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Results: 1 to 20 of 96

Similar articles for PubMed (Select 24391736)

1.

The contribution of diet and genotype to iron status in women: a classical twin study.

Fairweather-Tait SJ, Guile GR, Valdes AM, Wawer AA, Hurst R, Skinner J, Macgregor AJ.

PLoS One. 2013 Dec 31;8(12):e83047. doi: 10.1371/journal.pone.0083047. eCollection 2013.

2.

Blood loss is a stronger predictor of iron status in men than C282Y heterozygosity or diet.

Heath AL, Roe MA, Oyston SL, Gray AR, Williams SM, Fairweather-Tait SJ.

J Am Coll Nutr. 2008 Feb;27(1):158-67.

PMID:
18460494
3.

Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins.

Whitfield JB, Cullen LM, Jazwinska EC, Powell LW, Heath AC, Zhu G, Duffy DL, Martin NG.

Am J Hum Genet. 2000 Apr;66(4):1246-58. Epub 2000 Mar 15.

4.

CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients.

Pelucchi S, Mariani R, Calza S, Fracanzani AL, Modignani GL, Bertola F, Busti F, Trombini P, Fraquelli M, Forni GL, Girelli D, Fargion S, Specchia C, Piperno A.

Haematologica. 2012 Dec;97(12):1818-25. doi: 10.3324/haematol.2012.062661. Epub 2012 Jul 6.

5.

A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.

Constantine CC, Anderson GJ, Vulpe CD, McLaren CE, Bahlo M, Yeap HL, Gertig DM, Osborne NJ, Bertalli NA, Beckman KB, Chen V, Matak P, McKie AT, Delatycki MB, Olynyk JK, English DR, Southey MC, Giles GG, Hopper JL, Allen KJ, Gurrin LC.

Br J Haematol. 2009 Oct;147(1):140-9. doi: 10.1111/j.1365-2141.2009.07843.x. Epub 2009 Aug 10.

6.

Hemochromatosis gene mutations, body iron stores, dietary iron, and risk of colorectal adenoma in women.

Chan AT, Ma J, Tranah GJ, Giovannucci EL, Rifai N, Hunter DJ, Fuchs CS.

J Natl Cancer Inst. 2005 Jun 15;97(12):917-26.

7.

Diet and genetic factors associated with iron status in middle-aged women.

Cade JE, Moreton JA, O'Hara B, Greenwood DC, Moor J, Burley VJ, Kukalizch K, Bishop DT, Worwood M.

Am J Clin Nutr. 2005 Oct;82(4):813-20.

8.

Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.

Aranda N, Viteri FE, Montserrat C, Arija V.

Ann Hematol. 2010 Aug;89(8):767-73. doi: 10.1007/s00277-010-0901-9. Epub 2010 Jan 28.

9.

Relative importance of female-specific and non-female-specific effects on variation in iron stores between women.

Whitfield JB, Treloar S, Zhu G, Powell LW, Martin NG.

Br J Haematol. 2003 Mar;120(5):860-6.

PMID:
12614223
10.

Influence of diet, menstruation and genetic factors on iron status: a cross-sectional study in Spanish women of childbearing age.

Blanco-Rojo R, Toxqui L, López-Parra AM, Baeza-Richer C, Pérez-Granados AM, Arroyo-Pardo E, Vaquero MP.

Int J Mol Sci. 2014 Mar 6;15(3):4077-87. doi: 10.3390/ijms15034077.

11.

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

Benyamin B, McRae AF, Zhu G, Gordon S, Henders AK, Palotie A, Peltonen L, Martin NG, Montgomery GW, Whitfield JB, Visscher PM.

Am J Hum Genet. 2009 Jan;84(1):60-5. doi: 10.1016/j.ajhg.2008.11.011. Epub 2008 Dec 11.

12.

Heritability of serum iron, ferritin and transferrin saturation in a genetically isolated population, the Erasmus Rucphen Family (ERF) Study.

Njajou OT, Alizadeh BZ, Aulchenko Y, Zillikens MC, Pols HA, Oostra BA, Swinkels DW, van Duijn CM.

Hum Hered. 2006;61(4):222-8. Epub 2006 Jul 27.

13.

Phenotype and HFE genotype in a population with abnormal iron markers recruited from an Endocrinology Department.

Vantyghem MC, Fajardy I, Dhondt F, Girardot C, D'Herbomez M, Danze PM, Rousseaux J, Wemeau JL.

Eur J Endocrinol. 2006 Jun;154(6):835-41.

14.

Contribution of putative genetic factors and candidate gene variants to inter-individual variation of circulating fractalkine (CX3CL1) levels in a large UK twins' sample.

Franco L, Williams FM, Trofimov S, Surdulescu G, Spector TD, Livshits G.

Hum Immunol. 2013 Mar;74(3):358-63. doi: 10.1016/j.humimm.2012.12.002. Epub 2012 Dec 20.

PMID:
23261412
15.

Dilution of candidates: the case of iron-related genes in restless legs syndrome.

Oexle K, Schormair B, Ried JS, Czamara D, Heim K, Frauscher B, Högl B, Trenkwalder C, Martin Fiedler G, Thiery J, Lichtner P, Prokisch H, Specht M, Müller-Myhsok B, Döring A, Gieger C, Peters A, Wichmann HE, Meitinger T, Winkelmann J.

Eur J Hum Genet. 2013 Apr;21(4):410-4. doi: 10.1038/ejhg.2012.193. Epub 2012 Aug 29.

16.

Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis.

Valenti L, Pulixi EA, Arosio P, Cremonesi L, Biasiotto G, Dongiovanni P, Maggioni M, Fargion S, Fracanzani AL.

Haematologica. 2007 Aug;92(8):1037-42. Epub 2007 Jul 20.

17.

Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.

Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.

Isr Med Assoc J. 2004 Jan;6(1):30-3.

18.

Genetic determinants for body iron store and type 2 diabetes risk in US men and women.

He M, Workalemahu T, Manson JE, Hu FB, Qi L.

PLoS One. 2012;7(7):e40919. doi: 10.1371/journal.pone.0040919. Epub 2012 Jul 16.

19.

Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.

Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.

Eur J Immunogenet. 2000 Jun;27(3):129-34.

PMID:
10940080
20.

Lifestyle factors in monozygotic and dizygotic twins.

Heller RF, O'Connell DL, Roberts DC, Allen JR, Knapp JC, Steele PL, Silove D.

Genet Epidemiol. 1988;5(5):311-21.

PMID:
3215506
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