Akademisyen
İSMAİL REİSLİ
PROFESÖR
NECMETTİN ERBAKAN ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk İmmünolojisi ve Alerji Hastalıkları
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 109
- Proje 0
- Kitap 9
- Bildiri 0
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
48
Q2
15
Q3
13
Q4
4
WoS (JCR)
Q1
45
Q2
14
Q3
15
Q4
8
TR Index
12
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
2
Üst %10 makale
17
Ort. yüzdelik
66.7%
Üst %1 payı
2.3%
Üst %10 payı
19.5%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2026 Successful Treatment of POLD1 Deficiency With HSCT:Report of Two Years' Experience YÖKSİS SJR Q2 JCR Q3 OpenAlex 38.5%
- 2025 The effect of virtual reality on pain and fear levels of children with primary immunodeficiency applying intravenous immunoglobulin during intravenous access: A crossover randomized controlled trial YÖKSİS SJR Q1 JCR Q1 OpenAlex 34.8%
- 2025 Machine learning–assisted diagnosis classification of primary immune dysregulation using IDDA2.1 phenotype profiling YÖKSİS SJR Q1 JCR Q1 OpenAlex 71.1%
- 2025 CD19 Deficiency Leads to Dysregulation of Phosphoinositide 3-Kinase-Protein Kinase B (PI3K/AKT) and Nuclear Factor Kappa B (NF-κB) Pathways: Implications for B-Cell Maturation and Immune Function YÖKSİS TR Index JCR Q4 OpenAlex 55.6%
- 2025 Anticancer activity of thymoquinone in non-small cell lung cancer and possible involvement of PPAR- γ pathway YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 98.2%
- 2025 Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry YÖKSİS SJR Q2 JCR Q2 OpenAlex 57.4%
- 2025 Pediatric selective IgM deficiency: clinical features and a preliminary risk index for immunoglobulin replacement therapy YÖKSİS SJR Q3 JCR Q3 OpenAlex 46.4%
- 2025 Epidemiology and management of malignancies in patients with inborn errors of immunity—An ESID registry study of 19,959 patients YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 90.0%
- 2025 Expansion of Myeloid‐Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B‐Cell Deficiency in X‐Linked Agammaglobulinemia YÖKSİS SJR Q2 JCR Q3 OpenAlex 23.0%
- 2025 Evaluation of the Interaction Between Wharton’s Jelly-Derived Mesenchymal Stem Cells and β-Mercaptoethanol YÖKSİS JCR Q2 OpenAlex 68.6%
- 2025 Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia YÖKSİS SJR Q3 JCR Q3 OpenAlex 17.4%
- 2025 Multi-class machine learning-based classification of SCID-related genetic variants YÖKSİS SJR Q3 JCR Q3 OpenAlex 59.4%
- 2024 Investigation of Transcription Factor and Cytokine Gene Expression Levels in Helper T Cell Subsets Among Turkish Patients Diagnosed with ICF2 (Novel ZBTB24 gene Variant) and ICF3 (CDCA7 Variant) Syndrome YÖKSİS SJR Q1 JCR Q1 OpenAlex 60.3%
- 2024 MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort YÖKSİS SJR Q1 JCR Q1 OpenAlex 78.0%
- 2024 Chronic granulomatous disease: A single-center experience in Central Anatolia YÖKSİS SJR Q2 JCR Q2 OpenAlex 52.4%
- 2024 Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye YÖKSİS SJR Q1 JCR Q1 OpenAlex 86.5%
- 2024 Clinical efficacy of SARS‐CoV‐2 Omicron‐neutralizing antibodies in immunoglobulin preparations for the treatment of agammaglobulinemia in patients with primary antibody deficiency YÖKSİS SJR Q1 JCR Q1 OpenAlex 74.6%
- 2024 Molecular investigations on T cell subsets in patients affected by hypomorphic DCLRE1C mutation YÖKSİS SJR Q2 JCR Q2 OpenAlex 51.7%
- 2024 Molecular investigations on T cell subsets in patients affected by hypomorphic DCLRE1C mutation YÖKSİS SJR Q2 JCR Q2 OpenAlex 51.7%
- 2024 Variable clinical presentation of hypomorphic DCLRE1C deficiency from childhood to adulthood YÖKSİS SJR Q1 JCR Q1 OpenAlex 69.6%