| Infections in 252 patients with common variable immunodeficiency E Oksenhendler, L Gérard, C Fieschi, M Malphettes, G Mouillot, ... Clinical Infectious Diseases 46 (10), 1547-1554, 2008 | 557 | 2008 |
| Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect M Malphettes, L Gérard, M Carmagnat, G Mouillot, N Vince, D Boutboul, ... Clinical Infectious Diseases 49 (9), 1329-1338, 2009 | 256 | 2009 |
| B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the disease G Mouillot, M Carmagnat, L Gérard, JL Garnier, C Fieschi, N Vince, ... Journal of clinical immunology 30, 746-755, 2010 | 193 | 2010 |
| Autoimmunity in common variable immunodeficiency: correlation with lymphocyte phenotype in the French DEFI study J Boileau, G Mouillot, L Gérard, M Carmagnat, C Rabian, E Oksenhendler, ... Journal of autoimmunity 36 (1), 25-32, 2011 | 183 | 2011 |
| Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations M Daya, N Rafaels, TM Brunetti, S Chavan, AM Levin, A Shetty, ... Nature communications 10 (1), 880, 2019 | 93 | 2019 |
| Low circulating natural killer cell counts are associated with severe disease in patients with common variable immunodeficiency M Ebbo, L Gérard, S Carpentier, F Vély, S Cypowyj, C Farnarier, N Vince, ... EBioMedicine 6, 222-230, 2016 | 79 | 2016 |
| Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor V Gouilleux-Gruart, H Chapel, S Chevret, M Lucas, M Malphettes, ... Clinical & Experimental Immunology 171 (2), 186-194, 2013 | 71 | 2013 |
| Selective SIRPα blockade reverses tumor T cell exclusion and overcomes cancer immunotherapy resistance V Gauttier, S Pengam, J Durand, K Biteau, C Mary, A Morello, M Néel, ... The Journal of clinical investigation 130 (11), 6109-6123, 2020 | 60 | 2020 |
| Killer cell immunoglobulin–like receptor 3DL1 variation modifies HLA-B* 57 protection against HIV-1 MP Martin, V Naranbhai, PR Shea, Y Qi, V Ramsuran, N Vince, X Gao, ... The Journal of clinical investigation 128 (5), 1903-1912, 2018 | 59 | 2018 |
| HLA-C level is regulated by a polymorphic Oct1 binding site in the HLA-C promoter region N Vince, H Li, V Ramsuran, V Naranbhai, FM Duh, BP Fairfax, B Saleh, ... The American Journal of Human Genetics 99 (6), 1353-1358, 2016 | 59 | 2016 |
| Immune alterations in patients with type 1 autoimmune hepatitis persist upon standard immunosuppressive treatment A Renand, S Habes, JF Mosnier, H Aublé, JP Judor, N Vince, P Hulin, ... Hepatology communications 2 (8), 972-985, 2018 | 54 | 2018 |
| Diversity of the human LILRB3/A6 locus encoding a myeloid inhibitory and activating receptor pair AA Bashirova, R Apps, N Vince, Y Mochalova, XG Yu, M Carrington Immunogenetics 66, 1-8, 2014 | 50 | 2014 |
| The nature of genetic and environmental susceptibility to multiple sclerosis DS Goodin, P Khankhanian, PA Gourraud, N Vince PLoS One 16 (3), e0246157, 2021 | 45 | 2021 |
| Parental consanguinity is associated with a severe phenotype in common variable immunodeficiency C Rivoisy, L Gérard, D Boutboul, M Malphettes, C Fieschi, I Durieu, F Tron, ... Journal of clinical immunology 32, 98-105, 2012 | 40 | 2012 |
| Distribution of bacterial α1, 3-galactosyltransferase genes in the human gut microbiome E Montassier, GA Al-Ghalith, C Mathé, Q Le Bastard, V Douillard, ... Frontiers in Immunology 10, 3000, 2020 | 39 | 2020 |
| Defects in the CD19 complex predispose to glomerulonephritis, as well as IgG1 subclass deficiency N Vince, D Boutboul, G Mouillot, N Just, M Peralta, JL Casanova, ... Journal of allergy and clinical immunology 127 (2), 535-538. e2, 2011 | 39 | 2011 |
| Whole genome sequencing of SIV-infected macaques identifies candidate loci that may contribute to host control of virus replication AJ Ericsen, GJ Starrett, JM Greene, M Lauck, M Raveendran, DR Deiros, ... Genome biology 15, 1-14, 2014 | 36 | 2014 |
| Genome-wide association study identifies HLA-DPB1 as a significant risk factor for severe aplastic anemia SA Savage, M Viard, C O’huigin, W Zhou, M Yeager, SA Li, T Wang, ... The American Journal of Human Genetics 106 (2), 264-271, 2020 | 29 | 2020 |
| Lessons from CKD-related genetic association studies–moving forward S Limou, N Vince, A Parsa Clinical journal of the American Society of Nephrology 13 (1), 140-152, 2018 | 28 | 2018 |
| Highly conserved extended haplotypes of the major histocompatibility complex and their relationship to multiple sclerosis susceptibility DS Goodin, P Khankhanian, PA Gourraud, N Vince PLoS One 13 (2), e0190043, 2018 | 27 | 2018 |
Pierre-Antoine GourraudUniversity of California,USA - University of Nantes, France在 univ-nantes.fr 的电子邮件经过验证
