(Q34149136)

30 September 2017

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

1 reference

30 September 2017

0 references

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

PMC publication ID

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

1 reference

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

PMC publication ID

5555384

30 September 2017

PubMed publication ID

21068433

1 reference

PMC publication ID

5555384