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Franca Rosa Demartis

Observed names: Demartis F. R., Demartis F.R., F. Demartis, F. R. Demartis, F.-R. Demartis, F.R. Demartis, Franca R. Demartis, Franca Rosa De Martis
OpenAlex ID: A5089618257
KLF1 gene mutations cause borderline HbA2
2011 · Lucia Perseu, Stefania Satta, et al. · Blood · 107
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin
2011 · S. Satta, L. Perseu, et al. · Haematologica · 74
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A genetic score for the prediction of beta-thalassemia severity
2014 · F. Danjou, M. Francavilla, et al. · Haematologica · 56
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New analytical tools and epidemiological data for the identification of HbA2 borderline subjects in the screening for beta-thalassemia
2008 · Andrea Mosca, Renata Paleari, et al. · Bioelectrochemistry · 37
Thalassaemia and Glucose-6-Phosphate Dehydrogenase Screening in 13- to 14-Year-Old Students of the Sardinian Population: Preliminary Findings
2008 · A. Cao, R. Congiu, et al. · Public Health Genomics · 27
A validated cellular biobank for β-thalassemia
2016 · Lucia Carmela Cosenza, Laura Breda, et al. · Journal of Translational Medicine · 26
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The Problem of Borderline Hemoglobin A2 Levels in the Screening for β-Thalassemia Carriers in Sardinia
2016 · Maria Elisabetta Paglietti, Stefania Satta, et al. · Acta Haematologica · 25
Delta‐globin gene expression improves sickle cell disease in a humanised mouse model
2021 · Susanna Porcu, Michela Simbula, et al. · British Journal of Haematology · 18
Analytical evaluation of the Tosoh HLC-723 G7 automated HPLC analyzer for hemoglobin A2 and F determination
2004 · Renata Paleari, Monica Cannata, et al. · Clinical Biochemistry · 13
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation
2017 · Stefania Satta, Maria Elisabetta Paglietti, et al. · Blood Cells Molecules and Diseases · 9
Phenotype-Genotype Correlation in β-Thalassemia
2011 · R. Galanello, L. Perseu, et al. · Thalassemia Reports · 7
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IFNL3 polymorphisms and HCV infection in patients with beta thalassemia
2015 · Raffaella Origa, Giuseppe Marceddu, et al. · Annals of Hepatology · 6
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Low Impact of Genetic Modifiers on the Phenotype of Homozygous Beta Thalassemia in the Last Decennial Cohort of Thalassemia Newborns in Sardinia
2017 · Paolo Moi, Matteo Marcello, et al. · Blood
Contents Vol. 135, 2016
2016 · Dan Douer, Ruham Alshiekh-Nasany, et al. · Acta Haematologica
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The multicenter THALAMOSS cellular Biobank for β-Thalassemia
2016 · Lucia Carmela Cosenza, Laura Breda, et al. · Institutional Research Information System University of Ferrara (University of Ferrara)
Post GWAS analysis of a BCLA intronic region to define its role in regulating HbF levels
2012 · Francesca Anedda, Sanna Serena, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)
Eterogeneità molecolare delle emoglobinopatie e del difetto di G6PD in Sardegna
2006 · R. Congiu, M. C. Sollaino, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari)
Works count: 21
Citation count: 405
H-index: 9
I10-index: 9
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