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
Yıldırım, Y., Tolun, A., Tüysüz, B., “The phenotype caused by pycr1 mutations corresponds to geroderma osteodysplasticum rather than autosomal recessive cutis laxa type 2”, American Journal of Medical Genetics Part A, 155A, 1, 134-140, 2011. Dil Türkçe
Sin, B.A., Akdiş, M., Zumkehr, J., Bezzine, S., Bekpen, C., Lambeau, G., Akdiş, C.A., “T-cell and antibody responses to phospholipase A(2) from different species show distinct cross reactivity patterns”, Allergy, 66, 12, 1513-1521, 2011. Dil Türkçe
Giardine, B., Borg, Başak, A.N., et al., “Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach”, Nature Genetics, 43, 4, 295-302, 2011. Dil Türkçe
Deymeer, F., Matur, Z., Poyraz, M., Battaloğlu, E., Oflazer-Serdaroğlu, P., Parman, Y., “Nerve conduction studies in Charcot Marie tooth disease in a cohort from Turkey”, Muscle & Nerve, 43, 5, 657-664, 2011. Dil Türkçe
