Acun, T., Terzioğlu-Kara, E., Konu, O., Öztürk, M., Yakıcıer, M.C., “Mdm2 Snp309 G allele displays high frequency and inverse correlation with somatic p53 mutations in hepatocellular carcinoma”, Mutation Research Fundamental and Molecular Mechanisms of Mutagenesis, 684, 1-2, 106-108, 2010. Dil Türkçe
Bekpen, C., Xavier, R.J., Eichler, E.E., “Human IRGM gene "to be or not to be"”, Seminars in Immunopathology, 32, 4, 437-444, 2010. Dil Türkçe
Behunova, J., Zavadilikova, E., Bozoğlu, T.M., Gündüz, A., Tolun, A., Yalçınkaya, C., “Familial microhydranencephaly, a family that does not map to 16p13.13-p12.2: Relationship with hereditary fetal brain degeneration and fetal brain disruption sequence”, Clinical Dysmorphology, 19, 3, 107-118, 2010. Dil Türkçe
Duru, N., İşeri, S.A.U., Selçuk, N., Tolun, A., “Early onset progressive myoclonic epilepsy with dystonia mapping to 16pter-p13.3”, Journal of Neurogenetics, 24, 4, 207-215, 2010. Dil Türkçe
Sedjai, F., Acquaviva, C., Chevrier, V., Chauvin, J.P., Coppin, E., Aouane, A., Coulier, F., Tolun, A., Pierres, M., Birnbaum, D., Rosnet, O., “Control of ciliogenesis by for20, a novel centrosome and pericentriolar satellite protein”, Journal of Cell Science, 123, 14, 2391-2401, 2010. Dil Türkçe
Kurt, S., Karaer, H., Kaplan, Y., Akat, I., Battaloğlu, E., Eruslu, D., Başak, A.N., “Combination of myotonic dystrophy and hereditary motor and sensory neuropathy”, Journal of the Neurological Sciences, 288, 1-2, 197-199, 2010. Dil Türkçe
Berber, E., Rimoldi, V., Usluer, S., Aksu, S., Pekçelen, Y., Çağlayan, S.H., Duga, S., “Characterization of the genetic basis of FXI deficiency in two Turkish patients”, Haemophilia, 16, 3, 564-566, 2010. Dil Türkçe
Kavak, E., Najafov, A., Öztürk, N., Şeker, T., Çavuşoğlu, K., Aslan, T., Duru, A.D., Saygılı, T., Hoxhaj, G., Hiz, M.C., Ünal, D.O., Birgül-İyison, N., Öztürk, M., Koman, A., “Analysis of the wnt/b catenin/tcf4 pathway using sage, genome wide microarray and promoter analysis: identification of bri3 and hsf2 as novel targets”, Cellular Signalling, 22, 10, 1523-1535, 2010. Dil Türkçe
İşeri, S.A.U., Durlu, Y.K., Tolun, A., “A novel recessive gucy2d mutation causing cone rod dystrophy and not leber's congenital amaurosis”, European Journal of Human Genetics, 18, 10, 1121-1126, 2010. Dil Türkçe
Yiş, U., Dirik, E., Kurul, S.H., Eken, A.G., Başak, A.N., “Two young sisters with spinocerebellar ataxia type 2 showing different clinical progression of disease”, Cerebellum, 8, 2, 127-129, 2009. Dil Türkçe
