| MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability E Ylikallio, R Woldegebriel, M Tumiati, P Isohanni, MM Ryan, Z Stark, ... Brain 140 (8), 2093-2103, 2017 | 39 | 2017 |
| Evaluation techniques S Yesilkir-Baydar, ON Oztel, R Cakir-Koc, A Candayan Nanobiomaterials Science, Development and Evaluation, 211-232, 2017 | 24 | 2017 |
| The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype A Candayan, G Yunisova, A Çakar, H Durmuş, AN Başak, Y Parman, ... neurogenetics 21, 73-78, 2020 | 14 | 2020 |
| Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity A Kurolap, F Kreuder, C Gonzaga-Jauregui, MP Duvdevani, T Harel, ... The American Journal of Human Genetics 109 (3), 518-532, 2022 | 12 | 2022 |
| Clinical and genetic survey for Charcot-Marie-Tooth neuropathy based on the findings in Turkey, a country with a high rate of consanguineous marriages A Candayan, Y Parman, E Battaloğlu Balkan Medical Journal 39 (1), 3, 2022 | 8 | 2022 |
| Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features A Çakar, E Şahin, S Tezel, A Candayan, B Samancı, E Battaloğlu, ... Acta Neurologica Belgica 122 (4), 939-945, 2022 | 5 | 2022 |
| Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder A Çakar, M İnci, AN Özdağ Acarlı, S Çomu, A Candayan, E Battaloğlu, ... Acta Neurologica Scandinavica 145 (5), 619-626, 2022 | 4 | 2022 |
| Genetic survey of autosomal recessive peripheral neuropathy cases unravels high genetic heterogeneity in a Turkish cohort A Candayan, A Çakar, G Yunisova, AN Özdağ Acarlı, D Atkinson, ... Neurology: Genetics 7 (5), e621, 2021 | 4 | 2021 |
| Phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia S Perić, V Marković, A Candayan, E De Vriendt, N Momčilović, A Savić, ... Cells 11 (18), 2804, 2022 | 2 | 2022 |
| Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy C Armirola-Ricaurte, E De Vriendt, A Candayan, O Asenov, Y Parman, ... JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 26 (3), 426-426, 2021 | 1 | 2021 |
| Distinct Genetic Distribution of Distal Hereditary Motor Neuropathy in Turkey: A Single Centre Experience (P2-11.009) A Cakar, A Candayan, R Maroofian, H Durmus, H Houlden, E Battaloglu, ... Neurology 102 (17_supplement_1), 5907, 2024 | | 2024 |
| Genotypic And Phenotypic Features of Patients with GJB1 Mutations: Single Center Experience (P11-8.003) FY Parman, A Cakar, A Candayan, H Durmus, E Battaloglu Neurology 100 (17 Supplement 2), 2023 | | 2023 |
| Single Center Experience of SORD Neuropathy in Turkey (P1-1. Virtual) A Çakar, A Candayan, H Durmus, E Battaloglu, Y Parman Neurology 98 (18_supplement), 2529, 2022 | | 2022 |
| Central Nervous System Involvement in HINT1 Neuropathy: An Overlooked Phenotypical Feature?(P8-13.001) A Çakar, ANÖ Acarlı, A Candayan, S Ceylaner, E Battaloglu, H Durmuş, ... Neurology 98 (18 Supplement), 2022 | | 2022 |
| Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy C Armirola-Ricaurte, E de Vriendt, A Candayan, O Asenov, Y Parman, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 309-310, 2022 | | 2022 |
| Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort (vol 7, e621, 2021) A Candayan, cakar, Arman, G Yunisova, ozdag Acarli, Ayse Nur, ... NEUROLOGY-GENETICS 8 (1), 2022 | | 2022 |
| Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (Canvas) is an important cause of late-onset ataxia A Cakar, E Sahin, S Tezel, A Candayan, B Samanci, E Battaloglu, ... JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 26 (3), 364-364, 2021 | | 2021 |
| Investigation of novel recessive causative genes and gene/allele frequency for CMT disease in Turkey A Candayan Thesis (Ph. D.)-Bogazici University. Institute for Graduate Studies in …, 2021 | | 2021 |
| Genotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy AO Acarli, A Cakar, A Candayan, H Durmus, S Ceylaner, Z Matur, A Oge Wiley, 2021 | | 2021 |
| Clinical features of a homozygous missense mutation in the FXN gene resulting in a Charcot-Marie-Tooth-like phenotype A Cakar, A Candayan, G Yunisova, E Battaloglu, H Durmus, Y Parman JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 25 (4), 490-490, 2020 | | 2020 |
