| Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ... Functional & integrative genomics 22 (3), 291-315, 2022 | 16 | 2022 |
| Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion? B Durak Aras, S Isik, H Uskudar Teke, A Aslan, F Yavasoglu, Z Gulbas, ... Molecular cytogenetics 14, 1-7, 2021 | 16 | 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 … S Ilguy, O Cilingir, MD Bilgec, O Ozalp, E Erzurumluoglu Gokalp, S Arslan, ... Ophthalmic Genetics 42 (6), 725-731, 2021 | 12 | 2021 |
| A Turkish patient with novel AHCY variants and presumed diagnosis of S‐adenosylhomocysteine hydrolase deficiency H Bas, O Cilingir, N Tekin, S Saylisoy, B Durak Aras, E Uzay, ... American Journal of Medical Genetics Part A 182 (4), 740-745, 2020 | 11 | 2020 |
| Genetic variants associated with atrial fibrillation and long-term recurrence after catheter ablation for atrial fibrillation in Turkish patients T Ulus, M Dural, P Meşe, F Yetmiş, KU Mert, B Görenek, O Çilingir, ... Anatolian journal of cardiology 25 (2), 129, 2021 | 10 | 2021 |
| A novel SACS p. Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay B Samanci, EE Gokalp, B Bilgic, H Gurvit, S Artan, HA Hanagasi Neurological Sciences 42, 2969-2973, 2021 | 7 | 2021 |
| Future Treatment of Alzheimer AO Keskin, N Durmaz, G Uncu, E Erzurumluoglu, Z Yıldırım, N Tuncer, ... Geriatric medicine and gerontology, 83, 2019 | 7 | 2019 |
| The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degeneration E Erzurumluoglu, O Cilingir, BDO Adapinar, B Bilgic, S Kocagil, H Ozen, ... Neurobiology of Aging 76, 216. e1-216. e7, 2019 | 6 | 2019 |
| A novel mutation in RNF216 gene in a Turkish case with Gordon Holmes syndrome N Durmaz Çelik, E Erzurumluoğlu, S Özben, U Toprak, G Yorulmaz, ... BMC Medical Genomics 16 (1), 98, 2023 | 5 | 2023 |
| Frequency of frontotemporal dementia-related gene variants in Turkey S Artan, EE Gokalp, B Samanci, DO Adapinar, H Bas, F Tepgec, ... Neurobiology of Aging 106, 332. e1-332. e11, 2021 | 5 | 2021 |
| A new four-way complex translocation variant involving the t (8; 5; 21; 4)(q21; q13; q22; q31) and the relocalization of AML1/ETO fusion gene S Isik, HU Teke, G Gunden, EE Gokalp, O Cilingir, S Artan, BD Aras Cancer Genetics 256, 1-4, 2021 | 3 | 2021 |
| A novel PSEN2 p. Ser175Phe variant in a family with Alzheimer’s disease G Guven, B Samanci, C Gulec, H Hanagasi, H Gurvit, EE Gokalp, ... Neurological Sciences 42 (6), 2497-2504, 2021 | 3 | 2021 |
| Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey N Unlu, EE Gokalp, S Arslan, O Cilingir, M Bilgin, E Yildirim, H Gursoy International Journal of Ophthalmology 14 (6), 812, 2021 | 2 | 2021 |
| Ailesel Akdeniz Ateşi tanısı alan olgularda MEFV geni mutasyonlarının ve allel frekanslarının dağılımı-Tek Merkez Deneyimi O Çilingir, BD Aras, S Arslan, Ö Kutlay, E Erzurumluoğlu, S Kocagil, ... Osmangazi Tıp Dergisi 40 (2), 39-46, 2018 | 2 | 2018 |
| The relationship between glutathione-S-transferases polymorphisms and lichen planus susceptibility O Cilingir, I Bulur, BD Aras, O Kutlay, E Erzurumluoglu, K Haziyeva, ... International Journal of Research 3 (1), 15-22, 2018 | 2 | 2018 |
| Association of functional RAGE gene polymorphisms with Parkinson’s disease in a Turkish cohort. O Cilingir, S Ozkan, BD Aras, E Erzurumluoglu, O Kutlay, M Akinci, B Emir, ... Biomedical Research 28 (19), 8454-8460, 2017 | 2 | 2017 |
| Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus E Şimşek, O Çilingir, T Şimşek, S Kocagil, EE Gökalp, M Demiral, Ç Binay Journal of Clinical Research in Pediatric Endocrinology 16 (2), 137, 2024 | 1 | 2024 |
| Analyzing The Mutations Of Notch1 And Sf3b1 Genes In Cases With CLL Detected Isolated 13q Deletion G Günden, S Işık, HÜ Teke, O Çilingir, NO Davutoglu, E Erzurumluoğlu, ... Osmangazi Tıp Dergisi 45 (2), 480-484, 2023 | 1 | 2023 |
| An Anomaly with Potential as a New Prognostic Marker in CLL with del (13q): Gain of 16p13. 3 S Isik, G Gunden, E Gunduz, OM Akay, A Aslan, H Ozen, O Cilingir, ... Cytogenetic and Genome Research 161 (10-11), 479-487, 2022 | 1 | 2022 |
| Deep Brain Stimulation for Rare Neurodegenerative Diseases: Three-Center Experience ND Celik, B Samanci, GY Cakmakli, AA Gundogdu, E Erzurumluoglu, ... MOVEMENT DISORDERS 37, S148-S149, 2022 | 1 | 2022 |
