Publications by authors named "Ayse Candayan"

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Delineating the genetic landscape of Charcot-Marie-tooth disease in Türkiye: Distinct distribution, rare phenotypes, and novel variants.
Arman Cakar, Ayse Candayan, Gulandam Bagırova, Zehra Oya Uyguner, Serdar Ceylaner

Eur J Neurol· January 2025

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Identification and Characterization of Novel Founder Mutations in : Refining the Genetic Landscape of Charcot-Marie-Tooth Disease Type 4D in Bulgaria.
Derek Atkinson, Teodora Chamova, Ayse Candayan, Kristina Kastreva, Ognian Asenov

Int J Mol Sci· August 2024

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Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
Stojan Perić, Vladana Marković, Ayşe Candayan, Els De Vriendt, Nikola Momčilović

Cells· September 2022

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Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features.
Arman Çakar, Erdi Şahin, Seden Tezel, Ayşe Candayan, Bedia Samancı

Acta Neurol Belg· August 2022

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Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder.
Arman Çakar, Meltem İnci, Ayşe Nur Özdağ Acarlı, Sinan Çomu, Ayşe Candayan

Acta Neurol Scand· May 2022

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Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity.
Alina Kurolap, Florian Kreuder, Claudia Gonzaga-Jauregui, Morasha Plesser Duvdevani, Tamar Harel, Ayşe Candayan

Am J Hum Genet· March 2022

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Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages.
Ayşe Candayan, Yeşim Parman, Esra Battaloğlu

Balkan Med J· January 2022

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Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort.
Ayşe Candayan, Arman Çakar, Gulshan Yunisova, Ayşe Nur Özdağ Acarlı, Derek Atkinson

Neurol Genet· October 2021

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The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype.
Ayşe Candayan, Gulshan Yunisova, Arman Çakar, Hacer Durmuş, A Nazlı Başak

Neurogenetics· January 2020

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MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
Emil Ylikallio, Rosa Woldegebriel, Manuela Tumiati, Pirjo Isohanni, Monique M Ryan, Ayse Candayan

Brain· August 2017

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