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İşler, C., Tanrıverdi, T., Kavak, E., Sanus, G.Z., Ulu, M.O., Erkanlı, G., Koman, A., İyison, N.B., Uzan, M., “Prenatal Expressions of Hyperpolarization Activated Cyclic Nucleotide Gated Channel (HCN) Genes in Dysplastic Hippocampi in Rats”, Turkish Neurosurgery, 18, 4, 327-335, 2008. Dil Türkçe
Maljevic, S., Naros, G., Yalçın, O., Çağlayan, H., Steinlein, O., Lerche, H., “A trafficing defective kv7.2 mutation causing neonatal seizures”, Epilepsia, 50, 81-82, 2009. Dil Türkçe
Barış, I., Battaloğlu, E., “A multiplexed arms PCR approach for the detection of common MECP2 mutations”, Genetic Testing and Molecular Biomarkers, 13, 1, 19-22, 2009. Dil Türkçe
Pirkevi, C., Lesage, S., Condroyer, C., Tomiyama, H., Hattori, N., Ertan, S., Brice, A., Başak, A.N., “A lrrk2 g2019s mutation carrier from Turkey shares the Japanese haplotype”, Neurogenetics, 10, 3, 271-273, 2009. Dil Türkçe
Poyraz, M., Matur, Z., Battaloğlu, E., Oflazer, P., Parman, Y., Deymeer, F., “Nerve Conduction Studies in Demyelinating CMT”, Journal of Neurology, 255, 62-63, 2008. Dil Türkçe
Altıok, E., Taylan, F., Yenen, O.S., Demirkeser, G., Bozacı, M., Önel, D., Akçadağ, B., İyisan, A.S., Çıblak, M., Bozkaya, E., Yüksel, Ş., Badur, S., “Mutations in Influenza A Virus (H5N1) and Possible Limited Spread, Turkey, 2006”, Emerging Infectious Diseases, 14, 3, 491-492, 2008. Dil Türkçe
Uğur, S.A., Tolun, A., “Homozygous WNT10B Mutation and Complex Inheritance in Split Hand/Foot Malformation”, Human Molecular Genetics, 17, 17, 2644-2653, 2008. Dil Türkçe
Bingöl, C.A., Güçlü, B., Aktekin, B., Ağan, K., Akbaş, B.G., Karadeli, H.H., Karlıkaya, G., Çitçi, B., Türe, U., Bingöl, H., Yalçın, O., Salar, S., Çağlayan, H., “Febrile Seizure Plus Epilepsy: A Large Multi Generational Consanguineous Family, a Preliminary Study”, Epilepsia, 49, 310-310, 2008. Dil Türkçe
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