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Genome-wide association study identifies genetic loci associated with iron deficiency.

Genome-wide association study identifies genetic loci associated with iron deficiency.

http://www.wikidata.org/entity/Q33869815

about

Physiology of iron metabolism Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations.Systems Epidemiology: A New Direction in Nutrition and Metabolic Disease Research The contribution of diet and genotype to iron status in women: a classical twin study.Examining the clinical use of hemochromatosis genetic testing.Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?Systems genetic analysis of multivariate response to iron deficiency in mice.Associations between Common Variants in Iron-Related Genes with Haematological Traits in Populations of African Ancestry.Genome-wide association study of serum iron phenotypes in premenopausal women of European descent.Signatures of Evolutionary Adaptation in Quantitative Trait Loci Influencing Trace Element Homeostasis in Liver.GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.Toenail iron, genetic determinants of iron status, and the risk of glioma Association between celiac disease and iron deficiency in Caucasians, but not non-Caucasians.Profound morphological changes in the erythrocytes and fibrin networks of patients with hemochromatosis or with hyperferritinemia, and their normalization by iron chelators and other agents.Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin.Hamp1 mRNA and plasma hepcidin levels are influenced by sex and strain but don't predict tissue iron levels in inbred mice.Genetic factors influencing ferritin levels in 14,126 blood donors: results from the Danish Blood Donor Study.Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis.Transferrin polymorphism and opportunistic infections in HIV-infected women in Rwanda.Transferrin Level Before Treatment and Genetic Polymorphism in HFE Gene as Predictive Markers for Response to Adalimumab in Crohn's Disease Patients.Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis COMBINING INDIVIDUAL PARTICIPANT DATA AND SUMMARY STATISTICS FROM BOTH CONTINUOUSLY VALUED AND BINARY VARIABLES TO ESTIMATE REGRESSION PARAMETERS TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia

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Genome-wide association study identifies genetic loci associated with iron deficiency.

http://www.wikidata.org/entity/Q33869815

description

2011 nî lūn-bûn

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

@zh-hk

2011年論文

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2011年論文

@zh-tw

2011年论文

@wuu

name

Genome-wide association study identifies genetic loci associated with iron deficiency.

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Genome-wide association study identifies genetic loci associated with iron deficiency.

@en

type

label

Genome-wide association study identifies genetic loci associated with iron deficiency.

@ast

Genome-wide association study identifies genetic loci associated with iron deficiency.

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prefLabel

Genome-wide association study identifies genetic loci associated with iron deficiency.

@ast

Genome-wide association study identifies genetic loci associated with iron deficiency.

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JOURNAL.PONE.0017390

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Genome-wide association study identifies genetic loci associated with iron deficiency.

@en

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Anthony A Killeen

http://www.w3.org/2001/XMLSchema#string

Beverly M Snively

http://www.w3.org/2001/XMLSchema#string

Catherine Leiendecker-Foster

http://www.w3.org/2001/XMLSchema#string

Chad P Garner

http://www.w3.org/2001/XMLSchema#string

Chris D Vulpe

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Christine E McLaren

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Clare C Constantine

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Debbie A Nickerson

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Gordon D McLaren

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James D Cook

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P2860

Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance

Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults

Lack of the bone morphogenetic protein BMP6 induces massive iron overload

GenABEL: an R library for genome-wide association analysis

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

A genome-wide association analysis of serum iron concentrations

Role of matriptase-2 (TMPRSS6) in iron metabolism.

The roles of iron in health and disease.

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e17390

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10.1371/JOURNAL.PONE.0017390

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genome-wide association study

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