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Ceren Iskender Tunca
Ceren Iskender Tunca
Postdoctoral Researcher at Koç University Hospital, Research Center for Translational Medicine
Verified email at ku.edu.tr - Homepage
Title
Cited by
Cited by
Year
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
5882016
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
1052015
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
672019
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
362018
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
282018
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
282018
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
282016
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
182019
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
152015
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
122021
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
122020
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
72018
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
62018
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
42020
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
42016
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
22018
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
12018
Motor Nöron Hastalıklarına Örnek Olarak ALS: Charcot ve SOD1’den Post-Genomik Döneme
G ÇOBANOĞLU
Turkiye Klinikleri J Neurol-Special Topics 4 (2), 2011
12011
The Molecular Landscape of ALS in Türkiye.
E Bayraktar, V Çiftçi, C Tunca, AN Başak
Gazi Medical Journal 35, 2024
2024
CLINICAL, EPIDEMIOLOGICAL AND GENETIC FEATURES OF PATIENTS WITH AMYOTROPHIC LATERAL SCLEROS_IS IN TURKEY: DATA FROM A SINGLE CENTER
G Yunisova, E Bayraktar, V Ciftci, CI Tunca, AN Basak, P Oflazer
MUSCLE & NERVE 68, S76-S76, 2023
2023
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