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Yayınlar:

  • Rapid Analysis Of The Cystic Fibrosis Delta F508, Delta I507 And Deltaf508c Mutation By Real Time Multiplex PCR. (2008). Ege Journal Of Medicine, 47 (2), 103 -109.
  • Onay H, Ekmekci AY, Durmaz B, Sayın E, Cosar H, Bayram N, Can D, Akin H,  Ozkınay C, Ozkınay F. (2010). Interferon-γ gene and interferon-γ receptor-1 gene polymorphisms in children with tuberculosis from Turkey. Scandinavian Journal of Infectious Diseases, 42 (1), 39-42.
  • Kahraman S, Benkhalifa M, Donmez E, Biricik A, Sertyel S, Findikli N, Berkil H. (2004). The results of aneuploidy screening in 276 couples undergoing assisted reproductive techniques, Prenat Diagn. 24 (4), 307-11.
  • Banu Bingol, Seval Tasdemir, Ziya Gunenc, Faruk Abike, Semra Esenkaya, Safak Tavukcuoglu, Hakan Berkil. (2011). Prenatal diagnosis of Comel-Netherton syndrome with PGD, case report and review article, J Assist Reprod Genet. 28 (7), 615-20.
  • Ramesh Reddy, Ngoc M P Nguyen, Guillaume Sarrabay, Maryam Rezaei, Mayra C G Rivas, Aysenur Kavasoglu, Hakan Berkil. (2016). The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions, Eur J Hum Genet. 24 (10), 1445-52.
  • N Basaran, H Berkil, N Ay, B Durak, C Ataman, M Ozdemir, Y H Ozon, I Kaya. (2001). A rare case: mosaic trisomy 22, Ann Genet. 44 (4), 183-6.
  • Ramesh Reddy, Ngoc M P Nguyen, Guillaume Sarrabay, Maryam Rezaei, Mayra C G Rivas, Aysenur Kavasoglu, Hakan Berkil. (2016). The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions, Eur J Hum Genet. 24 (10), 1516.
  • Burak Hacıhanefioğlu, Bekir Aybey, Yavuz Hakan Özön, Hakan Berkil, Kubilay Karşıdağ. (2013). Association of anthropometric, androgenic and insulin-related features with polymorphisms in exon 8 of SHBG gene in women with polycystic ovary syndrome, Gynecol Endocrinol. 29 (4), 361-4.
  • N Findikli, S Kahraman, Y Kumtepe, E Donmez, M Benkhalifa, A Biricik, S Sertyel, H Berkil, N Oncu. (2004). Assessment of DNA fragmentation and aneuploidy on poor quality human embryos, Reprod Biomed Online, 8 (2), 196-206.
  • S Kahraman, N Findikli, H Berkil, E Bakircioglu, E Donmez, S Sertyel, A Biricik. (2003). Results of preimplantation genetic diagnosis in patients with Klinefelter's syndrome, Reprod Biomed Online, 7 (3), 346-52.
  • F Fiorentino, A Biricik, H Karadayi, H Berkil, G Karlikaya, S Sertyel, D Podini, M Baldi, M C Magli, L Gianaroli, S Kahraman. (2004). Development and clinical application of a strategy for preimplantation genetic diagnosis of single gene disorders combined with HLA matching, Mol Hum Reprod. 10 (6), 445-60.
  • N Fındıklı, S Kahraman, Y Kumtepe, E Donmez, A Biricik, S Sertyel, H Berkil, S Melil. (2003). Embryo development characteristics in Robertsonian and reciprocal translocations: a comparison of results with non-translocation cases, , Reprod Biomed Online, 7 (5), 563-71.
  • B Tuysuz, A Yavuz, M Ozdil, J Caferler, H Ozon, A typical Down syndrome phenotype in a girl with 21;21 translocation trisomy, 2010, Genet Couns. 21(1), 61-7.
  • Karagenc TI, Pasa S, Kirli G, Hosgor M, Bilgic HB, Ozon YH, Atasoy A, Eren H., A parasitological, molecular and serological survey of Hepatozoon canis infection in dogs around the Aegean coast of Turkey. 2006, Vet Parasitol. 135 (2), 113-9.
  • Durak B, Ozön YH, Ozdemir M, Artan S, Basaran N, Basaran S, Ozkinay C. FISH analysis with locus-specific probes in sperm from two translocation carrier men. 1999, Clin Genet. 56 (2), 129-35.
  • R Durmaz, A Arslantaş, S Artan, Y H Ozon, S Işıksoy, N Başaran, E Tel, The deletion of 22q13 region in both intracranial and spinal meningiomas in a patient (case report), 1998, Clin Neurol Neurosurg. 100 (3), 219-23.
  • N Basaran, H Berkil, N Ay, B Durak, C Ataman, M Ozdemir, Y H Ozon, I Kaya, A rare case: mosaic trisomy 22, 2001, Ann Genet. 44 (4), 183-6.
  • R Durmaz, A Arslantaş, Y H Ozön, E Tel, Double meningocele. Case report, 2000, Turk J Pediatr. 42 (4), 331-3.
  • Hacıhanefioğlu B, Aybey B, Hakan Özön Y, Berkil H, Karşıdağ K. (2013). Association of anthropometric, androgenic and insulin-related features with polymorphisms in exon 8 of SHBG gene in women with polycystic ovary syndrome. Gynecol Endocrinol. 29 (4), 361-4.
  • Köseoğlu RD, Müslehıddınoğlu A, Erkorkmaz U, Caferler JS, Dürer P, Özön YH. (2011).  An analysis of HER-2/neu gene status in invasive ductal carcinomas using immunohistochemistry and fluorescence in situ hybridization. Turkish Journal of Medical Sciences, 41 (5), 809.
  • Fiorentino F., Kahraman S., Karadayi H., Biricik A., Sertyel S., Karlıkaya G., Saglam Y., Nuccitelli A. and Baldi M. (2005). Short tandem repeats haplotyping of the HLA region in preimplatation HLA matching Eur J Hum Genet. 13: 953-958.
  • F.Fiorentino, A.Biricik, H.Karadayi, H.Berkil, G.Karlikaya, S.Sertyel, D.Podini, M.Baldi, M.C.Magli, L.Gianaroli and S.Kahraman. (2004). Development and clinical application of a strategy for preimplantation genetic diagnosis of single gene disorders combined with HLA matching Molecular Human Reproduction Vol.10, No.6 pp. 445-460.
  • Kahraman S, Karlikaya G, Sertyel S, Karadayi H, Findikli N. (2004). Clinical aspects of preimplantation genetic diagnosis for single gene disorders combined with HLA typing. Reprod Biomed Online. 9 (5):529-32.
  • S. Kahraman, G. Karlıkaya, Y. Kumtepe, S. Sertyel, H. Karadayı, N. Fındıklı, E. Enginsu, N. Oncu, A. Biricik, F. Fiorentino. (2004). Tek Gen Hastalıklarında Preimplantasyon Genetik Tanı Ve HLA Doku Tiplemesi Uygulamalarının Klinik Değerlendirmesi, Türk Fertilite Dergisi,12 (1).
  • H. Karadayi, S. Kahraman, Y. Saglam, G. Karlikaya, S. Sertyel, F. Fiorentino. (2005). Preimplantation Genetic Diagnoss For Single Gene Disorders, World IVF Congress Proceeding Book.
  • H. Karadayi, S. Özkan, Y. Saglam, A.Gür, S.Isin, H. Yekle, S. Unal, S. Kahraman. (2005). Outcome Of 817 Infertile Men For Y Chromosome Microdeletions And Karyotype Analysis, World IVF Congress Proceeding Book.
  • Azakli, H., Akkaya, A. D., Aygun, M. S., Demirkesen, C., Eraslan, S., & Kayserili, H. (2019). Terminal osseous dysplasia with pigmentary defects (TODPD) in a Turkish girl with new skin findings. Am J Med Genet A, 179(1), 123-129.
  • Sahakyan, H., Hooshiar Kashani, B., Tamang, R., Kushniarevich, A., Francis, A., Costa, M. D., . . . Azakli, H., …, Villems, R. (2017). Origin and spread of human mitochondrial DNA haplogroup U7. Sci Rep, 7, 46044.
  • Karimova, A., Oltulu, Y. M., Azakli, H., Kara, M., Ustek, D., Tutluoglu, B., & Onaran, I. (2017). Lack of association between increased mitochondrial DNA(4977) deletion and ATP levels of sputum cells from chronic obstructive pulmonary disease patients versus healthy smokers. Mitochondrial DNA A DNA Mapp Seq Anal, 28(3), 361-369.
  • Gurses, C., Azakli, H., Alptekin, A., Cakiris, A., Abaci, N., Arikan, M., . . . Ustek, D. (2014). Mitochondrial DNA profiling via genomic analysis in mesial temporal lobe epilepsy patients with hippocampal sclerosis. Gene, 538(2), 323-327.
  • Azakli, H., Gurses, C., Arikan, M., Aydoseli, A., Aras, Y., Sencer, A., . . . Ustek, D. (2013). Whole mitochondrial DNA variations in hippocampal surgical specimens and blood samples with high-throughput sequencing: a case of mesial temporal lobe epilepsy with hippocampal sclerosis. Gene, 529(1), 190-194.
  • Cosan, F., Emrence, Z., Erbag, G., Azakli, H., Yilmazer, B., Yazici, A., . . . Cefle, A. (2013). The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease. Rheumatol Int, 33(7), 1675-1680.
  • Ustek, D., Sirma, S., Gumus, E., Arikan, M., Cakiris, A., Abaci, N., Emrence, Z., Azakli, H., Cosan, F., Cakar, A., Parlak, M., Kursun O. (2012). A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology. Infect Genet Evol, 12(7), 1349-1354.
  • Remmers, E. F., Cosan, F., Kirino, Y., Ombrello, M. J., Abaci, N., Satorius, C., . . ., Azakli, H., … Gul, A. (2010). Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease. Nat Genet, 42(8), 698-702.
  • Abaci, N., Cosan, F., Gulec, C., Azakli, H., Emrence, Z., Sirma, S., Cakiris, A., Oku, B., Ustek, D. (2011) Hypoxia induces erythropoietin receptor expression on K562 cell line. Medical Biotechnology.
  • Akiva İ, Birgül Iyison N. (2018). Identification of IFITM3 and MGAT1 as novel interaction partners of BRI3 by yeast two-hybrid screening. Turk J Biol. 42 (6), 463-470.
  • Akiva İ, Birgül Iyison N. (2018). MGAT1 is a novel transcriptional target of Wnt/β-catenin signaling pathway. BMC Cancer. 18 (1), 60-68.
  • Even İ, Akiva İ, İyison NB. (2019). An in vivo RNAi mini-screen in Drosophila cancer models reveals novel potential Wnt targets in liver cancer. Turk J Gastroenterol. 30 (2), 198-207.