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]
Sılan, F., Paksoy, B., Karakaya, T., Yıldız, O., Urfalı, M., ÖZDEMİR, Ö. (2017) "Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?", BioDiscovery, 20 (0) Link DOI " data-bs-content-id="YazarBilgi-21408">
Sılan, F., Paksoy, B., Karakaya, T., Yıldız, O., Urfalı, M., ÖZDEMİR, Ö. (2017) "Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?", BioDiscovery, 20 (0) Link DOI Sılan, F., Paksoy, B., Karakaya, T., Yıldız, O., Urfalı, M., ÖZDEMİR, Ö. (2017) "Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?", BioDiscovery, 20 (0) Link DOI
Sılan, F., Karakaya, T., Yıldız, O., Paksoy, B., Urfalı, M., ÖZDEMİR, Ö. (2017) "A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report", Journal of Biotechnology, 256 (0) pp. 78-79 [SSCI] Link DOI " data-bs-content-id="YazarBilgi-21409">
Sılan, F., Karakaya, T., Yıldız, O., Paksoy, B., Urfalı, M., ÖZDEMİR, Ö. (2017) "A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report", Journal of Biotechnology, 256 (0) pp. 78-79 [SSCI] Link DOI Sılan, F., Karakaya, T., Yıldız, O., Paksoy, B., Urfalı, M., ÖZDEMİR, Ö. (2017) "A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report", Journal of Biotechnology, 256 (0) pp. 78-79 [SSCI] Link DOI
Sılan, F., Paksoy, B., Urfalı, M., Karakaya, T., Yıldız, O., ÖZDEMİR, Ö. (2017) "Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance", Journal of Biotechnology, 256 (0) pp. 78-78 [SSCI] Link DOI " data-bs-content-id="YazarBilgi-21410">
Sılan, F., Paksoy, B., Urfalı, M., Karakaya, T., Yıldız, O., ÖZDEMİR, Ö. (2017) "Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance", Journal of Biotechnology, 256 (0) pp. 78-78 [SSCI] Link DOI Sılan, F., Paksoy, B., Urfalı, M., Karakaya, T., Yıldız, O., ÖZDEMİR, Ö. (2017) "Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance", Journal of Biotechnology, 256 (0) pp. 78-78 [SSCI] Link DOI
ÖZDEMİR, Ö., Urfalı, M., Paksoy, B., Karakaya, T., Yıldız, O., Sılan, F. (2017) "A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when comparing to the MicroArray-CGH technique", Journal of Biotechnology, 256 (0) pp. 79-79 [SSCI] Link DOI " data-bs-content-id="YazarBilgi-21411">
ÖZDEMİR, Ö., Urfalı, M., Paksoy, B., Karakaya, T., Yıldız, O., Sılan, F. (2017) "A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when comparing to the MicroArray-CGH technique", Journal of Biotechnology, 256 (0) pp. 79-79 [SSCI] Link DOI ÖZDEMİR, Ö., Urfalı, M., Paksoy, B., Karakaya, T., Yıldız, O., Sılan, F. (2017) "A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when comparing to the MicroArray-CGH technique", Journal of Biotechnology, 256 (0) pp. 79-79 [SSCI] Link DOI
ÖZDEMİR, Ö., Yıldız, O., Karakaya, T., Paksoy, B., Urfalı, M., Sılan, F. (2017) "The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2 , and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), speech and motor delay", Journal of Biotechnology, 256 (0) pp. 78-78 [SSCI] Link DOI " data-bs-content-id="YazarBilgi-21412">
ÖZDEMİR, Ö., Yıldız, O., Karakaya, T., Paksoy, B., Urfalı, M., Sılan, F. (2017) "The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2 , and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), speech and motor delay", Journal of Biotechnology, 256 (0) pp. 78-78 [SSCI] Link DOI ÖZDEMİR, Ö., Yıldız, O., Karakaya, T., Paksoy, B., Urfalı, M., Sılan, F. (2017) "The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2 , and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), speech and motor delay", Journal of Biotechnology, 256 (0) pp. 78-78 [SSCI] Link DOI
Doğan, Ö.T., Özşahin, S.L., Gül, E., Arslan, S., Köksal, B., Berk, S., ÖZDEMİR, Ö., Akkurt, İ. (2010) "A frameshift mutation in SLC34A2 gene in three patients with pulmonary alveolar microlithiasis in an inbread family", INTERNAL MEDICINE, 49 (1) pp. 45-49 [SCI Expanded] DOI " data-bs-content-id="YazarBilgi-21413">
Doğan, Ö.T., Özşahin, S.L., Gül, E., Arslan, S., Köksal, B., Berk, S., ÖZDEMİR, Ö., Akkurt, İ. (2010) "A frameshift mutation in SLC34A2 gene in three patients with pulmonary alveolar microlithiasis in an inbread family", INTERNAL MEDICINE, 49 (1) pp. 45-49 [SCI Expanded] DOI Doğan, Ö.T., Özşahin, S.L., Gül, E., Arslan, S., Köksal, B., Berk, S., ÖZDEMİR, Ö., Akkurt, İ. (2010) "A frameshift mutation in SLC34A2 gene in three patients with pulmonary alveolar microlithiasis in an inbread family", INTERNAL MEDICINE, 49 (1) pp. 45-49 [SCI Expanded] DOI
Özen, F., Manduz, S., Katrancıoglu, N., Karahan, O., Köksal, B., Özdemir, Ö. (2009) "Role of prothrombotic gene polymorphism in patients with thromboangiitis obliterans", Türkiye Klinikleri Cardiovascular Sciences, 21 (2) pp. 160-164 [SSCI]
Arslan, S., Akkurt, I., Koksal, B., Karadayi, S., Ozdemir, O. (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 [SSCI]
