(Q28943510)

14 March 2017

title

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

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genome-wide association study

14 March 2017

main subject

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Chayanon Peerapittayamongkol

Surakameth Mahasirimongkol

object named as

Chayanon Peerapittayamongkol

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object named as

Surakameth Mahasirimongkol

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14 March 2017

Michiaki Kubo

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14 March 2017

Atsushi Takahashi

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14 March 2017

Yusuke Nakamura

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14 March 2017

Natsuhiko Kumasaka

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14 March 2017

Manit Nuinoon

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14 March 2017

Wattanan Makarasara

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14 March 2017

Iswari Setianingsih

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14 March 2017

Pustika Amalia Wahidiyat

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14 March 2017

Orapan Sripichai

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14 March 2017

Saovaros Svasti

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14 March 2017

Thongperm Munkongdee

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14 March 2017

Chayanon Peerapittayamongkol

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14 March 2017

Vip Viprakasit

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14 March 2017

Pranee Winichagoon

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14 March 2017

Suthat Fucharoen

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14 March 2017

publication date

1 March 2010

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14 March 2017

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14 March 2017

volume

127

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14 March 2017

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14 March 2017

page(s)

303–314

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A high-throughput SNP typing system for genome-wide association studies

14 March 2017

cites work

1 reference

12 December 2020

Chromosome Conformation Capture Carbon Copy (5C): a massively parallel solution for mapping interactions between genomic elements

1 reference

12 December 2020

Polymerase chain reaction amplification applied to the determination of beta-like globin gene cluster haplotypes

1 reference

12 December 2020

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

1 reference

12 December 2020

The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells

1 reference

12 December 2020

Phenotype score to grade the severity of thalassemia intermedia

1 reference

12 December 2020

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

1 reference

12 December 2020

Intergenic transcription, cell-cycle and the developmentally regulated epigenetic profile of the human beta-globin locus

1 reference

12 December 2020

The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans.

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular therapies in beta-thalassaemia

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12 December 2020

Genetic modifiers of beta-thalassemia.

1 reference

12 December 2020

Prenatal diagnosis of beta-thalassaemia by reverse dot-blot hybridization

1 reference

12 December 2020

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

1 reference

12 December 2020

Developmental biology. From genetic association to genetic switch

1 reference

12 December 2020

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

1 reference

12 December 2020

Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease

1 reference

12 December 2020

Severity differences in β‐thalassaemia/haemoglobin E syndromes: implication of genetic factors

1 reference

12 December 2020

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

1 reference

12 December 2020

Heterogeneity of the egammadeltabeta-thalassaemias: characterization of three novel English deletions

1 reference

12 December 2020

β-Globin gene cluster polymorphisms are strongly associated with severity of HbE/β0-thalassemia

1 reference

12 December 2020

Intergenic transcription and developmental remodeling of chromatin subdomains in the human beta-globin locus.

1 reference

12 December 2020

Genetic factors affecting clinical severity in beta-thalassemia syndromes

1 reference

12 December 2020

Deletion of a region that is a candidate for the difference between the deletion forms of hereditary persistence of fetal hemoglobin and deltabeta-thalassemia affects beta- but not gamma-globin gene expression

1 reference

12 December 2020

A scoring system for the classification of beta-thalassemia/Hb E disease severity.

1 reference

12 December 2020

Ethnic differences in F cell levels in Jamaica: a potential tool for identifying new genetic loci controlling fetal haemoglobin

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12 December 2020

Hemoglobin E beta-thalassemia: an increasingly common disease with some diagnostic pitfalls

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12 December 2020

Haemoglobin E beta thalassaemia in Sri Lanka.

1 reference

12 December 2020

Simplified multiplex-PCR diagnosis of common southeast asian deletional determinants of alpha-thalassemia

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12 December 2020

10.1007/S00439-009-0770-2

Identifiers

DOI

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Dimensions Publication ID

14 March 2017

1051213805

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