| 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 |
| 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 | 28 | 2018 |
| Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families C Kocoglu, A Gundogdu, G Kocaman, P Kahraman-Koytak, K Uluc, ... Neurology: Genetics 4 (1), e218, 2018 | 22 | 2018 |
| 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 | 15 | 2015 |
| 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 | 12 | 2021 |
| 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 | 12 | 2020 |
| Investigating the Endo-Lysosomal system in major neurocognitive disorders due to Alzheimer’s disease, frontotemporal lobar degeneration and lewy body disease: Evidence for … L Benussi, A Longobardi, C Kocoglu, M Carrara, S Bellini, C Ferrari, ... International journal of molecular sciences 22 (24), 13633, 2021 | 9 | 2021 |
| TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early‐onset autosomal dominant dementia with amyloid load and parkinsonism E Gómez‐Tortosa, Y Baradaran‐Heravi, L Dillen, NR Choudhury, ... Alzheimer's & Dementia 19 (7), 2805-2815, 2023 | 5 | 2023 |
| Protein interaction network analysis reveals genetic enrichment of immune system genes in frontotemporal dementia C Koçoğlu, R Ferrari, M Roes, G Vandeweyer, RF Kooy, ... Neurobiology of Aging 116, 67-79, 2022 | 3 | 2022 |
| Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis J van der Zee, L Dillen, Y Baradaran-Heravi, H Gossye, C Koçoğlu, I Cuyt, ... Neurobiology of Disease 156, 105421, 2021 | 3 | 2021 |
| No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers C Koçoğlu, H Gossye, L Dillen, S Van Mossevelde, JL De Bleecker, ... Neurobiology of Aging 97, 145. e1-145. e4, 2021 | 2 | 2021 |
| How network-based approaches can complement gene identification studies in frontotemporal dementia C Koçoğlu, C Van Broeckhoven, J van der Zee Trends in Genetics 38 (9), 944-955, 2022 | 1 | 2022 |
| Vestibulo-ocular reflex impairment in SPG7 hereditary spastic paraplegia G Akdal, K Kocoglu, C Koçoğlu, E Bora, AN Basak, GM Halmagyi Clinical neurophysiology.-Amsterdam 132 (1), 77-79, 2021 | 1 | 2021 |
| Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey S Sayan, D Kotan, A Gündoğdu-Eken, I Şahbaz, C Koçoğlu, AN Başak Archives of Neuropsychiatry 56 (2), 106, 2019 | 1 | 2019 |
| Analysis of endolysosomal pathway genes identifies AP2A2 as a candidate gene for dementia C Koçoğlu MEMBERS OF THE JURY, 91, 2022 | | 2022 |
| Molecular networks and gene identification studies in frontotemporal dementia C Koçoğlu University of Antwerp, 2022 | | 2022 |
| TRIM25 nonsense mutation (p. C168*) as the probable cause of early-onset autosomal dominant Alzheimer’s disease E Gómez-Tortosa, Y Baradaran-Heravi, L Dillen, P Agüero, MJ Sainz, ... DNA 2, 4, 2021 | | 2021 |
| Exploration of the endo‐lysosomal pathway genes in frontotemporal dementia: The use of protein‐protein interaction networks to prioritize rare‐variant association analysis … C Kocoglu, C Manzoni, R Ferrari, C Van Broeckhoven, J van der Zee Alzheimer's & Dementia 16, e043624, 2020 | | 2020 |
| Cover, Volume 41, Issue 8 C Tunca, T Şeker, F Akçimen, C Coşkun, E Bayraktar, R Palvadeau, S Zor, ... Human Mutation 41 (8), iv-iv, 2020 | | 2020 |
| Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database O Karakahya, U Norman, G Olgun, T Akgun, H Durmus, E Sahin, ... | | 2020 |
