The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency L Gámez-Díaz, D August, P Stepensky, S Revel-Vilk, MG Seidel, M Noriko, ... Journal of Allergy and Clinical Immunology 137 (1), 223-230, 2016 | 292 | 2016 |
Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia PJ Ancliff, MP Blundell, GO Cory, Y Calle, A Worth, H Kempski, S Burns, ... Blood 108 (7), 2182-2189, 2006 | 260 | 2006 |
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study F Barzaghi, LCA Hernandez, B Neven, S Ricci, ZY Kucuk, JJ Bleesing, ... Journal of Allergy and Clinical Immunology 141 (3), 1036-1049. e5, 2018 | 256 | 2018 |
Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype A Worth, AJ Thrasher, H Bobby Gaspar British journal of haematology 133 (2), 124-140, 2006 | 219 | 2006 |
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans P Tuijnenburg, HL Allen, SO Burns, D Greene, MH Jansen, E Staples, ... Journal of allergy and clinical immunology 142 (4), 1285-1296, 2018 | 210 | 2018 |
Whole-genome sequencing of a sporadic primary immunodeficiency cohort JED Thaventhiran, H Lango Allen, OS Burren, W Rae, D Greene, ... Nature 583 (7814), 90-95, 2020 | 166 | 2020 |
Human cytomegalovirus haplotype reconstruction reveals high diversity due to superinfection and evidence of within-host recombination J Cudini, S Roy, CJ Houldcroft, JM Bryant, DP Depledge, H Tutill, P Veys, ... Proceedings of the National Academy of Sciences 116 (12), 5693-5698, 2019 | 153 | 2019 |
WIP regulates the stability and localization of WASP to podosomes in migrating dendritic cells HC Chou, IM Antón, MR Holt, C Curcio, S Lanzardo, A Worth, S Burns, ... Current Biology 16 (23), 2337-2344, 2006 | 151 | 2006 |
Phage Therapy of Mycobacterium Infections: Compassionate Use of Phages in 20 Patients With Drug-Resistant Mycobacterial Disease RM Dedrick, BE Smith, M Cristinziano, KG Freeman, D Jacobs-Sera, ... Clinical infectious diseases 76 (1), 103-112, 2023 | 146 | 2023 |
The Wiskott-Aldrich syndrome: the actin cytoskeleton and immune cell function MP Blundell, A Worth, G Bouma, AJ Thrasher Disease markers 29 (3-4), 157-175, 2010 | 145 | 2010 |
T-cell receptor αβ+ and CD19+ cell–depleted haploidentical and mismatched hematopoietic stem cell transplantation in primary immune deficiency RM Shah, R Elfeky, Z Nademi, W Qasim, P Amrolia, R Chiesa, K Rao, ... Journal of Allergy and Clinical Immunology 141 (4), 1417-1426. e1, 2018 | 140 | 2018 |
Omission of in vivo T‐cell depletion promotes rapid expansion of naïve CD4+ cord blood lymphocytes and restores adaptive immunity within 2 months after … R Chiesa, K Gilmour, W Qasim, S Adams, AJJ Worth, H Zhan, ... British journal of haematology 156 (5), 656-666, 2012 | 139 | 2012 |
Thymus transplantation for complete DiGeorge syndrome: European experience EG Davies, M Cheung, K Gilmour, J Maimaris, J Curry, A Furmanski, ... Journal of Allergy and Clinical Immunology 140 (6), 1660-1670. e16, 2017 | 127 | 2017 |
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score VK Tesch, H Abolhassani, B Shadur, J Zobel, Y Mareika, S Sharapova, ... Journal of Allergy and Clinical Immunology 145 (5), 1452-1463, 2020 | 126 | 2020 |
Risk factors predisposing to the development of hypogammaglobulinemia and infections post-Rituximab EAA Christou, G Giardino, A Worth, F Ladomenou International Reviews of Immunology 36 (6), 352-359, 2017 | 116 | 2017 |
Inherited p40phox deficiency differs from classic chronic granulomatous disease A Van De Geer, A Nieto-Patlán, DB Kuhns, ATJ Tool, AA Arias, M Bouaziz, ... The Journal of clinical investigation 128 (9), 3957-3975, 2018 | 113 | 2018 |
Identifying functional defects in patients with immune dysregulation due to LRBA and CTLA-4 mutations TZ Hou, N Verma, J Wanders, A Kennedy, B Soskic, D Janman, ... Blood, The Journal of the American Society of Hematology 129 (11), 1458-1468, 2017 | 109 | 2017 |
Pre‐emptive rituximab based on viraemia and T cell reconstitution: a highly effective strategy for the prevention of Epstein–Barr virus‐associated lymphoproliferative disease … A Worth, R Conyers, J Cohen, M Jagani, R Chiesa, K Rao, N Goulden, ... British journal of haematology 155 (3), 377-385, 2011 | 102 | 2011 |
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations T Lorenzini, M Fliegauf, N Klammer, N Frede, M Proietti, A Bulashevska, ... Journal of Allergy and Clinical Immunology 146 (4), 901-911, 2020 | 97 | 2020 |
The United Kingdom primary immune deficiency (UKPID) registry 2012 to 2017 B Shillitoe, C Bangs, D Guzman, AR Gennery, HJ Longhurst, M Slatter, ... Clinical & Experimental Immunology 192 (3), 284-291, 2018 | 94 | 2018 |