Journal Publications

Publications

Lahut S, Gispert S, Ömür Ö, Depboylu C, Seidel K, Domínguez-Bautista JA, Brehm N, Tireli H, Hackmann K, Pirkevi C, Leube B, Ries V, Reim K, Brose N, den Dunnen W, Johnson M, Wolf Z, Schindewolf M, Schrempf W, Reetz K, Young P, Vadasz D, Frangakis AS, Schröck E, Steinmetz H, Jendrach M, Rüb U, Başak AN, Oertel W, Auburger G. (2015) Blood RNA Biomarkers In Prodromal Park4 And Rbd Show Role of Complexin-1 Loss For Risk Of Parkinson’s Disease. Submitted to Journal of Neuroscience. Supplementary material

Özoğuz, A., Uyan, Ö., Birdal, G., Iskender, C., Kartal, E., Lahut, S., Ömür, Ö., Agim, ZS., Gundogdu, A., Sen, N.E., Kavak, P., Saygi, C., Sapp, PC., Keagle, P., Parman, Y., Tan, E., Koç, F., Deymeer, F., Oflazer, P., Hanağası, H., Gürvit, H., Bilgiç, B., Durmuş, H., Ertaş, M., Kotan, D., Akalın, M.A., Güllüoğlu, H., Zarifoğlu, M., Aysal, F., Döşoğlu, N., Bilguvar, K., Günel, M., Keskin, Ö., Akgün, T., Özçelik, H., Landers, J.E., Brown, R.H., and Başak, A.N. (2015). The distinct genetic pattern of ALS in Turkey and novel mutations. Accepted in Neurobiology of Aging

Lahut, S., Vadasz, D., Depboylu, C., Ries, V., Krenzer, M., Stiasny-Kolster, K., Basak, A.N., Oertel, W. H., & Auburger, G. (2014). The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome. Neurogenetics, 15(3), 189–92. doi:10.1007/s10048-014-0407-z

Auburger, G., Gispert, S., Lahut, S., Omür, O., Damrath, E., Heck, M., & Başak, N. (2014). 12q24 locus association with type 1 diabetes: SH2B3 or ATXN2? World Journal of Diabetes, 5(3), 316–27. doi:10.4239/wjd.v5.i3.316

Gündüz, A., Eken, A. G., Bilgiç, B., Hanagasi, H. A., Bilgüvar, K., Günel, M., Basak, A.N., & Ertan, S. (2014). FBXO7-R498X mutation: Phenotypic variability from chorea to early onset parkinsonism within a family. Parkinsonism & Related Disorders, 20(11), 1253–6. doi:10.1016/j.parkreldis.2014.07.016

Uyan, Ö., Ömür, Ö., Ağım, Z. S., Özoğuz, A., Li, H., Parman, Y., Deymeer, F., Oflazer, P., Koc, F., Tan, E., Ozcelik, H., & Başak, A. N. (2013). Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor. PloS One, 8(8), e72381. doi:10.1371/journal.pone.0072381

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