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Academician profile · PROFESÖR

ESİN FİGEN DOĞU

ANKARA ÜNİVERSİTESİ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk İmmünolojisi ve Allerji Hastalıkları (Çocuk Sağlığı ve Hastalıkları)
  • TIP FAKÜLTESİ
  • DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Articles YÖKSİS 245 OpenAlex 82
Projects 1
Books 0
Proceedings 196
Patents 1
Artistic 1
Scopus (SJR)
Q1 99 Q2 31 Q3 29 Q4 11
WoS (JCR)
Q1 74 Q2 37 Q3 25 Q4 34
TR Index 30 articles

Scopus (SJR)

WoS (JCR)

TR Index

30 articles

YÖKSİS: 245 · OpenAlex: 82

Articles

  1. 2026 Nuclear Factor Kappa B ( NF ‐ κB )1 and NF ‐ κB2 Deficiency: An Unpredictable Defect With Wide Clinical and Immunologic Phenotype Scandinavian Journal of Immunology DOI 10.1111/sji.70142
  2. 2026 Clinical spectrum and survival outcomes of malignancies in pediatric patients with inborn errors of immunity Frontiers in Immunology DOI 10.3389/fimmu.2026.1904173
  3. 2026 Ichthyosis prematurity syndrome mimicking hyper‐ IgE syndrome due to a novel SLC27A4 variant Pediatric Allergy and Immunology DOI 10.1111/pai.70459
  4. 2025 Successful Use of Anakinra in a Patient with IL-10R Beta Deficiency: A Case Report Pediatric Allergy, Immunology, and Pulmonology DOI 10.1089/ped.2024.0116
  5. 2025 Double Trouble: A DOCK8- and CFI-Deficient Infant Presenting With Acute Necrotizing Meningoencephalitis Pediatric Infectious Disease Journal DOI 10.1097/INF.0000000000004766
  6. 2025 Comprehensive αβ T-Cell Receptor Repertoire Analysis Reveals a Unique CD8+ TCR Landscape in DOCK8-Deficient Patients. Allergy DOI 10.1111/all.16580
  7. 2025 Long-term outcome of bone marrow transplantation in NIK deficiency: non-redundant role of non-canonical NF-κB signaling in thymic reconstitution and secondary lymphoid organ development. Frontiers in immunology DOI 10.3389/fimmu.2025.1682642
  8. 2025 Hematopoietic stem cell transplantation for purine nucleoside phosphorylase deficiency: an EBMT-IEWP retrospective study Blood Journal DOI 10.1182/blood.2025029640
  9. 2025 Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry Frontiers in Genetics DOI 10.3389/fgene.2025.1584681
  10. 2025 Evaluation of Patients with Combined Immunodeficiency: A Single Center Experience Iranian Journal of Immunology DOI 10.22034/iji.2025.103499.2844
  11. 2025 Clinical and immunological spectrum of MHC class I deficiency: insights from a long-term cohort with two novel mutations Frontiers in Immunology DOI 10.3389/fimmu.2025.1675097
  12. 2025 Hematopoietic Stem Cell Transplantation in Severe Combined Immunodeficiency at the Pediatric Intensive Care Unit: Case Series of 5 Severe Combined Immunodeficiency Patients Turkish Archives of Pediatrics DOI 10.5152/turkarchpediatr.2025.24334
  13. 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 Journal of Clinical Immunology DOI 10.1007/s10875-024-01759-w
  14. 2024 Junctional Epidermolysis Bullosa Linked to Homozygous Mutation in LAMC2 Gene: A Case Report With Eosinophil-Rich Inflammatory Infiltrate American Journal of Dermatopathology DOI 10.1097/DAD.0000000000002714
  15. 2024 Varicella‐Zoster Virus Reactivation After Pediatric Allogeneic Hematopoietic Stem Cell Transplantation, Single‐Center Experience of Acyclovir Prophylaxis Pediatric Transplantation DOI 10.1111/petr.14819
  16. 2024 Two different diseases in two adolescent girls with the same clinic: Allergic bronchopulmonary aspergillosis Tuberk Toraks DOI 10.5578/tt.202404964
  17. 2024 Normal mean platelet volume and thrombocytopenia: It may still be Wiskott–Aldrich syndrome Pediatric Allergy and Immunology DOI 10.1111/pai.14206
  18. 2024 Pediatric Plasmablastic Lymphoma in the Setting of CD70 Deficiency Journal of Pediatric Hematology/Oncology DOI 10.1097/MPH.0000000000002948
  19. 2024 Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency? Turkish Archives of Pediatrics DOI 10.5152/TurkArchPediatr.2023.23157
  20. 2024 GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway Springer Science and Business Media LLC DOI 10.1038/s41590-023-01691-y

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