Bildiriler

• A CASE STUDY : GENETIC ANALYSIS OF NON-IMMUNE HYDROPS FETALIS (NIHF) PATIENTS. Lara Lembet1, Hakan Berkil2, İzzet Akiva2, Hande Ertürk2, Hülya Azaklı2, Eren Sayın2, Arda  Lembet3. 1University College London-Applied Medical Sciences (London, UK), 2Genetiks Genetic Diagnosis Center (Istanbul, Turkey), 3Femical Kadın Sağlığı ve Doğum Kliniği (Istanbul, Turkey) 18. Ulusal Perinatoloji Kongresi 8-10 Nisan 2021
• A Novel Mutation in GDAP1 Gene Causing Charcot-Marie-Tooth 4A, Duman N, Ekici B, Akyüz E, Taşar O, Bağcı F, Sayın E, Tatlı B, Yeşil G. (2016).  , XII. National Medical Genetics Congress.
• Vitamin D Receptor (Vdr) Gene Polymorphism And Susceptibility to Tuberculosis: A Case- Control Study, Keystone Symposia. (2007) İzmir - Turkey.
• Molecular Based Diagnostic Studies In The Department Of Medical Genetics, Facullty Of Medicine, Ege University. (2006). Bertinoro - Italy.
• Sağlıklı Türk Popülasyonundaki 4. ve 5. Kromozomlarda Yer Alan İki Önemli Mikrosatellite Ait Bilgilendiriciliğin Araştırılması. (2006). National Biology Congress, Aydın - Turkey.
• Huseyin Karadayi, Cigdem Aktas, Mert Alkac, Yavuz Hakan Ozon, Hakan Berkil. (2016). Molecular analysis of Kras and Nras mutations in a series of 720 patients for guiding the treatment of metastatic colorectal cancer in Turkey. American Society of Clinical Oncology (ASCO) 2016 Annual Meeting. June 3-7 2016, Chicago, Illinois.
• Y.H. Ozon, H. Karadayi, E. Atli, J. Caferler, M. Bahce, H. Berkil. (2013). Preimplantation genetic diagnosis for single gene disorders applied in GENETIKS Laboratory. 12. International Symposium on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Atli E., Karadayi H., Aktas, C., Caferler J., Ozon YH, Bahce, M., Berkil H. Preimplantation Genetic Diagnosis for Glycine Encephalopathy. (2013). 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H., Atli E., Aktas C., Caferler, J., Berkil H., Bahce M., Ozon, YH. (2013). Preimplantation Genetic Diagnosis for Epidermolysis Bullosa. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Atli E., Karadayi H., Arslan, A., Berkil, H., Caferler, J., Ozen, C., Ozon, YH. (2013). Preimplantation Genetic Diagnosis for Nemaline Myopathy. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H., Atli, E., Arslan A., Caferler, J., Ozon, YH. Berkil H., Bahce M. (2013).  Preimplantation Genetic Diagnosis for Hypoparathyroidism-Deafness-Renal Dysplasia Syndrome. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Atli E., Karadayi H., Aktas C., Caferler J., Ozon Y.H., Sertyel A., Berkil, H. (2013). Preimplantation Genetic Diagnosis for Glutaric Aciduria Type II. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H., Atli E., Aktas C., Berkil H., Ozon, YH, Budak E, Caferler J. (2013). Preimplantation Genetic Diagnosis for ARC Syndrome. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Atli E. Karadayi H, Aktas, C. Berkil H. Ulug M, Ulug, AA, Caferler, J. Ozon YH. (2013). Preimplantation Genetic Diagnosis for Lamellar Ichthyosis Type 2. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H., Atli, E., Aktas, C., Berkil H., Ozon YH, Ulug AA, Ulug M, Caferler J. (2013).  Preimplantation Genetic Diagnosis for Hereditary Motor and Sensory Neuropathy Type 1. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• 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 PGD of single gene disorders combined with HLA matching. 20th Annual Meeting of the European Society of Reproduction & Embryology. 27-30 June 2004, Berlin, Germany.
• Mustafa E. Bakırcıoğlu, Semra Kahraman, Semra Sertyel, Necati Fındıklı, Hakan Berkil, Sevil Ünal. (2003). Comparison of two tese procedures and PGD outcomes for patients with Kleinfelters syndrome. 59th Annual Meeting of the American Society for Reproductive Medicine, October 11-15, 2003, San Antonio, TX, US.
• Biricik A., Berkil H., Karadayı H., Bakırcıoğlu E., Kahraman S., Güney İ and Benkhalifa M. (2003). Chromosome and Y deletion analysis of non-obstructive azoospermic males and sperm retrieval with testicular sperm extraction technique. 19th Annual ESHRE Symposium, 29 June-2 July 2003, Madrid, Spain.
• Biricik A., Berkil H., Kahraman S., Oncu N., Gur A., Gurkan S., Sertyel S., Benkhalifa M. (2003). Chromosome segregation analysis in sperm cells from infertile males with abnormal karyotypes. 19th Annual ESHRE Symposium, 29 June-2 July 2003, Madrid, Spain.
• H. Berkil. (2003). Genetic Counselling. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• G. Karlıkaya, S. Kahraman, H. Berkil, A. Biricik, H. Karagözoğlu, E. Dönmez, S. (2003). Sertyel, F. Vanlıoğlu, M. Aygün, S. Melil, M. Benkhalifa. Preimplantation genetic diagnosis results for the recurrent implantation failure cases with or without advanced maternal age. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• F. Fiorentino, S. Kahraman, A Biricik, H. Karadayı, A. Nuccitelli, D. Podini, H. Berkil. (2003).  Preliminary data on the development of an alternative strategy for PGD of single gene disorders combined with HLA matching. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• G. Karlıkaya, S. Kahraman, N. Fındıklı, E. Dönmez, A. Biricik, H. Berkil. (2003). Efficiency of aneuploidy testing in patients with recurrent miscarriage: effect of maternal age. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• S. Sertyel, E. Bakırcıoğlu, S. Kahraman, A. Biricik, E. Dönmez, N. Fındıklı, S. Ünal, H. Yekle, S. Melil, H. Karagözoğlu, H. Berkil. (2003). Outcome of PGD in cases of severe sperm morphological defects. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• E. Dönmez, S. Kahraman, S. Sertyel, S. Melil, A. Biricik, N. Fındıklı, G. Karlıkaya, H. Karagözoğlu, H. Berkil. (2003). Couples in which embryo transfer was cancelled due to the lack of chromosomally normal embryos. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• N. Fındıklı, S. Kahraman, E. Dönmez, A. Biricik, H. Berkil, S. Sertyel, F. Vanlıoğlu. (2003). Embryo development and PGD outcome in translocations. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• A. Biricik, H. Berkil, S. Kahraman, M. Benkhalifa, N. Öncü, A. Gür, S. Gürkan, S. Sertyel, S. Ünal, H. Karagözoğlu. (2003). Detection of chromosomal abnormalities by FISH in infertile males with abnormal karyotypes. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya.
• N. Fındıklı, A. Biricik, N. Öncü, S. Kahraman, E. Dönmez, S Sertyel, S. Melil, M. Benkhalifa, F. Vanlıoğlu, H. Berkil. (2003). Assessment of DNA fragmantation and aneuploidy on slow growing embryos. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• E. Bakırcıoğlu, S. Kahraman, N. Fındıklı, A. Biricik, S. Sertyel, E. Dönmez, S. Ünal, H. Yelke, H. Berkil, N. Öncü, M. Aygün. (2003). Preimplantation genetic diagnosis for Klinefelters: Evidence for increased chromosomal abnormalities. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• Berkil H., Biricik A., Oncu N., Findikli N., Donmez E., Sertyel S., Vanlıoğlu, Karlikaya G., Aygun M., Oral E. and Kahraman S. (2003). Results of Preimplantation Genetic Diagnosis (PGD) for Aneuploidy Testing in Cases with Advanced Maternal Age (AMA), Repeated Implantation Faulure (RIF), Recurrent Early Miscarriage and Severe Male Infertility (SMI). ESHRE Campus 2003. PGD in 2003: A Genetic Odyssey. 5-6 December 2003. Brussels, Belgium.
• Findikli N., Oncu N., Biricik A., Berkil H, Sertyel S, Karagozoglu H, Aygun M, Unal S, Yelke H, Oral E and Kahraman S. (2003). The contribution of chromosomally abnormal spermatazoa in ART efficiency in severe male infertility cases. ESHRE Campus 2003. PGD in 2003: A Genetic Odyssey. 5-6 December 2003. Brussels, Belgium.
• Fiorentino F, Biricik A, Karadayi H, Berkil H, Karlikaya G, Sertyel S, Nucitelli A, Podini D, Baldi M, Magli MC, Gianaroli L and Kahraman S. (2003). Development and clinical application of a strategy for PGD of single gene disorders combined with HLA matching. ESHRE Campus 2003. PGD in 2003: A Genetic Odyssey. 5-6 December 2003. Brussels, Belgium.
• Melil S, Sertyel S, Bakircioglu E, Biricik A, Karlikaya G, Oncu N, Berkil H, Karagozoglu H, Vanlioglu F, Unal S, Yelke H, Findikli N and Kahraman S. (2003). Outcome of preimplantation genetic diagnosis in cases with severe sperm morphological defects. ESHRE Campus 2003. PGD in 2003: A Genetic Odyssey. 5-6 December 2003. Brussels, Belgium.
• Sertyel S, Bakircioglu E, Karlikaya G, Biricik A, Vanlioglu F, Findikli N, Oncu N, Gurkan S, Gur A, Berkil H, Oral E and Kahraman S. (2003). Results of preimplantation genetic diagnosis in patients with Klinefelters syndrome. ESHRE Campus 2003. PGD in 2003: A Genetic Odyssey. 5-6 December 2003. Brussels, Belgium.
• Semra Kahraman, Ersan Dönmez, Anıl Biricik, Semra Sertyel, Necati Fındıklı, Hakan Berkil. (2003). The results of aneuploidy screening in 276 couples undergoing assisted reproductive techniques. 59th Annual Meeting of the American Society for Reproductive Medicine, October 11-15, 2003, San Antonio, TX, USA.
• Bakırcıoğlu E., Kahraman S., Dönmez E., Fındıklı N., Sertyel S., Ünal S., Berkil H., Yekle H. and Melil S. (2003). Comparison of testicular sperm extraction of microdissection and multi-biopsy techniques in patients with Klinefelters Syndrome. 19th Annual ESHRE Symposium, 29 June-2 July 2003, Madrid, Spain.
• S. Melil, S. Kahraman, S. Sertyel, A. Biricik, E. Dönmez, N. Fındıklı, S. Ünal, H. Yekle, M. Aygün, H. Berkil. (2003). Increased sperm chromosomal abnormalities and possible contribution to preimplantation embryos: Case report. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• A. Biricik, H. Berkil, H. Karadayı, E. Bakırcıoğlu, S. Kahraman, F. Fiorentino, S. Sertyel, E. Dönmez, F. Vanlıoğlu, G. Karlıkaya. (2003). Molecular and cytogenetic analysis results in severe infertile males and their prognostic value for PGD in Turkish population. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• N.C. Yılanlıoğlu, S. Kahraman, E. Dönmez, B. Kumbak, H. Berkil, A. Biricik, S. Sertyel, F. Vanlıoğlu. (2003). Outcome of pregnancies achieved trough preimplantation genetic diagnosis. Fifth International Symposium on Preimplantation Genetics, 5-7 June 2003, Antalya, Turkey.
• Kahraman S., Biricik A., Yılanlıoğlu N.C., Vanlıoğlu F., Kumtepe Y., Berkil H. (2002). ART tedavisi gören 226 olguda preimplantasyon genetik tanı sonuçları ve elde edilen gebeliklerin endikasyonlara göre prognozları. II. World Congress of Perinatal medicine for Developing Countries & VIII. Ulusal Perinatoloji Kongresi. 1-5 Ekim 2002, Belek, Antalya, Türkiye.
• Kahraman S., Biricik A., Fiorentino F., Kumtepe Y., Berkil H. (2002). Embriyolarda beta Thalassemia yönünden preimplantasyon genetik tanı HLA genotiplemesi: Türkiyede elde edilen ilk gebelik ve doğum sonrası kord kanı stem cell ayrıştırılması. II. World Congress of Perinatal medicine for Developing Countries & VIII. Ulusal Perinatoloji Kongresi. 1-5 Ekim 2002, Belek, Antalya, Türkiye.
• Kahraman S., Kübelioğlu L., Biricik A., Berkil H., Kumtepe Y. (2002) . Tekrarlayan erken gebelik kayıplarında preimplantasyon genetik tanı sonuçları. II. World Congress of Perinatal medicine for Developing Countries & VIII. Ulusal Perinatoloji Kongresi. 1-5 Ekim 2002, Belek, Antalya, Türkiye.
• S. Kahraman, K. Yakin, M. Benkhalifa, S. Sertyel, H. Berkil, Y. Kumtepe. (2002). High aneuploidy rate in preimplantation embryos developed from macrocephalic sperm injection. Fourth International Symposium on Preimplantation Genetics”, Limassol, Cyprus, April 10-13, 2002.
• S. Kahraman, M. Benkhalifa, E. Dönmez, A. Biricik. H. Berkil, K. Yakin. (2002). Overall results of aneuploidy screening in a Turkish population undergoing assisted reproductive techniques. Fourth International Symposium on Preimplantation Genetics”, Limassol, Cyprus, April 10-13, 2002.
• S. Kahraman, K. Yakin, M. Benkhalifa, E. Dönmez, H. Berkil, Y. Kumtepe. (2002). Aneuploidy screening in embryos developed from centrally located granular oocytes improves implantation and clinical pregnancy rates, Fourth International Symposium on Preimplantation Genetics, Limassol, Cyprus, April 10-13, 2002.
• A. Guney, A. Biricik, E. Tetik, H. Berkil, S. Kahraman. (2002). Cytogenetic analysis and Y chromosome microdeletion results in infertile males undergoing assisted reproductive technology (ART). European Human Genetics Conference. May 25-29, 2002, Strasbourg, France.
• H Berkil, A Biricik, S. Kahraman, I Güney, K Yakın, E Dönmez, N Öncü, H Ozon. (2002). PGD for marker chromosome 15; case report. Fourth International Symposium on Preimplantation Genetics”, Limassol, Cyprus April 10-13, 2002.
• Berkil H, Durak B, Ataman C, Sabuncu I, Başaran N. (2001). Cytogenetics and Molecular Cytogenetic Analysis of the Patients with Psoriasis. 10th International Congress of Human Genetics, Vienna, Austria, 2001.
• Basaran N, Sener T, Durak B, Kaya I, Berkil H, Ozon YH. (2001). Prenatal Diagnosis of the Fetus with Mosaic Del(12)(q21.32q22): First Prenatal Case. 10th International Congress of Human Genetics, Vienna, Austria, 2001.
• Ozdemir M, Durak B, Berkil H, Kaya I, Basaran N. (2001). A rare a Mosaic Trisomy 22 Case. 10th International Congress of Human Genetics, Vienna, Austria, 2001.
• Kayhan Yakın, Semra Kahraman, Anıl Biricik, Nihal Öncü, Hakan Berkil, Moncef BenKhalifa. (2001). Is there a possible correlation between Chromosomal variants and spermatogenesis. Paris, 2001.
• Başaran, Nurettin; Koçak, A.; Berkil, H.</span>; Durak, B.; Kaya, I.; Özön, Y.H. (2000). Phenotipically Normal Mother and her Two Children with Translocation Type Down Syndrome. European Human Genetics Conferance, Amsterdam, Hollanda, 2000.
• Huseyin Karadayi, Cigdem Aktas, Mert Alkac, Yavuz Hakan Ozon, Hakan Berkil. (2016). Molecular analysis of Kras and Nras mutations in a series of 720 patients for guiding the treatment of metastatic colorectal cancer in Turkey. American Society of Clinical Oncology (ASCO) 2016 Annual Meeting. June 3-7 2016, Chicago, Illinois.
• Y.H. Ozon, H. Karadayi, E. Atli, J. Caferler, M. Bahce, H. Berkil. (2013). Preimplantation genetic diagnosis for single gene disorders applied in GENETIKS Laboratory. 12. International Symposium on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Atli, E.; Karadayi, H., Aktas, C.; Caferler, J.; Ozon, Y.H</span>.; Bahce, M., Berkil, H. (2013). Preimplantation Genetic Diagnosis for Glycine Encephalopathy. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H, Atli, E, Aktas C, Caferler J, Berkil H, Bahce M, Ozon YH. (2013). Preimplantation Genetic Diagnosis for Epidermolysis Bullosa. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Atli E, Karadayi H, Arslan A, Berkil H, Caferler J, Ozen C, Ozon YH. (2013) Preimplantation Genetic Diagnosis for Nemaline Myopathy. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H, Atli E, Arslan A, Caferler J, Ozon YH, Berkil H, Bahce M. (2013)  Preimplantation Genetic Diagnosis for Hypoparathyroidism-Deafness-Renal Dysplasia Syndrome. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Atli E, Karadayi H, Aktas C, Caferler J, Ozon YH, Sertyel A, Berkil H. (2013). Preimplantation Genetic Diagnosis for Glutaric Aciduria Type II. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H, Atli E, Aktas C, Berkil H, Ozon YH, Budak E, Caferler J. (2013). Preimplantation Genetic Diagnosis for ARC Syndrome. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey
• Atli E, Karadayi H, Aktas C, Berkil H, Ulug M, Ulug AA, Caferler J, Ozon YH. (2013). Preimplantation Genetic Diagnosis for Lamellar Ichthyosis Type 2. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• Karadayi H,  Atli E, Aktas C, Berkil H, Ozon Y.H, Ulug AA, Ulug, M, Caferler J. (2013). Preimplantation Genetic Diagnosis for Hereditary Motor and Sensory Neuropathy Type 1. 12. International Conference on Preimplantation Genetics, May 8-11 2013, Istanbul, Turkey.
• A.Biricik, I.Guney, S.Kahraman, K.Yakin, M.Benkhalifa, Y.H.Ozon. (2002). Recurrent spontaneus abortions due to 15;15 Robertsonian translocation in the male. Fourth International Symposium on Preimplantation Genetics, Abstract Book pp46; P15, Limasol Cyprus, April 10-13, 2002.
• H.Berkil, A.Biricik, S.Kahraman, I.Guney, K.Yakin, E.Donmez, N.Oncu, Y.H.Ozon. (2002). PGD for marker chromosome 15: case report. Fourth International Symposium on Preimplantation Genetics, Abstract Book pp46; P15, Limasol Cyprus, April 10-13,2002.
• Basaran N, Sener T, Durak B, Kaya I, Berkil H, Ozon YH. (2001). Prenatal Diagnosis of the Fetus with Mosaic Del(12)(q21.32q22): First Prenatal Case. 10th International Congress of Human Genetics, Vienna, Austria, 2001.
• Başaran N, Koçak A, Berkil H., Durak B, Kaya I, Ozon YH. (2000). A mosaic and phenotipically normal mother and her two children with translocation type down syndrome. European Human Genetics Conference 2000. 27-30 May 2000, Amsterdam, the Netherlands. European Journal of Human Genetics, 8(Suppl. 1), P-757, 2000.
• Durmaz R, Arslantaş A, Ozon YH, Tel E. (1999). Double Meningocele with Tethered Cord, 11th European Congress of  Neurosurgery Abstract Book, Copenhagen, Denmark, 19-24 Sept. 1999.
• Artan S, Ozon YH, Ozdemir M, Durak B, Başaran N, Başaran S, Ozkınay C. (1999). Segregation analyses in the sperm cells of the translocation carriers. 31st Annual Meeting of the European Society of Human Genetics, Geneva, Switzerland, Abstract Book, P-242: 71, 29 May-1 June 1999.
• Başaran N, Caferler J, Ozon YH, Ozdemir M, Durak B, Artan S, Başaran A. (1999). Isolation of fetal cells among endocervical canal cells. 31st Annual Meeting of the European Society of Human Genetics, Geneva, Switzerland, Final Programme and Abstracts, P-242: 79, 29 May-1 June 1999.
• Ozdemir M, Yavuz N, Durak B, Ozon YH, Çilingir O, Başaran N. (1997). Evaluation of abnormal karyotypes with physical features. 1st European Cytogenetics Conference, 22-25 June, 1997, Athens. Cytogenet. Cell Genet. 77: 118, 1997.
• Caferler J, Ozon YH, Ozdemir M, Tandogdu Ö, Durak B, Artan S, Başaran N. (1997). Isolation of fetal cells among endocervical canal cells. 1st European Cytogenetics Conference, 22-25 June, 1997, Athens.
• Genç J, Ozon YH, Ozdemir M, Artan S, Başaran N. (1996). Rapid detection of fetal sex and aneuploidy in uncultured amniocytes by FISH. 2nd Balkan Meeting on Human Genetics, İstanbul, 3-6 Eylül, 1996.
• Yesil, M.; Beyazyurek, C.;Umay,B.; Ozden,A.; Sabuncuoglu, Y.; Karadayi,H.</span>; Saglam,Y. (2007). Ozkan,S. and Kahraman,S. Results of cytogenetic and molecular screening in patients with non-obstructive azoospermia: 7 years experience, 6th European Cytogenetics Conference, İstanbul.
• Sabuncuoglu,Y.; Yesil,M.; Beyazyurek,C.; Ozden,A.; Saglam,Y.; Ozkan,S.; Umay,B.; Karadayi,H.</span>; Yekle,H. and Kahraman,S. (2007). Application of assisted reproductive techniques in patients with klinefelter’s syndrome, 6th European Cytogenetics Conference, İstanbul.
• Ozden,A.; Yesil,M.; Sabuncuoglu,Y.; Beyazyurek,C.; Isın,S.; Gur,A.; Umay,B.; Karadayi,H.</span>; Kahraman,S. and Saglam,Y. (2007). Result of 4680 cytogenetic studies: a retrospective study in karyotype abnormalities, 6th European Cytogenetics Conference, İstanbul .
• Umay B. Beyazyurek,C.; Yesil,M.; Karadayi, H.</span>; Ozden,A.; Sabuncuoglu,Y.; Yekle,H.; Saglam,Y.; Ozkan,S. and Kahraman, S. (2007). Unusal male karyotype with or without Y chromosome, 6th European Cytogenetics Conference, İstanbul.
• Taser Guney, A., Yesil, M.; Sabuncuoglu, Y.Ozden, A.; Umay, B.; Yılanlıoglu, N.C. Beyazyurek, C. Karadayi, H. Kahraman, S. and Saglam, Y. (2007). A case report : Prenatal diagnosis of 47,XX,der-15-t-4;15--q35;q21.3-, 6th European Cytogenetics Conference, İstanbul.
• Semiz,A.; Umay,B.; Yesil,M.;  Karadayi,H.</span>; Ozden,A.; Sabuncuoglu,Y.; Saglam,Y.; Yılanlıoglu,N.C. and Kahraman,S. (2007). QF_PCR in preimplantation diagnosis, 6th European Cytogenetics Conference, İstanbul.
• Zeynep Özkan, Burcu Umay Kara, Hüseyin Karadayı, Didem Savaş, Bihter Mergen, Nazan Emruşi, Hakan Yurt, Rıdvan Seçkin Özen. (2012). Bare lenfosit sendromu tip II / major Histocompatibility Complex Class II eksikliği - kompleman grup b nin blastomer analizi ile preimplantasyon genetik tanısı. 10. Ulusal Tıbbi Genetik Kongresi 0451. İstanbul Genetik Grubu, İstanbul.
• Bihter Mergen, Didem Savaş, Burcu Umay Kara, Hüseyin Karadayı, Nazan Emruşi, Zeynep Özkan, Hakan Yurt, Rıdvan Seçkin Özen. (2012). Akromatopsi tip 3 (siklik Nükleotid-kapılı kanal beta 3 - CNgb3) ün blastomer analizi ile preimplantasyon genetik tanısı. 10. Ulusal Tıbbi Genetik Kongresi 0449, İstanbul Genetik Grubu, İstanbul.
• Burcu Umay Kara, Hüseyin Karadayı, Didem Savaş, Bihter Mergen, Nazan Emruşi, Zeynep Özkan, Hakan Yurt, Rıdvan Seçkin Özen. Berardinelli-seip konjenital lipodistrofi tip 2 (bsCl2) nin blastomer analizi ile preimplantasyon genetik tanısı. İstanbul Genetik Grubu, İstanbul.
• B. Umay, C. B. Ogur, Y. Saglam, S. Isin, H. Karadayi, S. Ozkan Males With Female Karyotypes ASRM 2006 Annual Meeting Posters.
• Azakli, H., Yücel, E., Arıkan, Ç., Armutlu, Ç., Eraslan, S., Kayserili, H. (2019). “TRMU-related transient liver failure of infancy presents with microcephaly and neurodevelopmental delay.”. European Human Genetics Conference, Gothenburg, Sweden.
• Azakli, H., Akkaya, D., Aygun, SM., Demirkesen, C., Kayserili, H. (2018). “Pigment defektli terminal osseöz displazi olgusu; tanı yaklaşımı ve ek bulguların varlığı.” 13. Ulusal Tıbbi Genetik Kongresi, Antalya.
• Hirose, M., Azakli, H., Ibrahim, SM. (2012). “Impact of a single mitochondrial DNA mutation on variety of phenotype and mitochondrial function in aging.” The 17^th European Bioenergetics Conference Freiburg, Germany.
• Azakli, H., Emrence, Z., Cakiris, A., Arikan, M., Abaci, N., Ustek, D. (2011). “A novel ND5 gene mutation giving mitochondrial myopathy.” Mitochondrial Medicine 2011 Chicago, USA.
• Azakli, H., Cakar, A., Emrence, Z., Abaci, N., Cakiris, A., Ustek, D., Gurses, C. (2010). “The role of mitochondrial DNA in drug resistant Mesial Temporal Lobe Epilepsy.” John Wiley&Sons A/S, Clinical Genetics, 78:112-133.
• Gedikbasi, A., Azakli, H., Ozturk, S., Cakiris, A., Cefle K, Abaci N, Palandüz S, Emrence Z, Cakar A, Ustek D. (2010). “Ultra-deep pyrosequencing of whole mitochondrial DNA: A report of Leber’s Hereditary  Optic Neuropathy.” John Wiley&Sons A/S, Clinical Genetics 2010;78 (Suppl. 1):95-103.
• Kalay, S., Turkan, A., Zergeroglu, AD., Azakli, H., Ustek, D. (2010). “Investigation of PDC, A-KGDC, SDH and IDH activities In SPC111 and SPC212 malignant mesothelioma cells.” 22th National  Biochemistry Congress, Eskişehir, Turkey.
• Haciosmanoglu, E., Unlü,  A., Azakli, H., Ustek, D., Bektas, M. (2009). “FB cloning from toxin fragments and obtaining antibody.” 2. International Biophyics Congress and Biotechnology at GAP & 21st National Biophyics Congress, Diyarbakır, Turkey
• Hatemi, A., Cakiris, A., Ceviker, K., Canikoglu, M., Abaci, N., Cosan, F., Ozbalci, C., Aglar, O., Azakli, H., Okten, Z., Kazan, D., Kansız, E., Ustek, D. (2009) “Blood surface interaction and aggregation of serum proteins during extracorporeal circulation with phosphorylcholine –coated tubing lines: S100 A8/A9 is it the trigger for inflammation.” 2nd National Congress of Artificial Organs and Support Systems, Antalya, Turkey
• Azakli, H., Müller, S., Hirose, M., Yu, X., Ludwig, R., Zillikens, D., Ibrahim, S. (2012). “The role of mitochondrial genome in autoimmunity to type VII collagen.” 42^nd Annual ESDR Meeting Venice, Italy.
• Emrence, Z., Abaci, N., Cosan, F., Azakli, H., Cakiris, A., Cakar, A., Erman, B., Gül, A., Ustek, D. (2010) “MEFV gene 3’UTR Region Alu-Repeats may have an effect on the gene expression.” Autoinfallamation 2010 6^th International Congress on FMF and SAID, Amsterdam, Holland.
• Ustek, D., George, J., Cakiris, A., Abaci, N., Sirma, S., Emrence, Z., Azakli, H., Cosan, F., Cakar, A., Parlak, M., Arikan, M. (2010). “Whole genome screening of lentiviral vector integration sites using next generation sequencing technology”. Viral Vectors in Gene Therapy: Applications and Novel Production Methods Advanced Symposium and EMBO Practical Course A.I. Virtanen Institute, Kuopio, Finland.
• Ciftci, S., Cakiris, A., Abaci, N., Keskin, F., Akyüz, F., Dincer, E., Aglar, O., Okten, Z., Azakli, H., Badur, S., Kaymakoglu, S., Ustek, D. (2010). “Ultra-deep whole genome sequencing of naive HBV-infected patients.” 26^th National Gastroentrology Congress, 2010, Ankara.
• Akiva İ, Birgül Iyison N. (2010). Identification of novel Wnt/B-catenin pathway targets. 4th International EACR Conference of European Association for Cancer Research,  Antalya, Turkey.
• Akiva İ, Birgül Iyison N. (2012). Identification of novel Wnt/B-catenin pathway targets. International EMBO (European Molecular Biology Organization) Congress,  Istanbul, Turkey.
• Akiva İ, Birgül Iyison N. (2015). Characterization of novel Wnt/B-catenin pathway targets. 3rd MBD Conference of Molecular Biology Association, Ankara, Turkey.
• Akiva İ, Birgül Iyison N. (2016). Characterization of IFITM3 and MGAT1 as novel transcriptional targets of Wnt/B-catenin pathway. 4th MBD Conference of Molecular Biology Association, Istanbul, Turkey.