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Neslihan Edeer Karaca

Observed names: EDEER KARACA, NESLİHAN, KARACA, NESLİHAN, KARACA, Neslihan EDEER, Karaca N. Edeer, Karaca, Neslihan E., Karaca, Neslihan Edeer, N Karaca, N Karaca Edeer, N. E. Karaca, N. Edeer Karaca, N. Karaca, N.E. Karaca, NESLİHAN KARACA, Neslihan E Karaca, Neslihan E. Karaca, Neslihan EDEER KARACA, Neslihan Edeer, Neslihan Edeer KARACA, Neslihan Edeer-Karaca, Neslihan Edeer-karaca, Neslihan Karaca, edeer karaca, neslihan, karaca edeer, neslihan, neslihan karaca edeer
Institution: Ege University
ORCID: 0000-0002-2202-7082
Observed ORCID: 0000-0002-2202-7082
OpenAlex ID: A5004336829
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
2015 · On behalf of the inborn errors working party of EBMT, Susanne E. Aydin, et al. · Journal of Clinical Immunology · 318
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Inherited and acquired immunodeficiencies underlying tuberculosis in childhood
2015 · Stéphanie Boisson‐Dupuis, Jacinta Bustamante, et al. · Immunological Reviews · 224
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score
2019 · Victoria Katharina Tesch, Hassan Abolhassani, et al. · Journal of Allergy and Clinical Immunology · 160
Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency
2019 · Ayca Kiykim, Ismail Ogulur, et al. · The Journal of Allergy and Clinical Immunology In Practice · 153
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases
2016 · Francesca Conti, Saul Oswaldo Lugo-Reyes, et al. · Journal of Allergy and Clinical Immunology · 145
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Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency
2013 · Monia Ouederni, Ozden Sanal, et al. · Clinical Infectious Diseases · 101
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Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation
2016 · Sevgi Keles, Louis Marie Charbonnier, et al. · Journal of Allergy and Clinical Immunology · 95
The Prevalances and Patient Characteristics of Primary Immunodeficiency Diseases in Turkey—Two Centers Study
2012 · Sara S. Kilic, Mustafa Ozel, et al. · Journal of Clinical Immunology · 85
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity
2021 · Asghar Aghamohammadi, Nima Rezaei, et al. · Journal of Clinical Immunology · 78
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Increases in serum immunoglobulins to age‐related normal levels in children with IgA and/or IgG subclass deficiency
2007 · Necil Kutukculer, Neslihan Edeer Karaca, et al. · Pediatric Allergy and Immunology · 68
Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children from western Anatolia, Turkey
2011 · Can Ozturk, Oya Halıcıoglu, et al. · Clinical Rheumatology · 67
Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency
2023 · Nigar Taghizade, Royala Babayeva, et al. · Journal of Allergy and Clinical Immunology · 61
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Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report
2015 · Ezgi Ulusoy, Neslihan Edeer Karaca, et al. · Journal of Medical Case Reports · 45
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CD4 + CD25 + Foxp3 + T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency
2015 · Necil Kutukculer, Elif Azarsiz, et al. · International Journal of Immunopathology and Pharmacology · 43
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Gain-of-Function Mutations inSTAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies
2017 · Sanem Eren Akarcan, Ezgi Ulusoy Severcan, et al. · Case Reports in Immunology · 39
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Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival
2024 · Tanja C. Vallée, Jannik S. Glasmacher, et al. · Blood · 37
Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency
2022 · Mehmet C. Catak, Bengu Akcam, et al. · Allergy · 31
Three Different Classifications, B Lymphocyte Subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) Gene Mutations, CTLA-4 and ICOS Gene Polymorphisms in Turkish Patients with Common Variable Immunodeficiency
2012 · Necil Kutukculer, Nesrin Gulez, et al. · Journal of Clinical Immunology · 31
Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea
2017 · Britt-Sabina Petersen, Dietrich August, et al. · Inflammatory Bowel Diseases · 30
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Psychological burden of pediatric primary immunodeficiency
2018 · Binay Kayan Ocakoglu, Neslihan Edeer Karaca, et al. · Pediatrics International · 28
Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases
2016 · Neslihan Edeer Karaca, Guzide Aksu, et al. · Case Reports in Immunology · 26
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Successful management of colchicine resistant familial Mediterranean fever patients with a standardized canakinumab treatment protocol: a case series and literature review
2019 · Sanem Eren Akarcan, Seyda Dogantan, et al. · Rheumatology International · 24
Novel mutatıons and diverse clinical phenotypes in recombınase-activating gene 1 deficiency
2012 · Necil Kutukculer, Nesrin Gulez, et al. · ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics · 24
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New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy.
2010 · Neslihan Edeer Karaca, Guzide Aksu, et al. · PubMed · 24
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages
2018 · Necil Kutukculer, Ayca Aykut, et al. · Scandinavian Journal of Immunology · 23
Works count: 162
Citation count: 2,658
H-index: 24
I10-index: 53
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