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Title
Genetic modifiers of severity in sickle cell disease
Authors
Keywords
-
Journal
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION
Volume 68, Issue 2-3, Pages 147-164
Publisher
IOS Press
Online
2018-03-30
DOI
10.3233/ch-189004
References
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Note: Only part of the references are listed.- Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors
- (2018) Graham R. Serjeant et al. BLOOD CELLS MOLECULES AND DISEASES
- UGT1A1 (TA)ngenotype is not the major risk factor of cholelithiasis in sickle cell disease children
- (2017) Philippe Joly et al. EUROPEAN JOURNAL OF HAEMATOLOGY
- Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes
- (2017) Céline Renoux et al. PEDIATRIC BLOOD & CANCER
- Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia
- (2016) André Rolim Belisário et al. ANNALS OF HEMATOLOGY
- Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction?
- (2016) Keyne Charlot et al. BLOOD CELLS MOLECULES AND DISEASES
- The role of blood rheology in sickle cell disease
- (2016) Philippe Connes et al. BLOOD REVIEWS
- Original Research: Use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC disease
- (2016) Carly C Ginter Summarell et al. EXPERIMENTAL BIOLOGY AND MEDICINE
- Endothelial nitric oxide synthase gene polymorphisms and the risk of vasculopathy in sickle cell disease
- (2016) Sherif M. Yousry et al. Hematology
- Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategies
- (2016) Guillaume Lettre et al. LANCET
- Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study
- (2016) Céline Renoux et al. PLoS One
- Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia
- (2016) Beverly A. Schaefer et al. PLoS One
- Osteonecrosis in Sickle Cell Disease
- (2016) Zan A. Naseer et al. SOUTHERN MEDICAL JOURNAL
- Genome-Wide Analysis Identifies IL-18 and FUCA2 as Novel Genes Associated with Diastolic Function in African Americans with Sickle Cell Disease
- (2016) Julio D. Duarte et al. PLoS One
- Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients
- (2015) Tite Minga Mikobi et al. PLoS One
- The glomerulopathy of sickle cell disease
- (2014) Kenneth I. Ataga et al. AMERICAN JOURNAL OF HEMATOLOGY
- Haemolysis and abnormal haemorheology in sickle cell anaemia
- (2014) Philippe Connes et al. BRITISH JOURNAL OF HAEMATOLOGY
- Thinking beyond sickling to better understand pain in sickle cell disease
- (2014) Deepika S. Darbari et al. EUROPEAN JOURNAL OF HAEMATOLOGY
- Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease
- (2014) N. Lemonne et al. HAEMATOLOGICA
- Sickle cell disease
- (2014) Duyen Ngo et al. Hematology
- HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers
- (2014) Ralph Stadhouders et al. JOURNAL OF CLINICAL INVESTIGATION
- Association of Xmn1 −158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia
- (2014) Sneha Dadheech et al. MOLECULAR BIOLOGY REPORTS
- Impact ofVEGFA−583C > T polymorphism on serum VEGF levels and the susceptibility to acute chest syndrome in pediatric patients with sickle cell disease
- (2014) Noor A. Redha et al. PEDIATRIC BLOOD & CANCER
- Endothelial nitric oxide synthase gene intron 4 VNTR polymorphism in sickle cell disease: Relation to vasculopathy and disease severity
- (2014) Azza Abdel Gawad Tantawy et al. PEDIATRIC BLOOD & CANCER
- Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia
- (2014) Vivien A. Sheehan et al. PLoS One
- Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians
- (2013) Paolo Rigano et al. AMERICAN JOURNAL OF HEMATOLOGY
- Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes
- (2013) Vivien A. Sheehan et al. AMERICAN JOURNAL OF HEMATOLOGY
- Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia
- (2013) J. M. Flanagan et al. BLOOD
- Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?
- (2013) N. Lemonne et al. BLOOD
- Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients
- (2013) G. Galarneau et al. BLOOD
- Genetic determinants of haemolysis in sickle cell anaemia
- (2013) Jacqueline N. Milton et al. BRITISH JOURNAL OF HAEMATOLOGY
- Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia
- (2013) Philippe Connes et al. BRITISH JOURNAL OF HAEMATOLOGY
- Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study
- (2013) Malika Benkerrou et al. BRITISH JOURNAL OF HAEMATOLOGY
- Genetic variation inCD36,HBA,NOS3andVCAM1is associated with chronic haemolysis level in sickle cell anaemia: a longitudinal study
- (2013) Andreia Coelho et al. EUROPEAN JOURNAL OF HAEMATOLOGY
- Endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in India
- (2013) Sudhansu Sekhar Nishank et al. JOURNAL OF HUMAN GENETICS
- Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A
- (2013) J. Xu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Search for Genetic Modifiers of Disease Severity in the -Hemoglobinopathies
- (2013) G. Lettre Cold Spring Harbor Perspectives in Medicine
- The Natural History of Sickle Cell Disease
- (2013) G. R. Serjeant Cold Spring Harbor Perspectives in Medicine
- Genetic modifiers of sickle cell disease
- (2012) Martin H. Steinberg et al. AMERICAN JOURNAL OF HEMATOLOGY
- Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis
- (2012) P. Bartolucci et al. BLOOD
- The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and Europe
- (2012) M. Nouraie et al. HAEMATOLOGICA
- A Genome-Wide Association Study of Total Bilirubin and Cholelithiasis Risk in Sickle Cell Anemia
- (2012) Jacqueline N. Milton et al. PLoS One
- Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia
- (2011) R. E. Ware et al. BLOOD
- Transcriptional regulation of fetal to adult hemoglobin switching: new therapeutic opportunities
- (2011) A. Wilber et al. BLOOD
- MYH9 and APOL1 are both associated with sickle cell disease nephropathy
- (2011) Allison E. Ashley-Koch et al. BRITISH JOURNAL OF HAEMATOLOGY
- c-myb supports erythropoiesis through the transactivation of KLF1 and LMO2 expression
- (2010) E. Bianchi et al. BLOOD
- Association of variant alleles of MBL2 gene with vasoocclusive crisis in children with sickle cell anemia
- (2010) T.F. Mendonça et al. BLOOD CELLS MOLECULES AND DISEASES
- A Review of the Literature on the Multiple Dimensions of Chronic Pain in Adults with Sickle Cell Disease
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- Sickle-cell disease
- (2010) David C Rees et al. LANCET
- Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment
- (2010) Kleber Yotsumoto Fertrin et al. Expert Review of Hematology
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- (2009) M.C.V.C. Oliveira et al. ACTA HAEMATOLOGICA
- Glucose 6 phosphate dehydrogenase deficiency is not associated with cerebrovascular disease in children with sickle cell anemia
- (2009) D. C. Rees et al. BLOOD
- Renal Function in Infants with Sickle Cell Anemia: Baseline Data from the BABY HUG Trial
- (2009) Russell E. Ware et al. JOURNAL OF PEDIATRICS
- UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia
- (2008) Shannon L. Carpenter et al. AMERICAN JOURNAL OF HEMATOLOGY
- Association of sickle avascular necrosis with bone morphogenic protein 6
- (2008) Pinar Ulug et al. ANNALS OF HEMATOLOGY
- Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease
- (2008) A. E. Ashley-Koch et al. BLOOD
- G6PD deficiency, absence of -thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia
- (2008) F. Bernaudin et al. BLOOD
- Chronic Hyper-Hemolysis in Sickle Cell Anemia: Association of Vascular Complications and Mortality with Less Frequent Vasoocclusive Pain
- (2008) James G. Taylor et al. PLoS One
- 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
- Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific RepressorBCL11A
- (2008) Vijay G. Sankaran et al. SCIENCE
- Prediction of adverse outcomes in children with sickle cell anemia: a study of the Dallas Newborn Cohort
- (2007) C. T. Quinn et al. BLOOD
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