Kara B, Ayhan Özgecan, Gökçay G, Başboğa N, Tolun Aslıhan, Adult phenotype and further phenotypic variability in SRD5A3-CDG, BMC Med Genet, 15, 10, online dergi, 2014 Dil Türkçe
Erken E, Köroğlu Ç, Yıldız F, Ozer HT, Gülek B, Tolun A, A novel recessive 15-hydroxyprostaglandin dehydrogenase mutation in a family with primary hypertrophic osteoarthropathy, Modern Rheumatology, 0, 1-9, 2014 Dil Türkçe
Durlu YK, Köroğlu Ç, Tolun A, Novel Recessive Cone-Rod Dystrophy Caused by POC1B Mutation, JAMA Ophthalmology, 0, 1-7, 2014 Dil Türkçe
Potier D, Davie K, Hulselmans G, Naval Sanchez M, Haagen L, Huynh-Thu VA, Duygu Koldere D, Celik A, Geurts P, Christiaens V, Aerts S, Mapping Gene Regulatory Networks in Drosophila Eye Development by Large-Scale Transcriptome Perturbations and Motif Inference, Cell Reports, 9, 1-14, 2014 Dil Türkçe
Özoğuz, A., Uyan, O., Birdal, G., İskender, C., Omur, O., Lahut, S., Agim, Z.S., Kartal, E., Başak, A.N. et al. 'The distinct genetic pattern of ALS in Turkey', Journal of Neurology, Meeting Abstract: OS2207, 261, S47-S47, 2014. Dil Türkçe
Özoğuz, A., Uyan, O., Birdal, G., İskender, C., Omur, O., Lahut, S., Agim, Z.S., Kartal, E., Basak, A.N. et al. 'The distinct genetic pattern of ALS in Turkey', European Journal of Neurology, Meeting Abstract: OS2207, 21, 63-63, 2014. Dil Türkçe
Lahut, S.; Vadasz, D.; Depboylu, C.; Basak, A.N.; et al.,'The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome',Neurogenetics, 15, 3, 1-19, 2014. Dil Türkçe
Lahut, S., Omur, O., Gispert, S., Pirkevi, C., Tireli, H., Herrmann, E., Brehm, N., Başak, A.N., Auburger, G., 'A large Turkish Parkinson pedigree with alpha-synuclein duplication: blood expression biomarker profile for predictive diagnostics', European Journal of Neurology, Meeting Abstract: OS2114, 21, 54-54, 2014. Dil Türkçe
Lahut, S., Omur, O., Gispert, S., Pirkevi, C., Tireli, H., Herrmann, E., Brehm, A.N., Başak, N., Auburger, G., 'A large Turkish Parkinson pedigree with alpha-synuclein duplication: blood expression biomarker profile for predictive diagnostics', Journal of Neurology, Meeting Abstract: OS2114, 261, S41-S41, 2014. Dil Türkçe
Kurt, S., Kartal, E., Aksoy, D., Çevik, B., Eken, A.G., Şahbaz, I., Başak, N., 'Coexistance of autosomal recessive spastic ataxia of charlevoix saguenay and spondyloepiphyseal dysplasia in a Turkish patient', Journal of Neurology, Meeting Abstract:PP4196, 261, S448-S448, 2014. Dil Türkçe
