| Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey P Gresele, P Harrison, L Bury, E Falcinelli, C Gachet, CP Hayward, ... Journal of Thrombosis and Haemostasis 12 (9), 1562-1569, 2014 | 200 | 2014 |
| A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders I Simeoni, JC Stephens, F Hu, SVV Deevi, K Megy, TK Bariana, ... Blood, The Journal of the American Society of Hematology 127 (23), 2791-2803, 2016 | 196 | 2016 |
| Megakaryocytes differentially sort mRNAs for matrix metalloproteinases and their inhibitors into platelets: a mechanism for regulating synthetic events L Cecchetti, ND Tolley, N Michetti, L Bury, AS Weyrich, P Gresele Blood, The Journal of the American Society of Hematology 118 (7), 1903-1911, 2011 | 185 | 2011 |
| Bleeding risk of surgery and its prevention in patients with inherited platelet disorders S Orsini, P Noris, L Bury, PG Heller, C Santoro, RA Kadir, NC Butta, ... haematologica 102 (7), 1192, 2017 | 130 | 2017 |
| Association of neutrophil activation, more than platelet activation, with thrombotic complications in coronavirus disease 2019 E Petito, E Falcinelli, U Paliani, E Cesari, G Vaudo, M Sebastiano, ... The Journal of infectious diseases 223 (6), 933-944, 2021 | 115 | 2021 |
| Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: a communication from the Platelet Physiology SSC P Gresele, S Orsini, P Noris, E Falcinelli, MC Alessi, L Bury, M Borhany, ... Journal of Thrombosis and Haemostasis 18 (3), 732-739, 2020 | 91 | 2020 |
| A novel mechanism regulating human platelet activation by MMP-2–mediated PAR1 biased signaling M Sebastiano, S Momi, E Falcinelli, L Bury, MF Hoylaerts, P Gresele Blood, The Journal of the American Society of Hematology 129 (7), 883-895, 2017 | 82 | 2017 |
| Inherited platelet function disorders: algorithms for phenotypic and genetic investigation P Gresele, L Bury, E Falcinelli Seminars in thrombosis and hemostasis 42 (03), 292-305, 2016 | 77 | 2016 |
| Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia P Noris, N Schlegel, C Klersy, PG Heller, E Civaschi, N Pujol-Moix, ... haematologica 99 (8), 1387, 2014 | 77 | 2014 |
| Outside-In Signalling Generated by a Constitutively Activated Integrin αIIbβ3 Impairs Proplatelet Formation in Human Megakaryocytes L Bury, A Malara, P Gresele, A Balduini PloS one 7 (4), e34449, 2012 | 76 | 2012 |
| Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: communication from the SSC of the ISTH K Megy, K Downes, I Simeoni, L Bury, J Morales, R Mapeta, ... Journal of Thrombosis and Haemostasis 17 (8), 1253, 2019 | 67 | 2019 |
| Cytoskeletal perturbation leads to platelet dysfunction and thrombocytopenia in variant forms of Glanzmann thrombasthenia L Bury, E Falcinelli, D Chiasserini, TA Springer, JE Italiano Jr, P Gresele haematologica 101 (1), 46, 2016 | 58 | 2016 |
| Maraviroc intensification modulates atherosclerotic progression in HIV-suppressed patients at high cardiovascular risk. A randomized, crossover pilot study D Francisci, M Pirro, E Schiaroli, MR Mannarino, S Cipriani, V Bianconi, ... Open forum infectious diseases 6 (4), ofz112, 2019 | 56 | 2019 |
| Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome MC Sims, L Mayer, JH Collins, TK Bariana, K Megy, C Lavenu-Bombled, ... Blood, The Journal of the American Society of Hematology 136 (17), 1956-1967, 2020 | 48 | 2020 |
| Mechanisms of thrombocytopenia in platelet-type von Willebrand disease L Bury, A Malara, S Momi, E Petito, A Balduini, P Gresele Haematologica 104 (7), 1473, 2019 | 46 | 2019 |
| Platelet function assays in diagnosis: an update P Gresele, L Bury, AM Mezzasoma, E Falcinelli Expert review of hematology 12 (1), 29-46, 2019 | 41 | 2019 |
| Laboratory diagnosis of clinically relevant platelet function disorders P Gresele, E Falcinelli, L Bury International journal of laboratory hematology 40, 34-45, 2018 | 41 | 2018 |
| GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in … K Megy, K Downes, MC Morel‐Kopp, JM Bastida, S Brooks, L Bury, ... Journal of Thrombosis and Haemostasis 19 (10), 2612-2617, 2021 | 37 | 2021 |
| Next‐generation sequencing for the diagnosis of MYH9‐RD: Predicting pathogenic variants L Bury, K Megy, JC Stephens, L Grassi, D Greene, N Gleadall, K Althaus, ... Human Mutation 41 (1), 277-290, 2020 | 37 | 2020 |
| Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders E Civaschi, C Klersy, F Melazzini, N Pujol‐Moix, C Santoro, M Cattaneo, ... British Journal of Haematology 170 (4), 559-563, 2015 | 37 | 2015 |
