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
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
Jacobs, J., Atkins, M., Davie, K., Taşkıran, İ.İ., et al., “The Transcription FacTor GraIny Head Primes Epithelial Enhancers for Spatiotemporal Activation by Displacing Nucleosomes“, Nature Genetıcs, 50, 7, 1011, 2018. Dil Türkçe
Heyne, H.O., Singh, T., Stamberger, H., Çağlayan, H., et al., “De Novo Variants in Neurodevelopmental Disorders with Epilepsy“, Nature Genetıcs, 50, 7, 1048, 2018. Dil Türkçe
Hamzeiy, H., Savaş, D., Tunca, C., Şen, N.E., Gündoğdu-Eken, A., Sahbaz, I., CalIni, D., Tiloca, C., Ticozzi, N., Ratti, A., Silani, V., Başak, A.N., “Elevated Global Dna Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in SpInocerebellar ataxia Types 1 and 2“, Neurodegeneratıve Diseases, 18, 1, 38-48, 2018. Dil Türkçe
Fattahi, Z., Sheikh, T.I., Musante, L., Rasheed, M., Taşkıran, İ.İ., et al., “Biallelic Missense Variants in Zbtb11 Can Cause Intellectual Disability in Humans“, Human Molecular Genetıcs, 27, 18, 3177-3188, 2018. Dil Türkçe
Corrado, L., Tiloca, C., Locci, C., Başak, A.N., et al., “Characterization of The C9orf72 Gc-Rich Low Complexity Sequence in Two Cohorts of Italian and Turkish Als Cases“, Amyotrophic Lateral Sclerosis and FronTotemporal Degeneration, 19, 5-6, 426-431, 2018. Dil Türkçe
Bölükbaşı, E.Y., Mumtaz, S., Afzal, M., Woehlbier, U., Malik, S., Tolun, A., “Homozygous Mutation in Cep19, A Gene Mutated in Morbid Obesity, in Bardet-Biedl Syndrome with PredomInant Postaxial Polydactyly“, Journal of Medical Genetıcs, 55, 3, 189-197, 2018. Dil Türkçe