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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 17, 2018
Three novel mutations in 20 patients with hereditary spastic paraparesisMehmet Bugrahan Duz, Selcuk Dasdemir, Aysel Kalayci Yigin, et al.
Psychiatric Genetics|June 6, 2024
Comparison of microRNA expression levels in patients with schizophrenia before and after electroconvulsive therapyNazife Gamze Usta Saglam, Mehmet Bugrahan Duz, Seda Salman Yilmaz, et al.
Cellular Oncology (Dordrecht, Netherlands)|December 10, 2015
Identification of miR-139-5p as a saliva biomarker for tongue squamous cell carcinoma: a pilot studyMehmet Bugrahan Duz, Omer Faruk Karatas, Esra Guzel, et al.
Gene|November 10, 2015
Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndromeByeonghyeon Lee, Mehmet Bugrahan Duz, Borum Sagong, et al.
American Journal of Medical Genetics. Part A|January 9, 2026
Homozygous MGME1 Variant in Turkish Siblings: First Reported Case With Successful Heart Transplantation, Expanding the Clinical Spectrum of MGME1-Related Mitochondrial DiseaseNazli Busra Acikgoz, Gizem Urel Demir, Yilmaz Yildiz, et al.
The British Journal of Dermatology|January 3, 2026
Genotype-Phenotype Associations in a Robust Cohort of 69 Xeroderma Pigmentosum Patients across Türkiye: A Multicenter StudyDefne Baskurt, Şule Altıner, Tuğba Atcı, et al.
Neuron|November 6, 2015
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic DiseaseEnder Karaca, Tamar Harel, Davut Pehlivan, et al.
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