Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha)). by Viprakasit, V, Green, S, Height, S, Ayyub, H, Higgs, D

Mutations in a general transcription factor, TFIIH result in a novel unlinked form of beta thalassaemia in individuals with trichothiodystrophy. by Viprakasit, V, Gibbons, R, Broughton, B, Lehmann, A, Higgs, D

Genetic study and haplotype analysis of alpha hemoglobin stabilizing protein (AHSP) in beta thalassaemia/Hb E disease with variable clinical severity. by Viprakasit, V, Tanphaichitr, V, Chinchang, W, Weiss, M, Higgs, D

De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia. by Viprakasit, V, Kidd, A, Ayyub, H, Horsley, S, Hughes, J, Higgs, D

Estimating the burden of α-thalassaemia in Thailand using a comprehensive prevalence database for Southeast Asia by Hockham, C, Ekwattanakit, S, Bhatt, S, Penman, B, Gupta, S, Viprakasit, V, Piel, F

Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia. by Viprakasit, V, Tanphaichitr, V, Chinchang, W, Sangkla, P, Weiss, M, Higgs, D

Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome. by Steensma, D, Viprakasit, V, Hendrick, A, Goff, D, Leach, J, Gibbons, R, Higgs, D

A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element. by Viprakasit, V, Harteveld, C, Ayyub, H, Stanley, J, Giordano, P, Wood, W, Higgs, D

Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease. by Viprakasit, V, Tanphaichitr, V, Veerakul, G, Chinchang, W, Petrarat, S, Pung-Amritt, P, Higgs, D

Clinical phenotypes and molecular characterization of Hb H-Pakse disease. by Viprakasit, V, Tanphaichitr, V, Pung-Amritt, P, Petrarat, S, Suwantol, L, Fisher, C, Higgs, D

An entirely novel form of a thalassemia in patients from the south pacific linked to chromosome 16 by Viprakasit, V, De Gobbi, M, Ayyub, H, Ragoussis, L, Wood, W, Bowden, D, Higgs, D

Identification of mutations in a trans-acting factor with different effects on alpha and beta globin expression. by Viprakasit, V, Gibbons, R, Tolmie, J, Lunt, P, Winter, R, Broughton, B, Lehmann, A, Higgs, DR

Identification of mutations in a trans-acting factor with different effects on alpha and beta globin expression. by Viprakasit, V, Gibbons, R, Tolmie, J, Lunt, P, Winter, R, Broughton, B, Lehmann, A, Higgs, DR

Recent advances in understanding haemochromatosis: a transition state. by Robson, K, Merryweather-Clarke, A, Cadet, E, Viprakasit, V, Zaahl, MG, Pointon, J, Weatherall, D, Rochette, J

Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload. by Pointon, J, Viprakasit, V, Miles, K, Livesey, K, Steiner, M, O'Riordan, S, Hien, T, Merryweather-Clarke, A, Robson, K

Molecular diagnosis of the first ferroportin mutation (C326Y) in the far east causing a dominant form of inherited iron overload by Viprakasit, V, Merryweather-Clarke, A, Chinthammitr, Y, Schimanski, L, Drakesmith, H, Srichairatanakool, S, Limwongse, C, Townsend, A, Robson, K

Identification of a gain-of-function SNP causing a new model of alpha-thalassaemia. by De Gobbi, M, Viprakasit, V, de Jong, P, Yoshinaga, Y, Cheng, J, Hughes, J, Fisher, C, Wood, W, Bowden, D, Higgs, D

Analysis of DNA Methylation at the Human Alpha Globin Cluster during Hematopoiesis by Ekwattanakit, S, Ayyub, H, Clark, K, Marques-Kranc, F, Butler, S, Sloane-Stanley, J, Sharpe, J, Colella, S, Ragoussis, J, Viprakasit, V, Gibbons, R, Higgs, D

What is the evidence of a role for host genetics in susceptibility to influenza A/H5N1? by Horby, P, Sudoyo, H, Viprakasit, V, Fox, A, Thai, P, Yu, H, Davila, S, Hibberd, M, Dunstan, S, Monteerarat, Y, Farrar, J, Marzuki, S, Hien, N

Mutations in the general transcription factor TFIIH result in beta-thalassaemia in individuals with trichothiodystrophy. by Viprakasit, V, Gibbons, R, Broughton, B, Tolmie, J, Brown, D, Lunt, P, Winter, R, Marinoni, S, Stefanini, M, Brueton, L, Lehmann, A, Higgs, D