| 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 | 138 | 2019 |
| Human AGR2 deficiency causes mucus barrier dysfunction and infantile inflammatory bowel disease AA Al-Shaibi, UM Abdel-Motal, SZ Hubrack, AN Bullock, AA Al-Marri, ... Cellular and molecular gastroenterology and hepatology 12 (5), 1809-1830, 2021 | 32 | 2021 |
| Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome N Agrebi, I Ben-Mustapha, N Matoussi, N Dhouib, M Ben-Ali, N Mekki, ... Clinical Immunology 183, 17-23, 2017 | 19 | 2017 |
| Comprehensive review of autoantibodies in patients with hyper-IgM syndrome MR Barbouche, Q Chen, M Carbone, I Ben-Mustapha, Z Shums, M Trifa, ... Cellular & Molecular Immunology 15 (6), 610-617, 2018 | 18 | 2018 |
| Autoantibodies in patients with interleukin 12 receptor beta 1 deficiency V Ronca, QB Chen, V Lygoura, I Ben‐Mustapha, Z Shums, M Trifa, ... Journal of Digestive Diseases 20 (7), 363-370, 2019 | 15 | 2019 |
| Novel insights into FAS defects underlying autoimmune lymphoproliferative syndrome revealed by studies in consanguineous patients I Ben-Mustapha, N Agrebi, MR Barbouche Journal of Leukocyte Biology 103 (3), 501-508, 2018 | 15 | 2018 |
| Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression N Agrebi, LS Ben-Mansour, M Medhaffar, S Hadiji, F Fedhila, M Ben-Ali, ... Journal of Allergy and Clinical Immunology 140 (1), 298-301. e3, 2017 | 13 | 2017 |
| In vitro Interleukin-7 treatment partially rescues MAIT cell dysfunction caused by SARS-CoV-2 infection S Hubrack, MA Al-Nesf, N Agrebi, C Raynaud, MA Khattab, M Thomas, ... Scientific reports 11 (1), 14090, 2021 | 10 | 2021 |
| Novel ORAI1 mutation disrupts channel trafficking resulting in combined immunodeficiency F Yu, N Agrebi, R Mackeh, K Abouhazima, K KhudaBakhsh, M Adeli, B Lo, ... Journal of Clinical Immunology 41, 1004-1015, 2021 | 9 | 2021 |
| Biallelic TLR4 deficiency in humans M Capitani, AA Al-Shaibi, S Pandey, L Gartner, H Taylor, SZ Hubrack, ... Journal of Allergy and Clinical Immunology 151 (3), 783-790. e5, 2023 | 6 | 2023 |
| Sfaihi Ben-Mansour L, Medhaffar M, Hadiji S, Fedhila F, Ben-Ali M, et al. Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual … N Agrebi J Allergy Clin Immunol 140, 298-301, 2017 | 6 | 2017 |
| Case Report: FOXP3 Mutation in a Patient Presenting With ALPS A Rais, N Mekki, F Fedhila, MF Alosaimi, M Ben Khaled, A Zameli, ... Frontiers in Immunology 12, 692107, 2021 | 4 | 2021 |
| Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migration F Yu, S Hubrack, CM Raynaud, A Elmi, R Mackeh, N Agrebi, G Thareja, ... Journal of Allergy and Clinical Immunology, 2024 | | 2024 |
| Burden of Mendelian disorders in a large Middle Eastern biobank W Aamer, A Al-Maraghi, N Syed, GD Gandhi, E Aliyev, AA Al-Kurbi, ... Genome Medicine 16 (1), 46, 2024 | | 2024 |
| X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase N Agrebi, G Gentilcore, JC Grivel, G Alkhayer, J Hassoun, A Hassan, ... Journal of Clinical Immunology 41 (4), 825-828, 2021 | | 2021 |
| AUTOANTIBODIES IN PATIENTS WITH IL12 beta 1 RECEPTOR DEFICIENCY V Ronca, QB Chen, V Lygoura, I Ben-Mustapha, Z Shums, M Trifa, ... HEPATOLOGY 70, 868A-869A, 2019 | | 2019 |
