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Hysom, S.J., Fişek, M.H., “Situational determinants of reward allocation: The equity equality equilibrium model”, Social Science Research, 40, 4, 1263-1285, 2011. Dil Türkçe
Öner, D., Adadan, E., “Use of web based portfolios as tools for reflection in preservice teacher education”, Journal of Teacher Education, 62, 5, 477-492, 2011. Dil Türkçe
Sayar-Türet, M., Dreisigacker, S., Braun, H.J., Hede, A., Maccormack, R., Boyd, L.A., “Genetic variation within and between winter wheat genotypes from Turkey, Kazakhstan and Europe as determined by nucleotide binding site profiling”, Genome, 54, 5, 419-430, 2011. Dil Türkçe
Baets, J., Deconinck, T., Bilir, B., Battaloğlu E., et al., “Genetic spectrum of hereditary neuropathies with onset in the first year of life”, Brain, 134, , 2664-2676, 2011. Dil Türkçe
Wang, H.J., Li, Z.Y., Liu, Y., Persson, J., Beyer, I., Moller, T., Koyuncu, D., Drescher, M.R., Strauss, R., Zhang, X.B., Wahl, J.K., Urban, N., Drescher, C., Hemminki, A., Fender, P., Lieber, A., “Desmoglein 2 is a receptor for adenovirus serotypes 3, 7, 11 and 14”, Nature Medicine, 17, 1, 96-U273, 2011. Dil Türkçe
Galy, A., Schenck, A., Sahin, H.B., Qurashi, A., Sahel, J.A., Diebold, C., Giangrande, A., “Cyfip dependent actin remodeling controls specific aspects of drosophila eye morphogenesis”, Developmental Biology, 359, 1, 37-46, 2011. Dil Türkçe
Yalçın, Ö., Baykan, B., Agan, K., Yapıcı, Z., Yalçın, D., Dizdarer, G., Türkdoğan, D., Özkara, C., Ünalp, A., Uluduz, D., Gül, G., Kuşcu, D., Ayta, S., Tutkavul, K., Comu, S., Tatlı, B., Meral, C., Bebek, N., Cağlayan, S.H., “An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic clonic seizures”, Epilepsia, 52, 5, 975-983, 2011. Dil Türkçe
Enünlü, I., Ozansoy, M., Başak, A.N., “Alfaclass prefoldin protein UXT is a novel interacting partner of amyotrophic lateral sclerosis 2 (ALS2) Protein”, Biochemical and Biophysical Research Communications, 413, 3, 471-475, 2011. Dil Türkçe
Yıldırım, Y., Orhan, E.K., İşeri, S.A.U., Serdaroglu-Oflazer, P., Kara, B., Solakoğlu, S., Tolun, A., “A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures”, Human Molecular Genetics, 20, 10, 1886-1892, 2011. Dil Türkçe
