| 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, C Liu, LYA Chai, M Migaud, F Hauck, ... Proceedings of the National Academy of Sciences 113 (51), E8277-E8285, 2016 | 174 | 2016 |
| Monogenic early-onset lymphoproliferation and autoimmunity: natural history of STAT3 gain-of-function syndrome JW Leiding, TP Vogel, VGJ Santarlas, R Mhaskar, MR Smith, A Carisey, ... Journal of allergy and clinical immunology 151 (4), 1081-1095, 2023 | 85 | 2023 |
| Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots G La Marca, C Canessa, E Giocaliere, F Romano, S Malvagia, S Funghini, ... Journal of allergy and clinical immunology 134 (1), 155-159. e3, 2014 | 68 | 2014 |
| Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency T Le Voyer, AV Parent, X Liu, A Cederholm, A Gervais, J Rosain, ... Nature 623 (7988), 803-813, 2023 | 61 | 2023 |
| Successful granulocyte colony-stimulating factor treatment of relapsing Candida albicans meningoencephalitis caused by CARD9 deficiency F Celmeli, N Oztoprak, D Turkkahraman, D Seyman, E Mutlu, N Frede, ... The Pediatric infectious disease journal 35 (4), 428-431, 2016 | 59 | 2016 |
| Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance T Asano, J Khourieh, P Zhang, F Rapaport, AN Spaan, J Li, WT Lei, ... Journal of Experimental Medicine 218 (8), e20202592, 2021 | 45 | 2021 |
| Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease MY Köker, K Van Leeuwen, M De Boer, F Celmeli, A Metin, TT Özgür, ... European journal of clinical investigation 39 (4), 311-319, 2009 | 43 | 2009 |
| Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations MY Köker, Ö Sanal, K Van Leeuwen, M De Boer, A Metin, T Patıroğlu, ... European journal of clinical investigation 39 (10), 942-951, 2009 | 42 | 2009 |
| Primary immunodeficiency associated with chromosomal aberration–an ESID survey E Schatorjé, M Van Der Flier, M Seppänen, M Browning, M Morsheimer, ... Orphanet journal of rare diseases 11, 1-14, 2016 | 35 | 2016 |
| CTLA-4 (+ 49A/G) polymorphism and type-1 diabetes in Turkish children F Çelmeli, D Türkkahraman, D Özel, S Akçurin, O Yeğin Journal of clinical research in pediatric endocrinology 5 (1), 40, 2013 | 34 | 2013 |
| Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency MC Catak, B Akcam, S Bilgic Eltan, R Babayeva, IS Karakus, G Akgun, ... Allergy 77 (10), 3108-3123, 2022 | 23 | 2022 |
| PCR-based national bacterial meningitis surveillance in Turkey: years 2006 to 2009 D Toprak, A Soysal, MA Torunoglu, M Turgut, S Türkoglu, FC Pimenta, ... The Pediatric infectious disease journal 33 (10), 1087-1089, 2014 | 23 | 2014 |
| Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency N Taghizade, R Babayeva, A Kara, IS Karakus, MC Catak, A Bulutoglu, ... Journal of Allergy and Clinical Immunology 152 (6), 1634-1645, 2023 | 21 | 2023 |
| Does gastroesophageal reflux scintigraphy correlate with clinical findings in children with chronic cough? AB Boz, F Aydn, F Celmeli, A Boz, R Artan, F Gungor Nuclear Medicine Communications 30 (10), 802-806, 2009 | 19 | 2009 |
| A case of allergic bronchopulmonary aspergillosis following active pulmonary tuberculosis AB Boz, F Celmeli, AG Arslan, A Cilli, C Ogus, T Ozdemir Pediatric pulmonology 44 (1), 86-89, 2009 | 15 | 2009 |
| Genetic analysis of a cohort of 275 patients with hyper-IgE syndromes and/or chronic mucocutaneous candidiasis N Frede, J Rojas-Restrepo, A Caballero Garcia de Oteyza, M Buchta, ... Journal of clinical immunology 41 (8), 1804-1838, 2021 | 13 | 2021 |
| A successful unrelated peripheral blood stem cell transplantation with reduced intensity‐conditioning regimen in a patient with late‐onset purine nucleoside phosphorylase … F Celmeli, D Turkkahraman, V Uygun, G la Marca, M Hershfield, ... Pediatric Transplantation 19 (2), E47-E50, 2015 | 13 | 2015 |
| Cockroach (Blattella Germanica) Sensitization is Associated with Coexistence of Asthma and Allergic Rhinitis in Childhood F Celmeli, ST Yavuz, D Turkkahraman, O Simsek, A Kılınc, BE Sekerel Pediatric Allergy, Immunology, and Pulmonology 29 (1), 38-43, 2016 | 10 | 2016 |
| Impaired thymic AIRE expression underlies autoantibodies against type I IFNs in humans with inborn errors of the alternative NF-kB pathway T Le Voyer, A Gervais, J Rosain, A Parent, A Cederholm, D Rinchai, ... Authorea Preprints, 2023 | 6 | 2023 |
| Selective IgM deficiency in a boy with ring chromosome 18 F Celmeli, D Turkkahraman, Z Cetin, E Mihci, O Yegin Journal of investigational allergology & clinical immunology 24 (6), 442-444, 2014 | 6 | 2014 |
Mustafa Yavuz kökerDepartment of Immunology, University of Erciyes, KayseriEmail verificata su erciyes.edu.tr