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Acta Neurochirurgica|March 6, 2012
Intracranial arachnoid cyst family with autosomal recessive trait mapped to chromosome 6q22.31-23.2Fatih Bayrakli, Ali Ihsan Okten, Ugur Kartal, et al.Turkish Neurosurgery|February 6, 2020
Analyses of Copy Number Variations in Myxopapillary Ependymomas of Cauda EquinaAli Ozen, Fatih Bayrakli, Ozcan Sonmez, et al.Omics : a Journal of Integrative Biology|February 16, 2022
Past, Present, and Future of Therapies for Pituitary Neuroendocrine Tumors: Need for Omics and Drug Repositioning GuidanceBusra Aydin, Esra Yildirim, Onur Erdogan, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 26, 2015
Neural tube defect family with recessive trait linked to chromosome 9q21.12-21.31Yasar Bayri, Burcak Soylemez, Askin Seker, et al.BMC Genetics|October 1, 2013
Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtypeFatih Bayrakli, Bulent Guclu, Cengiz Yakicier, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 2, 2009
A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family groupFatih Bayrakli, Ilter Guney, Yasar Bayri, et al.Human Mutation|August 7, 2007
Rapid identification of disease-causing mutations using copy number analysis within linkage intervalsFatih Bayrakli, Kaya Bilguvar, Christopher E Mason, et al.Journal of Neurosurgery|December 25, 2007
A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigationKaya Bilguvar, Mohamad Bydon, Fatih Bayrakli, et al.Journal of Child Neurology|January 30, 2010
Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI)Zulfikar Arlier, Yasar Bayri, Luis E Kolb, et al.Neurogenetics|March 7, 2008
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationBeyhan Tüysüz, Fatih Bayrakli, Michael L DiLuna, et al.Pageof 4