Holme, S. Alexander, Worwood, Mark, Anstey, Alexander Vincent ![]() |
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Goringe, Andrew, Ellis, Richard, McDowell, Ian Frederick, Vidal-Alaball, Josep ![]() ![]() |
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McCune, Catherine Anne, Ravine, D., Carter, K., Jackson, H. A., Dutton, D., Hedderich, J., Krawczak, M. and Worwood, Mark 2006. Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients. Gut 55 (4) , pp. 554-562. 10.1136/gut.2005.070342 |
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Bharadwaj, A., Prior, L., Atkinson, P., Clarke, Angus John ![]() |
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Feeney, G. P., Ashfield-Watt, P. A. L., Burr, Michael Leslie, Dunstan, F. D. J., McDowell, I. F. W. and Worwood, Mark 2004. Heterozygosity for the haemochromatosis mutation HFE C282Y is not a risk factor for angina [Letter]. Heart 90 (8) , pp. 939-940. 10.1136/hrt.2003.014480 |
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Carter, Kymberley, Bowen, Derrick John, McCune, Catherine Anne and Worwood, Mark 2004. Response to Langlois et al (LE 01059). British Journal of Haematology 124 (4) , pp. 556-557. 10.1046/j.1365-2141.2003.04798.x |
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Carter, Kymberley, Bowen, Derrick John, McCune, Catherine Anne and Worwood, Mark 2003. Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysis. British Journal of Haematology 122 (2) , pp. 326-332. 10.1046/j.1365-2141.2003.04436.x |
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McCune, Catherine Anne, Al-Jader, Layla N., May, Alison, Hayes, Sara Lindsay, Jackson, Helen A. and Worwood, Mark 2002. Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload. Human Genetics 111 (6) , pp. 538-543. 10.1007/s00439-002-0824-1 |
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Devalia, Vinod, Carter, Kymberley, Walker, Ann P., Perkins, Stephen J., Worwood, Mark, May, Alison and Dooley, James S. 2002. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3). Blood 100 (2) , pp. 695-697. 10.1182/blood-2001-11-0132 |
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Jackson, H. A., Carter, Kymberley, Darke, C., Guttridge, M. G., Ravine, D., Hutton, R. D., Napier, J. A. and Worwood, Mark 2001. HFE mutations, iron deficiency and overload in 10,500 blood donors. British Journal of Haematology 114 (2) , pp. 474-484. 10.1046/j.1365-2141.2001.02949.x |
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Dorak, M. Tevfik, Burnett, Alan Kenneth, Worwood, Mark, Sproul, Anne M. and Gibson, Brenda E. S. 1999. The C282Y mutation of HFE is another male-specific risk factor for childhood acute lymphoblastic leukemia [Letter]. Blood 94 (11) , pp. 3957-3958. |
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MacLean, R. M., Feeney, G. P., Bowley, S. J., Bowen, Derrick John, Worwood, Mark and Collins, Peter William ![]() |
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Jackson, H. A., Bowen, Derrick John and Worwood, Mark 1997. Rapid genetic screening for haemochromatosis using heteroduplex technology. British Journal of Haematology 98 (4) , pp. 856-859. 10.1046/j.1365-2141.1997.3193136.x |
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White, A. D., Jones, B. M., Worwood, Mark, Webb, D. K. H., Davies, K. R., Clark, V. and Burnett, Alan Kenneth 1996. Monitoring disease status in paediatric acute lymphoblastic leukemia (ALL) using conventional cytogenetic techniques, fluorescence in situ hybridisation (FISH) and PCR detection of IgH gene rearrangements (CDR3) [Abstract]. Blood 88 (10) , p. 285. |
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Worwood, M., Evans, W. D. ![]() |
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Bowen, Derrick John, Raha-Chowdhury, R. and Worwood, Mark 1996. A new highly polymorphic marker in the 5' untranslated region of HLA-F shows strong allelic association with haemochromatosis. Human Genetics 97 (2) , pp. 228-231. 10.1007/BF02265271 |
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Raha-Chowdhury, Ruma, Bowen, Derrick John, Stone, Caroline, Pointon, Jennifer J., Terwilliger, Joseph D., Shearman, Jeremy D., Robson, Kathryn J. H., Bomford, Adrian and Worwood, Mark 1995. New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105. Human Molecular Genetics 4 (10) , pp. 1869-1874. 10.1093/hmg/4.10.1869 |
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Raha-Chowdhury, R., Bowen, Derrick John, Burnett, Alan Kenneth and Worwood, Mark 1995. Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis. Journal of Medical Genetics 32 (6) , pp. 446-452. 10.1136/jmg.32.6.446 |
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Dorak, M. Tevfik, Wilson, David W. L., Galbraith, Ian, Henderson, Nancy, Burnett, Alan Kenneth and Worwood, Mark 1995. A molecular analysis of the telomeric end of the major histocompatibility complex: DNA typing of HLA-A3 subtypes and -B7. Human Immunology 42 (1) , pp. 1-8. 10.1016/0198-8859(94)00054-T |
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Dorak, M. Tevfik, Burnett, Alan Kenneth and Worwood, Mark 1994. Thymus-leukaemia antigens: The haemochromatosis gene product? Immunology and Cell Biology 72 (5) , pp. 435-439. 10.1038/icb.1994.64 |
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Worwood, Mark, Raha-Chowdhury, Ruma, Dorak, M. Tevfik, Darke, C., Bowen, Derrick John and Burnett, Alan Kenneth 1994. Alleles at D6S265 and D6S105 define a haemochromatosis-specific genotype. British Journal of Haematology 86 (4) , pp. 863-866. 10.1111/j.1365-2141.1994.tb04843.x |
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Dorak, M. T., Chalmers, E. A., Gaffney, D., Wilson, D. W., Glabraith, I., Henderson, N., Worwood, Mark, Mills, K. I. and Burnett, Alan Kenneth 1994. Human major histocompatibility complex contains several leukemia susceptibility genes. Leukemia and Lymphoma 12 (3-4) , pp. 211-222. 10.3109/10428199409059592 |
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Dorak, M. T., Raha-Chowdhury, R., Worwood, Mark, Mills, Kenneth I. and Burnett, Alan Kenneth 1993. A molecular investigation of homozygosity for HLA-A3 [Abstract]. British Journal of Haematology 84 (Sup.1) , p. 59. 10.1111/j.1365-2141.1993.tb06831.x |
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Dorak, M. Trevfik, Raha-Chowdhury, R., Owen, G., Worwood, Mark, Mills, K. I. and Burnett, Alan Kenneth 1993. A molecular analysis of HLA-A3 subtypes: Relevance to disease associations. Human Immunology 37 (S1) , p. 19. 10.1016/0198-8859(93)90221-L |
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