Gao, F., Schon, K. R., Vandrovcova, J., Köken, Ö. Y., Raga, S., Naidu, K., Schoonen, M., Rani, N., Tomaselli, P., Baskar, D., Kapapa, M., Polat, I., Wilson, L. A., Thangaraj, K., Yiş, U., Nandeesh, B. N., Bearden, D., Kvalsund, M., Henning, F., Vengalil, S., … Horvath, R. (2025). Mitochondrial DNA disorders in neuromuscular diseases in diverse populations. Annals of clinical and translational neurology, 12(8), 1680–1688. https://doi.org/10.1002/acn3.52141
Mehpare, S. Y., Furkan, D., Şakir, G., Sait, A., Özlem, Y. K., & Şenay, H. (2025). What is the right choice? Is the answer sodium channel blockers?. Epileptic disorders : international epilepsy journal with videotape, 10.1002/epd2.70063. Advance online publication. https://doi.org/10.1002/epd2.70063
Akinci, G., Ozyilmaz, B., Ozturk, G., Komur, M., Onel, E., Ardicli, D., Gerik-Celebi, H. B., Ozcelik, A., Yilmaz, S., Cetin, I. D., Gunay, C., Tuncer, G. O., Aydin, H., Gunes, A. S., Koken, O. Y., Polat, I., Degerliyurt, A., Celik, T., Cetinoglu, Y. K., Karti, O., … Topaloglu, H. (2025). Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients. Neuromuscular disorders : NMD, 53, 105423. Advance online publication. https://doi.org/10.1016/j.nmd.2025.105423
Uğur, F., Gürbüz, İ., Köken, Ö. Y., Kurt, A. N. Ç., & Yılmaz, Ö. (2024). Pelvic obliquity, trunk control, and motor function: an exploratory study in a non-ambulatory Duchenne muscular dystrophy cohort. Revista da Associacao Medica Brasileira (1992), 70(12), e20241109. https://doi.org/10.1590/1806-9282.20241109
Şanlidağ, B., Donbaloğlu, F., Sari Yanartaş, M., Şekeroğlu, B., Yilmaz, A., & Köken, Ö. Y. (2025). High-frequency oscillations in autism spectrum disorder: are they related to clinical severity?. Cerebral cortex (New York, N.Y. : 1991), 35(4), bhaf068. https://doi.org/10.1093/cercor/bhaf068
Yayıcı Köken, Ö., Şekeroğlu, B., Şanlıdağ, B., Sarı Yanartaş, M., & Yılmaz, A. (2024). Focality in childhood absence epilepsy. Neurological research, 46(7), 626–633. https://doi.org/10.1080/01616412.2024.2339114
Bulut, N., Aydın Yağcıoğlu, G., Uğur, F., Yayıcı Köken, Ö., Gürbüz, İ., Yılmaz, Ö., Topaloğlu, H., & Karaduman, A. (2024). Sleep quality and daytime sleepiness amongst family caregivers of children with Spinal Muscular Atrophy. Research in developmental disabilities, 152, 104811. https://doi.org/10.1016/j.ridd.2024.104811
Ceylan, G. G., Habiloğlu, E., Çavdarlı, B., Tuncez, E., Bilen, S., Köken, Ö. Y., & Gündüz, C. N. S. (2023). High diagnostic yield with algorithmic molecular approach on hereditary neuropathies. Revista da Associacao Medica Brasileira (1992), 69(2), 233–239. https://doi.org/10.1590/1806-9282.20220929
Çavdarlı, B., Köken, Ö. Y., Satılmış, S. B. A., Bilen, Ş., Ardıçlı, D., Ceylan, A. C., Gündüz, C. N. S., & Topaloğlu, H. (2023). High diagnostic yield of targeted next-generation sequencing panel as a first-tier molecular test for the patients with myopathy or muscular dystrophy. Annals of human genetics, 87(3), 104–114. https://doi.org/10.1111/ahg.12492
Wilson, L. A., Macken, W. L., Perry, L. D., Record, C. J., Schon, K. R., Frezatti, R. S. S., Raga, S., Naidu, K., Köken, Ö. Y., Polat, I., Kapapa, M. M., Dominik, N., Efthymiou, S., Morsy, H., Nel, M., Fassad, M. R., Gao, F., Patel, K., Schoonen, M., Bisschoff, M., … Hanna, M. G. (2023). Neuromuscular disease genetics in under-represented populations: increasing data diversity. Brain : a journal of neurology, 146(12), 5098–5109. https://doi.org/10.1093/brain/awad254