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The International Journal of Neuroscience|April 29, 2006
GAA repeat polymorphism in Turkish Friedreich's ataxia patientsM Bertan Yilmaz, A Filiz Koç, Halil Kasap, et al.
Plos One|August 31, 2013
Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factorÖzgün Uyan, Özgür Ömür, Zeynep Sena Ağım, et al.
Plos One|August 24, 2012
ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish populationSuna Lahut, Özgür Ömür, Özgün Uyan, et al.
Noro Psikiyatri Arsivi|December 20, 2021
Neuropathic Pain Frequency in Neurology Outpatients: A Multicenter StudyCan Ebru Bekircan-Kurt, Berin Inan, Onur Bulut, et al.
Neurobiology of Aging|February 16, 2015
The distinct genetic pattern of ALS in Turkey and novel mutationsAslıhan Özoğuz, Özgün Uyan, Güneş Birdal, et al.
Human Mutation|June 25, 2020
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant databaseCeren Tunca, Tuncay Şeker, Fulya Akçimen, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2025
Identification of a presymptomatic and early disease signature for Amyotrophic Lateral Sclerosis (ALS): protocol of the premodiALS studyLaura Tzeplaeff, Ana Galhoz, Clara Meijs, et al.
Neurological Research and Practice|August 20, 2025
Identification of a presymptomatic and early disease signature for amyotrophic lateral sclerosis (ALS): protocol of the premodiALS studyLaura Tzeplaeff, Ana Galhoz, Clara Meijs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2021
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical PracticeAtay Vural, Gülşah Şimşir, Şeyma Tekgül, et al.
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