Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia (Q34149136)

30 September 2017

Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia (English)

1 reference

30 September 2017

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0 references

0 references

12

1 reference

30 September 2017

Sharon E Cox

4

0 references

Stephan Menzel

object named as

Stephan Menzel

series ordinal

2

0 references

Julie Makani

object named as

Julie Makani

series ordinal

1

0 references

Josephine Mgaya

series ordinal

8

object named as

Josephine Mgaya

1 reference

30 September 2017

14

Swee Lay Thein

1 reference

30 September 2017

3

Siana Nkya

1 reference

30 September 2017

7

Albert N Komba

1 reference

30 September 2017

6

Deogratius Soka

1 reference

30 September 2017

9

Helen Rooks

1 reference

30 September 2017

10

Nisha Vasavda

1 reference

30 September 2017

5

Emma Drasar

1 reference

30 September 2017

Martin Farrall

13

1 reference

PMCID

5555384

30 September 2017

language of work or name

English

0 references

publication date

10 November 2010

1 reference

30 September 2017

3

1 reference

based on heuristic

inferred from page(s)

published in

Blood

1 reference

30 September 2017

117

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30 September 2017

4

1 reference

30 September 2017

1390-1392

1 reference

The inherited diseases of hemoglobin are an emerging global health burden

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association 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=5555384

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

The genetic structure and history of Africans and African Americans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Global epidemiology of haemoglobin disorders and derived service indicators

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Genetic modifiers of the beta-haemoglobinopathies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in 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=5555384

Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

Whole genome amplification from a single cell: implications for genetic 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=5555384

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555384

The molecular basis of HPFH in a British family identified by heteroduplex formation

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21068433

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Pain in sickle cell disease. Rates and risk factors

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21068433

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1182/BLOOD-2010-08-302703

1 reference

30 September 2017

1 reference

30 September 2017

1 reference

PMCID

5555384