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C. Aytekin · SciRah

Researcher profile · Semantic Scholar

C. Aytekin

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C. Aytekin — researcher profile on SciRah

h-index: 25
Works: 88
Citations: 2,908

Most-cited papers

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
S. Aydin, S. Kilic, C. Aytekin, Ashish R. Kumar +58 more
2015Journal of Clinical Immunology295 citations Open access
Semantic Scholar
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood
S. Boisson-Dupuis, J. Bustamante, Jamila El-Baghdadi, Y. Camcıoğlu +37 more
2015Immunological Reviews207 citations Open access
Semantic Scholar
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis
Y. Ling, Sophie Cypowyj, C. Aytekin, M. Galicchio +17 more
2015Journal of Experimental Medicine183 citations Open access
Semantic Scholar
The extended clinical phenotype of 64 patients with DOCK8 deficiency
K. Engelhardt, E. Gertz, S. Keleş, A. Schäffer +53 more
2015Journal of Allergy and Clinical Immunology181 citations Open access
Semantic Scholar
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.
J. D. de Greef, Jun Wang, J. Balog, J. D. den Dunnen +21 more
2011American Journal of Human Genetics177 citations Open access
Semantic Scholar
Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23
R. Martinez-Barricarte, J. Markle, Cindy S. Ma, E. Deenick +49 more
2018Science immunology173 citations Open access
Semantic Scholar
Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency
R. Lévy, S. Okada, V. Béziat, K. Moriya +38 more
2016Proceedings of the National Academy of Sciences of the United States of America162 citations Open access
Semantic Scholar
SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
V. Sancho-Shimizu, P. Brodin, A. Cobat, C. Biggs +147 more
2021Journal of Experimental Medicine133 citations Open access
Semantic Scholar
Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects
C. Weemaes, M. V. van Tol, Jun Wang, M. M. van Ostaijen-ten Dam +19 more
2013European Journal of Human Genetics126 citations Open access
Semantic Scholar
IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey
S. Boisson-Dupuis, J. El Baghdadi, N. Parvaneh, A. Bousfiha +24 more
2011PLoS ONE125 citations Open access
Semantic Scholar
Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.
M. Ouederni, O. Sanal, A. Ikincioğullari, I. Tezcan +38 more
2014Clinical Infectious Diseases105 citations Open access
Semantic Scholar
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child
Masato Ogishi, Rui Yang, C. Aytekin, D. Langlais +51 more
2021Nature Medicine96 citations Open access
Semantic Scholar
Disruption of an anti-mycobacterial circuit between dendritic and Th cells in human SPPL2a deficiency
Xiao-Fei Kong, R. Martinez-Barricarte, J. Kennedy, F. Mele +37 more
2018Nature Immunology88 citations Open access
Semantic Scholar
Multiple Presentations of LRBA Deficiency: a Single-Center Experience
Sevgi Kostel Bal, Şule Haskoloğlu, N. Serwas, Candan Islamoğlu +11 more
2017Journal of Clinical Immunology71 citations Open access
Semantic Scholar
Selective IgA Deficiency: Clinical and Laboratory Features of 118 Children in Turkey
C. Aytekin, N. Tuygun, Selim Gokçe, F. Doğu +1 more
2012Journal of Clinical Immunology69 citations
Semantic Scholar
Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals.
Hao-Yu Wu, P. E. Thijssen, Eleonora de Klerk, Kelly K D Vonk +5 more
2016Human Molecular Genetics60 citations
Semantic Scholar
Therapeutic Modalities and Clinical Outcomes in a Large Cohort with LRBA Deficiency and CTLA4 Insufficiency.
Nigar Taghizade, Royala Babayeva, Altan Kara, Ibrahim Serhat Karakus +51 more
2023Journal of Allergy and Clinical Immunology48 citations Open access
Semantic Scholar
Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association
C. Yee, M. Massaad, Wayne Bainter, T. Ohsumi +9 more
2015Journal of Allergy and Clinical Immunology48 citations Open access
Semantic Scholar
Hypomorphic mutation in TTC7A causes combined immunodeficiency with mild structural intestinal defects.
Stavroula Woutsas, C. Aytekin, E. Salzer, C. Conde +11 more
2015Blood41 citations Open access
Semantic Scholar
Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2
M. L. van den Boogaard, P. E. Thijssen, C. Aytekin, F. Licciardi +17 more
2017Clinical Genetics35 citations Open access
Semantic Scholar
Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling
Masato Ogishi, Koji Kitaoka, K. Good-Jacobson, Darawan Rinchai +60 more
2024Immunity34 citations Open access
Semantic Scholar
B-cell subsets in patients with transient hypogammaglobulinemia of infancy, partial IgA deficiency, and selective IgM deficiency.
F. Cipe, F. Doğu, Deniz Guloglu, C. Aytekin +3 more
2013Journal of investigational allergology & clinical immunology31 citations
Semantic Scholar
A novel mutation for TAP deficiency and its possible association with Toxoplasmosis.
F. Doğu, A. Ikincioğullari, D. Fricker, Gunseli Bozdoğan +5 more
2006Parasitology international27 citations
Semantic Scholar
Homozygous missense VPS16 variant is associated with a novel disease, resembling mucopolysaccharidosis‐plus syndrome in two siblings
Y. Yıldız, C. Koşukcu, Damla Aygün, M. Akçaboy +8 more
2021Clinical Genetics25 citations
Semantic Scholar
Purine nucleoside phosphorylase deficiency with fatal course in two sisters
C. Aytekin, F. Doğu, G. Tanır, Deniz Guloglu +3 more
2010European Journal of Pediatrics25 citations
Semantic Scholar
An unconditioned bone marrow transplantation in a child with purine nucleoside phosphorylase deficiency and its unique complication
C. Aytekin, Mutlu Yuksek, F. Doğu, A. Yağmurlu +6 more
2008Pediatric Transplantation25 citations
Semantic Scholar
Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency
Şule Haskoloğlu, Sevgi Kostel Bal, Candan Islamoğlu, C. Aytekin +7 more
2020Pediatric Allergy and Immunology22 citations Open access
Semantic Scholar
Inherited IL-17 RC deficiency in patients with chronic mucocutaneous candidiasis
Y. Ling, Sophie Cypowyj, C. Aytekin, Miguel Galicchio +17 more
201522 citations
Semantic Scholar
Complete deficiency of the IL-12 receptor β1 chain: three unrelated Turkish children with unusual clinical features
G. Tanır, F. Doğu, N. Tuygun, A. Ikincioğullari +9 more
2006European Journal of Pediatrics21 citations
Semantic Scholar
Bacille Calmette-Guérin Lymphadenitis and Recurrent Oral Candidiasis in an Infant With a New Mutation Leading to Interleukin-12 Receptor ß-1 Defi ciency
C. Aytekin, F. Doğu, N. Tuygun, G. Tanır +6 more
201119 citations
Semantic Scholar
Analyzing the Effectiveness of Marketing Strategies in the Presence of Word of Mouth: Agent-Based Modeling Approach
Çiğdem Karakaya, B. Badur, C. Aytekin
201119 citations Open access
Semantic Scholar
Renpenning Syndrome in a Turkish Patient: de novo Variant c.607C>T in PACS1 and Hypogammaglobulinemia Phenotype
Fatma Kurt Colak, Nilnur Eyerci, C. Aytekin, A. Ekşioğlu
2020Molecular Syndromology18 citations Open access
Semantic Scholar
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study
Ş. Çekiç, A. Meti̇n, C. Aytekin, Neslihan Edeer Karaca +10 more
2020Pediatric Allergy and Immunology17 citations
Semantic Scholar
Recurrent bacterial meningitis in children: our experience with 14 cases.
N. Tuygun, G. Tanır, C. Aytekin
2010Turkish Journal of Pediatrics16 citations Open access
Semantic Scholar
GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway
Ann Y. Park, Michael A. Leney-Greene, Matthew Lynberg, Justin Q. Gabrielski +70 more
2024Nature Immunology15 citations
Semantic Scholar
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
B. Erman, Umran Aba, Canberk Ipsir, Damla Pehlivan +42 more
2024Journal of Clinical Immunology13 citations Open access
Semantic Scholar
BCG Lymphadenitis and Recurrent Oral Candidiasis in an Infant with a New Mutation Leading to Interleukin-12 Receptor Beta-1 Deficiency
C. Aytekin, F. Doğu, N. Tuygun, G. Tanır +6 more
2011Journal of investigational allergology & clinical immunology13 citations
Semantic Scholar
Inherited IRAK-4 Deficiency in Acute Human Herpesvirus-6 Encephalitis
Zeynep Güneş Tepe, Y. Yazıcı, Umut Tank, Ladin Işık Köse +3 more
2022Journal of Clinical Immunology12 citations Open access
Semantic Scholar
Kostmann disease with developmental delay in three patients
C. Aytekin, M. Germeshausen, N. Tuygun, G. Tanır +2 more
2010European Journal of Pediatrics12 citations
Semantic Scholar
A Novel G6PC3 Gene Mutation in a Patient With Severe Congenital Neutropenia
C. Aytekin, M. Germeshausen, N. Tuygun, F. Doğu +1 more
2013Journal of pediatric hematology/oncology11 citations
Semantic Scholar
Eponym
C. Aytekin, M. Germeshausen, N. Tuygun, G. Tanır +2 more
2010European Journal of Pediatrics10 citations
Semantic Scholar
Single-Center Study of 72 Patients with Severe Combined Immunodeficiency: Clinical and Laboratory Features and Outcomes
O. Bayram, Şule Haskoloğlu, Deniz Bayrakoğlu, S. Bal +14 more
2021Journal of Clinical Immunology6 citations Open access
Semantic Scholar
Pseudomonas Aeruginosa Sepsis in a Previously Healthy Infant with Subcutaneous Nodules and Mastoid Bone Destruction
E. Azapağası, F. Öz, Mutlu Uysal Yazıcı, Dilara Ceylan +3 more
2020Journal of Pediatric Intensive Care6 citations Open access
Semantic Scholar
Glycogen storage disease type 1b: an early onset severe phenotype associated with a novel mutation (IVS4) in the glucose 6-phosphate translocase (SLC37A4) gene in a Turkish patient.
M. Oğuz, E. Aykan, G. Yilmaz, C. Aytekin +2 more
2014Genetic Counseling6 citations
Semantic Scholar
HLA‐haploidentical transplantations for primary immunodeficiencies: A single‐center experience
F. Cipe, F. Doğu, C. Aytekin, Mutlu Yuksek +8 more
2012Pediatric Transplantation6 citations
Semantic Scholar
[TGF-Beta1-915G/C and TNF-alpha-308G/A polymorphisms in children with asthma].
C. Aytekin, F. Doğu, A. Ikincioğullari, Y. Eğin +4 more
2009Turkish Journal of Tuberculosis & Thorax6 citations
Semantic Scholar
Successful Use of Anakinra in a Patient with IL-10R Beta Deficiency: A Case Report
S. Doğan, R. Selen, Ferda Özbay Hoşnut, S. Ozdel +3 more
2025Pediatric Allergy, Immunology, and Pulmonology5 citations
Semantic Scholar
Drug-induced enterocolitis syndrome in children: report of two cases and a literature review.
M. Özer, E. Bahadır, B. C. Duran, C. Aytekin +1 more
2025Turkish Journal of Pediatrics5 citations Open access
Semantic Scholar
COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report
John C McDonnell, K. Cousins, M. E. Younger, Adam Lane +154 more
2024Journal of Clinical Immunology5 citations Open access
Semantic Scholar
Whole‐exome sequencing for genetic diagnosis of idiopathic liver injury in children
Aysima Atılgan Lülecioğlu, Y. Yazıcı, Alperen Baran, K. Warasnhe +6 more
2024Journal of Cellular and Molecular Medicine5 citations Open access
Semantic Scholar

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A. Meti̇n — researcher profile on SciRah