Suls, A., Jaehn, J.A., Kecskes, A., Çağlayan, S.A. et al, “De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome”, American Journal of Human Genetics, 93, 5, 967-975, 2013. Dil Türkçe
Scholey, J.M., “Cilium Assembly: Delivery of Tubulin by Kinesin-2-Powered Trains”, Current Biology, 23, 21, R956-R959, 2013. Dil Türkçe
Praetorius, C., Grill, C., Stacey, S.N., Emre, N.C.T. et al., “A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway”, Cell, 155, 1022-1033, 2013. Dil Türkçe
Ozansoy, M., Başak, A.N., “The central theme of Parkinson’s disease: -synuclein”, Molecular Neurobiology , 47, 2, 460-465, 2013. Dil Türkçe
Onat, O.E., Gülsüner, S., Bilguvar, K., Başak, A.N., Topaloğlu, H., Tan, M., Tan, Ü., Günel, M., Özçelik, T., “Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion”, European Journal of Human Genetics 21, 3, 281-285, 2013. Dil Türkçe
Mishra, A.K., Tsachaki, M., Rister, J., Ng, J., Celik, A., Sprecher, S.G., “Binary cell fate decisions and fate transformation in the Drosophila larval eye”, PLoS Genetics, 9, 12, Article Number: e10040, 2013. Dil Türkçe
Li, X., Erclik, T., Bertet, C., Chen, Z., Voutev, R., Venkatesh, S., Morante, J., Celik, A., Desplan, C., “Temporal patterning of Drosophila medulla neuroblasts controls neural fates.”, Nature, 498, 7455, 456-462, 2013 Dil Türkçe
Lamy, L., Ngo, V. N., Emre, N. C.T., Shaffer, A. L. III, Yang, Y., Tian, E., Nair, V., Kruhlak, M. J., Zingone, A., Landgren, O., Staudt, L. M., “Control of autophagic cell death by caspase-10 in multiple myeloma.”, Cancer Cell, 23, 4, 435-449, 2013. Dil Türkçe
Küser-Abalı, G., Özcan, F., Uğurlu, A., Uysal, A., Fuss, S.H., Buğra-Bilge, K., “SIK2 is involved in the negative modulation of insulin-dependent müller cell survival and implicated in hyperglycemia-induced cell death”, Investigative Ophthalmology & Visual Science, 54, 5, 3526-3537, 2013. Dil Türkçe
Köroğlu, Ç., Seven, M., Tolun, A., “Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism”, Journal of Medical Genetics, 50, 8, 515-520, 2013 Dil Türkçe