Durmuş, H., Özoğuz, A., Deymeer, F., Serdaroğlu, P., Aysal, F., Ertaş, M., Günel, M., Başak, N., Parman, Y., “Clinical and Genetic Characteristics of Five Turkish Families with UBQLN2 Mutations”, Neurology, 80, Meeting Abstract: P05078, 2013. Dil Türkçe
Yalçınkaya, M., Yüksel, Ş., “Investigation of LL-37 mediated transfection”, Turkish Journal of Biology, 37, 4, 426-432, 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
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
Köroğlu, Ç., Baysal, L., Çetinkaya, M., Karasoy, H., Tolun, A., “DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability”, Parkinsonism & Related Disorders, 19, 3, 320-324, 2013. Dil Türkçe
Güven, A., Tolun, A., “TBC1D24 truncating mutation resulting in severe neurodegeneration”, Journal of Medical Genetics, 50, 3, 199-202, 2013. Dil Türkçe
Gökçe, M., Gümrük, F., Haliloğlu, G., Serdaroğlu, E., Çağlayan, H., “Double trouble: Duchenne muscular dystrophy and hemophilia”, Pediatric Blood & Cancer, 60, 3, 525-525, 2013. Dil Türkçe
Fuss, S.H., Zhu, Y., Mombaerts, P., “Odorant receptor gene choice and axonal wiring in mice with deletion mutations in the odorant receptor gene SR1”, Molecular and Cellular Neuroscience”, 56, 212-224, 2013. Dil Türkçe
Berber, E., Pehlevan, F., Akın, M., Çapan, Ö.Y., Kavaklı, K., Çağlayan, S.H., “A Common VWF Exon 28 Haplotype in the Turkish Population”, Clinical and Applied Thrombosis-Hemostasis, 19, 5, 550-556, 2013. Dil Türkçe