PubMed (OMIM) for id: 854011

Year	Number of Results
1952	1
1958	1
1959	1
1962	1
1965	1
1966	1
1967	2
1973	1
1974	1
1976	2
1977	5
1978	4
1979	7
1980	5
1981	1
1982	3
1983	4
1984	3
1985	3
1986	5
1987	6
1988	5
1989	4
1990	8
1991	6
1992	8
1993	4
1994	3
1995	4
1996	8
1997	19
1998	14
1999	14
2000	5
2001	12
2002	8
2003	8
2004	8
2005	1
2024	0

1

The Q283P amino-acid change in HFE leads to structural and functional consequences similar to those described for the mutated 282Y HFE protein.

Ka C, Le Gac G, Dupradeau FY, Rochette J, Férec C. Ka C, et al. Hum Genet. 2005 Sep;117(5):467-75. doi: 10.1007/s00439-005-1307-y. Epub 2005 Jun 18. Hum Genet. 2005. PMID: 15965644

2

The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis.

Valenti L, Conte D, Piperno A, Dongiovanni P, Fracanzani AL, Fraquelli M, Vergani A, Gianni C, Carmagnola L, Fargion S. Valenti L, et al. J Med Genet. 2004 Dec;41(12):946-50. doi: 10.1136/jmg.2004.019588. J Med Genet. 2004. PMID: 15591282 Free PMC article.

3

Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis.

Lee PL, Barton JC, Brandhagen D, Beutler E. Lee PL, et al. Br J Haematol. 2004 Oct;127(2):224-9. doi: 10.1111/j.1365-2141.2004.05165.x. Br J Haematol. 2004. PMID: 15461631 Free article.

4

The origin and spread of the HFE-C282Y haemochromatosis mutation.

Distante S, Robson KJ, Graham-Campbell J, Arnaiz-Villena A, Brissot P, Worwood M. Distante S, et al. Hum Genet. 2004 Sep;115(4):269-79. doi: 10.1007/s00439-004-1152-4. Hum Genet. 2004. PMID: 15290237

5

Hereditary hemochromatosis--a new look at an old disease.

Pietrangelo A. Pietrangelo A. N Engl J Med. 2004 Jun 3;350(23):2383-97. doi: 10.1056/NEJMra031573. N Engl J Med. 2004. PMID: 15175440 Review. No abstract available.

6

An Hfe-dependent pathway mediates hyposideremia in response to lipopolysaccharide-induced inflammation in mice.

Roy CN, Custodio AO, de Graaf J, Schneider S, Akpan I, Montross LK, Sanchez M, Gaudino A, Hentze MW, Andrews NC, Muckenthaler MU. Roy CN, et al. Nat Genet. 2004 May;36(5):481-5. doi: 10.1038/ng1350. Epub 2004 Apr 18. Nat Genet. 2004. PMID: 15098034

7

Hemochromatosis mutations in the general population: iron overload progression rate.

Andersen RV, Tybjaerg-Hansen A, Appleyard M, Birgens H, Nordestgaard BG. Andersen RV, et al. Blood. 2004 Apr 15;103(8):2914-9. doi: 10.1182/blood-2003-10-3564. Epub 2003 Dec 4. Blood. 2004. PMID: 15070663 Free article.

8

Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.

Robson KJ, Lehmann DJ, Wimhurst VL, Livesey KJ, Combrinck M, Merryweather-Clarke AT, Warden DR, Smith AD. Robson KJ, et al. J Med Genet. 2004 Apr;41(4):261-5. doi: 10.1136/jmg.2003.015552. J Med Genet. 2004. PMID: 15060098 Free PMC article.

9

The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.

Livesey KJ, Wimhurst VL, Carter K, Worwood M, Cadet E, Rochette J, Roberts AG, Pointon JJ, Merryweather-Clarke AT, Bassett ML, Jouanolle AM, Mosser A, David V, Poulton J, Robson KJ. Livesey KJ, et al. J Med Genet. 2004 Jan;41(1):6-10. doi: 10.1136/jmg.2003.008805. J Med Genet. 2004. PMID: 14729817 Free PMC article.

10

Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis.

Tomatsu S, Orii KO, Fleming RE, Holden CC, Waheed A, Britton RS, Gutierrez MA, Velez-Castrillon S, Bacon BR, Sly WS. Tomatsu S, et al. Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15788-93. doi: 10.1073/pnas.2237037100. Epub 2003 Dec 12. Proc Natl Acad Sci U S A. 2003. PMID: 14673107 Free PMC article.

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