| Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy N Cartier, S Hacein-Bey-Abina, CC Bartholomae, G Veres, M Schmidt, ... Science 326 (5954), 818-23, 2009 | 1821 | 2009 |
| B cell–helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen I Puga, M Cols, CM Barra, B He, L Cassis, M Gentile, L Comerma, ... Nature immunology 13 (2), 170-180, 2012 | 855 | 2012 |
| Clinical picture and treatment of 2212 patients with common variable immunodeficiency B Gathmann, N Mahlaoui, L Gérard, E Oksenhendler, K Warnatz, ... Journal of Allergy and Clinical Immunology 134 (1), 116-126. e11, 2014 | 685 | 2014 |
| The European Society for Immunodeficiencies (ESID) registry working definitions for the clinical diagnosis of inborn errors of immunity MG Seidel, G Kindle, B Gathmann, I Quinti, M Buckland, J van Montfrans, ... The Journal of Allergy and Clinical Immunology: In Practice 7 (6), 1763-1770, 2019 | 551 | 2019 |
| Primary immunodeficiency diseases worldwide: more common than generally thought AA Bousfiha, L Jeddane, F Ailal, I Benhsaien, N Mahlaoui, JL Casanova, ... Journal of clinical immunology 33, 1-7, 2013 | 447 | 2013 |
| Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells M Côte, MM Ménager, A Burgess, N Mahlaoui, C Picard, C Schaffner, ... The Journal of clinical investigation 119 (12), 3765-3773, 2009 | 424 | 2009 |
| Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency) JP Schmid, D Canioni, D Moshous, F Touzot, N Mahlaoui, F Hauck, ... Blood, The Journal of the American Society of Hematology 117 (5), 1522-1529, 2011 | 405 | 2011 |
| Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ... Nature genetics 48 (9), 1071-1076, 2016 | 378 | 2016 |
| Coronavirus disease 2019 in patients with inborn errors of immunity: an international study I Meyts, G Bucciol, I Quinti, B Neven, A Fischer, E Seoane, ... Journal of Allergy and Clinical Immunology 147 (2), 520-531, 2021 | 372 | 2021 |
| X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease C Booth, KC Gilmour, P Veys, AR Gennery, MA Slatter, H Chapel, ... Blood, The Journal of the American Society of Hematology 117 (1), 53-62, 2011 | 371 | 2011 |
| Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey MO Chandesris, I Melki, A Natividad, A Puel, C Fieschi, L Yun, ... Medicine 91 (4), e1-e19, 2012 | 354 | 2012 |
| Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an … D Moratto, S Giliani, C Bonfim, E Mazzolari, A Fischer, HD Ochs, AJ Cant, ... Blood, The Journal of the American Society of Hematology 118 (6), 1675-1684, 2011 | 346 | 2011 |
| Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis: a single-center report of 48 patients M Ouachee-Chardin, C Elie, G de Saint Basile, F Le Deist, N Mahlaoui, ... Pediatrics 117 (4), e743-e750, 2006 | 340 | 2006 |
| Evidence of innate lymphoid cell redundancy in humans F Vély, V Barlogis, B Vallentin, B Neven, C Piperoglou, M Ebbo, T Perchet, ... Nature immunology 17 (11), 1291-1299, 2016 | 335 | 2016 |
| Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase δ … ME Maccari, H Abolhassani, A Aghamohammadi, A Aiuti, O Aleinikova, ... Frontiers in immunology 9, 543, 2018 | 328 | 2018 |
| Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies A Fischer, J Provot, JP Jais, A Alcais, N Mahlaoui, D Adoue, N Aladjidi, ... Journal of Allergy and Clinical Immunology 140 (5), 1388-1393. e8, 2017 | 328 | 2017 |
| Neutrophil depletion impairs natural killer cell maturation, function, and homeostasis BN Jaeger, J Donadieu, C Cognet, C Bernat, D Ordoñez-Rueda, ... Journal of Experimental Medicine 209 (3), 565-580, 2012 | 296 | 2012 |
| Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: a single-center retrospective report of 38 patients N Mahlaoui, M Ouachée-Chardin, G de Saint Basile, B Neven, C Picard, ... Pediatrics 120 (3), e622-e628, 2007 | 295 | 2007 |
| MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival NT Nehme, JP Schmid, F Debeurme, I André-Schmutz, A Lim, P Nitschke, ... Blood, The Journal of the American Society of Hematology 119 (15), 3458-3468, 2012 | 294 | 2012 |
| Congenital neutropenia: diagnosis, molecular bases and patient management J Donadieu, O Fenneteau, B Beaupain, N Mahlaoui, CB Chantelot Orphanet journal of rare diseases 6, 1-28, 2011 | 293 | 2011 |