Existence of HbF Enhancer Haplotypes atHBS1L-MYBIntergenic Region in Transfusion-Dependent Saudiβ-Thalassemia Patients

A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia

(2016) Vinod Vathipadiekal et al.   AMERICAN JOURNAL OF HEMATOLOGY

Mutations in the β-globin gene from a Saudi population: an update

(2016) J. F. Borgio et al.   International Journal of Laboratory Hematology

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

(2015) P. Sebastiani et al.   BLOOD CELLS MOLECULES AND DISEASES

Polymorphic variations influencing fetal hemoglobin levels: Association study in beta-thalassemia carriers and in normal individuals of Portuguese origin

(2015) Clara Pereira et al.   BLOOD CELLS MOLECULES AND DISEASES

Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients

(2015) Awatif N. Al-Nafie et al.   BLOOD CELLS MOLECULES AND DISEASES

Genomic approaches to identifying targets for treating β hemoglobinopathies

(2015) Duyen A. Ngo et al.   BMC Medical Genomics

DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil

(2014) Greice Lemos Cardoso et al.   BLOOD CELLS MOLECULES AND DISEASES

A novel HBA2 gene conversion in cis or trans: “α12 allele” in a Saudi population

(2014) J. Francis Borgio et al.   BLOOD CELLS MOLECULES AND DISEASES

HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers

(2014) Ralph Stadhouders et al.   JOURNAL OF CLINICAL INVESTIGATION

Spectrum ofα-Thalassemia Mutations in Transfusion-Dependent β-Thalassemia Patients from the Eastern Province of Saudi Arabia

(2013) Mohammed Shakil Akhtar et al.   HEMOGLOBIN

Analysis of rs4671393 Polymorphism in Hemoglobin E/β-thalassemia Major in Guangxi Province of China

(2013) Yunyan He et al.   JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY

An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level

(2013) D. E. Bauer et al.   SCIENCE

EFFECT OF CIS ACTING POTENTIAL REGULATORS IN THE ß GLOBIN GENE CLUSTER ON THE PRODUCTION OF HBF IN THALASSEMIA PATIENTS

(2013) Anita Nadkarni   Mediterranean Journal of Hematology and Infectious Diseases

Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans

(2011) Abdulrahman Alsultan et al.   AMERICAN JOURNAL OF HEMATOLOGY

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

(2011) J. J. Farrell et al.   BLOOD

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

(2010) J. Makani et al.   BLOOD

The XmnI Gγ polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 β-thalassemia intermedia patients

(2010) Thi Khanh Tien Nguyen et al.   BLOOD CELLS MOLECULES AND DISEASES

Studies in haemoglobin E beta-thalassaemia

(2010) Nancy F. Olivieri et al.   BRITISH JOURNAL OF HAEMATOLOGY

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

(2010) Joseph Borg et al.   NATURE GENETICS

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

(2010) Geneviève Galarneau et al.   NATURE GENETICS

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

(2009) N. Solovieff et al.   BLOOD

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

(2009) S. L. Thein et al.   HUMAN MOLECULAR GENETICS

Genetic Variation on Chromosome 6 Influences F Cell Levels in Healthy Individuals of African Descent and HbF Levels in Sickle Cell Patients

(2009) Lisa E. Creary et al.   PLoS One

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

(2008) Amanda E. Sedgewick et al.   BLOOD CELLS MOLECULES AND DISEASES

Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand

(2008) L NUNTAKARN et al.   BLOOD CELLS MOLECULES AND DISEASES

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

(2008) M. Uda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

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

(2008) G. Lettre et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA