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Ebru Erzurumluoglu Gokalp
Ebru Erzurumluoglu Gokalp
Verified email at ogu.edu.tr
Title
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Cited by
Year
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
142021
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
102022
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
102021
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
102021
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
72020
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
62021
Future Treatment of Alzheimer
AO Keskin, N Durmaz, G Uncu, E Erzurumluoglu, Z Yıldırım, N Tuncer, ...
Geriatric medicine and gerontology, 83, 2019
62019
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
62019
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
42023
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
42021
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
32021
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
32021
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
22021
Dijital Dönüşümün İstihdama Etkisi: Mesleki Açıdan Fırsatlar ve Tehditler
E Gökalp, MO Gökalp, S Çoban, PE Eren
IMISC, 2019
22019
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
22018
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
22017
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
12023
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
12022
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
12022
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
12018
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