(Q37156198)

18 August 2017

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

1 reference

18 August 2017

1 reference

11

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18 August 2017

Beben Benyamin

1

0 references

Allan F McRae

Allan F McRae

2

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Anjali K. Henders

Anjali K Henders

5

0 references

Grant W. Montgomery

Grant W Montgomery

9

0 references

Nick Martin

Nicholas G Martin

8

0 references

Aarno Palotie

6

Aarno Palotie

1 reference

18 August 2017

Leena Peltonen-Palotie

7

Leena Peltonen

1 reference

18 August 2017

Gu Zhu

3

1 reference

18 August 2017

Scott Gordon

4

1 reference

18 August 2017

John B Whitfield

10

1 reference

18 August 2017

language of work or name

English

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publication date

11 December 2008

1 reference

American Journal of Human Genetics

18 August 2017

6

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published in

1 reference

18 August 2017

84

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18 August 2017

1

1 reference

18 August 2017

60-65

1 reference

The serine protease TMPRSS6 is required to sense iron deficiency

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

WGAViewer: software for genomic annotation of whole genome association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

A genome-wide association study of global gene expression

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

PLINK: a tool set for whole-genome association and population-based linkage analyses

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

A haplotype map of the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

Population structure, differential bias and genomic control in a large-scale, case-control association study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

GenomEUtwin: A Strategy to Identify Genetic Influences on Health and Disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

A general test of association for quantitative traits in nuclear families

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

The beta subunit of the signal recognition particle receptor is a transmembrane GTPase that anchors the alpha subunit, a peripheral membrane GTPase, to the endoplasmic reticulum membrane

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

Sizing up human height variation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668053

The effect of transferrin polymorphisms on iron metabolism

4 December 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

12 December 2020

Human transferrin G277S mutation and iron deficiency in pregnancy

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1016/J.AJHG.2008.11.011

Identifiers

DOI

1 reference

18 August 2017

1 reference

18 August 2017

PubMed publication ID

19084217

1 reference