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
Leon-Mediavilla, J., Senovilla, M., Montiel, J., Gil-Diez, P., Saez, A., Kryvoruchko, I.S., Reguera, M., Udvardi, M.K., Imperial, J., Gonzalez-Guerrero, M., “Mtmtp2-Facilitated ZInc Transport Into Intracellular Compartments İs Essential for Nodule Development in Medicago Truncatula“, Frontıers in Plant Science, 9, 2018. Dil Türkçe
Kryvoruchko, I.S., Routray, P., SInharoy, S., Torres-Jerez, I., Tejada-Jimenez, M., FInney, L.A., Nakashima, J., Pislariu, C.I., BenediTo, V.A., Gonzalez-Guerrero, M., Roberts, D.M., Udvardi, M.K., “An Iron-Activated Citrate Transporter, Mtmate67, Is Required for Symbiotic Nitrogen Fixation“, Plant Physıology, 176, 3, 2315-2329, 2018. Dil Türkçe
Koçoğlu, C., Gündoğdu, A., Kocaman, G., Kahraman-Koytak, P., Uluc, K., Kızıltan, G., Çağlayan, A.O., Bilguv, K., Vural, A., Başak, A.N., “Homozygous Capn1 Mutations Causing A Spastic-ataxia Phenotype in 2 Families“, Neurology-Genetıcs, 4, 1, 2018. Dil Türkçe
KazemInasab, S., Taşkıran, İ.İ., Fattahi, Z., Bazazzadegan, N., HosseIni, M., Rahimi, M., Oladnabi, M., Haddadi, M., Çelik, A., Ropers, H.H., Najmabadi, H., Kahrizi, K., “Cnksr1 Gene Defect Can Cause Syndromic AuTosomal Recessive Intellectual Disability“, American Journal of Medical Genetıcs Part B-Neuropsychiatric Genetics, 177, 8, 691-699, 2018. Dil Türkçe
Karacan, İ., Uğurlu, S., ŞahIn, S., Everest, E., Kasapcopur, Ö., Tolun, A., Özdoğan, H., Turanlı, E.T., “Lacc1 Gene Defects in Familial form of Juvenile Arthritis“, Journal of Rheumatology, 45, 5, 726-728, 2018. Dil Türkçe
Karacan, I., Uğurlu, S., Tolun, A., Tahir Turanlı, E., Özdoğan, H., “Other AuToInflammatory Disease Genes in an FMF-prevalent Population: A Homozygous MVK Mutation and a Novel Heterozygous TNFRSF1A Mutation in Two Different Turkish Families with ClInical FMF“, Clinical and Experimental Rheumatology, 108, 6, S75-S81, 2018. Dil Türkçe