Academician profile · PROFESÖR
ÖZTÜRK ÖZDEMİR
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
- TIP FAKÜLTESİ
- DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Scopus (SJR)
Q1
6
Q2
46
Q3
26
Q4
16
WoS (JCR)
Q1
5
Q2
18
Q3
15
Q4
51
TR Index
18
articles
Articles
- 2023 Reanalysis of genetic variants detected by next generation sequencing in Parkinson’s disease with two novel variants. Twin Res Hum Genet.
- 2023 Evaluating of colchicine use patterns and attack frequency of familial Mediterranean fever patients in the COVID-19 pandemic.Int J Rheum Dis. 2023 May;26(5):988-991
- 2022 A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation
- 2022 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
- 2022 Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
- 2022 Copy number variations in patients with idiopathic recurrent pregnancy loss: an array- CGH approach
- 2022 Are P-glycoprotein (ABCB1/MDR1) and endothelial nitric oxide synthase (eNOS) polymorphisms related to severity of the coronary artery disease?
- 2022 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
- 2021 The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients
- 2021 Prognostic Prediction of BRCA Mutations by 18F-FDG PET/CT SUVmax in Breast Cancer
- 2021 Delayed time of atrial conduction in children with Familial Mediterranean Fever
- 2021 The comparison of telomere length in cancer patients Plasma, whole blood and tumor tissue
- 2020 Tedaviyi Etkileyen Tarama Testleri
- 2020 Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma
- 2020 Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report
- 2020 Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay
- 2019 The Genomics of Arthrogryposis, a Complex Trait:Candidate Genes and Further Evidence for Oligogenic Inheritance
- 2019 Warfarin Resistance: A Case Report
- 2019 Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in CentralAnatolia
- 2019 The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas