Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients-Reference-Cited by-同舟云学术

Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients

Published:2015-01 Issue:1 Volume:54 Page:4-8
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Bhanushali Aparna A.,Patra P.K.,Nair D.,Verma H.,Das B.R.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference52 articles.

1. Inherited haemoglobin disorders: an increasing global health problem;Weatherall;Bull. World Health Organ.,2001

2. The inherited disorders of hemoglobin are an emerging global health burden;Weatherall;Blood,2010

3. Epidemiology of sickle cell disorder in the state of Maharashtra;Kate;Int. J. Hum. Genet.,2002

4. Gene mutations in human haemoglobin: the chemical difference between normal and sickle haemoglobin;Ingram;Nature,1957

5. Sickle cell disease in the Post Genomic Era: a monogenic disease with a polygenic phenotype;Driss;Genomics Insights,2009

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18

2. Infection and Potential Challenge of Childhood Mortality in Sickle Cell Disease: A Comprehensive Review of the Literature from a Global Perspective;Thalassemia Reports;2023-08-30

3. Effects of Quantitative Trait Loci (QTLs) of BCL11A and HBS1L-MYB genes on clinical-biological variability of sickle cell disease in a Senegalese pediatric population;African Journal of Biochemistry Research;2022-11-30

4. A Versatile and Efficient Novel Approach for Mendelian Randomization Analysis with Application to Assess the Causal Effect of Fetal Hemoglobin on Anemia in Sickle Cell Anemia;Mathematics;2022-10-12

5. Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine;Scientific Reports;2021-10-22