Viprakasit, Vip
Siriraj Hospital · University of Milan · University of Campania "Luigi Vanvitelli" · Mahidol University · Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · Ente Ospedaliero Ospedali Galliera · Azienda Ospedaliera G. Brotzu
6 papers on CoChatORCID 0000-0003-3162-1849
Most cited papers
- Verified
A phase 3 trial of luspatercept in patients with transfusion-dependent β-thalassemia.
Cappellini, M. D., Viprakasit, V., Taher, A. T., Georgiev, P., Kuo, K. H. M., Coates, T., Voskaridou, E., Liew, H.-K., Pazgal-Kobrowski, I., Forni, G. L., et al. (2020) · New England Journal of Medicine
Hemoglobinopathies and Related DisordersBlood transfusion and management
Cited by 332
- Verified
Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin
Drakesmith, H., Schimanski, L. M., Ormerod, E., Merryweather-Clarke, A. T., Viprakasit, V., Edwards, J. P., Sweetland, E., Bastin, J. M., Cowley, D., Chinthammitr, Y., et al. (2005) · Blood
Iron Metabolism and DisordersNeurological diseases and metabolism
Cited by 264
- Verified
In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations
Schimanski, L. M., Drakesmith, H., Merryweather-Clarke, A. T., Viprakasit, V., Edwards, J. P., Sweetland, E., Bastin, J. M., Cowley, D., Chinthammitr, Y., Robson, K. J. H., et al. (2005) · Blood
Iron Metabolism and DisordersNeurological diseases and metabolism
Cited by 212
- Verified
Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition
Lower, K. M., Hughes, J. R., De Gobbi, M., Henderson, S., Viprakasit, V., Fisher, C., Goriely, A., Ayyub, H., Sloane-Stanley, J., Vernimmen, D., et al. (2009) · Proceedings of the National Academy of Sciences
Genomics and Chromatin DynamicsHemoglobinopathies and Related Disorders
Cited by 92
- Verified
Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions
Puehringer, H., Najmabadi, H., Law, H.-Y., Krugluger, W., Viprakasit, V., Pissard, S., Baysal, E., Taher, A., Farra, C., Al-Ali, A., et al. (2007) · Clinical Chemical Laboratory Medicine
Hemoglobinopathies and Related DisordersBlood groups and transfusion
Cited by 45
- Verified
Molecular Diagnosis of the First Ferroportin Mutation (C326Y) in the Far East Causing a Dominant Form of Inherited Iron Overload.
Viprakasit, V., Merryweather-Clarke, A. T., Chinthammitr, Y., Schimanski, L., Drakesmith, H., Srichairatanakool, S., Limwongse, C., Townsend, A., & Robson, K. J. H. (2004) · Blood
Iron Metabolism and DisordersNeurological diseases and metabolism
Cited by 13
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