Stefania Satta
University of Cagliari(IT)
Publications by Year
Research Areas
Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Prenatal Screening and Diagnostics, Blood groups and transfusion, Neonatal Health and Biochemistry
Most-Cited Works
- → Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia(2008)661 cited
- → Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach(2011)160 cited
- → KLF1 gene mutations cause borderline HbA2(2011)100 cited
- → Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum(1996)31 cited
- → A validated cellular biobank for β-thalassemia(2016)29 cited
- → Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation(2011)25 cited
- → The Problem of Borderline Hemoglobin A2 Levels in the Screening for β-Thalassemia Carriers in Sardinia(2016)22 cited
- Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [alpha50(CD8)His-->Asn-->Asp].(1999)
- → Homozygosity for nondeletion δ-β0 thalassemia resulting in a silent clinical phenotype(2002)13 cited
- → Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation(2017)7 cited