Associated Papers
Association of cell adhesion molecules levels & single nucleotide polymorphisms with vaso-occlusive crisis in sickle cell disease: A cross sectional study.
Gupta P et al.
The Indian Journal of Medical Research, 2025
Global analysis of suppressor mutations that rescue human genetic defects.
Ünlü B et al.
Genome Medicine, 2023
Genetic Variation and Sickle Cell Disease Severity: A Systematic Review and Meta-Analysis.
Kirkham JK et al.
Jama Network Open, 2023
Somatic mutations reveal hyperactive Notch signaling and racial disparities in prurigo nodularis.
Rajeh A et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
Co-Inheritance of alpha-thalassemia and sickle cell disease in a cohort of Angolan pediatric patients.
Santos B et al.
Molecular Biology Reports, 2020
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.
Belisário AR et al.
Annals of Hematology, 2016
Association of alpha-thalassemia, TNF-alpha (-308G>A) and VCAM-1 (c.1238G>C) gene polymorphisms with cerebrovascular disease in a newborn cohort of 411 children with sickle cell anemia.
Belisário AR et al.
Blood Cells, Molecules & Diseases, 2015
Genetic variation in CD36, HBA, NOS3 and VCAM1 is associated with chronic haemolysis level in sickle cell anaemia: a longitudinal study.
Coelho A et al.
European Journal of Haematology, 2014
Increased monocyte adhesion by endothelial expression of VCAM-1 missense variation in vitro.
Schmitz B et al.
Atherosclerosis, 2013
Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia.
Connes P et al.
British Journal of Haematology, 2013
Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment.
Fertrin KY et al.
Expert Review of Hematology, 2010
Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
Driss A et al.
Genomics Insights, 2009
Genetic etiologies for phenotypic diversity in sickle cell anemia.
Steinberg MH
Thescientificworldjournal, 2009
Expression of ICAM1 and VCAM1 serum levels in rheumatoid arthritis clinical activity. Association with genetic polymorphisms.
Navarro-Hernández RE et al.
Disease Markers, 2009
Genetic modifiers of the beta-haemoglobinopathies.
Thein SL
British Journal of Haematology, 2008
Sickle cell disease: a multigenic perspective of a single gene disorder.
Kutlar A
Hemoglobin, 2007
Functional nsSNPs from carcinogenesis-related genes expressed in breast tissue: potential breast cancer risk alleles and their distribution across human populations.
Savas S et al.
Human Genomics, 2006
Sickle cell disease: a multigenic perspective of a single-gene disorder.
Kutlar A
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre, 2005
New advances in identifying genetic anomalies in stroke-prone probands.
Meschia JF et al.
Current Neurology and Neuroscience Reports, 2004
New advances in identifying genetic anomalies in stroke-prone probands.
Meschia JF et al.
Current Atherosclerosis Reports, 2003
Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease.
Taylor JG et al.
Blood, 2002