Prof. Dr. Ferah GENEL

1. Clinical, Immunological Findings, and Outcomes of Children with Ataxia-Telangiectasia: A Single Center Experience

Cetinoglu S., Ozen S., Haci I. A., Taskirdi I., AKÇAL Ö., Kaya M. S., et al.

Pediatric, Allergy, Immunology, and Pulmonology , cilt.39, sa.1-2, ss.30-35, 2026 (SCI-Expanded, Scopus)

2. Tuberculosis in Children With Primary Immunodeficiencies: A 13-Year Retrospective Experience

Ozbakir H., Yuksel N. C., Ergun D., Kacar P., Kahraman Cetin B., Ozer A., et al.

Pediatric Pulmonology , cilt.61, sa.1, 2026 (SCI-Expanded, Scopus)

3. Abatacept restores dysregulated transcriptomic and proteomic profile in disorders of CTLA-4 insufficiency

Catak M. C., Surucu N., Bayram Catak F., Kara A., Cildir S., Babayeva R., et al.

Journal of Allergy and Clinical Immunology , cilt.156, sa.6, ss.1725-1742, 2025 (SCI-Expanded, Scopus)

4. Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia

Artac H., Ceylan A., Kulhas Celik I., Celebi Celik F., KARALI Y., Meric Z., et al.

Immunologic Research , cilt.73, sa.1, 2025 (SCI-Expanded, Scopus)

5. Expansion of Myeloid-Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B-Cell Deficiency in X-Linked Agammaglobulinemia

Ceylan A., Kulhas Celik I., Keles S., Celebi Celik F., KARALI Y., Meric Z., et al.

Scandinavian Journal of Immunology , cilt.102, sa.5, 2025 (SCI-Expanded, Scopus)

6. Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry

Chavoshzadeh Z., Fallah S., Zeinali V., Sharafian S., Delavari S., Mesdaghi M., et al.

Frontiers in Genetics , cilt.16, 2025 (SCI-Expanded, Scopus)

7. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort

Gulec Koksal Z., BİLGİÇ ELTAN S., Topyildiz E., Sezer A., Keles S., Celebi Celik F., et al.

Journal of Allergy and Clinical Immunology: In Practice , cilt.12, sa.9, ss.2490, 2024 (SCI-Expanded, Scopus)

8. Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants

Aykut A., Durmaz A., Karaca N., GÜLEZ N., GENEL F., ÇELMELİ F., et al.

Immunologic Research , cilt.72, sa.4, ss.714-726, 2024 (SCI-Expanded, Scopus)

9. Extended Phenotype of VPS45 Defect with Additional Features of Combined Immunodeficiency and Neuromotor Developmental Delay Along with Severe Congenital Neutropenia

Kostel Bal S., İSLAMOĞLU C., HASKOLOĞLU Z. Ş., Karaman S., Jimenez-Heredia R., Segarra Roca A., et al.

Asthma Allergy Immunology , cilt.22, sa.3, ss.269-276, 2024 (ESCI, Scopus, TRDizin)

10. Successful management of delayed-onset adenosine deaminase deficiency with novel mutation

Çelik F. Ç., Soyöz Ö., Bölük S. Ö., Taşklrdl I., Hacl I. A., Kaya M. Å., et al.

Personalized Medicine , cilt.21, sa.1, ss.11-19, 2024 (SCI-Expanded, Scopus)

11. Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency

Taghizade N., Babayeva R., Kara A., Karakus I. S., Catak M. C., Bulutoglu A., et al.

Journal of Allergy and Clinical Immunology , cilt.152, sa.6, ss.1634-1645, 2023 (SCI-Expanded, Scopus)

12. Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1

Erdem S., HASKOLOĞLU Z. Ş., Haliloglu Y., Celikzencir H., Arik E., Keskin O., et al.

Clinical Immunology , cilt.253, 2023 (SCI-Expanded, Scopus)

13. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity

BARIŞ S., Abolhassani H., Massaad M. J., Al-Nesf M., Chavoshzadeh Z., Keles S., et al.

Journal of Allergy and Clinical Immunology: In Practice , cilt.11, sa.1, ss.158, 2023 (SCI-Expanded, Scopus)

14. Symptoms, clinical profile and management of pediatric hereditary angioedema: A single-centre

Bölük S. Ö., Akçal Ö., Taşkırdı İ., Hacı İ. A., Kaya M. Ş., Çelik F. Ç., et al.

Trends in Pediatrics , cilt.4, sa.3, ss.192-198, 2023 (Scopus, TRDizin)

15. The effect of subcutaneous immunoglobulin replacement therapy on serum IgG levels in patients with primary immunodeficiency

Bölük S. Ö., Akçal Ö., Taşkırdı İ., Hacı İ. A., Kaya M. Ş., Çelik F. Ç., et al.

Trends in Pediatrics , cilt.4, sa.2, ss.103-108, 2023 (Scopus, TRDizin)

16. Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency

Ogishi M., Arias A. A., Yang R., Han J., Zhang P., Rinchai D., et al.

Journal of Experimental Medicine , cilt.219, sa.10, 2022 (SCI-Expanded, Scopus)

17. Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency

Catak M. C., Akcam B., BİLGİÇ ELTAN S., Babayeva R., Karakus I. S., Akgun G., et al.

Allergy: European Journal of Allergy and Clinical Immunology , cilt.77, sa.10, ss.3108-3123, 2022 (SCI-Expanded, Scopus)

18. Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants

Aykut A., Durmaz A., Karaca N., GÜLEZ N., GENEL F., ÇELMELİ F., et al.

Scandinavian Journal of Immunology , cilt.95, sa.6, 2022 (SCI-Expanded, Scopus)

19. Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

Aghamohammadi A., Rezaei N., Yazdani R., Delavari S., Kutukculer N., Topyildiz E., et al.

Journal of Clinical Immunology , cilt.41, sa.6, ss.1339-1351, 2021 (SCI-Expanded, Scopus)

20. Autoimmune and inflammatory manifestations in pediatric patients with primary immunodeficiencies and their importance as a warning sign

KAPLAN M., Ozen S., Akcal O., GÜLEZ N., GENEL F.

Allergologia et Immunopathologia , cilt.48, sa.6, ss.701-710, 2020 (SCI-Expanded, Scopus)

21. Molecular analysis and clinical findings of griscelli syndrome patients

Durmaz A., Ozkinay F., Onay H., Tombuloglu M., Atay A., GÜRSEL O., et al.

Journal of Pediatric Hematology/Oncology , cilt.34, sa.7, ss.541-544, 2012 (SCI-Expanded, Scopus)

Prof. Dr. Ferah GENEL

Yayınlar & Eserler

1. Clinical, Immunological Findings, and Outcomes of Children with Ataxia-Telangiectasia: A Single Center Experience

2. Tuberculosis in Children With Primary Immunodeficiencies: A 13-Year Retrospective Experience

3. Abatacept restores dysregulated transcriptomic and proteomic profile in disorders of CTLA-4 insufficiency

4. Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia

5. Expansion of Myeloid-Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B-Cell Deficiency in X-Linked Agammaglobulinemia

6. Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry

7. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort

8. Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants

9. Extended Phenotype of VPS45 Defect with Additional Features of Combined Immunodeficiency and Neuromotor Developmental Delay Along with Severe Congenital Neutropenia

10. Successful management of delayed-onset adenosine deaminase deficiency with novel mutation

11. Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency

12. Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1

13. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity

14. Symptoms, clinical profile and management of pediatric hereditary angioedema: A single-centre

15. The effect of subcutaneous immunoglobulin replacement therapy on serum IgG levels in patients with primary immunodeficiency

16. Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency

17. Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency

18. Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants

19. Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

20. Autoimmune and inflammatory manifestations in pediatric patients with primary immunodeficiencies and their importance as a warning sign

21. Molecular analysis and clinical findings of griscelli syndrome patients

Yayın

Yayın (WoS)

Yayın (Scopus)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Atıf (TrDizin)

H-İndeks (TrDizin)

Atıf (Diğer Toplam)

Tez Danışmanlığı

Açık Erişim