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Tunca, C., Işık, S., Dönmez, M.Y., Ersoy, C., 'Distributed Mobile Sink Routing for Wireless Sensor Networks: A Survey', IEEE Communications Surveys and Tutorials, 16, 2, 877-897, 2014. Dil Türkçe
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Demirkol-Ertürk, Ş., Paker, S.,'Beyoglu/Pera as a translating site in Istanbul', Translation Studies, 7, 1870-185, 2014. Dil Türkçe
Weckhuysen, S., Suls, A., Djemie, T., Sterbova, K., Hoffman-Zacharska, D., Talvik, T., Çağlayan, H. et al. 'Trio Exome Sequencing in 31 Patients with SCN1A Negative Dravet Syndrome Leads to the Detection of Another Recessive SCN1B Mutation and the Discovery of at Least Two Novel Epilepsy Genes', Epilepsia, 55, 2, 81-81 Meeting Abstract: p239, 2014. Dil Türkçe
Suls, A., Jaehn, J.J., Kecskes, A., Weber, Y., Weckhuysen, S., Craiu, D.C., Siekierska, A., Djemie, T., Afrikanova, T., Gormley, P., von Spiczak, S., Kluger, G., Iliescu, C.M., Talvik, T., Talvik, I., Meral, C., Çağlayan, S.H. et al. 'De Novo Loss-of-Function Mutations in CHD2 Cause A Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features With Dravet Syndrome', Epilepsia, 55, 2, 79-80, Meeting Abstract: p239, 2014. Dil Türkçe
Altındağ, E., Gündoğdu, A., Usluer, S., Çağlayan, H., Baykara, B., 'Down syndrome and late onset myoclonic epilepsy in Down syndrome: investigation of EPM1 gene mutations in two cases', Journal of Neurology, Meeting Abstract: PP2050, 261, S328-S328, 2014. Dil Türkçe
Altındağ, E., Gündoğdu, A., Usluer, S., Çağlayan, H., Baykan, B., 'Down syndrome and late onset myoclonic epilepsy in Down syndrome: investigation of EPM1 gene mutations in two casesP.M., Başak, A.N., 'C9orf72 hexanucleotide repeat expansion in Turkish ALS patients', European Journal of Neurology, Meeting Abstract: PP2050, 21, 496-496, 2014. Dil Türkçe
Fidancı İD, Zülfikar B, Kavaklı K, Ar MC, Kılınç Y, Başlar Z, Çağlayan SH, A Polymorphism in the IL-5 Gene is Associated with Inhibitor Development in Severe Hemophilia A Patients, Turkish Journal of Hematology, 31, 17-24, 2014 Dil Türkçe