| RETRACTED ARTICLE: Increased Gut Redox and Depletion of Anaerobic and Methanogenic Prokaryotes in Severe Acute Malnutrition M Million, M Tidjani Alou, S Khelaifia, D Bachar, JC Lagier, N Dione, ... Scientific reports 6 (1), 26051, 2016 | 219 | 2016 |
| The SKIV2L RNA exosome limits activation of the RIG-I-like receptors SC Eckard, GI Rice, A Fabre, C Badens, EE Gray, JL Hartley, YJ Crow, ... Nature immunology 15 (9), 839-845, 2014 | 207 | 2014 |
| Clinical aspects of STAT3 gain-of-function germline mutations: a systematic review A Fabre, S Marchal, V Barlogis, B Mari, P Barbry, PS Rohrlich, LR Forbes, ... The Journal of Allergy and Clinical Immunology: In Practice 7 (6), 1958-1969. e9, 2019 | 192 | 2019 |
| SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome A Fabre, B Charroux, C Martinez-Vinson, B Roquelaure, E Odul, E Sayar, ... The American Journal of Human Genetics 90 (4), 689-692, 2012 | 185 | 2012 |
| COVID-19 virus and children: What do we know? A Morand, A Fabre, P Minodier, A Boutin, N Vanel, E Bosdure, ... Archives de pediatrie 27 (3), 117-118, 2020 | 129 | 2020 |
| Component‐resolved diagnosis with commercially available D. pteronyssinus Der p 1, Der p 2 and Der p 10: relevant markers for house dust mite allergy M Bronnert, J Mancini, J Birnbaum, C Agabriel, V Liabeuf, F Porri, ... Clinical & Experimental Allergy 42 (9), 1406-1415, 2012 | 124 | 2012 |
| Diagnostic yield of next-generation sequencing in very early-onset inflammatory bowel diseases: a multicentre study F Charbit-Henrion, M Parlato, S Hanein, R Duclaux-Loras, J Nowak, ... Journal of Crohn's and Colitis 12 (9), 1104-1112, 2018 | 98 | 2018 |
| Monogenic early-onset lymphoproliferation and autoimmunity: natural history of STAT3 gain-of-function syndrome JW Leiding, TP Vogel, VGJ Santarlas, R Mhaskar, MR Smith, A Carisey, ... Journal of allergy and clinical immunology 151 (4), 1081-1095, 2023 | 85 | 2023 |
| Microbiome and the immune system: From a healthy steady-state to allergy associated disruption S Mezouar, Y Chantran, J Michel, A Fabre, JC Dubus, M Leone, ... Human Microbiome Journal 10, 11-20, 2018 | 80 | 2018 |
| Syndromic diarrhea/Tricho-hepato-enteric syndrome A Fabre, C Martinez-Vinson, O Goulet, C Badens Orphanet journal of rare diseases 8, 1-7, 2013 | 79 | 2013 |
| Novel mutations in TTC37 associated with tricho‐hepato‐enteric syndrome A Fabre, C Martinez‐Vinson, B Roquelaure, C Missirian, N Andre, ... Human mutation 32 (3), 277-281, 2011 | 76 | 2011 |
| Why and when was lactase persistence selected for? Insights from Central Asian herders and ancient DNA L Segurel, P Guarino-Vignon, N Marchi, S Lafosse, R Laurent, C Bon, ... PLoS biology 18 (6), e3000742, 2020 | 74 | 2020 |
| Assessment of quality of life of the children and parents affected by inborn errors of metabolism with restricted diet: preliminary results of a cross-sectional study A Fabre, K Baumstarck, A Cano, A Loundou, J Berbis, B Chabrol, ... Health and quality of life outcomes 11, 1-8, 2013 | 73 | 2013 |
| Tricho‐Hepato‐Enteric Syndrome mutation update: Mutations spectrum of TTC37 and SKIV2L, clinical analysis and future prospects P Bourgeois, C Esteve, C Chaix, C Béroud, N Lévy, ... Human Mutation 39 (6), 774-789, 2018 | 63 | 2018 |
| Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome A Fabre, A Breton, ME Coste, V Colomb, B Dubern, A Lachaux, J Lemale, ... Archives of disease in childhood 99 (1), 35-38, 2014 | 63 | 2014 |
| Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity S Jägle, M Heeg, S Grün, A Rensing-Ehl, ME Maccari, C Klemann, ... Clinical Immunology 210, 108316, 2020 | 60 | 2020 |
| Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature … P Maillard, S Baer, É Schaefer, B Desnous, N Villeneuve, A Lépine, ... Epilepsia 63 (10), 2519-2533, 2022 | 55 | 2022 |
| Tissue-specific regulation of Drosophila NF-κB pathway activation by peptidoglycan recognition protein SC D Costechareyre, F Capo, A Fabre, D Chaduli, C Kellenberger, A Roussel, ... Journal of innate immunity 8 (1), 67-80, 2016 | 55 | 2016 |
| Ageing of polyvinylidene fluoride hollow fiber membranes in sodium hypochlorite solutions J Ravereau, A Fabre, A Brehant, R Bonnard, C Sollogoub, J Verdu Journal of Membrane Science 505, 174-184, 2016 | 54 | 2016 |
| Loss-of-function mutations in UNC45A cause a syndrome associating cholestasis, diarrhea, impaired hearing, and bone fragility C Esteve, L Francescatto, PL Tan, A Bourchany, C De Leusse, E Marinier, ... The American Journal of Human Genetics 102 (3), 364-374, 2018 | 53 | 2018 |
Joana VitteImmunology, Reims-Champagne-Ardenne Univ; IHU Méditerranée Infection; IDESP, Montpellier, Franceبريد إلكتروني تم التحقق منه على inserm.fr
