Journal Publications

Publications

Cemile Kocoglu,  Asli Gundogdu, Gulsen Kocaman, Pinar Kahraman-Koytak, Kayihan Uluc, Gunes Kiziltan, Ahmet Okay Caglayan, Kaya Bilguvar, Atay Vural, A. Nazli Basak; 
Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in two families; Neurology: Genetics 2018 Feb; 4(1): e218. Doi: 10.1212/NXG.0000000000000218

Hamid Hamzeiy, Doruk Savaş, Ceren Tunca, Nesli Ece Şen, Aslı Gündoğdu Eken, Irmak Şahbaz, Daniela Calini, Nicola Ticozi, Antonia Ratti, Vincenzo Silani, A. Nazlı Başak; Elevated Global DNA Methylation is not exclusive to Amyotrophic Lateral Sclerosis and is also observed in Spinocerebellar Ataxia Types 1 and 2; Karger Neurodegenerative DiseasesNeurodegener Dis. 2018;18(1):38-48. Doi: 10.1159/000486201. Epub 2018 Feb 9.

Ceren Tunca, Cemre Coşkun, Fulya Akçimen, Cemile Koçoğlu, Aslı Gündoğdu Eken, Betül Çevik, Ersin Tan, A. Nazlı Başak; ERLIN1 Mutations Cause Teenage-onset Slow Progressive ALS in a Large Turkish Pedigree; European Journal of Neurology 2018 Feb 16. Doi: 10.1038/s41431-018-0107-5

Auburger G, Sen NE, Meierhofer D, Başak AN, Gitler AD.; Efficient Prevention of Neurodegenerative Diseases by Depletion of Starvation Response Factor Ataxin-2; Trends Neurosci. 2017 Aug; 40 (8):507-516.doi: 10.1016/j.tins.2017.06.004.

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.; Blood RNA Biomarkers In Prodromal Park4 And Rbd Show Role of Complexin-1 Loss For Risk Of Parkinson’s Disease; Dis. Model Mech, 2017, 10(5):619-631

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; The distinct genetic pattern of ALS in Turkey and novel mutations. Neurobiology of Aging, 2015, 36 (4):1764.e9–1764.e18

Lahut, S., Vadasz, D., Depboylu, C., Ries, V., Krenzer, M., Stiasny-Kolster, K., Basak, A.N., Oertel, W. H., & Auburger, G; The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome. Neurogenetics, 2014, 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; 12q24 locus association with type 1 diabetes: SH2B3 or ATXN2? World Journal of Diabetes, 2014, 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 FBXO7-R498X mutation: Phenotypic variability from chorea to early onset parkinsonism within a family. Parkinsonism & Related Disorders, 2014, 20(11), 1253–6. doi:10.1016/j.parkreldis.2014.07.016

For a complete publication list please visit