| Pyogenic bacterial infections in humans with MyD88 deficiency H Von Bernuth, C Picard, Z Jin, R Pankla, H Xiao, CL Ku, M Chrabieh, ... Science 321 (5889), 691-696, 2008 | 881 | 2008 |
| The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response A Baroja-Mazo, F Martín-Sánchez, AI Gomez, CM Martínez, ... Nature immunology 15 (8), 738-748, 2014 | 841 | 2014 |
| 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 | 827 | 2012 |
| Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency C Picard, H Von Bernuth, P Ghandil, M Chrabieh, O Levy, PD Arkwright, ... Medicine 89 (6), 403-425, 2010 | 482 | 2010 |
| Classification criteria for autoinflammatory recurrent fevers M Gattorno, M Hofer, S Federici, F Vanoni, F Bovis, I Aksentijevich, ... Annals of the rheumatic diseases 78 (8), 1025-1032, 2019 | 347 | 2019 |
| MCC950 closes the active conformation of NLRP3 to an inactive state A Tapia-Abellán, D Angosto-Bazarra, H Martínez-Banaclocha, ... Nature chemical biology 15 (6), 560-564, 2019 | 319 | 2019 |
| High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: Results of an international multicenter … N Tanaka, K Izawa, MK Saito, M Sakuma, K Oshima, O Ohara, ... Arthritis & Rheumatism 63 (11), 3625-3632, 2011 | 314 | 2011 |
| Innate lymphoid cells integrate stromal and immunological signals to enhance antibody production by splenic marginal zone B cells G Magri, M Miyajima, S Bascones, A Mortha, I Puga, L Cassis, CM Barra, ... Nature immunology 15 (4), 354-364, 2014 | 309 | 2014 |
| Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence M Alvarez-Lobos, JI Arostegui, M Sans, D Tassies, S Plaza, S Delgado, ... Annals of surgery 242 (5), 693-700, 2005 | 259 | 2005 |
| NOD2 gene–associated pediatric granulomatous arthritis: Clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin‐1 … JI Aróstegui, C Arnal, R Merino, C Modesto, M Antonia Carballo, ... Arthritis & Rheumatism: Official Journal of the American College of …, 2007 | 243 | 2007 |
| Heterogeneity among patients with tumor necrosis factor receptor–associated periodic syndrome phenotypes E Aganna, L Hammond, PN Hawkins, A Aldea, SA McKee, ... Arthritis & Rheumatism: Official Journal of the American College of …, 2003 | 243 | 2003 |
| An international registry on autoinflammatory diseases: the Eurofever experience N Toplak, J Frenkel, S Ozen, HJ Lachmann, P Woo, I Koné-Paut, ... Annals of the rheumatic diseases 71 (7), 1177-1182, 2012 | 222 | 2012 |
| A novel Pyrin-Associated Autoinflammation with Neutrophilic Dermatosis mutation further defines 14-3-3 binding of pyrin and distinction to Familial Mediterranean Fever F Moghaddas, R Llamas, D De Nardo, H Martinez-Banaclocha, ... Annals of the rheumatic diseases 76 (12), 2085-2094, 2017 | 152 | 2017 |
| Plasma Stromal Cell–Derived Factor (SDF)-1 Levels, SDF1-3′ A Genotype, and Expression of CXCR4 on T Lymphocytes: their Impact on Resistance to Human Immunodeficiency Virus … A Soriano, C Martínez, F García, M Plana, E Palou, M Lejeune, ... The Journal of infectious diseases 186 (7), 922-931, 2002 | 151 | 2002 |
| Blau syndrome: cross-sectional data from a multicentre study of clinical, radiological and functional outcomes CD Rosé, S Pans, I Casteels, J Anton, B Bader-Meunier, P Brissaud, ... Rheumatology 54 (6), 1008-1016, 2015 | 150 | 2015 |
| New workflow for classification of genetic variants’ pathogenicity applied to hereditary recurrent fevers by the International Study Group for Systemic Autoinflammatory … ME Van Gijn, I Ceccherini, Y Shinar, EC Carbo, M Slofstra, JI Arostegui, ... Journal of medical genetics 55 (8), 530-537, 2018 | 142 | 2018 |
| Evaluating the genetics of common variable immunodeficiency: monogenetic model and beyond G de Valles-Ibáñez, A Esteve-Sole, M Piquer, EA González-Navarro, ... Frontiers in Immunology 9, 636, 2018 | 141 | 2018 |
| IL36RN mutations define a severe autoinflammatory phenotype of generalized pustular psoriasis S Hussain, DM Berki, SE Choon, AD Burden, MH Allen, JI Arostegui, ... Journal of Allergy and Clinical Immunology 135 (4), 1067-1070. e9, 2015 | 140 | 2015 |
| Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes K Nakagawa, E Gonzalez-Roca, A Souto, T Kawai, H Umebayashi, ... Annals of the rheumatic diseases 74 (3), 603-610, 2015 | 134 | 2015 |
| NOD2‐associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain CD Rosé, JI Aróstegui, TM Martin, G Espada, L Scalzi, J Yagüe, ... Arthritis & Rheumatism: Official Journal of the American College of …, 2009 | 134 | 2009 |
