Erdik M, Uckan E,, Earthquake Damage and Fragilities of Industrial Facilities, Seismic Design on Industrial Facilities, -, 3-13, 2014 Dil Türkçe
Wenzel F, Erdik M, Köhler N, Zschau J, Milkereit C, Picozzi M, Fischer J, Redlich JP, Kühnlenz F, Lichtblau B, Eveslage I, Christ I, Lessing R, Kiehle C, , EDIM: Earthquake Disaster Information System for the Marmara Region, Turkey, Early Warning for Geological Disasters: Scientific Methods and Current Practice, -, 103-116, 2014 Dil Türkçe
Cinar, Kenan; Ozturk, Umud Esat; Ersoy, Nuri; Wisnom, Michael R., 'Modelling manufacturing deformations in corner sections made of composite materials',Journal Of Composite Materials Volume: 48 Issue: 7 Dil Türkçe
Türköz, E., Çelik, M., '2-D Electromagnetic and Fluid Models for Inductively Coupled Plasma for RF Ion Thruster Performance Evaluation', IEEE Transactions on Plasma Science, 418, 235-240, 2014. Dil Türkçe
Korkmaz, O., Çelik, M., 'Global Numerical Model for the Assessment of the Effect of Geometry and Operation Conditions on Insert and Orifice Region Plasmas of a Thermionic Hollow Cathode Electron Source', Contributions to Plasma Physics, 54, 10, 838-850, 2014. Dil Türkçe
Sönmez, Ç., Durmaz Incel, Ö., Işık, S., Dönmez, M.Y., Ersoy, C., 'Fuzzy-based congestion control for wireless multimedia sensor networks', EURASIP Journal on Wireless Communications and Networking, 63, Article Number: 63, 2014. Dil Türkçe
Selamet, S., Garlock, M.E., 'Fire Resistance of Steel Shear Connections', Fire Safety Journal, 68, 52-60, 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
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
