Merryweather-Clarke AT - Search Results

1

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.

Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ. Merryweather-Clarke AT, et al. Hum Mol Genet. 2003 Sep 1;12(17):2241-7. doi: 10.1093/hmg/ddg225. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915468

2

Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload.

Pointon JJ, Viprakasit V, Miles KL, Livesey KJ, Steiner M, O'Riordan S, Hien TT, Merryweather-Clarke AT, Robson KJ. Pointon JJ, et al. Blood Cells Mol Dis. 2003 May-Jun;30(3):302-6. doi: 10.1016/s1079-9796(03)00041-x. Blood Cells Mol Dis. 2003. PMID: 12737949

3

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.

Viprakasit V, Vathesathokit P, Chinchang W, Tachavanich K, Pung-Amritt P, Wimhurst VL, Yenchitsomanus PT, Merryweather-Clarke AT, Tanphaichitr VS. Viprakasit V, et al. Eur J Haematol. 2004 Jul;73(1):43-9. doi: 10.1111/j.1600-0609.2004.00246.x. Eur J Haematol. 2004. PMID: 15182337

4

Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload.

Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ. Zaahl MG, et al. Hum Genet. 2004 Oct;115(5):409-17. doi: 10.1007/s00439-004-1166-y. Epub 2004 Aug 24. Hum Genet. 2004. PMID: 15338274

5

A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient.

Pointon JJ, Lok CY, Shearman JD, Suckling RJ, Rochette J, Merryweather-Clarke AT, Robson KJ. Pointon JJ, et al. Among authors: merryweather clarke at. Blood Cells Mol Dis. 2009 Sep-Oct;43(2):194-8. doi: 10.1016/j.bcmd.2009.04.007. Epub 2009 May 24. Blood Cells Mol Dis. 2009. PMID: 19477142

6

Haemochromatosis: a gene at last?

Robson KJ, Shearman JD, Merryweather-Clarke AT, Pointon JJ, Rosenberg WM, Walker AP, Dooley JS, Bomford A, Raha-Chowdhury R, Worwood M. Robson KJ, et al. J Med Genet. 1997 Feb;34(2):148-51. doi: 10.1136/jmg.34.2.148. J Med Genet. 1997. PMID: 9039993 Free PMC article. No abstract available.

7

Global prevalence of putative haemochromatosis mutations.

Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ. Merryweather-Clarke AT, et al. J Med Genet. 1997 Apr;34(4):275-8. doi: 10.1136/jmg.34.4.275. J Med Genet. 1997. PMID: 9138148 Free PMC article.

8

A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations.

Merryweather-Clarke AT, Simonsen H, Shearman JD, Pointon JJ, Nørgaard-Pedersen B, Robson KJ. Merryweather-Clarke AT, et al. Hum Mutat. 1999;13(2):154-9. doi: 10.1002/(SICI)1098-1004(1999)13:2<154::AID-HUMU8>3.0.CO;2-E. Hum Mutat. 1999. PMID: 10094552

9

Detection of C282Y and H63D in the HFE gene.

Pointon JJ, Merryweather-Clarke AT, Carella M, Robson KJ. Pointon JJ, et al. Genet Test. 2000;4(2):115-20. doi: 10.1089/10906570050114803. Genet Test. 2000. PMID: 10953949 Review.

10

Uncommon mutations and polymorphisms in the hemochromatosis gene.

Pointon JJ, Wallace D, Merryweather-Clarke AT, Robson KJ. Pointon JJ, et al. Genet Test. 2000;4(2):151-61. doi: 10.1089/10906570050114867. Genet Test. 2000. PMID: 10953955

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