİR, Ö. (2017) "Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation", Family Practice and Palliative Care, (0) pp. 23-28 Link DOI  

2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

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]   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]  

2016 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

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  " 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  

2019 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus

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  " 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  

2010 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

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  

2011 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

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]   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]  

2011 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

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  " 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  

2018 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

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  

2018 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

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  

2018 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus