(Q34165031)

28 February 2018

title

Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients (English)

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28 February 2018

genome-wide association study

main subject

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Pallav Bhatnagar

1

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28 February 2018

Shirley Purvis

2

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28 February 2018

Emily Barron-Casella

3

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28 February 2018

Michael R DeBaun

4

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28 February 2018

James F Casella

5

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28 February 2018

Dan E Arking

6

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28 February 2018

Jeffrey R Keefer

7

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28 February 2018

publication date

17 February 2011

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28 February 2018

Journal of Human Genetics

published in

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28 February 2018

volume

56

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28 February 2018

issue

4

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28 February 2018

page(s)

316-323

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28 February 2018

describes a project that uses

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1038/jhg.2011.12

inferred from title

exact match

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cites work

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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

5 July 2018

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5 July 2018

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Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype

5 July 2018

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5 July 2018

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5 July 2018

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A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E

5 July 2018

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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster

5 July 2018

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5 July 2018

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5 July 2018

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Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A.

5 July 2018

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BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies

5 July 2018

1 reference

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DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

5 July 2018

1 reference

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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

5 July 2018

1 reference

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A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

5 July 2018

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5 July 2018

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Whole genome genotyping technologies on the BeadArray platform

5 July 2018

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Principal components analysis corrects for stratification in genome-wide association studies

5 July 2018

1 reference

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A haplotype map of the human genome

5 July 2018

1 reference

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Haploview: analysis and visualization of LD and haplotype maps

5 July 2018

1 reference

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The structure of haplotype blocks in the human genome

5 July 2018

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Genomic control for association studies

5 July 2018

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A New Statistical Method for Haplotype Reconstruction from Population Data

5 July 2018

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Frequency of Sickling Disorders in U.S. Blacks

5 July 2018

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X-linked dominant control of F-cells in normal adult life: characterization of the Swiss type as hereditary persistence of fetal hemoglobin regulated dominantly by gene(s) on X chromosome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5825003

DNA sequence variation associated with elevated fetal G gamma globin production

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5825003

Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5825003

Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human 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=5825003

Genetic control of F cells in human 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=5825003

Individual Variation in the Production and Survival of F Cells in Sickle-Cell 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=5825003

Mortality in sickle cell disease. Life expectancy and risk factors for early death.

5 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.12

Genetics of Hb F/F cell variance in adults and heterocellular hereditary persistence of fetal hemoglobin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.12

Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach.

21 January 2018

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https://api.crossref.org/works/10.1038%2FJHG.2011.12

Interaction between two quantitative trait loci affects fetal haemoglobin expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.12

Fetal haemoglobin level--effect of gender, age and haemoglobin disorders

21 January 2018

1 reference

12 December 2020

The estimation of fetal haemoglobin in healthy adults by radioimmunoassay

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12 December 2020

Hereditary persistence of foetal haemoglobin production, and its interaction with the sickle-cell trait

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12 December 2020

Genetic influences on F cells and other hematologic variables: a twin heritability study

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12 December 2020

The significance of the paucity of sickle cells in newborn Negro infants

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12 December 2020

Pain in sickle cell disease. Rates and risk factors

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12 December 2020

Identifiers

DOI

10.1038/JHG.2011.12

1 reference

28 February 2018

PMC publication ID

5825003

1 reference

28 February 2018

PubMed ID

21326311

1 reference

28 February 2018