Akademisyen
DENİZ ASLAN
PROFESÖR
GAZİ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk Hematolojisi ve Onkolojisi (Çocuk Sağlığı ve Hastalıkları)
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 54
- Proje 0
- Kitap 0
- Bildiri 0
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
11
Q2
23
Q3
17
Q4
0
WoS (JCR)
Q1
6
Q2
11
Q3
12
Q4
23
TR Index
10
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
3
Ort. yüzdelik
55.3%
Üst %1 payı
0.0%
Üst %10 payı
6.4%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2026 Increased Red Blood Cell Count With High Hemoglobin Indicates a Different Diagnosis From Beta-thalassemia Trait, Regardless of Mean Corpuscular Volume YÖKSİS SJR Q3 JCR Q3 OpenAlex 38.5%
- 2025 Cobalamin J disorder in a teenage boy with recurrent abdominal pain attacks: A case report and literature review YÖKSİS SJR Q3 JCR Q4 OpenAlex 4.8%
- 2025 DNA damage in children with β-thalassemia minor: genotoxicity assessment by comet assay YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 78.4%
- 2024 HbA2 levels in children with β-thalassemia trait associated with iron deficiency: A perspective for pediatricians YÖKSİS SJR Q1 JCR Q3 OpenAlex 83.9%
- 2022 Fresh Frozen Plasma Plus Iron Therapy in Congenital Hypotransferrinemia in the Second Decade: A Dynamic Approach to Maintaining Hematological Stability YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 19.4%
- 2021 A Novel Mutation p.Asp374Val of SERPINC1 in a Turkish Family with İnherited Antithrombin Deficiency YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 79.3%
- 2020 Is Hemoglobin D Trait Hematologically Silent YÖKSİS SJR Q3 JCR Q4 OpenAlex 51.3%
- 2019 Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome YÖKSİS SJR Q2 JCR Q4 OpenAlex 11.2%
- 2018 Formulas for the Detection β-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters YÖKSİS SJR Q3 JCR Q4 OpenAlex 4.8%
- 2018 The search for new approaches to treating type 1 plasminogen deficiency YÖKSİS SJR Q1 JCR Q1 OpenAlex 47.0%
- 2018 Addition of oral iron to plasma transfusion in human congenital hypotransferrinemia: A 10-year observational follow-up with the effects on hematological parameters and growth YÖKSİS SJR Q1 JCR Q1 OpenAlex 54.6%
- 2017 Maternal serum alpha-fetoprotein levels are normal in Fanconi anemia: Can it be a lack of postnatal inhibition of iAFP/i gene resulting in the elevation? YÖKSİS SJR Q1 JCR Q1 OpenAlex 63.4%
- 2017 title Protein modelling to understand iFGB/i mutations leading to congenital hypofibrinogenaemia/title YÖKSİS SJR Q1 JCR Q2 OpenAlex 84.2%
- 2016 Recessive congenital methemoglobinemia in immediate generations YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex üst %10 OpenAlex 90.1%
- 2016 "Silent" beta-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A(2) YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 61.3%
- 2016 Harris Platelet Syndrome in Patients of Non-Indian Origin YÖKSİS SJR Q2 JCR Q4 OpenAlex 4.9%
- 2016 title Specific mosaic iKRAS/i mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis/title YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 96.5%
- 2014 Oculoectodermal syndrome: report of a new case with a broad clinical spectrum YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.7%
- 2013 Leukopenia in Familial Mediterranean Fever: Case Series and Literature Review with Special Emphasis on Pathogenesis YÖKSİS SJR Q2 JCR Q3 OpenAlex 60.2%
- 2009 Primary Hemophagocytic Lymphohistiocytosis in Turkish Children YÖKSİS SJR Q2 JCR Q4 OpenAlex 50.0%