| The signaling role of CD40 ligand in platelet biology and in platelet component transfusion C Aoui, A Prigent, C Sut, S Tariket, H Hamzeh-Cognasse, B Pozzetto, ... International journal of molecular sciences 15 (12), 22342-22364, 2014 | 200 | 2014 |
| The non-hemostatic aspects of transfused platelets C Sut, S Tariket, C Aubron, C Aloui, H Hamzeh-Cognasse, P Berthelot, ... Frontiers in medicine 5, 42, 2018 | 78 | 2018 |
| Transfusion as an inflammation hit: knowns and unknowns O Garraud, S Tariket, C Sut, A Haddad, C Aloui, T Chakroun, S Laradi, ... Frontiers in Immunology 7, 534, 2016 | 74 | 2016 |
| Platelet components associated with adverse reactions: predictive value of mitochondrial DNA relative to biological response modifiers F Cognasse, C Aloui, K Anh Nguyen, H Hamzeh‐Cognasse, J Fagan, ... Transfusion 56 (2), 497-504, 2016 | 57 | 2016 |
| Transfusion-associated hazards: a revisit of their presentation O Garraud, C Sut, A Haddad, S Tariket, C Aloui, S Laradi, ... Transfusion Clinique et Biologique 25 (2), 118-135, 2018 | 42 | 2018 |
| Clinical and molecular features of 5 European multigenerational families with moyamoya angiopathy L Grangeon, S Guey, JC Schwitalla, F Bergametti, M Arnould, ... Stroke 50 (4), 789-796, 2019 | 31 | 2019 |
| Levels of human platelet-derived soluble CD40 ligand depend on haplotypes of CD40LG-CD40-ITGA2 C Aloui, A Prigent, S Tariket, C Sut, J Fagan, F Cognasse, T Chakroun, ... Scientific reports 6 (1), 24715, 2016 | 26 | 2016 |
| Are polymorphisms of the immunoregulatory factor CD40LG implicated in acute transfusion reactions? C Aloui, C Sut, A Prigent, J Fagan, F Cognasse, V Granados-Herbepin, ... Scientific Reports 4 (1), 7239, 2014 | 26 | 2014 |
| Soluble CD40L and CD62P levels differ in single‐donor apheresis platelet concentrates and buffy coat–derived pooled platelet concentrates C Sut, S Tariket, C Aloui, CA Arthaud, MA Eyraud, J Fagan, P Chavarin, ... Transfusion 59 (1), 16-20, 2019 | 14 | 2019 |
| Differential protein expression of blood platelet components associated with adverse transfusion reactions C Aloui, C Barlier, S Claverol, J Fagan, D Awounou, E Tavernier, ... Journal of proteomics 194, 25-36, 2019 | 13 | 2019 |
| Genetic basis of cystinosis in Tunisian patients: Identification of novel mutation in CTNS gene L Chkioua, S Khedhiri, O Grissa, C Aloui, HB Turkia, S Ferchichi, A Miled, ... Meta Gene 5, 144-149, 2015 | 12 | 2015 |
| Leucocyte cytokines dominate platelet cytokines overtime in non-leucoreduced platelet components C Aloui, T Chakroun, A Prigent, S Jemni-Yacoub, F Cognasse, S Laradi, ... Blood Transfusion 16 (1), 63, 2018 | 11 | 2018 |
| From donor to recipient: current questions relating to humoral alloimmunization A Prigent, N Maillard, L Absi, C Aloui, F Cognasse, S Laradi, C Mariat, ... Antibodies 3 (1), 130-152, 2014 | 11 | 2014 |
| Assessment of soluble platelet CD40L and CD62P during the preparation process and the storage of apheresis platelet concentrates: absence of factors related to donors and donations C Sut, C Aloui, S Tariket, CA Arthaud, MA Eyraud, J Fagan, P Chavarin, ... Transfusion Clinique et Biologique 25 (3), 192-196, 2018 | 10 | 2018 |
| COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage T Coste, C Vincent‐Delorme, M Stichelbout, L Devisme, A Gelot, ... Prenatal diagnosis 42 (5), 601-610, 2022 | 9 | 2022 |
| Development of a highly resolutive method, using a double quadruplex tetra-primer-ARMS-PCR coupled with capillary electrophoresis to study CD40LG polymorphisms C Aloui, C Sut, F Cognasse, V Granados, M Hassine, T Chakroun, ... Molecular and cellular probes 29 (6), 335-342, 2015 | 9 | 2015 |
| Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome C Aloui, S Guey, E Pipiras, M Kossorotoff, S Guéden, M Corpechot, ... Journal of Medical Genetics 57 (5), 339-346, 2020 | 8 | 2020 |
| End‐truncated LAMB1 causes a hippocampal memory defect and a leukoencephalopathy C Aloui, D Hervé, G Marenne, F Savenier, K Le Guennec, F Bergametti, ... Annals of Neurology 90 (6), 962-975, 2021 | 7 | 2021 |
| Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease A Pinard, W Ye, SM Fraser, JA Rosenfeld, P Pichurin, SE Hickey, D Guo, ... Brain 146 (9), 3616-3623, 2023 | 6 | 2023 |
| Genetic heterogeneity of 72 patients with Mucopolysaccharidosis in Tunisia L Chkioua, C Aloui, S Laradi, O Grissa, HB Turkia, S Ouesleti, S Ferchichi, ... International Journal of New Technology and Research 1 (3), 263696, 2015 | 6 | 2015 |
