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| Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome Y Minegishi, M Saito, S Tsuchiya, I Tsuge, H Takada, T Hara, ... Nature 448 (7157), 1058-1062, 2007 | 1187 | 2007 |
| Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity Y Minegishi, M Saito, T Morio, K Watanabe, K Agematsu, S Tsuchiya, ... Immunity 25 (5), 745-755, 2006 | 807 | 2006 |
| Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome KR Engelhardt, S McGhee, S Winkler, A Sassi, C Woellner, ... Journal of Allergy and Clinical Immunology 124 (6), 1289-1302. e4, 2009 | 583 | 2009 |
| Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy D Kotlarz, R Beier, D Murugan, J Diestelhorst, O Jensen, K Boztug, ... Gastroenterology 143 (2), 347-355, 2012 | 534 | 2012 |
| Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation L Svensson, K Howarth, A McDowall, I Patzak, R Evans, S Ussar, ... Nature medicine 15 (3), 306-312, 2009 | 439 | 2009 |
| DOCK8 deficiency: clinical and immunological phenotype and treatment options-a review of 136 patients SE Aydin, SS Kilic, C Aytekin, A Kumar, O Porras, L Kainulainen, ... Journal of clinical immunology 35, 189-198, 2015 | 296 | 2015 |
| Inherited and acquired immunodeficiencies underlying tuberculosis in childhood S Boisson‐Dupuis, J Bustamante, J El‐Baghdadi, Y Camcioglu, ... Immunological reviews 264 (1), 103-120, 2015 | 239 | 2015 |
| Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients MY Köker, Y Camcıoğlu, K Van Leeuwen, SŞ Kılıç, I Barlan, M Yılmaz, ... Journal of allergy and clinical immunology 132 (5), 1156-1163. e5, 2013 | 211 | 2013 |
| WASP regulates suppressor activity of human and murine CD4+CD25+FOXP3+ natural regulatory T cells F Marangoni, S Trifari, S Scaramuzza, C Panaroni, S Martino, ... The Journal of experimental medicine 204 (2), 369-380, 2007 | 206 | 2007 |
| The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency KR Engelhardt, ME Gertz, S Keles, AA Schäffer, EC Sigmund, C Glocker, ... Journal of Allergy and Clinical Immunology 136 (2), 402-412, 2015 | 195 | 2015 |
| Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination S Péron, A Metin, P Gardès, MA Alyanakian, E Sheridan, CP Kratz, ... The Journal of experimental medicine 205 (11), 2465-2472, 2008 | 168 | 2008 |
| Abatacept as a long-term targeted therapy for LRBA deficiency A Kiykim, I Ogulur, E Dursun, LM Charbonnier, E Nain, S Cekic, ... The Journal of Allergy and Clinical Immunology: In Practice 7 (8), 2790-2800 …, 2019 | 140 | 2019 |
| Transient hypogammaglobulinemia of infancy: clinical and immunologic features of 40 new cases SŞ Kiliç, İ Tezcan, Ö Sanal, A Metin, F Ersoy Pediatrics International 42 (6), 647-650, 2000 | 131 | 2000 |
| IL‐12Rβ1 Deficiency: Mutation Update and Description of the IL12RB1 Variation Database E van de Vosse, MH Haverkamp, N Ramirez‐Alejo, M Martinez‐Gallo, ... Human mutation 34 (10), 1329-1339, 2013 | 107 | 2013 |
| Griscelli disease: genotype–phenotype correlation in an array of clinical heterogeneity O Sanal, F Ersoy, I Tezcan, A Metin, L Yel, G Ménasché, A Gürgey, ... Journal of clinical immunology 22, 237-243, 2002 | 104 | 2002 |
| Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia–telangiectasia O Sanal, F Ersoy, L Yel, I Tezcan, A Metin, H Özyürek, S Gariboglu, ... Journal of clinical immunology 19, 326-334, 1999 | 84 | 1999 |
| Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency S Ghosh, S Köstel Bal, ESJ Edwards, B Pillay, R Jiménez Heredia, ... Blood, The Journal of the American Society of Hematology 136 (23), 2638-2655, 2020 | 81 | 2020 |
| The prevalence of dyslipidemia and associated factors in children and adolescents with type 1 diabetes T Bulut, F Demirel, A Metin Journal of Pediatric Endocrinology and Metabolism 30 (2), 181-187, 2017 | 81 | 2017 |
| Hematopoietic stem cell transplantation as treatment for patients with DOCK8 deficiency SE Aydin, AF Freeman, W Al-Herz, HA Al-Mousa, RK Arnaout, RC Aydin, ... The Journal of Allergy and Clinical Immunology: In Practice 7 (3), 848-855, 2019 | 70 | 2019 |
Ilhan TezcanProfessor of Pediatrics, Hacettepe UniversityVerified email at hacettepe.edu.tr
