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ŞÜKRÜ NAİL GÜNER
PROFESÖR
NECMETTİN ERBAKAN ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk İmmünolojisi ve Allerji Hastalıkları (Çocuk Sağlığı ve Hastalıkları)
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 130
- Proje 0
- Kitap 0
- Bildiri 0
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
46
Q2
22
Q3
23
Q4
26
WoS (JCR)
Q1
39
Q2
13
Q3
21
Q4
38
TR Index
20
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
2
Üst %10 makale
4
Ort. yüzdelik
83.9%
Üst %1 payı
28.6%
Üst %10 payı
57.1%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2025 Expansion of Myeloid‐Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B‐Cell Deficiency in X‐Linked Agammaglobulinemia YÖKSİS SJR Q2 JCR Q3
- 2025 Pediatric selective IgM deficiency: clinical features and a preliminary risk index for immunoglobulin replacement therapy YÖKSİS SJR Q3 JCR Q3
- 2025 Chronic granulomatous disease: A single-center experience in Central Anatolia YÖKSİS SJR Q2 JCR Q2
- 2025 Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia YÖKSİS SJR Q3 JCR Q3
- 2025 Enhancing the Prediction of Inborn Errors of Immunity: Integrating Jeffrey Modell Foundation Criteria with Clinical Variables Using Machine Learning YÖKSİS SJR Q1 JCR Q1
- 2025 Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry YÖKSİS SJR Q2 JCR Q2
- 2025 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 Q2
- 2024 Association of NK cell subsets and cytotoxicity with FCGR3A gene polymorphism in functional NK cell deficiency YÖKSİS SJR Q3 JCR Q2
- 2024 Molecular investigations on T cell subsets in patients affected by hypomorphic DCLRE1C mutation YÖKSİS SJR Q2 JCR Q2
- 2024 Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency YÖKSİS SJR Q1 JCR Q1
- 2024 Newborn screening for SCID: the very first prospective pilot study from Türkiye YÖKSİS SJR Q1 JCR Q1
- 2024 MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort YÖKSİS SJR Q1 JCR Q1
- 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
- 2024 Variable clinical presentation of hypomorphic DCLRE1C deficiency from childhood to adulthood YÖKSİS SJR Q1 JCR Q1
- 2023 Retrospective analysis of patients with severe combined immunodeficiency and alternative diagnostic criteria: A 20‐year single centre experience YÖKSİS SJR Q2 JCR Q3
- 2023 Could immune cells be associated with nephropathy in Fabry disease patients? YÖKSİS SJR Q2 JCR Q3
- 2023 Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome YÖKSİS SJR Q3 JCR Q4
- 2023 Clinical and laboratory evaluation of Turkish children with IgG subclass deficiency YÖKSİS SJR Q2 JCR Q2
- 2023 The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.4%
- 2023 Identification of the Mutation in DCLRE1C Gene by PCR-RFLP YÖKSİS