| Updates of the HbVar database of human hemoglobin variants and thalassemia mutations B Giardine, J Borg, E Viennas, C Pavlidis, K Moradkhani, P Joly, ... Nucleic acids research 42 (D1), D1063-D1069, 2014 | 455 | 2014 |
| Blood rheology: key parameters, impact on blood flow, role in sickle cell disease and effects of exercise E Nader, S Skinner, M Romana, R Fort, N Lemonne, N Guillot, A Gauthier, ... Frontiers in physiology 10, 1329, 2019 | 332 | 2019 |
| Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach B Giardine, J Borg, DR Higgs, KR Peterson, S Philipsen, D Maglott, ... Nature genetics 43 (4), 295-301, 2011 | 185 | 2011 |
| Quantitative Real-Time Legionella PCR for Environmental Water Samples: Data Interpretation P Joly, PA Falconnet, J André, N Weill, M Reyrolle, F Vandenesch, ... Applied and environmental microbiology 72 (4), 2801-2808, 2006 | 183 | 2006 |
| Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease C Badens, P Joly, I Agouti, I Thuret, K Gonnet, S Fattoum, A Francina, ... haematologica 96 (11), 1712, 2011 | 100 | 2011 |
| The XmnI Gγ polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 β-thalassemia intermedia patients TKT Nguyen, P Joly, C Bardel, M Moulsma, N Bonello-Palot, A Francina Blood Cells, Molecules, and Diseases 45 (2), 124-127, 2010 | 91 | 2010 |
| Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations BM Giardine, P Joly, S Pissard, H Wajcman, DH K. Chui, RC Hardison, ... Nucleic acids research 49 (D1), D1192-D1196, 2021 | 78 | 2021 |
| Impact of COVID‐19 on red blood cell rheology. C Renoux, R Fort, E Nader, C Boisson, P Joly, E Stauffer, M Robert, ... British journal of haematology 192 (4), 2021 | 76 | 2021 |
| A genetic score for the prediction of beta-thalassemia severity F Danjou, M Francavilla, F Anni, S Satta, FR Demartis, L Perseu, M Manca, ... Haematologica 100 (4), 452, 2015 | 70 | 2015 |
| Impact of surface-area-to-volume ratio, internal viscosity and membrane viscoelasticity on red blood cell deformability measured in isotonic condition C Renoux, M Faivre, A Bessaa, L Da Costa, P Joly, A Gauthier, P Connes Scientific reports 9 (1), 6771, 2019 | 67 | 2019 |
| Increased blood viscosity and red blood cell aggregation in patients with COVID‐19 E Nader, C Nougier, C Boisson, S Poutrel, J Catella, F Martin, J Charvet, ... American journal of hematology 97 (3), 283-292, 2022 | 62 | 2022 |
| Hydroxyurea therapy modulates sickle cell anemia red blood cell physiology: Impact on RBC deformability, oxidative stress, nitrite levels and nitric oxide synthase signalling … E Nader, M Grau, R Fort, B Collins, G Cannas, A Gauthier, K Walpurgis, ... Nitric Oxide 81, 28-35, 2018 | 57 | 2018 |
| Blood rheological abnormalities in sickle cell anemia P Connes, C Renoux, M Romana, M Abkarian, P Joly, C Martin, ... Clinical hemorheology and microcirculation 68 (2-3), 165-172, 2018 | 50 | 2018 |
| Effect of age on blood rheology in sickle cell anaemia and sickle cell haemoglobin C disease: a cross-sectional study C Renoux, M Romana, P Joly, S Ferdinand, C Faes, N Lemonne, ... PloS one 11 (6), e0158182, 2016 | 48 | 2016 |
| G 6 PD deficiency and absence of α‐thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia P Joly, N Garnier, K Kebaili, C Renoux, A Dony, N Cheikh, C Renard, ... European Journal of Haematology 96 (4), 404-408, 2016 | 48 | 2016 |
| Importance of methodological standardization for the ektacytometric measures of red blood cell deformability in sickle cell anemia C Renoux, N Parrow, C Faes, P Joly, M Hardeman, J Tisdale, M Levine, ... Clinical hemorheology and microcirculation 62 (2), 173-179, 2016 | 43 | 2016 |
| Association between nitric oxide, oxidative stress, eryptosis, red blood cell microparticles, and vascular function in sickle cell anemia E Nader, M Romana, N Guillot, R Fort, E Stauffer, N Lemonne, Y Garnier, ... Frontiers in immunology 11, 551441, 2020 | 41 | 2020 |
| Alpha‐thalassaemia promotes frequent vaso‐occlusive crises in children with sickle cell anaemia through haemorheological changes C Renoux, P Connes, E Nader, S Skinner, C Faes, M Petras, Y Bertrand, ... Pediatric Blood & Cancer 64 (8), e26455, 2017 | 39 | 2017 |
| Identification and molecular characterization of four new large deletions in the β-globin gene cluster P Joly, P Lacan, C Garcia, N Couprie, A Francina Blood Cells, Molecules, and Diseases 43 (1), 53-57, 2009 | 39 | 2009 |
| Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects P Joly, C Pondarre, C Badens Annales de biologie clinique 72 (6), 639-668, 2014 | 38 | 2014 |
