The impact of HFE mutations on haemoglobin and iron status in individuals experiencing repeated iron loss through blood donation*. (Q36430010)

14 August 2017

The impact of HFE mutations on haemoglobin and iron status in individuals experiencing repeated iron loss through blood donation*. (English)

1 reference

14 August 2017

13

Michael P Busch

1 reference

14 August 2017

2

Tzong-Hae Lee

1 reference

14 August 2017

9

Simone A Glynn

1 reference

14 August 2017

3

Karen S Schlumpf

1 reference

Danielle Mercatante Carrick

14 August 2017

6

object named as

Danielle M Carrick

1 reference

NHLBI Retrovirus Epidemiology Donor Study-II (REDS-II)

14 August 2017

14

object named as

NHLBI Retrovirus Epidemiology Donor Study-II (REDS-II)

1 reference

14 August 2017

1

Alan E Mast

1 reference

14 August 2017

David J Wright

4

1 reference

14 August 2017

Bryce Johnson

5

1 reference

14 August 2017

Ritchard G Cable

7

1 reference

14 August 2017

Joseph E Kiss

8

1 reference

14 August 2017

Whitney R Steele

10

1 reference

14 August 2017

Edward L Murphy

11

1 reference

14 August 2017

Ronald Sacher

12

1 reference

14 August 2017

language of work or name

English

0 references

publication date

25 November 2011

1 reference

British Journal of Haematology

14 August 2017

1 reference

14 August 2017

156

1 reference

14 August 2017

3

1 reference

14 August 2017

388-401

1 reference

Iron deficiency in blood donors: analysis of enrollment data from the REDS-II Donor Iron Status Evaluation (RISE) study

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

Demographic correlates of low hemoglobin deferral among prospective whole blood donors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

A genome-wide association analysis of serum iron concentrations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

The serine protease TMPRSS6 is required to sense iron deficiency

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

The TNF (-308A) polymorphism is associated with microchimerism in transfused trauma patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

Regulation of iron metabolism by hepcidin

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

Hematologic differences between African-Americans and whites: the roles of iron deficiency and alpha-thalassemia on hemoglobin levels and mean corpuscular volume

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3508695

A study of the iron and HFE status of blood donors, including a group who failed the initial screen for anaemia.

30 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2011.08952.X

International variation in volunteer whole blood donor eligibility criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2011.08952.X

Behavioral, biochemical, and genetic analysis of iron metabolism in high-intensity blood donors

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2011.08952.X

Reticulocyte hemoglobin content.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2011.08952.X

Immunoassay for human serum hepcidin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2011.08952.X

HFE mutations, iron deficiency and overload in 10,500 blood donors

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22118647

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22118647

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22118647

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1365-2141.2011.08952.X

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

22118647

1 reference