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Toplam 27769 kayıt

The prevalence of Familial Mediterranean Fever common gene mutations in patients with simple febrile seizures.

Link   Özen, F., Koçak, N., Kelekçi, S., Yıldırım, İ.H., Hacimuto, G., Özdemir, 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., Özdemir, 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., Özdemir, 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  
2014 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
European review for medical and pharmacological sciences

A mosaic infertile case of isodicentric Y-chromosome with duplicated SRY, SHOX and deleted AZF locus

Özdemir, 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   Özdemir, 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  
2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Biomedical Genetics and Genomics

Çok Parametreli ve Çoklu Bilinmeyenli Kanser

Özdemir, Ö. (2017) "Çok Parametreli ve Çoklu Bilinmeyenli Kanser", Türkiye Klinikleri Journal of Medical Genetics-Special Topics, 2 (2) pp. 60-68   Özdemir, Ö. (2017) "Çok Parametreli ve Çoklu Bilinmeyenli Kanser", Türkiye Klinikleri Journal of Medical Genetics-Special Topics, 2 (2) pp. 60-68  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Türkiye Klinikleri Journal of Medical Genetics-Special Topics

Günümüzde Kanser Tanısında Kullanılan Geçerli ve Güvenilir Moleküler Tetkikler

Yalcintepe, S., Özdemir, 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   Yalcintepe, S., Özdemir, 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  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Turkiye Klinikleri Journal of Medical Genetics-Special Topics

Kanser Etyolojisinde Tetikleyici Moleküler Mekanizmalar

Özdemir, 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   Özdemir, 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  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Turkiye Klinikleri Journal of Medical Genetics-Special Topics

Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension

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) pp. 340-345 [SCI Expanded] DOI  " data-bs-content-id="YazarBilgi-21406"> 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) pp. 340-345 [SCI Expanded] 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) pp. 340-345 [SCI Expanded] DOI  
2014 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
ANNALS OF SAUDI MEDICINE

Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?

Link DOI   Sılan, F., Paksoy, B., Karakaya, T., Yıldız, O., Urfalı, M., Özdemir, 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., Özdemir, 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., Özdemir, 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  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
BioDiscovery

A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report

Link DOI   Sılan, F., Karakaya, T., Yıldız, O., Paksoy, B., Urfalı, M., Özdemir, 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., Özdemir, 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., Özdemir, 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  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance

Link DOI   Sılan, F., Paksoy, B., Urfalı, M., Karakaya, T., Yıldız, O., Özdemir, 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., Özdemir, 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., Özdemir, 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  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

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

Link DOI   Özdemir, 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"> Özdemir, 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   Özdemir, 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  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

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

Link DOI   Özdemir, 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"> Özdemir, 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   Özdemir, 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  
2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

A frameshift mutation in SLC34A2 gene in three patients with pulmonary alveolar microlithiasis in an inbread family

DOI   Doğan, Ö.T., Özşahin, S.L., Gül, E., Arslan, S., Köksal, B., Berk, S., Özdemir, 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., Özdemir, 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., Özdemir, 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  
2010 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
INTERNAL MEDICINE

Role of prothrombotic gene polymorphism in patients with thromboangiitis obliterans

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]   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]  
2009 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Türkiye Klinikleri Cardiovascular Sciences

Alterations in Promoter Methylation Status of Tumor Suppressor HIC1, SFRP2, and DAPK1 Genes in Prostate Carcinomas , iSFRP2/i , and iDAPK1/i Genes in Prostate Carcinomas/title

Link DOI   Kılınç, D., Özdemir, Ö., Özdemir, S., Korgalı, E., Köksal, B., Uslu, A., Gültekin, E.Y. (2012) "Alterations in Promoter Methylation Status of Tumor Suppressor HIC1, SFRP2, and DAPK1 Genes in Prostate Carcinomas , iSFRP2/i , and iDAPK1/i Genes in Prostate Carcinomas/title", DNA and Cell Biology, 31 (5) pp. 826-832 [SCI] Link DOI  " data-bs-content-id="YazarBilgi-21416"> Kılınç, D., Özdemir, Ö., Özdemir, S., Korgalı, E., Köksal, B., Uslu, A., Gültekin, E.Y. (2012) "Alterations in Promoter Methylation Status of Tumor Suppressor HIC1, SFRP2, and DAPK1 Genes in Prostate Carcinomas , iSFRP2/i , and iDAPK1/i Genes in Prostate Carcinomas/title", DNA and Cell Biology, 31 (5) pp. 826-832 [SCI] Link DOI   Kılınç, D., Özdemir, Ö., Özdemir, S., Korgalı, E., Köksal, B., Uslu, A., Gültekin, E.Y. (2012) "Alterations in Promoter Methylation Status of Tumor Suppressor HIC1, SFRP2, and DAPK1 Genes in Prostate Carcinomas , iSFRP2/i , and iDAPK1/i Genes in Prostate Carcinomas/title", DNA and Cell Biology, 31 (5) pp. 826-832 [SCI] Link DOI  
2012 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
DNA and Cell Biology

Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis

Link DOI   Özdemir, Ö., Kayataş, M., Çetinkaya, S., Yıldırım, M.E., Sılan, F., Kurtulgan, H.K., Urfalı, M., Candan, F. (2015) "Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis", RENAL FAILURE, 37 (2) pp. 292-296 [SSCI] Link DOI  " data-bs-content-id="YazarBilgi-21417"> Özdemir, Ö., Kayataş, M., Çetinkaya, S., Yıldırım, M.E., Sılan, F., Kurtulgan, H.K., Urfalı, M., Candan, F. (2015) "Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis", RENAL FAILURE, 37 (2) pp. 292-296 [SSCI] Link DOI   Özdemir, Ö., Kayataş, M., Çetinkaya, S., Yıldırım, M.E., Sılan, F., Kurtulgan, H.K., Urfalı, M., Candan, F. (2015) "Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis", RENAL FAILURE, 37 (2) pp. 292-296 [SSCI] Link DOI  
2015 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
RENAL FAILURE