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Fuss, S.H., Bayramlı, X., Çoban, B., Çapar, S., Balı, B., "Birth and Migration of Sensory Neurons in the Adult Zebrafish Olfactory System", Chemical Senses, 40, 3, 229, 2015. Dil Türkçe
Erten, N., Battaloğlu, E., Erdoğan, A., Seren, E., "A Family with Vocal Cord Paralysis Associated with GDAP1 Mutation in Giresun, Turkey", Turkish Journal of Neurology, 21, 3, 124-126, 2015. Dil Türkçe
Erken, E., Köroğlu, C., Yıldız, F., Özer, H.T.E., Gülek, B., Tolun, A., "A Novel Recessive 15-Hydroxyprostaglandin Dehydrogenase Mutation in A Family With Primary Hypertrophic Osteoarthropathy", Modern Rheumatology, 25, 2, 315-321, 2015. Dil Türkçe
Dede, H.O., Gelişin, O., Baykan, B., Çağlayan, H., Topaloğlu, P., Gürses, C., Bebek, N., Gökyiğit, A., "Definite Sudep in Dravet Syndrome: An Adult Case Report", Journal ff Neurological Sciences-Turkish, 32, 3, 610-616, 2015. Dil Türkçe
Corell, M., Wicher, G., Radomska, K.J., Dağlıkoca, E.D., Godskesen, R.E., Fredriksson, R., Benedikz, E., Magnaghi, V., Svenningsen, A.F., "GABA and Its B-Receptor Are Present at the Node of Ranvier in a Small Population of Sensory Fibers, Implicating a Role in Myelination", Journal of Neuroscience Research, 93, 2, 285-295, 2015. Dil Türkçe
Bayrak, A.O., Bayrak, I.K., Battaloüglu, E., Özes, B., Yıldız, O., Onar, M.K., "Ultrasonographic Findings in Hereditary Neuropathy With Liability to Pressure Palsies", Neurological Research, 37, 2, 106-111, 2015. Dil Türkçe
Batini, C.,Hallast, P., Zadik, D., Delser, P.M., Benazzo, A., Ghirotto, S., Arroyo-Pardo, E., Cavalleri, G.L., de Knijff, P., Dupuy, B.M., Eriksen, H.A., King, T.E., de Munain, A.L., Lopez-Parra, A.M., Loutradis, A., Milasin, J., Novelletto, A., Pamjav, H., Sajantila, A., Tolun, A., Winney, B., Jobling, M.A., "Large-Scale Recent Expansion of European Patrilineages Shown by Population Resequencing", Nature Communications, 6, 7152, 2015. Dil Türkçe
Atkinson, D., Kancheva, D., Zimon, M., De Rijk, P., Chamova, T., Mitev, V., Fabrizi, G.M., Topaloğlu, H., Tourney, I., Parman, Y., Battaloğlu, E., Estrada-Cuzcano, A., Jordanova, A., " Novel Mutatıons in Genes Causıng Charcot-Marıe-Tooth Neuropathy and Heredıtary Spastıc Paraplegıa Identıfıed by Homwes", Journal of the Peripheral Nervous System, 20, 2, 98, 2015. Dil Türkçe
Mümtaz, S., Yıldız, E., Jabeen, S., Khan, A., Tolun, A., Malik, S., "RBBP8 Syndrome with Microcephaly, Intellectual Disability, Short Stature and Brachydactyly", American Journal of Medical Genetics Part A, 167, 12, 3148-3152, 2015. Dil Türkçe
