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SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Diverse Clinical and Immunological Profiles in Patients with IPEX Syndrome: a Multicenter Analysis from Turkey

Bekis Bozkurt H., Bayram Catak F., Sahin A., Yalcin Gungoren E., Gemici Karaarslan B., Yakici N., et al.
Journal of Clinical Immunology , cilt.45, sa.1, 2025 (SCI-Expanded) identifier identifier
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    • Readers: 16
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Inborn Errors of Immunity in Pediatric Intensive Care: Prevalence, Characteristics, and Prognosis

Celmeli 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) identifier identifier
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  • Citations
    • Citation Indexes: 1
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    • Readers: 7
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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) identifier
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    • Abstract Views: 6
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    • Readers: 3
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Insights into Patient Experiences with Facilitated Subcutaneous Immunoglobulin Therapy in Primary Immune Deficiency: A Prospective Observational Cohort

Yalcin Gungoren E., YORĞUN ALTUNBAŞ M., Dikici U., Meric Z., ESER ŞİMŞEK I., KIYKIM A., et al.
Journal of Clinical Immunology , cilt.44, sa.8, 2024 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 4
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TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome

Werren E. A., LaForce G. R., Srivastava A., Perillo D. R., Li S., Johnson K., et al.
Nature Communications , cilt.15, sa.1, 2024 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 2
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    • Abstract Views: 1
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    • Readers: 10
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    • News Mentions: 1
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DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans

Azizoglu Z. B., Babayeva R., HASKOLOĞLU Z. Ş., Acar M. B., Ayaz-Guner S., Okus F. Z., et al.
Journal of Clinical Immunology , cilt.44, sa.8, 2024 (SCI-Expanded) identifier identifier
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    • Readers: 5
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    • Shares, Likes & Comments: 18
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Long-term immunological changes after corrective cardiac surgery

Bilgic-Eltan S., Amirov R., Babayeva R., Yorgun Altunbas M., Karakurt T., Can S., et al.
Scandinavian Journal of Immunology , cilt.100, sa.6, 2024 (SCI-Expanded) identifier identifier
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    • Citation Indexes: 1
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    • Readers: 3
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Delineating the Clinical and Immunologic Characteristics: A Comparative Study of Inborn Errors of Immunity in Adult versus Pediatric Diagnosed

Karabiber E., BARIŞ S.
International Archives of Allergy and Immunology , cilt.185, sa.11, ss.1123-1135, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier
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  • Citations
    • Citation Indexes: 2
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    • Readers: 12
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    • News Mentions: 1
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DOCK8 deficiency due to a deep intronic variant in two kindreds with hyper-IgE syndrome

Oktelik F. B., Wang M., Keles S., Eke Gungor H., Cansever M., CAN S., et al.
Clinical Immunology , cilt.268, 2024 (SCI-Expanded) identifier identifier
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    • Readers: 1
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LTβR deficiency causes lymph node aplasia and impaired B cell differentiation

Ransmayr B., Bal S. K., Thian M., Svaton M., van de Wetering C., Hafemeister C., et al.
Science Immunology , cilt.9, sa.101, 2024 (SCI-Expanded) identifier identifier
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    • Readers: 4
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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) identifier identifier
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    • Readers: 6
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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, ss.157, 2024 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 1
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    • Readers: 10
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Neurocognitive Impairment in Patients With Ataxia Telangiectasia and Their Unaffected Parents: Is It Similar?

UYAR E., Akturk H., Usanmaz S., KIYKIM A., Tufan A. E., Alibas H., et al.
Pediatric Neurology , cilt.156, ss.85-90, 2024 (SCI-Expanded) identifier identifier
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    • Readers: 7
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Regulatory T-cell dysfunction and cutaneous exposure to Staphylococcus aureus underlie eczema in DOCK8 deficiency.

Wilkie H., Das M., Pelovitz T., Bainter W., Woods B., Alasharee M., et al.
The Journal of allergy and clinical immunology , cilt.154, sa.1, ss.143-156, 2024 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 6
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    • Readers: 6
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Artemis deficiency: A large cohort including a novel variant with increased radiosensitivity

Meric Z., Gemici Karaaslan B., Yalcin Gungoren E., Bektas Hortoglu M., Cavas T., Aydemir S., et al.
Pediatric Allergy and Immunology , cilt.35, sa.6, 2024 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 2
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    • Readers: 6
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Rapamycin Controls Lymphoproliferation and Reverses T-Cell Responses in a Patient with a Novel STIM1 Loss-of-Function Deletion.

Karakus I. S., Catak M. C., Frohne A., Bayram Catak F., Yorgun Altunbas M., Babayeva R., et al.
Journal of clinical immunology , cilt.44, sa.4, ss.94, 2024 (SCI-Expanded) Creative Commons License identifier identifier
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  • Citations
    • Citation Indexes: 2
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    • Readers: 3
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Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease: an open-label phase 2 and 3 study

ÖZEN A. O., Chongsrisawat V., Sefer A. P., KOLUKISA B., Jalbert J. J., Meagher K. A., et al.
The Lancet , cilt.403, sa.10427, ss.645-656, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 14
  • Captures
    • Readers: 34
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GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway

Park A. Y., Leney-Greene M., Lynberg M., Gabrielski J. Q., Xu X., Schwarz B., et al.
Nature Immunology , cilt.25, sa.2, ss.282-293, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier
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  • Citations
    • Citation Indexes: 7
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    • Readers: 11
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    • News Mentions: 1
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Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond

Sharma M., Suratannon N., Leung D., BARIŞ S., Takeuchi I., Samra S., et al.
Trends in Immunology , cilt.45, sa.2, ss.138-153, 2024 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 16
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    • Readers: 26
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Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study

Hägele P., Staus P., Scheible R., Uhlmann A., Heeg M., Klemann C., et al.
The Lancet Haematology , cilt.11, sa.2, 2024 (SCI-Expanded) identifier identifier identifier
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    • Citation Indexes: 1
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    • Readers: 18
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Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome

Bilgic Eltan S., Nain E., Catak M. C., Ezen E., Sefer A. P., Karimi N., et al.
Journal of Clinical Immunology , cilt.44, sa.1, 2024 (SCI-Expanded) identifier identifier
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    • Citation Indexes: 5
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    • Readers: 15
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Intrafamilial clinical variability of CTLA-4 insufficiency hindering early diagnosis.

Karadaǧ Ş., Hancloǧlu G., Akçam B., Altundağ E., Barlś S., Ylldlran A.
Klinische Padiatrie , cilt.236, sa.1, ss.39-42, 2024 (SCI-Expanded) identifier identifier
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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.
The Journal of allergy and clinical immunology , cilt.152, ss.1634-1645, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 16
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    • Readers: 44
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Atypical Localization of Eczema Discriminates DOCK8 or STAT3 Deficiencies from Atopic Dermatitis

Kasap N., Kara A., Celik V., Bilgic Eltan S., Akay Haci I., KÖSE H., et al.
Journal of Clinical Immunology , cilt.43, sa.8, ss.1882-1890, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 2
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    • Readers: 7
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Outcomes of Hematopoietic Stem Cell Gene Therapy for Wiskott-Aldrich Syndrome.

Labrosse R., Chu J., Armant M., Everett J. K., Pellin D., Kareddy N., et al.
Blood , cilt.142, ss.1281-1296, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 13
  • Captures
    • Readers: 77
  • Mentions
    • News Mentions: 1
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    • Shares, Likes & Comments: 10
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Activated phosphoinositide 3-kinase d syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

Maccari M., Wolkewitz M., Schwab C., Lorenzini T., Leiding J., Aladjdi N., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.152, sa.4, 2023 (SCI-Expanded) identifier

Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients.

Yakici N., Kreins A. Y., Catak M. C., Babayeva R., Erman B., Kenney H., et al.
Clinical immunology (Orlando, Fla.) , cilt.255, ss.109757, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 7
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    • Readers: 7
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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

Maccari M. E., Wolkewitz M., Schwab C., Lorenzini T., Leiding J. W., Aladjdi N., et al.
The Journal of allergy and clinical immunology , cilt.152, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 12
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    • Readers: 49
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    • Shares, Likes & Comments: 23
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Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis

Kostel Bal S., Giuliani S., Block J., Repiscak P., Hafemeister C., Shahin T., et al.
Blood , cilt.142, sa.9, ss.827-845, 2023 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier
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  • Citations
    • Citation Indexes: 4
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    • Readers: 28
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    • News Mentions: 1
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Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1

Erdem S., Haskologlu S., Haliloglu Y., Celikzencir H., Arik E., Keskin O., et al.
Clinical Immunology , cilt.253, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 2
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    • Readers: 6
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    • Shares, Likes & Comments: 15
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Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6

BARIŞ S., Benamar M., Chen Q., Catak M. C., Martínez-Blanco M., Wang M., et al.
Journal of Allergy and Clinical Immunology , cilt.152, sa.1, ss.182, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 38
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    • Readers: 30
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    • News Mentions: 2
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    • Shares, Likes & Comments: 22
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Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

Oftedal B. E., Assing K., BARIŞ S., Safgren S. L., Johansen I. S., Jakobsen M. A., et al.
iScience , cilt.26, sa.6, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 15
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    • Readers: 26
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    • Shares, Likes & Comments: 27
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Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.

Leiding J. W., Vogel T. P., Santarlas V. G. J., Mhaskar R., Smith M. R., Carisey A., et al.
The Journal of allergy and clinical immunology , cilt.151, ss.1081-1095, 2023 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 33
  • Usage
    • Downloads: 3
    • Abstract Views: 1
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    • Readers: 95
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    • News Mentions: 1
    • References: 1
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    • Shares, Likes & Comments: 1
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The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children

Benamar M., Chen Q., Chou J., Julé A. M., Boudra R., Contini P., et al.
JOURNAL OF CLINICAL INVESTIGATION , cilt.133, sa.1, 2023 (SCI-Expanded) Creative Commons License identifier identifier identifier
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  • Citations
    • Citation Indexes: 19
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    • Readers: 17
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    • News Mentions: 1
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    • Shares, Likes & Comments: 25
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The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity

Baris 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, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 37
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    • Readers: 44
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    • Shares, Likes & Comments: 1
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Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency

Lévy R., Gothe F., Momenilandi M., Magg T., Materna M., Peters P., et al.
JOURNAL OF EXPERIMENTAL MEDICINE , cilt.220, sa.2, 2022 (SCI-Expanded) Creative Commons License identifier identifier identifier
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  • Citations
    • Citation Indexes: 10
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    • Readers: 22
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Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry

Jamee M., Azizi G., BARIŞ S., Karakoc-Aydiner E., ÖZEN A. O., KILIÇ GÜLTEKİN S. Ş., et al.
CLINICAL IMMUNOLOGY , cilt.244, 2022 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 13
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    • Readers: 49
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Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency

Catak M. C., Akcam B., Bilgic Eltan S., Babayeva R., Karakus I. S., Akgun G., et al.
ALLERGY , cilt.77, sa.10, ss.3108-3123, 2022 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 20
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    • Readers: 19
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A Stk4-Foxp3-NF-κB p65 transcriptional complex promotes Treg cell activation and homeostasis

Cui Y., Benamar M., Schmitz-Abe K., Poondi-Krishnan V., Chen Q., Jugder B., et al.
Science immunology , cilt.7, sa.75, 2022 (SCI-Expanded) identifier identifier identifier
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    • Citation Indexes: 14
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    • Readers: 24
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Increased radiosensitivity and impaired DNA repair in patients with STAT3-LOF and ZNF341 deficiency, potentially contributing to malignant transformations

Cekic S., Huriyet H., Hortoglu M., Kasap N., Ozen A. O., Karakoc-Aydiner E., et al.
CLINICAL AND EXPERIMENTAL IMMUNOLOGY , cilt.209, sa.1, ss.83-89, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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    • Citation Indexes: 5
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Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency

Ozturk E., Catak M. C., Kiykim A., Baser D., Bilgic Eltan S., Yalcin K., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, sa.5, ss.1036-1050, 2022 (SCI-Expanded) identifier identifier identifier
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    • Citation Indexes: 11
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    • Readers: 8
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Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency

Sefer A. P., Abolhassani H., Ober F., KAYAOĞLU B., Eltan S. B., Kara A., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, sa.3, ss.634-652, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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    • Citation Indexes: 22
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    • Readers: 25
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Expanding the clinical and immunological phenotypes and natural history of MALT1 deficiency

Sefer A. P., Abolhassani H., KAYAOĞLU B., Ober F., Bilgic-Eltan S., Kara A., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, sa.SUPPL 1, 2022 (SCI-Expanded) identifier

Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency

Yilmaz N. S., Eltan S. B., KAYAOĞLU B., Geckin B., Heredia R. J., Sefer A. P., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, ss.582-596, 2022 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 5
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    • Readers: 16
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    • Shares, Likes & Comments: 24
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Mucus sialylation determines intestinal host-commensal homeostasis.

Yao Y., Kim G., Shafer S., Chen Z., Kubo S., Ji Y., et al.
Cell , cilt.185, sa.7, 2022 (SCI-Expanded) Creative Commons License identifier identifier identifier
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  • Citations
    • Citation Indexes: 128
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    • Readers: 203
  • Social Media
    • Shares, Likes & Comments: 22
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Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency

Kolukisa B., Baser D., Akcam B., Danielson J., Bilgic Eltan S., Haliloglu Y., et al.
ALLERGY , cilt.77, sa.3, ss.1004-1019, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 34
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    • Readers: 51
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    • News Mentions: 1
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A boy with a novel homozygous ZAP70 mutation presenting with a dermatological phenotype and postnatal decrease in CD8(+) T cells

Babayeva R., Mongellaz C., Karakus I. S., Cansever M., Bilgic Eltan S., Catak M. C., et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.33, sa.3, 2022 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 6
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Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls

Senturk G., Ng Y. Y., Eltan S. B., Baser D., Ogulur I., Altindirek D., et al.
SCANDINAVIAN JOURNAL OF IMMUNOLOGY , cilt.95, 2022 (SCI-Expanded) identifier identifier identifier
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    • Citation Indexes: 6
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    • Readers: 16
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A Novel ATM Gene Mutation Affecting Splicing in an Ataxia-Telangiectasia Patient

Ates E. A., TÜRKYILMAZ A., Eltan S. B., BARIŞ S., GÜNEY A. İ.
MOLECULAR SYNDROMOLOGY , cilt.13, sa.1, ss.80-84, 2022 (SCI-Expanded) identifier identifier identifier
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    • Readers: 7
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Primary antibody deficiencies in Turkey: molecular and clinical aspects

Firtina S., Ng Y. Y., HATIRNAZ NG Ö., Kiykim A., Ozek E. Y., Kara M., et al.
IMMUNOLOGIC RESEARCH , cilt.70, sa.1, ss.44-55, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 3
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Adverse COVID-19 outcomes in immune deficiencies: Inequality exists between subclasses.

AYDINER E., Eltan S., Babayeva R., Aydiner O., KEPENEKLİ KADAYİFCİ E., KOCAMIŞ B., et al.
Allergy , cilt.77, sa.1, ss.282-295, 2022 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 36
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    • Readers: 54
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    • Shares, Likes & Comments: 36
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Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease

Kubo S., Fritz J. M., Raquer-McKay H. M., Kataria R., Vujkovic-Cvijin I., Al-Shaibi A., et al.
NATURE IMMUNOLOGY , cilt.23, sa.1, ss.75-101, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 9
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    • Readers: 42
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Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

Thalhammer J., Kindle G., Nieters A., Rusch S., Seppanen M. R. J., Fische A., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.148, sa.5, ss.1332-1346, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier
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  • Citations
    • Citation Indexes: 53
  • Captures
    • Readers: 137
  • Mentions
    • News Mentions: 1
    • References: 1
  • Social Media
    • Shares, Likes & Comments: 6
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Impaired respiratory burst contributes to infections in PKC-deficient patients

Neehus A., Moriya K., Nieto-Patlán A., Le Voyer T., Lévy R., Özen A. O., et al.
JOURNAL OF EXPERIMENTAL MEDICINE , cilt.218, sa.9, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 25
  • Captures
    • Readers: 50
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Reversal clinical and immunological effects of abatacept in patients with LRBA and CTLA4 deficiencies

BARIŞ S., Babayeva R., Catak M. C., Baser D., Eltan S. B., Akgun G., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.77, 2021 (SCI-Expanded) identifier

Autoinflammatory manifestations as a result of an elevated type I IFN signature in a case of NEMO deficiency

Yilmaz N. S., Eltan S. B., KAYAOĞLU B., Geckin B., Sozeri B., KIYKIM A., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.370, 2021 (SCI-Expanded) identifier

CHAPLE disease and non-CHAPLE protein losing enteropathies: natural history and immune characteristics

Selcuk M., Sefer A. P., Baser D., Ogulur I., Eltan S. B., Dursun E., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.83, 2021 (SCI-Expanded) identifier

Impaired respiratory burst contributes to infections in PKC delta-deficient patients

Neehus A. L., Moriya K., Patlan A. N., Le Voyer T., Levy R., Yildiran A., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.348, 2021 (SCI-Expanded) identifier

A novel frameshift mutation in Malt1 gene resulted in defective TCR signaling and impaired immune response to fungal ligands

KAYAOĞLU B., Yilmaz N., Baydemir I., Aydin Y., Yilmaz A. P., ERMAN B., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.329, 2021 (SCI-Expanded) identifier

The mechanism of LRBA dependent CTLA-4 surface expression in regulatory T cell lymphocytes

Zahedimaram P., Erman B., Baris S.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.359, 2021 (SCI-Expanded) identifier

Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency

ÇAĞDAŞ AYVAZ D. N., Mayr D., BARIŞ S., Worley L., Langley D. B., Metin A., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.6, ss.1272-1290, 2021 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 25
  • Captures
    • Readers: 47
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Genomic investigation into early onset protein-losing enteropathies: therapeutic implications and insights into clusters of shared pathomechanisms

Sefer A. P., AYDINER E., Urganci N., Kiykim E., Baysoy G., Fisher M., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.371, 2021 (SCI-Expanded) identifier

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

Aghamohammadi A., Rezaei N., Yazdani R., Delavari S., KÜTÜKÇÜLER N., Topyildiz E., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, ss.1339-1351, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 22
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    • Readers: 41
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Development of a pseudovirus-based assay for analysis of neutralizing activity against SARS-CoV-2 in convalescent plasma

Aras M., Pamukcu C., Celik E., Ergun E. Z., Karahan Z. S., Turkoz G., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.368, 2021 (SCI-Expanded) identifier

Characterization of Th17 and Treg cells in leucocyte adhesion deficiency 1 patients

Erdem S., Haliloglu Y., Haskaloglu S., Arik E., Keskin O., Karadag S. I. K., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.298, 2021 (SCI-Expanded) identifier

Adverse COVID outcomes in youngsters with immune deficiencies; inequality exists between subclasses

AYDINER E., Eltan S. B., Babayeva R., Aydiner O., KEPENEKLİ KADAYİFCİ E., KOLUKISA B., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.285, 2021 (SCI-Expanded) identifier

Reference values for T and B lymphocyte subpopulations in Turkish children and adults.

Besci Ö., Başer D., Öğülür İ., Berberoğlu A. C., Kıykım A., Besci T., et al.
TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.30, sa.51 (4), ss.1814-1824, 2021 (SCI-Expanded)

Single cell sequencing of peripheral mononuclear cells reveals CHAPLE-specific distinct signaling pathways

Ogulur I., Kim J., Ruckert B., Pat Y., AYDINER E., BARIŞ S., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.372, 2021 (SCI-Expanded) identifier

Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

Aydemir S., Islek A., Nepesov S., Yaman Y., Baysoy G., Beser O. F., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.6, ss.1406-1410, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 4
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    • Readers: 5
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GIMAP5 maintains liver endothelial cell homeostasis and prevents portal hypertension

Drzewiecki K., Choi J., Brancale J., Leney-Greene M. A., Sari S., Dalgiç B., et al.
JOURNAL OF EXPERIMENTAL MEDICINE , cilt.218, sa.7, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 29
  • Captures
    • Readers: 28
  • Mentions
    • News Mentions: 2
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Two patients with chronic mucocutaneous candidiasis caused by TRAF3IP2 deficiency

Shafer S., Yao Y., Comrie W., Cook S., Zhang Y., Yesil G., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.148, sa.1, ss.256-263, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 12
  • Captures
    • Readers: 11
  • Social Media
    • Shares, Likes & Comments: 2
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Lymphopenia with Low T and NK Cells in a Patient with USB1 Mutation, Rare Findings in Clericuzio-Type Poikiloderma with Neutropenia

Bilgic Eltan S., Sefer A. P., Karakus İ. S., ÖZEN A. O., Karakoc-Aydiner E., BARIŞ S.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.5, ss.1106-1111, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 4
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Comprehensive comparison between 222 CTLA-4 haploinsufficiency and 212 LRBA deficiency patients: a systematic review.

Jamee M., Hosseinzadeh S., Sharifinejad N., Zaki-Dizaji M., Matloubi M., Hasani M., et al.
Clinical and experimental immunology , cilt.205, sa.1, ss.28-43, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 52
    • Patent Family Citations: 1
  • Captures
    • Readers: 54
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Mesenchymal stem cells derived from human dental follicle modulate the aberrant immune response in atopic dermatitis

Zibandeh N., Genc D., Özgen Z., Duran Y., Goker K., Barış S., et al.
IMMUNOTHERAPY , cilt.13, ss.825-840, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 4
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    • Readers: 15
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Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4(+) T cell perturbations

Zemmour D., Charbonnier L., Leon J., Six E., KELEŞ S., Delville M., et al.
NATURE IMMUNOLOGY , cilt.22, sa.5, ss.607-619, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 38
  • Captures
    • Readers: 133
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Stepwise Reversal of Immune Dysregulation Due to STAT1 Gain-of-Function Mutation Following Ruxolitinib Bridge Therapy and Transplantation

Kayaoglu B., Kasap N., Yilmaz N. S., Charbonnier L. M., Geckin B., Akcay A., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.4, ss.769-779, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 34
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    • Readers: 26
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CARMIL2 Deficiency And Various Clinical Phenotypes: Warning Signs For Early Diagnosis

Kolukisa B. K., Kasap N., Eltan S. B., Baser D., Akgun G., Sefer A. P., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, 2021 (SCI-Expanded) identifier

Heterozygous AIRE Mutation in a Family with Multiple Autoimmune Organ Involvement

Sefer A. P., Kolukisa B. K., Akcam B., Demirkol Y. K., Aydiner E., Ozen A., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.SUPPL 1, 2021 (SCI-Expanded) identifier

The evaluation of radiosensitivity in patients with STAT3 deficiency

ÇEKİÇ Ş., Huriyet H., BEKTAŞ HORTOĞLU M., Baris S., Metin A., Ozen A. O., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, 2021 (SCI-Expanded) identifier

Homozygous IL37 mutation associated with infantile inflammatory bowel disease

Zhang Z. Z., Zhang Y., He T., Sweeney C. L., Baris S., Karakoc-Aydiner E., et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.118, sa.10, 2021 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 20
  • Captures
    • Readers: 34
  • Social Media
    • Shares, Likes & Comments: 125
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Primary Immune Regulatory Disorders and Targeted Therapies

Kolukısa B., Barış S.
Turkish journal of haematology : official journal of Turkish Society of Haematology , cilt.38, sa.1, ss.1-14, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier identifier
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  • Citations
    • Citation Indexes: 13
  • Captures
    • Readers: 35
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Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimickingATM-mutated patients

ÖĞÜLÜR İ., Ertuzun T., KOCAMIŞ B., Kendir Demirkol Y., UYAR E., KIYKIM A., et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.32, sa.2, ss.349-357, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 5
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    • Readers: 9
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Broadly effective metabolic and immune recovery with C5 inhibition in CHAPLE disease

Ozen A. O., Kasap N., Vujkovic-Cvijin I., Apps R., Cheung F., Karakoc-Aydiner E., et al.
NATURE IMMUNOLOGY , cilt.22, sa.2, ss.128-151, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier
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  • Citations
    • Citation Indexes: 38
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    • Readers: 59
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A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis

Kasap N., Celik V., Isik S., Cennetoglu P., Kiykim A., Eltan S. B., et al.
CLINICAL IMMUNOLOGY , cilt.223, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 9
  • Captures
    • Readers: 31
  • Social Media
    • Shares, Likes & Comments: 200
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Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

Meyts I., Bucciol G., Quinti I., Neven B., Fischer A., Seoane E., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.147, sa.2, ss.520-531, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 297
    • Policy Citations: 2
  • Captures
    • Readers: 449
  • Mentions
    • Blog Mentions: 1
    • News Mentions: 5
  • Social Media
    • Shares, Likes & Comments: 15
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Immune alterations in subacute sclerosing panencephalitis reflect an incompetent response to eliminate the measles virus

Yentur S. P., Demirbilek V., Gurses C., BARIŞ S., Kuru U., Ayta S., et al.
PLOS ONE , cilt.16, sa.1, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 2
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    • Readers: 13
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Novel Frameshift Autosomal Recessive Loss-of-Function Mutation inSMARCD2Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

Yucel E., Karakus I. S., Krolo A., KIYKIM A., Heredia R. J., Tamay Z., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.1, ss.59-65, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 8
  • Captures
    • Readers: 24
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Reference values for T and B lymphocyte subpopulations in Turkish children and adults

Bescİ Ö., BaŞer D., ÖĞÜlÜr İ., BerberoĞlu A. C., Kiykim A., Bescİ T., et al.
TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.51, sa.4, ss.1814-1824, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier identifier
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  • Citations
    • Citation Indexes: 20
  • Usage
    • Downloads: 665
    • Abstract Views: 237
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    • Readers: 26
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Immune dysfunction in inborn errors of immunity causing malignancies

BARIŞ S., KOCAMIŞ B.
EXPERT REVIEW OF CLINICAL IMMUNOLOGY , cilt.17, ss.695-699, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 7
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    • Readers: 7
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A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells

Sefer A. P., Charbonnier L. M., Kasap N., Akcam B., Demirkol Y. K., Eltan S. B., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.1, ss.251-255, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 6
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    • Readers: 3
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Prevalence of allergic disorders and risk factors associated with food allergy in Turkish preschoolers

Aksoy A. G., BORAN P., Karakoc-Aydiner E., Gokcay G., TAMAY Z. Ü., Devecioglu E., et al.
ALLERGOLOGIA ET IMMUNOPATHOLOGIA , cilt.49, sa.1, ss.11-16, 2021 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 14
  • Captures
    • Readers: 32
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Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

Ghosh S., Köstel B., Edwards E., Pillay B., Jiménez H., Erol C., et al.
BLOOD , cilt.136, sa.23, ss.2638-2655, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 72
  • Captures
    • Readers: 147
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Mutational landscape of severe combined immunodeficiency patients from Turkey

Firtina S., Ng Y. Y., Ng O. H., Kiykim A., AYDINER E., Nepesov S., et al.
INTERNATIONAL JOURNAL OF IMMUNOGENETICS , cilt.47, sa.6, ss.529-538, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 17
  • Captures
    • Readers: 21
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Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort

Baris H. E., Ogulur I., Akcam B., Kiykim A., Karagoz D., Saraymen B., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , cilt.8, sa.10, ss.3525-3535, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 11
  • Captures
    • Readers: 17
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A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma

Harb H., Stephen-Victor E., Crestani E., Benamar M., Massoud A., Cui Y., et al.
NATURE IMMUNOLOGY , cilt.21, sa.11, ss.1359-1386, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 86
    • Patent Family Citations: 1
  • Captures
    • Readers: 103
  • Mentions
    • News Mentions: 1
  • Social Media
    • Shares, Likes & Comments: 47
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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

Lorenzini T., Fliegauf M., Klammer N., Frede N., Proietti M., Bulashevska A., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.146, sa.4, ss.901-911, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 29
    • Policy Citations: 2
  • Captures
    • Readers: 126
  • Social Media
    • Shares, Likes & Comments: 11
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Hematopoietic stem cell transplantation in CD40 ligand deficiency: A single-center experience

KOCACIK UYGUN D. F., Uygun V., Karasu G. T., Daloglu H., Ozturkmen S. I., Celmeli F., et al.
PEDIATRIC TRANSPLANTATION , cilt.24, sa.6, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 1
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    • Readers: 16
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The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study

Cekic S., Metin A., Aytekin C., Edeer Karaca N., Baris S., Karali Y., et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.31, sa.5, ss.528-536, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 14
  • Captures
    • Readers: 25
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Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty

Kirkgoz T., Karakoc-Aydiner E., Bugrul F., Yavas Abali Z., Helvacioglu D., Kiykim A., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.93, sa.1, ss.66-72, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 8
  • Captures
    • Readers: 17
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All together to Fight COVID-19

Momtazmanesh S., Ochs H. D., Uddin L. Q., Perc M., Routes J. M., Vieira D. N., et al.
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE , cilt.102, sa.6, ss.1181-1183, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 83
  • Captures
    • Readers: 289
  • Social Media
    • Shares, Likes & Comments: 47
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Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.

Tesch V., Abolhassani H., Shadur B., Zobel J., Mareika Y., Sharapova S., et al.
The Journal of allergy and clinical immunology , cilt.145, ss.1452-1463, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 116
  • Captures
    • Readers: 135
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ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients

Eken A., Cansever M., Okus F. Z., Erdem S., Nain E., Azizoglu Z. B., et al.
Allergy: European Journal of Allergy and Clinical Immunology , cilt.75, sa.4, ss.921-932, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 18
  • Captures
    • Readers: 28
  • Social Media
    • Shares, Likes & Comments: 29
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Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

Kiykim A., Eker N., Surekli O., Nain E., Kasap N., Aktürk H., et al.
Pediatric Blood and Cancer , cilt.67, sa.2, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 16
  • Captures
    • Readers: 16
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Immediate adverse reactions to intravenous immunoglobulin in primary immune deficiencies: A single center experience

Nain E., Kıykım A., Kasap N. A., BARIŞ S., Özen A. O., Aydıner E. K.
Turkish Journal of Pediatrics , cilt.62, sa.3, ss.379-386, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 8
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Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype

Nain E., ÜLGEN Ö., Kiykim A., Aydiner E., Ozen A. O., BARIŞ S.
CLINICAL IMMUNOLOGY , cilt.210, 2020 (SCI-Expanded) identifier identifier identifier
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    • Readers: 2
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Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency.

Ogulur I., Kiykim A., Baser D., Karakoc-Aydiner E., Ozen A. O., Baris S.
International archives of allergy and immunology , cilt.181, sa.3, ss.228-237, 2020 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 17
  • Captures
    • Readers: 15
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Multiple Brain Abscesses Due to Actinomyces Odontolyticus: A Rare Infection In a Previously Healthy Child

Saritas B., Duramaz B. B., Yesilbas O., Nizam O. G., ÖZTANIR M. N., Tekin A., et al.
EUROPEAN JOURNAL OF PEDIATRICS , cilt.178, sa.11, ss.1720, 2019 (SCI-Expanded) identifier

Immune system defects in DiGeorge syndrome and association with clinical course.

Nain E., Kiykim A., ÖĞÜLÜR İ., Kasap N., Karakoc-Aydiner E., Ozen A. O., et al.
Scandinavian journal of immunology , cilt.90, sa.5, 2019 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 9
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    • Readers: 30
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Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress.

Conde C. D., Petronczki Ö. Y., Baris S., Willmann K. L., Girardi E., Salzer E., et al.
The Journal of clinical investigation , cilt.129, sa.10, ss.4194-4206, 2019 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 41
  • Captures
    • Readers: 63
  • Social Media
    • Shares, Likes & Comments: 16
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How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty

KIRKGÖZ T., Karakoc E., Kiykim A., Bugrul F., Helvacioglu D., Eltan S. B., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.185, 2019 (SCI-Expanded) identifier

A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency

Firtina S., Cipe F., Ng Y. Y., KIYKIM A., Ng O. H., Sudutan T., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.39, sa.2, ss.144-147, 2019 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 6
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    • Readers: 6
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Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency.

Farmer J. R., Foldvari Z., Ujhazi B., De Ravin S. S., Chen K., Bleesing J. J., et al.
The journal of allergy and clinical immunology. In practice , cilt.7, sa.6, 2019 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 70
  • Captures
    • Readers: 116
  • Mentions
    • News Mentions: 1
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Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation.

Kiykim A., Charbonnier L. M., Akcay A., Karakoc-Aydiner E., Ozen A. O., Ozturk G., et al.
Journal of clinical immunology , cilt.39, sa.1, ss.37-44, 2019 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 35
    • Policy Citations: 1
  • Captures
    • Readers: 52
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Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies

Kiykim A., Karakoc-Aydiner E., Gunes E., Nain E., Öğülür İ., Yazici D., et al.
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.178, sa.1, ss.1-9, 2019 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 4
    • Policy Citations: 1
  • Captures
    • Readers: 50
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Basic immunology-humoral

BARIŞ S.
Turkish Journal of Hematology , cilt.36, ss.3, 2019 (SCI-Expanded) identifier identifier

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency.

Kiykim A., Ogulur I., Dursun E., Charbonnier L. M., Nain E., Cekic S., et al.
The journal of allergy and clinical immunology. In practice , cilt.7, sa.8, 2019 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 127
  • Captures
    • Readers: 89
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Group 3 innate Iymphoid cells are absent DOCK8- defective HIES patients

EKEN A., Okuş F. Z., PATIROĞLU T., Erdem Ş., Karakükçü m., CANSEVER M., et al.
Journal Of Immunology , cilt.200, ss.17025, 2018 (SCI-Expanded)

ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome

Cagdas D., Gur Cetinkaya P., Karaatmaca B., Esenboga S., TAN Ç., Yılmaz T., et al.
Journal of Clinical Immunology , cilt.38, sa.4, ss.484-493, 2018 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 30
  • Captures
    • Readers: 70
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Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry.

Maccari M. E., Abolhassani H., Aghamohammadi A., Aiuti A., Aleinikova O., Bangs C., et al.
Frontiers in immunology , cilt.9, ss.543, 2018 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 163
    • Policy Citations: 1
  • Captures
    • Readers: 132
  • Mentions
    • News Mentions: 2
  • Social Media
    • Shares, Likes & Comments: 45
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Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation

Alroqi F. J., Charbonnier L., BARIŞ S., Kiykim A., Chou J., Platt C. D., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.141, sa.3, ss.1050-1069, 2018 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 87
    • Patent Family Citations: 1
  • Captures
    • Readers: 86
  • Mentions
    • News Mentions: 1
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Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.

Barzaghi F., Hernandez L. C. A., Neven B., Ricci S., Kucuk Z. Y., Bleesing J. J., et al.
The Journal of allergy and clinical immunology , cilt.141, sa.3, 2018 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 251
  • Captures
    • Readers: 297
  • Mentions
    • News Mentions: 1
    • References: 2
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A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity.

Béziat V., Li J., Lin J., Ma C., Li P., Bousfiha A., et al.
SCIENCE IMMUNOLOGY , cilt.3, 2018 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 150
    • Policy Citations: 1
  • Captures
    • Readers: 127
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Acute myeloid leukemia in a child with dedicator of cytokinesis 8 (DOCK8) deficiency

Kuskonmaz B., Ayvaz D., BARIŞ S., Unal S., Tezcan I., Uckan D.
PEDIATRIC BLOOD & CANCER , cilt.64, sa.12, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 7
  • Captures
    • Readers: 14
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Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

Petersen B., August D., Abt R., Alddafari M., Atarod L., BARIŞ S., et al.
Inflammatory bowel diseases , cilt.23, sa.12, ss.2109-2120, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 27
  • Captures
    • Readers: 57
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A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients

Pronicka E., Ropacka-Lesiak M., Trubicka J., Pajdowska M., Linke M., Ostergaard E., et al.
JOURNAL OF INHERITED METABOLIC DISEASE , cilt.40, sa.6, ss.853-860, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 25
    • Policy Citations: 1
  • Captures
    • Readers: 58
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Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2

van den Boogaard M. L., Thijssen P. E., Aytekin C., Licciardi F., Kiykim A. A., Spossito L., et al.
CLINICAL GENETICS , cilt.92, sa.4, ss.380-387, 2017 (SCI-Expanded) identifier
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  • Citations
    • Citation Indexes: 30
  • Captures
    • Readers: 37
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IL12R beta 1 defect presenting with massive intra-abdominal lymphadenopathy due to Mycobacterium intracellulare infection

KepenekliKadayifci E., Karaaslan A., Atici S., Akkoc G., BARIŞ S., YAKUT N., et al.
ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY , cilt.35, sa.3, ss.161-165, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 6
  • Captures
    • Readers: 58
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Predictive risk factors for relapse after cessation of inhaled corticosteroids in well-controlled childhood asthma

akturk h., Karakoc-Aydiner E., ÖZEN A. O., Baris S., akkoc T., bahceciler n., et al.
MINERVA PEDIATRICA , cilt.69, sa.4, ss.274-280, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 2
  • Captures
    • Readers: 32
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CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

Ozen A. O., Comrie W. A., Ardy R. C., Conde C. D., Dalgıç B., Beser O. F., et al.
The New England journal of medicine , cilt.377, sa.1, ss.52-61, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 155
    • Patent Family Citations: 2
    • Policy Citations: 2
  • Captures
    • Readers: 183
  • Mentions
    • News Mentions: 13
    • References: 3
  • Social Media
    • Shares, Likes & Comments: 1
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Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication.

Aghamohammadi A., Hassan A., KÜTÜKÇÜLER N., Wassilak S. G., Pallansch M. A., Kluglein S., et al.
Frontiers in immunology , cilt.8, ss.685, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 50
    • Policy Citations: 14
  • Captures
    • Readers: 78
  • Social Media
    • Shares, Likes & Comments: 19
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Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide.

Shah N. N., Freeman A. F., Su H., Cole K., Parta M., Moutsopoulos N. M., et al.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation , cilt.23, sa.6, ss.980-990, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 44
  • Captures
    • Readers: 64
  • Social Media
    • Shares, Likes & Comments: 12
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Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis.

ÖĞÜLÜR İ., Kiykim A., BARIŞ S., Ozen A. O., Yuce E. G., Karakoc-Aydiner E.
International journal of pediatric otorhinolaryngology , cilt.97, ss.197-201, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 11
  • Captures
    • Readers: 21
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Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?

Kiykim A., MUMCU G., ÖĞÜLÜR İ., Karakoc-Aydiner E., Direskeneli H., BARIŞ S., et al.
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.174, sa.1, ss.52-56, 2017 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 2
  • Captures
    • Readers: 44
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Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

Baris S., Alroqi F., Kiykim A., Karakoc-Aydiner E., ÖĞÜLÜR İ., Ozen A. O., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.36, sa.7, ss.641-648, 2016 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 77
  • Captures
    • Readers: 103
  • Mentions
    • References: 3
  • Social Media
    • Shares, Likes & Comments: 12
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School Board Policies on Prevention and Management of Anaphylaxis in İstanbul: Where Do We Stand?

ÖZEN A. O., BORAN P., torlak f., Karakoc-Aydiner E., barış s., KARAVUŞ M., et al.
Balkan medical journal , cilt.33, sa.5, ss.539-542, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 6
  • Captures
    • Readers: 38
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House Dust Mites Confer a Distinct Immunological Feature among Dermatitis

BARIŞ S., Ozen A. O., Akdeniz T., Karakoc-Aydiner E., Aydin O., ERCAN SARIÇOBAN H., et al.
IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY , cilt.15, sa.4, ss.264-274, 2016 (SCI-Expanded) identifier identifier identifier

The effect of systemic corticosteroids on the innate and adaptive immune system in children with steroid responsive nephrotic syndrome.

Baris H. E., BARIŞ S., Karakoc-Aydiner E., GÖKCE İ., YILDIZ N., Cicekkoku D., et al.
European journal of pediatrics , cilt.175, sa.5, ss.685-93, 2016 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 30
  • Captures
    • Readers: 44
  • Mentions
    • News Mentions: 1
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Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.

Kiykim A., Garncarz W., Karakoc-Aydiner E., Ozen A. O., KIYKIM E., Yesil G., et al.
Clinical immunology (Orlando, Fla.) , cilt.165, ss.1-3, 2016 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 19
  • Captures
    • Readers: 21
  • Mentions
    • References: 2
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Two patients with novel missense mutation in the purine nucleoside phosphorylase gene without serious or recurrent infections

Kiykim A., Simsek I. E., Kiykim E., Karakoc-Aydiner E., BARIŞ S., ÖZEN A. O., et al.
Clinical and Experimental Neuroimmunology , cilt.7, sa.1, ss.79-82, 2016 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 4
  • Captures
    • Readers: 3
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G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

Kiykim A., BARIŞ S., Karakoc-Aydiner E., ÖZEN A. O., ÖĞÜLÜR İ., Bozkurt S., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.37, sa.8, ss.616-622, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 23
    • Patent Family Citations: 1
  • Captures
    • Readers: 51
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Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study.

Demirca B. P., Cagan H., Kiykim A., Arig U., Arpa M., Tulunay A., et al.
Respiratory medicine , cilt.109, sa.9, ss.1120-5, 2015 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 7
    • Policy Citations: 3
  • Captures
    • Readers: 59
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Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.

Kiykim A., ÖĞÜLÜR İ., BARIŞ S., Salzer E., Karakoc-Aydiner E., ÖZEN A. O., et al.
Journal of clinical immunology , cilt.35, sa.6, ss.523-6, 2015 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 33
  • Captures
    • Readers: 32
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JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family.

Baris S., Karakoc-Aydiner E., Ozen A. O., Delil K., Kiykim A., Ogulur I., et al.
Journal of clinical immunology , cilt.35, sa.4, ss.339-43, 2015 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 20
  • Captures
    • Readers: 20
  • Social Media
    • Shares, Likes & Comments: 27
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The Association of TLR4 and NOD2 Polymorphisms and Febrile Neutropenia in Children with Burkitt Lymphoma

Ozdemir N., Guven M., Batar B., BARIŞ S., Tun O., Celkan T.
UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.25, sa.1, ss.70-71, 2015 (SCI-Expanded) identifier identifier
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  • Captures
    • Readers: 2
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Long-Term Effect of Sublingual and Subcutaneous Immunotherapy in Dust Mite-Allergic Children With Asthma/Rhinitis: A 3-Year Prospective Randomized Controlled Trial.

Karakoc-Aydiner E., Eifan A., BARIŞ S., Gunay E., Akturk E., AKKOÇ T., et al.
Journal of investigational allergology & clinical immunology , cilt.25, sa.5, ss.334-42, 2015 (SCI-Expanded) identifier identifier identifier

Granzyme B gene polymorphism associated with subacute sclerosing panencephalitis

Yentur S. P., Aydin H. N., Gurses C., Demirbilek V., Kuru U., Uysal S., et al.
Neuropediatrics , cilt.45, sa.5, ss.309-313, 2014 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 12
  • Captures
    • Readers: 6
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Clinical Heterogeneity of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked: Pulmonary Involvement as a Non-Classical Disease Manifestation

BARIŞ S., Schulze I., Ozen A. O., AYDINER E., Altuncu E., Karasu G. T., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.34, sa.6, ss.601-606, 2014 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 32
  • Captures
    • Readers: 47
  • Social Media
    • Shares, Likes & Comments: 1
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Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite.

Baris S., Kiykim A., Ozen A. O., Tulunay A., Karakoc-Aydiner E., Barlan I. B.
Allergy , cilt.69, sa.2, ss.246-53, 2014 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 82
    • Policy Citations: 4
  • Captures
    • Readers: 113
  • Social Media
    • Shares, Likes & Comments: 2
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Alteration in humoral immunity is common among family members of patients with common variable immunodeficiency.

Karakoc-Aydiner E., ÖZEN A. O., Bans S., ercan h., ozdemir c., barlan i. b.
Journal of investigational allergology & clinical immunology , cilt.24, sa.5, ss.346-51, 2014 (SCI-Expanded) identifier identifier identifier

Performance comparison of machine learning methods for prognosis of hormone receptor status in breast cancer tissue samples

KALINLI A., Sarikoc F., AKGÜN H., ÖZTÜRK F.
COMPUTER METHODS AND PROGRAMS IN BIOMEDICINE , cilt.110, sa.3, ss.298-307, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 15
  • Captures
    • Readers: 46
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Predictors of atopic dermatitis phenotypes and severity: Roles of serum immunoglobulins and filaggrin gene mutation R501X

Ercan H., Ispir T., Kirac D., Baris S., Ozen A. O., Oztezcan S., et al.
ALLERGOLOGIA ET IMMUNOPATHOLOGIA , cilt.41, sa.2, ss.86-93, 2013 (SCI-Expanded) identifier
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  • Citations
    • Citation Indexes: 13
  • Captures
    • Readers: 21
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Inhaled alpha 1-Antitrypsin Administered to Treat Pneumatocele in Autosomal Dominant Hyperimmunoglobulin E Syndrome

Karakoc-Aydiner E., Baris S., Keles S., Ozdemir C., Chatila T., Barlan I.
JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY , cilt.23, sa.5, ss.359-361, 2013 (SCI-Expanded) identifier

The phenotype-genotype relationship in severe congenital neutropenia patients

BARIŞ S., Aydiner E., Kiykim A., Çaǧan H. H., Boztug K., Barlan I.
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.47, sa.4, ss.272-277, 2012 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 3
  • Captures
    • Readers: 11
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Childhood urticaria and angioedema: pathogenesis, diagnosis and therapy

Barlan I., Baris S.
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.47, sa.4, ss.235-239, 2012 (SCI-Expanded) identifier identifier
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  • Captures
    • Readers: 2
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DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation

Jabara H. H., McDonald D. R., Janssen E., Massaad M. J., Ramesh N., Borzutzky A., et al.
NATURE IMMUNOLOGY , cilt.13, sa.6, ss.612-622, 2012 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 192
    • Policy Citations: 1
  • Usage
    • Abstract Views: 14
  • Captures
    • Readers: 186
  • Social Media
    • Shares, Likes & Comments: 13
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DNA repair gene XPD and XRCC1 polymorphisms and the risk of febrile neutropenia and mucositis in children with leukemia and lymphoma

Ozdemir N., Celkan T., BARIŞ S., Batar B., Guven M.
LEUKEMIA RESEARCH , cilt.36, sa.5, ss.565-569, 2012 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 17
  • Captures
    • Readers: 21
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Abnormal IL-7 signaling may lead to the loss of bone mineral density in common variable immunodeficiency

Khan S.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.23, sa.2, ss.202, 2012 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 1
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    • Readers: 3
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Experience with intravenous immunoglobulin in severe childhood atopic dermatitis

Ozen A. O., BARIŞ S., AYDINER E., Yucelten D., Bahceciler N. N.
ALLERGOLOGIA ET IMMUNOPATHOLOGIA , cilt.40, sa.2, ss.131-133, 2012 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 10
  • Captures
    • Readers: 13
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Abnormal IL-7 signaling may lead to the loss of bone mineral density in common variable immunodeficiency Reply

BARIŞ S., Barlan I.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.23, sa.2, ss.204, 2012 (SCI-Expanded) identifier identifier
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    • Readers: 1
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Comparison of Color Doppler US and CT Portography in Evaluating Portal Hypertension in Children

Adaletli I., Baris S., Gulsen G., Kurugoglu S., Kantarci F., Mihmanli I., et al.
SOUTHERN MEDICAL JOURNAL , cilt.105, sa.1, ss.6-10, 2012 (SCI-Expanded) identifier
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  • Citations
    • Citation Indexes: 3
  • Captures
    • Readers: 8
  • Social Media
    • Shares, Likes & Comments: 153
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THE ASSOCIATION OF TOLL-LIKE 4 (TLR-4) AND NOD2 POLYMORPHISMS AND FEBRILE NEUTROPENIA IN CHILDREN WITH BURKITT LYMPHOMA

Ozdemir N., Guven M., Batar B., Apak H., Tuysuz G., BARIŞ S., et al.
PEDIATRIC BLOOD & CANCER , cilt.57, sa.5, ss.844, 2011 (SCI-Expanded) identifier

Osteoporosis: An ignored complication of CVID

BARIŞ S., Ozen A. O., ERCAN SARIÇOBAN H., Karakoc-Aydiner E., Cagan H., Ozdemir C., et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.22, sa.7, ss.676-683, 2011 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 17
    • Policy Citations: 1
  • Captures
    • Readers: 24
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Papaverine chloride as a topical vasodilator in accidental injection of adrenaline into a digital finger

Baris S., Saricoban H. E., Ak K., Ozdemir C.
ALLERGY , cilt.66, sa.11, ss.1495-1496, 2011 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 5
  • Captures
    • Readers: 6
  • Mentions
    • News Mentions: 1
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Multislice computed tomography angiography is a sufficient method for detecting native aortic coarctation in children

ADALETLİ İ., BARIŞ S., Kilic F., Ozdil M., Guzeltas A., Demir T., et al.
TURK GOGUS KALP DAMAR CERRAHISI DERGISI-TURKISH JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY , cilt.19, sa.3, ss.361-365, 2011 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 2
  • Captures
    • Readers: 1
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Serum immunoglobulin levels as a predictive factor for a better outcome of non-atopic childhood asthma

BARIŞ S., Karakoc-Aydiner E., Ozen A. O., Ozdemir C., Bahceciler N. N., Barlan I. B.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.22, sa.3, ss.298-304, 2011 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 10
    • Policy Citations: 1
  • Captures
    • Readers: 17
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An Adolescent with Hyperimmunoglobulinemia D and Periodic Fever Syndrome Responding to Simvastatin Treatment

Karakoç-Aydiner E., Özdemir C., Keleş S., BARIŞ S., Bahçeciler N. N., Barlan I. B.
TURKISH JOURNAL OF RHEUMATOLOGY , cilt.26, sa.2, ss.167-170, 2011 (SCI-Expanded) identifier identifier
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    • Readers: 7
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Efficacy of Intravenous Immunoglobulin Treatment in Children with Common Variable Immunodeficiency

BARIŞ S., ercan h., cagan h., ÖZEN A. O., Karakoc-Aydiner E., Ozdemir C., et al.
JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY , cilt.21, sa.7, ss.514-521, 2011 (SCI-Expanded) identifier identifier identifier

Current and future concepts in treatment of childhood atopic dermatitis Çocukluklarda atopik dermatit tedavisinde güncel ve gelecek yaklaşımlar

Aydiner E. K., BARIŞ S., Özdemir C.
Guncel Pediatri , cilt.9, sa.1, ss.39-43, 2011 (SCI-Expanded) identifier

Acquired origin of the left anterior descending coronary artery from the pulmonary artery: A complication of the arterial switch operation

Saltik L., BARIŞ S., Ozyilmaz I., Eroǧlu A. G.
Annals of Pediatric Cardiology , cilt.4, sa.1, ss.60-61, 2011 (SCI-Expanded) identifier identifier
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    • Readers: 3
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Outcome of hypogammaglobulinemia in children: Immunoglobulin levels as predictors

ÖZEN A. O., Baris S., Karakoc-Aydiner E., Ozdemir C., Bahceciler N., Barlan I.
CLINICAL IMMUNOLOGY , cilt.137, sa.3, ss.374-383, 2010 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 32
  • Captures
    • Readers: 29
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Treatment of Pediatric Burkitt Lymphoma in Turkey

Celkan T. T., BARIŞ S., Ozdemir N., Ozkan A., Apak H., Dogru Ö., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.32, sa.7, 2010 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 7
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    • Readers: 22
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Acute Promyelocytic Leukemia Treated With Idarubicin Complicated by Focal Segmental Glomerulosclerosis

Bariş S., Özdil M., Topal N., Doğru Ö., Özdemir N., Sever L., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.32, sa.2, 2010 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 10
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    • Readers: 12
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Renovascular hypertension in a child with marfan syndrome Marfan sendromlu bir çocukta renovasküler hipertansiyon

Çivilibal M., Çalişkan S., Numan F., Bariş S., Doǧan D., Kasapçopur Ö., et al.
Anadolu Kardiyoloji Dergisi , cilt.10, sa.3, 2010 (SCI-Expanded) identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 13
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Intractable atrial flutter presented with severe bradycardia in an infant

Bariş S., Güzeltaş A., Seymen G., Özyilmaz I., Eroǧlu A. G., Öztunç F.
Anadolu Kardiyoloji Dergisi , cilt.9, sa.6, ss.515-517, 2009 (SCI-Expanded) identifier identifier identifier

Thiamine-responsive megaloblastic anemia: Early diagnosis may be effective in preventing deafness

Önal H., Bariş S., Özdil M., Yeşil G., Altun G., Özyilmaz I., et al.
Turkish Journal of Pediatrics , cilt.51, sa.3, ss.301-304, 2009 (SCI-Expanded) identifier identifier identifier

Duration and dispersion of the P wave after the senning operation

Özylmaz I., Eroglu A. G., Güzeltaş A., Öztunç F., Saltk L., Özdil M., et al.
Cardiology in the Young , cilt.19, sa.6, ss.615-619, 2009 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 3
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Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma

Bariş S., Celkan T., Batar B., Güven M., Özdil M., Özkan A., et al.
Pediatric Hematology and Oncology , cilt.26, sa.6, ss.467-472, 2009 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 15
  • Captures
    • Readers: 5
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Clinical variability of asphyxiating thoracic dystrophy (Jeune) syndrome: Evaluation and classification of 13 patients

Tüuysüz B., Bariş S., Aksoy F., Madazli R., Üngür S., Sever L.
American Journal of Medical Genetics, Part A , cilt.149, sa.8, ss.1727-1733, 2009 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 60
  • Captures
    • Readers: 43
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DNA repair gene XPD and XRCC1 polymorphisms and the risk of childhood acute lymphoblastic leukemia

Batar B., Güven M., Bariş S., Celkan T., Yildiz I.
Leukemia Research , cilt.33, sa.6, ss.759-763, 2009 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 62
  • Captures
    • Readers: 29
  • Social Media
    • Shares, Likes & Comments: 17
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Coronary events and anatomy after arterial switch operation for transposition of the great arteries: Detection by 16-row multislice computed tomography angiography in pediatric patients

Öztunç F., BarIş S., Adaletli I., Önol N. Ö., Olgun D. C., Güzeltaş A., et al.
CardioVascular and Interventional Radiology , cilt.32, sa.2, ss.206-212, 2009 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 21
  • Captures
    • Readers: 22
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A rare cause of ischemic stroke: fibromuscular dysplasia

Ödil M., Bariş S., Özyilmaz I., Doǧru Ö., Celkan T., Albayram S.
NEUROLOGICAL SCIENCES , cilt.30, sa.1, ss.77-79, 2009 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 7
  • Captures
    • Readers: 28
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A rare cause of ischemic stroke: fibromuscular dysplasia

Baris S., Ozdil M., Topal N., Dogru Ö., Ozyilmaz I., Celkan T., et al.
ACTA PAEDIATRICA , cilt.97, ss.158-159, 2008 (SCI-Expanded) identifier

Our cases with Scimitar syndrome

Baris S., Guzeltas A., Ozdil M., Eroglu A. G., Saltik L., Oztunc F., et al.
ACTA PAEDIATRICA , cilt.97, ss.93, 2008 (SCI-Expanded) identifier

Two cases with atrioventricular septal defect: double-orifice mitral valve and single mitral papillary muscle

Guzeltas A., Eroglu A. G., Ozdil M., Baris S., Hatemi A., Turkoglu H., et al.
ACTA PAEDIATRICA , cilt.97, ss.91, 2008 (SCI-Expanded) identifier

Giant coronary sinus aneurysm with additional cardiac anomalies

Guzeltas A., Saltik L., Ozdil M., Baris S., Eroglu A. G.
ACTA PAEDIATRICA , cilt.97, ss.92-93, 2008 (SCI-Expanded) identifier

The difference between pre-B cell acute lymphoblastic leukemia and Burkitt lymphoma in relation to DNA damage repair gene polymorphisms in childhood

Celkan T., Guven M., Batar B., Alhaj S.
LEUKEMIA & LYMPHOMA , cilt.49, sa.8, ss.1638-1640, 2008 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 14
  • Captures
    • Readers: 9
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A new parameter in the differential diagnosis of bacterial and viral meningitis

Onal H., Onal Z., Ozdil M., Alhaj S.
NEUROSCIENCES , cilt.13, sa.1, ss.91-92, 2008 (SCI-Expanded) identifier identifier identifier

Prenatal diagnosis of hereditary spherocytosis with osmotic fragility test

Celkan T., Alhaj S.
INDIAN PEDIATRICS , cilt.45, sa.1, ss.63-64, 2008 (SCI-Expanded) identifier

Eyelid, facial and presternal edema in mumps

Alhaj S., Ozyylmaz I., Altun G., Cam H.
PEDIATRIC INFECTIOUS DISEASE JOURNAL , cilt.26, sa.7, ss.661, 2007 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 3
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    • Readers: 3
  • Social Media
    • Shares, Likes & Comments: 15
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Encephalopathy in type I hyperlipidemia

Onal H., Atugluzeybek C., Alhaj S., Altun G.
INDIAN PEDIATRICS , cilt.44, sa.4, ss.306-308, 2007 (SCI-Expanded) identifier identifier identifier

Capillary leak syndrome in a 5-month-old infant associated with intractable diarrhoea

Onal H., Aktuglu-Zeybek C., Altun G., Ozyilmaz I., Alhaj S., Aydin A.
ANNALS OF TROPICAL PAEDIATRICS , cilt.27, sa.1, ss.81-86, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
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  • Citations
    • Citation Indexes: 17
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    • Readers: 11
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Control of bleeding associated with hemophagocytic syndrome in children: An audit of the clinical use of recombinant activated factor VII

Celkan T., Alhaj S., Civilibal M., Elicevik M.
PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.24, sa.2, ss.117-121, 2007 (SCI-Expanded) identifier identifier identifier
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  • Citations
    • Citation Indexes: 12
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    • Readers: 9
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Metrikler

Yayın

507

Atıf (WoS)

2664

H-İndeks (WoS)

26

Atıf (Scopus)

4122

H-İndeks (Scopus)

33

Atıf (Scholar)

1099

H-İndeks (Scholar)

5

Atıf (TrDizin)

1115

H-İndeks (TrDizin)

2

Atıf (Diğer Toplam)

1129

Proje

19

Açık Erişim

17
BM Sürdürülebilir Kalkınma Amaçları