Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations (Q34325709)

1 August 2017

Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations (English)

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single-nucleotide polymorphism

1 August 2017

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12

Lisa F Barcellos

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1 August 2017

Christine E McLaren

1

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1 August 2017

Stela McLachlan

2

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1 August 2017

Chad P Garner

3

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1 August 2017

Chris D Vulpe

4

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1 August 2017

Victor R Gordeuk

5

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1 August 2017

John H Eckfeldt

6

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1 August 2017

Paul C Adams

7

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1 August 2017

Ronald T Acton

8

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1 August 2017

Joseph A Murray

9

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1 August 2017

Catherine Leiendecker-Foster

10

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1 August 2017

Beverly M Snively

11

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1 August 2017

James D Cook

13

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1 August 2017

Gordon D McLaren

14

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1 August 2017

language of work or name

English

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publication date

22 June 2012

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1 August 2017

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1 August 2017

7

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6

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1 August 2017

e38339

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Creative Commons Attribution 4.0 International

1 August 2017

start time

22 June 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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

1 reference

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CUBN is a gene locus for albuminuria

6 July 2018

1 reference

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Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

A genome-wide association analysis of serum iron concentrations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

Iron absorption and metabolism.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

Blood iron homeostasis: newly discovered proteins and iron imbalance.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

GenABEL: an R library for genome-wide association analysis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

The ins and outs of iron homeostasis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

Categorization of humans in biomedical research: genes, race and disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

Megalin-dependent cubilin-mediated endocytosis is a major pathway for the apical uptake of transferrin in polarized epithelia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

The roles of iron in health and disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

Association mapping in structured populations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

A genetic developmental model of iron deficiency: biological aspects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

Serum transferrin receptor: a quantitative measure of tissue iron deficiency.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382217

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

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0038339

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

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0038339

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0038339

The quantitative assessment of body iron

21 January 2018

1 reference

12 December 2020

A serum ferritin assay for prevalence studies of iron deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Summary of a report on assessment of the iron nutritional status of the United States population. Expert Scientific Working Group

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0038339

Identifiers

DOI

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1 August 2017

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1 August 2017

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