Number of items: 24.
Goringe, Andrew, Ellis, Richard, McDowell, Ian Frederick, Vidal-Alaball, Josep ORCID: https://orcid.org/0000-0002-3527-4242, Jenkins, Christopher, Butler, Christopher Collett ORCID: https://orcid.org/0000-0002-0102-3453 and Worwood, Mark
2006.
The limited value of methylmalonic acid, homocysteine and holotranscobalamin in the diagnosis of early B12 deficiency.
Haematologica
91
(2)
, pp. 231-234.
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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 ORCID: https://orcid.org/0000-0002-1200-9286 and Worwood, Mark
2006.
The genetic iceberg: risk and uncertainty.
Webster, A., ed.
New Technologies in Health Care: Challenge, Change and Innovation,
Health, Technology and Society,
Basingstoke:
Palgrave MacMillan,
pp. 11-24.
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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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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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MacLean, R. M., Feeney, G. P., Bowley, S. J., Bowen, Derrick John, Worwood, Mark and Collins, Peter William ORCID: https://orcid.org/0000-0002-6410-1324
1999.
Factor V Leiden and the common haemochromatosis mutation HFE C282Y: is there an association in familial venous thromboembolic disease?
British Journal of Haematology
107
(1)
, pp. 210-212.
10.1046/j.1365-2141.1999.01663.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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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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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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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. 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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This list was generated on Sat Nov 8 11:51:26 2025 GMT.