| Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ... Nature genetics 48 (9), 1043-1048, 2016 | 616 | 2016 |
| The distinct genetic pattern of ALS in Turkey and novel mutations A Özoğuz, Ö Uyan, G Birdal, C Iskender, E Kartal, S Lahut, Ö Ömür, ... Neurobiology of aging 36 (4), 1764. e9-1764. e18, 2015 | 110 | 2015 |
| The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public RAA van der Spek, W van Rheenen, SL Pulit, KP Kenna, ... Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 20 (5-6), 432-440, 2019 | 73 | 2019 |
| Elevated global DNA methylation is not exclusive to amyotrophic lateral sclerosis and is also observed in spinocerebellar ataxia types 1 and 2 H Hamzeiy, D Savaş, C Tunca, NE Şen, A Gündoğdu Eken, I Şahbaz, ... Neurodegenerative Diseases 18 (1), 38-48, 2018 | 37 | 2018 |
| ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree C Tunca, F Akçimen, C Coşkun, A Gündoğdu-Eken, C Kocoglu, B Çevik, ... European Journal of Human Genetics 26 (5), 745-748, 2018 | 30 | 2018 |
| CHCHD10 variants in amyotrophic lateral sclerosis: Where is the evidence? Project MinE ALS Sequencing Consortium, GHP Tazelaar, ... Annals of neurology 84 (1), 110-116, 2018 | 28 | 2018 |
| PARALS Registry; SLALOM Group; SLAP Registry; FALS Sequencing Consortium; SLAGEN Consortium; NNIPPS Study Group. Genome-wide association analyses identify new risk variants and … W van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ... Nat Genet 48 (9), 1043-1048, 2016 | 27 | 2016 |
| A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification Y Forouhideh, K Müller, W Ruf, M Assi, T Şeker, C Tunca, A Knehr, ... Brain 142 (2), e4-e4, 2019 | 18 | 2019 |
| Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11 C Iskender, E Kartal, F Akcimen, C Kocoglu, A Ozoguz, D Kotan, ... Neurology: Genetics 1 (3), e25, 2015 | 17 | 2015 |
| Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database C Tunca, T Şeker, F Akcimen, C Coşkun, E Bayraktar, R Palvadeau, S Zor, ... Human mutation 41 (8), e7-e45, 2020 | 15 | 2020 |
| The complex genetic landscape of hereditary ataxias in Turkey and implications in clinical practice A Vural, G Şimşir, Ş Tekgül, C Koçoğlu, F Akcimen, E Kartal, NE Şen, ... Movement Disorders 36 (7), 1676-1688, 2021 | 13 | 2021 |
| Clinical and molecular characterization and response to acitretin in three families with Sjögren‐Larsson syndrome S Vural, A Vural, F Akçimen, IS Bağci, C Tunca, A Gündoğdu Eken, ... International Journal of Dermatology 57 (7), 843-848, 2018 | 7 | 2018 |
| A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy NH Akçakaya, Z Yapıcı, Cİ Tunca, P Tektürk, F Akçimen, AN Başak Journal of Neurology, Neurosurgery & Psychiatry 89 (10), 1123-1125, 2018 | 6 | 2018 |
| A Turkish family with a familial ALS-positive UBQLN2-S340I mutation D Kotan, C Iskender, AÖ Erimiş, AN Başak Archives of Neuropsychiatry 53 (3), 283, 2016 | 5 | 2016 |
| Phenotypic and genotypic features of patients diagnosed with ALS in the city of Sakarya, Turkey D Kotan, Z Özözen Ayas, C Tunca, BD Gungen, F Akcimen, AN Başak Acta Neurologica Belgica, 1-8, 2020 | 4 | 2020 |
| SOD1 (L144F) ve C9orf72 Gen Mutasyonları Saptanan İki Aile ve Amiyotrofik Lateral Skleroza Genel Bakış GB Nazlı, Y Seçil, N Başak, Y Beckmann, HS Türe, C Tunca, A Özoğuz Turk Noroloji Dergisi 24 (2), 159, 2018 | 2 | 2018 |
| MRI‐ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study A Scaravilli, D Negroni, C Senatore, L Ugga, M Cosottini, I Ricca, ... Movement Disorders, 2024 | 1 | 2024 |
| A combined clinical and computational approach to understand the SOD1A4T-mediated pathogenesis of rapidly progressive familial amyotrophic lateral sclerosis S Diker, P Gelener, K Teralı, MC Ergoren, C Tunca, AN Başak, E Tan Acta Neurologica Belgica, 1-6, 2022 | 1 | 2022 |
| Two families with SOD1 (L144F) and C9orf72 gene mutations and an overview of amyotrophic lateral sclerosis NG Bülbül, Y Seçil, N Başak, Y Beckmann, HS Türe, C Tunca, A Özoğuz Turkish Journal of Neurology 24 (2), 159-164, 2018 | 1 | 2018 |
| Motor Nöron Hastalıklarına Örnek Olarak ALS: Charcot ve SOD1’den Post-Genomik Döneme G ÇOBANOĞLU Turkiye Klinikleri J Neurol-Special Topics 4 (2), 2011 | 1 | 2011 |
Ayşe Nazlı BaşakVerified email at ku.edu.tr
