Akademisyen
BEYHAN DURAK ARAS
PROFESÖR
ESKİŞEHİR OSMANGAZİ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 86
- Proje 0
- Kitap 7
- Bildiri 107
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
6
Q2
6
Q3
12
Q4
12
WoS (JCR)
Q1
2
Q2
5
Q3
7
Q4
21
TR Index
28
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
2
Ort. yüzdelik
44.8%
Üst %1 payı
0.0%
Üst %10 payı
4.2%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2026 Evaluation of Stromal Fibrosis in Triple-Negative Breast Carcinomas YÖKSİS TR Index OpenAlex 29.8%
- 2025 Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 91.1%
- 2025 A rare case of Hodgkin lymphoma transformed from follicular lymphoma demonstrating 14;18 translocation YÖKSİS SJR Q3 JCR Q4 OpenAlex 22.0%
- 2025 Chromosomal abnormalities in couples with recurrent pregnancy loss: a 16-year cross-sectional study of 4030 cases from Turkey YÖKSİS SJR Q3 JCR Q2 OpenAlex üst %10 OpenAlex 96.9%
- 2025 Evaluation of Genomic Variants in Non-syndromic Congenital Heart Disease in Turkish Pediatric Group YÖKSİS OpenAlex 12.9%
- 2024 KLL Olgularında NOTCH1 Gen Amplifikasyonu YÖKSİS TR Index OpenAlex 48.9%
- 2023 Genetic Investigations in Turkish Idiopathic Pancreatitis Patients Show Unique Characteristics YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 72.2%
- 2023 ERCC8 related Cockayne syndrome type-1: A rare entity diagnosed in a Turkish boy YÖKSİS OpenAlex 8.7%
- 2022 Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.1%
- 2022 An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3 YÖKSİS SJR Q3 JCR Q4 OpenAlex 48.7%
- 2022 NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly YÖKSİS SJR Q2 JCR Q3 OpenAlex 10.7%
- 2022 Flow Cytometric Analysis of Chronic Phase Chronic Myeloid Leukemia Patients YÖKSİS TR Index OpenAlex 11.3%
- 2022 The Impact of Cytogenetic Aberrations in the Clonal Evolution of Chronic Myeloid Leukemia: A Single-Center Experience Among 450 Turkish Patients (Cohort Study) YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 49.6%
- 2021 Frequency of frontotemporal dementia-related gene variants in Turkey YÖKSİS SJR Q1 JCR Q2 OpenAlex 63.4%
- 2021 Which Prognostic Marker is Responsible For the Clinical Heterogenity in CLL with 13q Deletion? YÖKSİS SJR Q1 JCR Q4 OpenAlex 82.4%
- 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 YÖKSİS SJR Q3 JCR Q4 OpenAlex 62.4%
- 2021 A Pediatric BAL Case with Double Ph Chromosomes and Trisomy 5 YÖKSİS SJR Q3 JCR Q4 OpenAlex 43.5%
- 2021 Analyzing the Mutations of NOTCH1 and SF3B1 Genes in Cases with CLL Detected Isolated 13q Deletion YÖKSİS TR Index OpenAlex 6.6%
- 2021 The Importance of FISH Test Targeting EGFR, CCND1and RREB1 Genes in Differentiating Malignant Melanomas from Melanocytic Nevus YÖKSİS TR Index OpenAlex 4.4%
- 2020 A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency YÖKSİS SJR Q2 JCR Q3 OpenAlex 73.9%