A. Nazli Basak, PhD
Affiliations: | 1987- | Molecular Biology and Genetics | Bogazici University, Istanbul, Turkey |
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"A. Basak"Cross-listing: Neurotree
Parents
Sign in to add mentor| Friedrich Cramer | grad student | 1977 | Max-Planck-Institut für experimentelle Medizin (Chemistry Tree) |
Children
Sign in to add trainee| Hilmi Özcelik | grad student | 1991 | Bogazici University (Chemistry Tree) |
| Ayse Ozer | grad student | 1992 | Bogazici University (Chemistry Tree) |
| Sukru Tuzmen | grad student | 1995 | Bogazici University (Chemistry Tree) |
| Hamdi Jarjanazi | grad student | 1999 | Bogazici University (Chemistry Tree) |
| Ghazi Omar Tadmouri | grad student | 1999 | Bogazici University (Chemistry Tree) |
| Onur Bilenoglu | grad student | 2002 | Bogazici University (Chemistry Tree) |
| Nagehan Ersoy | grad student | 2005 | Bogazici University (Chemistry Tree) |
| Mehmet Baki Yokes | grad student | 2005 | Bogazici University (Chemistry Tree) |
| Mehmet Ozansoy | grad student | 2006 | Bogazici University (Chemistry Tree) |
| Caroline Pirkevi | grad student | 2009 | Bogazici University (Chemistry Tree) |
| Aslihan Ozoguz | grad student | 2010 | Bogazici University (Chemistry Tree) |
| Zeynep Sena Agim | grad student | 2009-2012 | Bogazici University (Neurotree) |
| Suna Lahut | grad student | 2015 | Bogazici University (Chemistry Tree) |
| Kadir Ozkan | grad student | 2016 | (Neurotree) |
| Ceren Iskender | grad student | 2017 | Bogazici University (Chemistry Tree) |
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Publications
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| Bayraktar E, Çiftçi V, Uysal H, et al. (2023) Another mutation in the gene: the first Turkish patient with -His47Arg, a case report. Frontiers in Genetics. 14: 1208673 |
| Öztop-Çakmak Ö, Şimşir G, Tekgül Ş, et al. (2022) VPS13D-based disease: Expansion of the clinical phenotype in two brothers and mutation diversity in the Turkish population. Revue Neurologique. 178: 907-913 |
| Güler S, Gül T, Güler Ş, et al. (2021) Early-Onset Parkinson's Disease: A Novel Deletion Comprising the DJ-1 and TNFRSF9 Genes. Movement Disorders : Official Journal of the Movement Disorder Society |
| Johnson JO, Chia R, Miller DE, et al. (2021) Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis. Jama Neurology |
| Vural A, Şimşir G, Tekgül Ş, et al. (2021) The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice. Movement Disorders : Official Journal of the Movement Disorder Society |
| Diker S, Gelener P, Teralı K, et al. (2021) A combined clinical and computational approach to understand the SOD1-mediated pathogenesis of rapidly progressive familial amyotrophic lateral sclerosis. Acta Neurologica Belgica |
| Emekli AS, Samanci B, Şimşir G, et al. (2020) A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology |
| Yetim E, Gul T, Basak AN, et al. (2020) An Unusual Familial Dementia Associated with G131V PRNP Mutation. European Journal of Neurology |
| Tunca C, Şeker T, Akçimen F, et al. (2020) Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database. Human Mutation |
| Reichenstein I, Eitan C, Diaz-Garcia S, et al. (2019) Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology. Science Translational Medicine. 11 |