Citations (13)
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Eng K Gan, Debbie Trinder, Oyekoya T Ayonrinde & John K Olynyk. (2009) Genetics of hereditary hemochromatosis: a clinical perspective. Expert Review of Endocrinology & Metabolism 4:3, pages 225-239.
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Enrico Rossi, John K Olynyk & Gary P Jeffrey. (2008) Clinical penetrance of C282Y homozygous HFE hemochromatosis. Expert Review of Hematology 1:2, pages 205-216.
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S. Distante. (2006) Genetic predisposition to iron overload: Prevalence and phenotypic expression of hemochromatosis‐associated HFE‐C282Y gene mutation. Scandinavian Journal of Clinical and Laboratory Investigation 66:2, pages 83-100.
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Articles from other publishers (10)
James C. Barton, J. Clayborn Barton & Ronald T. Acton. (2022) HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity. Hereditas 159:1.
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Andreia Soares da Silva, Tatiana Lins Carvalho, Kleyton Palmeira do Ó, Débora Nascimento da Nóbrega, Roberta dos Santos Souza, Victor Fernando da Silva Lima, Isabela Cristina Cordeiro Farias, Taciana Furtado de Mendonça Belmont, Maria do Socorro de Mendonça Cavalcanti & Demócrito de Barros Miranda-Filho. (2020) Association of the polymorphisms of the genes APOC3 (rs2854116), ESR2 (rs3020450), HFE (rs1799945), MMP1 (rs1799750) and PPARG (rs1801282) with lipodystrophy in people living with HIV on antiretroviral therapy: a systematic review. Molecular Biology Reports 47:6, pages 4779-4787.
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Constance Delaby, Vincent Oustric, Caroline Schmitt, Francoise Muzeau, Anne-Marie Robreau, Philippe Letteron, Eric Couchi, Angel Yu, Saïd Lyoumi, Jean-Charles Deybach, Herve Puy, Zoubida Karim, Carole Beaumont, Bernard Grandchamp, Peter Demant & Laurent Gouya. (2013) Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in mice. Mammalian Genome 24:11-12, pages 427-438.
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James E. Nelson, Debbie Trinder & Kris V. Kowdley. 2011. Molecular Pathology of Liver Diseases. Molecular Pathology of Liver Diseases
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Ronald T. Acton, James C. Barton, Catherine Leiendecker-Foster, Christopher Zaun, Christine E. McLaren & John H. Eckfeldt. (2010) Tumor necrosis factor-alpha promoter variants and iron phenotypes in 785 Hemochromatosis and Iron Overload Screening (HEIRS) Study participants. Blood Cells, Molecules, and Diseases 44:4, pages 252-256.
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Sarah H. AtkinsonKirk A. RockettGareth MorganPhilip A. BejonGiorgio SirugoMaria A. O'Connell, Neil HanchardDominic P. Kwiatkowski & Andrew M. Prentice. (2008) Tumor necrosis factor SNP haplotypes are associated with iron deficiency anemia in West African children. Blood 112:10, pages 4276-4283.
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Marnie J. Wood, Lawrie W. Powell & Grant A. Ramm. (2008) Environmental and genetic modifiers of the progression to fibrosis and cirrhosis in hemochromatosis. Blood 111:9, pages 4456-4462.
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Todd Hulgan, Pablo Tebas, Jeffrey A. Canter, Kathleen Mulligan, David W. Haas, Michael Dubé, Steven Grinspoon, Gregory K. Robbins, Alison A. Motsinger & Asha R. Kallianpur. (2008) Hemochromatosis Gene Polymorphisms, Mitochondrial Haplogroups, and Peripheral Lipoatrophy during Antiretroviral Therapy. The Journal of Infectious Diseases 197:6, pages 858-866.
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RT Acton, BM Snively, JC Barton, CE McLaren, PC Adams, SS Rich, JH Eckfeldt, RD Press, P Sholinsky, C Leiendecker-Foster, GD McLaren, MR Speechley, EL Harris, FW Dawkins & VR Gordeuk. (2007) A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study. Clinical Genetics 71:6, pages 518-529.
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Pierre-Alexandre Krayenbuehl, Friedrich E Maly, Martin Hersberger, Peter Wiesli, Andreas Himmelmann, Karim Eid, Peter Greminger, Wilhelm Vetter & Georg Schulthess. (2006) Tumor Necrosis Factor-α −308G>A Allelic Variant Modulates Iron Accumulation in Patients with Hereditary Hemochromatosis. Clinical Chemistry 52:8, pages 1552-1558.
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