Prof. Dr. Fatih ÇELMELİ

1. Multidimensional Assessment of Patient-Reported-Outcomes in a Multicenter Cohort of Inborn Errors of Immunity

Yorgun Altunbas M., Sefer A. P., Bilgic-Eltan S., Yildirimcakar C., Ozturk P., Dikici Ü., et al.

Journal of Clinical Immunology , cilt.46, sa.1, 2026 (SCI-Expanded, Scopus)

2. Inborn Errors of Immunity in Pediatric Intensive Care: Prevalence, Characteristics, and Prognosis

ÇELMELİ F., Oz A., KIHTIR H. S., ONGUN E. A., Tekmenuray-Unal A., CEYLANER S., et al.

Journal of Clinical Immunology , cilt.45, sa.1, 2025 (SCI-Expanded, Scopus)

3. Ruxolitinib treatment ameliorates clinical, immunologic, and transcriptomic aberrations in patients with STAT3 gain-of-function disease

Bayram Catak F., Catak M. C., Babayeva R., Toubia J., Warnock N. I., ÇELMELİ F., et al.

Journal of Allergy and Clinical Immunology , cilt.155, sa.3, ss.784-791, 2025 (SCI-Expanded, Scopus)

4. Evaluation of Meibography Findings and Ocular Surface Parameters in Children with Atopic Dermatitis Without Eye Complaints

Sabancı Ş., Küçükkeleş H., ÇELMELİ F., Yavuz S.

Children , cilt.12, sa.2, 2025 (SCI-Expanded, Scopus)

5. Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature

Bosticardo M., Dobbs K., Delmonte O. M., Martins A. J., Pala F., Kawai T., et al.

Science Immunology , cilt.10, sa.103, 2025 (SCI-Expanded, Scopus)

6. 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

ERMAN B., Aba U., Ipsir C., Pehlivan D., Aytekin C., Cildir G., et al.

Journal of Clinical Immunology , cilt.44, sa.7, 2024 (SCI-Expanded, Scopus)

7. 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)

8. 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)

9. 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)

10. 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)

11. Human stat3 variants underlie autosomal dominant hyper-igesyndromebynegativedominance

Asano T., Khourieh J., Zhang P., Rapaport F., Spaan A. N., Li J., et al.

Journal of Experimental Medicine , cilt.218, sa.8, 2021 (SCI-Expanded, Scopus)

12. CARD9 mutation in a patient with Candida albicans meningoencephalitis; A case report Candida albicans meningoensefaliti olan bir hastada CARD9 mutasyonu; Bir olgu raporu

Kuruoğlu T., Çelik M., ÇELMELİ F., Tanyel E.

Mikrobiyoloji Bulteni , cilt.55, sa.4, ss.656-664, 2021 (SCI-Expanded, Scopus, TRDizin)

13. Hematopoietic stem cell transplantation in CD40 ligand deficiency: A single-center experience

KOCACIK UYGUN D. F., Uygun V., Karasu G. T., Daloğlu H., Öztürkmen S. I., ÇELMELİ F., et al.

Pediatric Transplantation , cilt.24, sa.6, 2020 (SCI-Expanded, Scopus)

14. Transient anisocoria during wheezy infant treatment due to ipratropium-bromide Hışıltılı İnfant tedavisinde İpratropium-bromide baǧlı geçici anizokori

ÇELMELİ F., ÇELİK T., Özkiraz S., ÇELİK Ü.

Cocuk Enfeksiyon Dergisi , cilt.6, sa.1, ss.30-31, 2012 (Scopus, TRDizin)

Prof. Dr. Fatih ÇELMELİ

Yayınlar & Eserler

1. Multidimensional Assessment of Patient-Reported-Outcomes in a Multicenter Cohort of Inborn Errors of Immunity

2. Inborn Errors of Immunity in Pediatric Intensive Care: Prevalence, Characteristics, and Prognosis

3. Ruxolitinib treatment ameliorates clinical, immunologic, and transcriptomic aberrations in patients with STAT3 gain-of-function disease

4. Evaluation of Meibography Findings and Ocular Surface Parameters in Children with Atopic Dermatitis Without Eye Complaints

5. Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature

6. 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

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

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

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

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

11. Human stat3 variants underlie autosomal dominant hyper-igesyndromebynegativedominance

12. CARD9 mutation in a patient with Candida albicans meningoencephalitis; A case report Candida albicans meningoensefaliti olan bir hastada CARD9 mutasyonu; Bir olgu raporu

13. Hematopoietic stem cell transplantation in CD40 ligand deficiency: A single-center experience

14. Transient anisocoria during wheezy infant treatment due to ipratropium-bromide Hışıltılı İnfant tedavisinde İpratropium-bromide baǧlı geçici anizokori

Yayın

Yayın (WoS)

Yayın (Scopus)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Proje

Tez Danışmanlığı

Açık Erişim