Turanlı, E.T., Karacan, I., Esatlıoğlu, S. N., ŞahIn, S., Kasapcopur, O., Tolun, A., Seyahi, E., “Whole Genome Linkage and Exome Sequencing Analyses in Takayasu Arteritis Familirs”, Annals of the Rheumatic Diseases, 77, 231-232, 2018. Dil Türkçe
Turan, M., Kuran, M.Ş., Yılmaz, H.B., Chae, C.B., Tuğcu, T., “MOL-Eye: A New Metric for the Performance Evaluation of a Molecular Signal“, IEEE Wireless Communications and Networking Conference, 2018. Dil Türkçe
Solmaz, B., Özyurt, M.G., Ata, D.B., Akçimen, F., Shabsog, M., Türker, K.S., Alçık, H., AlgIn, O., Başak, A.N., Özgür, M., Çavdar, S., “Assessment of the CorticospInal Fiber Integrity in Mirror Movement Disorder“, Journal of ClInical Neuroscience, 54, 69-76, 2018. Dil Türkçe
Shabbir, R.M.K., Nalbant, G., Ahmad, N., Malik, S., Tolun, A., “Homozygous CHST11 Mutation in Chondrodysplasia, Brachydactyly, Overriding Digits, ClIno-symphalangism and Synpolydactyly“, Journal of Medical Genetics, 55, 7, 489-496, 2018. Dil Türkçe
Parman, Y., Durmuş, H., Candayan, A., Akçay, H.İ., Yunisova, G., Ulukan, Ç., Serdaroğlu, P., Deymeer, F., Battaloğlu, E., “ClInical and Genetic Features in X-Linked Charcot-Marie-Tooth Neuropathy (Cmt-X) Patients from Turkey“, Neurology, 90, 2018. Dil Türkçe
Niron, H., Türet, M., “Functional Role of Pvchomt in Salt Stress Tolerance“, Journal of Biotechnology, 280, S82-S83, 2018. Dil Türkçe
Nicolas, A., Kenna, K.P., RenTon, A.E., Başak, A.N., “Genome-Wide Analyses Identify Kıf5A as a Novel Als Gene“, Neuron, 97, 6, 1268, 2018. Dil Türkçe
Naseem, M., Bencurova, E., Dandekar, T., “The CyTokInIn-Activating Log-Family ProteIns Are Not LysIne Decarboxylases“, Trends in Biochemical Sciences, 43, 4, 232-236, 2018. Dil Türkçe
Mitropoulos, K., Papadima, E.M., Xeromerisiou, G., Balasopoulou, A., Başak, A.N., et al., “Genomic Variants in The Fto Gene Are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients“, Publıc Health Genomıcs, 21, 17-17, 2018. Dil Türkçe
May, P., Girard, S., Harrer, M., Çağlayan, H., “Rare Coding Variants in Genes Encoding Gaba(A) RecepTors in Genetic Generalised Epilepsies: An Exome-Based Case-Control Study“, Lancet Neurology, 17, 8, 699-708, 2018. Dil Türkçe