Prof.Dr.Öztürk ÖZDEMİR
Çanakkale Onsekiz Mart Üniversitesi
H-index: 22
Asia-Turkey
Top articles of Prof.Dr.Öztürk ÖZDEMİR
Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method
Cumhuriyet Medical Journal
2022/3/30
A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels
Hemoglobin
2022/3/4
Copy number variations in patients with idiopathic recurrent pregnancy loss: an arrayCGH approach
Turkish Journal of Medical Sciences
2022
COVID-19 pandemic in patients with familial mediterranean fever; The possible protective role of colchicine in COVID-19 symptoms
Gazi Medical Journal
2022
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
Functional & integrative genomics
2022/6
Munis Dundar
H-Index: 14
Umut Fahrioglu
H-Index: 5
Haluk Akin
H-Index: 7
Sevilhan Artan
H-Index: 9
Ahmet Dursun
H-Index: 9
Ahmet Arman
H-Index: 8
Mahmut Cerkez Ergoren
H-Index: 6
Bilge Dundar
H-Index: 1
Ayca Dundar
H-Index: 3
Sevda Yesim Ozdemir
H-Index: 3
Adem Alemdar
H-Index: 2
Burak Durmaz
H-Index: 11
Beyhan Durak Aras
H-Index: 5
Ebru Erzurumluoglu Gokalp
H-Index: 2
Sinem Kocagil
H-Index: 1
Hasan Bas
H-Index: 4
Ezgi Susam
H-Index: 0
Elif Sarac
H-Index: 2
Yunus Kasim Terzi
H-Index: 8
Gunes Cakmak Genc
H-Index: 4
Serbulent Yigit
H-Index: 14
Mustafa Yilmaz
H-Index: 6
Mehmet Ali Ergun
H-Index: 8
A New Case of Rare Microdeletion 10q22. 3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor …
Molecular Syndromology
2022/5/2
Are P-glycoprotein (ABCB1/MDR1) and endothelial nitric oxide synthase (eNOS) polymorphisms related to severity of the coronary artery disease?
Journal of Surgery and Medicine
2022/4/1
Prognostic Prediction of BRCA Mutations by 18F-FDG PET/CT SUVmax in Breast Cancer
Mol Imaging Radionucl Ther
2021
Delayed time of atrial conduction in children with Familial Mediterranean Fever
Family Practice and Palliative Care
2021/5/5
The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients
Clinical Neurology and Neurosurgery
2021/3/1
The comparison of telomere length in cancer patients: Plasma, whole blood and tumor tissue
Med. Sci
2021
Diagnostic Outcomes for Genetic Testing of 54 Genes in Pregnancy Loss Using Array CGH Method: A Two-Year Retrospective Study
Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi
2020/12/12
Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report
Cumhuriyet Medical Journal
2020/10/27
Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay
Cumhuriyet Medical Journal
2020/5/20
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