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Scientific Reports|May 14, 2025
Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathiesM Arda Temena, Ebru Erzurumluoglu Gokalp, Ezgi Susam, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 15, 2021
A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's diseaseGamze Guven, Bedia Samanci, Cagri Gulec, et al.
Annals of Saudi Medicine|June 7, 2025
Chromosomal abnormalities in couples with recurrent pregnancy loss: a 16-year cross-sectional study of 4030 cases from TurkeySabri Aynaci, Sinem Kocagil, Esfun Tosumoglu, et al.
Turkish Neurosurgery|January 19, 2026
Evaluation of the Role of miRNAs Expression Profiles in AneurysmSara Khadem Ansari, Ebru Erzurumluoglu Gokalp, Emre Ozkara, et al.
Biomedicines|June 26, 2026
MicroRNAs in Aneurysmal Subarachnoid Hemorrhage: A Stage-Specific Model Linking Rupture, Vasospasm, and OutcomeEmre Ozkara, Ebru Erzurumluoglu Gokalp, Ozlem Aykac, et al.
Ophthalmic Genetics|August 4, 2021
The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphismsSerdar Ilguy, Oguz Cilingir, Mustafa Deger Bilgec, et al.
Cytogenetic and Genome Research|December 16, 2021
An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3Sevgi Isik, Gulcin Gunden, Eren Gunduz, et al.
Genes|September 27, 2025
Cerebrospinal Fluid MicroRNAs as Early Biomarker Candidates for Predicting Vasospasm Following Aneurysmal Subarachnoid HemorrhageEmre Ozkara, Ozlem Aykac, Ebru Erzurumluoglu Gokalp, et al.
Anatolian Journal of Cardiology|February 15, 2021
Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patientsTaner Ulus, Muhammet Dural, Pelin Meşe, et al.
Neurobiology of Aging|June 24, 2021
Frequency of frontotemporal dementia-related gene variants in TurkeySevilhan Artan, Ebru Erzurumluoglu Gokalp, Bedia Samanci, et al.
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