Genome-wide association study identifies genetic loci associated with iron deficiency (Q33869815)

29 July 2017

title

Genome-wide association study identifies genetic loci associated with iron deficiency (English)

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genome-wide association study

29 July 2017

main subject

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13

Lisa F Barcellos

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29 July 2017

5

Chris D Vulpe

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29 July 2017

Christine E McLaren

1

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29 July 2017

Chad P Garner

2

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29 July 2017

Clare C Constantine

3

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29 July 2017

Stela McLachlan

4

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29 July 2017

Beverly M Snively

6

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29 July 2017

Victor R Gordeuk

7

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29 July 2017

Debbie A Nickerson

8

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29 July 2017

James D Cook

9

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29 July 2017

Catherine Leiendecker-Foster

10

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29 July 2017

Kenneth B Beckman

11

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29 July 2017

John H Eckfeldt

12

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29 July 2017

Joseph A Murray

14

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29 July 2017

Paul C Adams

15

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29 July 2017

Ronald T Acton

16

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29 July 2017

Anthony A Killeen

17

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29 July 2017

Gordon D McLaren

18

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29 July 2017

language of work or name

English

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publication date

31 March 2011

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29 July 2017

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29 July 2017

volume

6

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29 July 2017

issue

3

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29 July 2017

page(s)

e17390

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Creative Commons CC0 License

29 July 2017

copyright license

start time

31 March 2011

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April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

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describes a project that uses

genome-wide association study

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

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Role of matriptase-2 (TMPRSS6) in iron metabolism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

A genome-wide association analysis of serum iron concentrations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Iron absorption and metabolism.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Blood iron homeostasis: newly discovered proteins and iron imbalance.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Lack of the bone morphogenetic protein BMP6 induces massive iron overload

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

5 July 2018

Non-HFE haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

GenABEL: an R library for genome-wide association analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

The ins and outs of iron homeostasis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Hemochromatosis and iron-overload screening in a racially diverse population.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

The roles of iron in health and disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

A genetic developmental model of iron deficiency: biological aspects

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Normal Serum Iron and Elevated Total Iron-binding Capacity in Iron-deficiency States

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

Evaluation of an automated soluble transferrin receptor (sTfR) assay on the Roche Hitachi analyzer and its comparison to two ELISA assays

5 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

Polymorphisms in the transferrin 5' flanking region associated with differences in total iron binding capacity: possible implications in iron homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

BMP6 is a key endogenous regulator of hepcidin expression and iron metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

BMP6 orchestrates iron metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

Two nonsense mutations in the TMPRSS6 gene in a patient with microcytic anemia and iron deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

Mixture distribution analysis of phenotypic markers reflecting HFE gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

Population norms for serum ferritin

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069025

The G277S transferrin mutation does not affect iron absorption in iron deficient women

29 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0017390

Human transferrin G277S mutation: a risk factor for iron deficiency anaemia

21 January 2018

1 reference

12 December 2020

HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes

1 reference

12 December 2020

A serum ferritin assay for prevalence studies of iron deficiency

1 reference

12 December 2020

The g277s mutation in transferrin does not disturb function

1 reference

12 December 2020

Selective genotyping for determination of linkage between a marker locus and a quantitative trait locus

1 reference

12 December 2020

Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: a protective role against iron deficiency?

1 reference

12 December 2020

Dissociation between tissue iron concentrations and transferrin saturation among inbred mouse strains

1 reference

12 December 2020

Serum ferritin in healthy Danes: relation to marrow haemosiderin iron stores

1 reference

12 December 2020

The effect of transferrin polymorphisms on iron metabolism

1 reference

12 December 2020

The quantitative assessment of body iron

1 reference

12 December 2020

Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0017390

Identifiers

DOI

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29 July 2017

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29 July 2017

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