CNR Institutional Research Information System

PERSEU, LUCIA
 Distribuzione geografica
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Continente #
NA - Nord America 104
AS - Asia 60
EU - Europa 9
Totale 173
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Nazione #
US - Stati Uniti d'America 104
SG - Singapore 55
IT - Italia 7
KR - Corea 3
CN - Cina 2
FI - Finlandia 1
NL - Olanda 1
Totale 173
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Città #
Santa Clara 94
Singapore 41
Assemini 4
Seoul 3
Guangzhou 2
Cagliari 1
Helsinki 1
Totale 146
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Nome #
Genome-wide association scan for serum bilirubin levels in a Sardinian cohort. 8
BCL11A is associated with persistent HbF and ameliorates the ²-thalassemia phenotype. 7
Genome-wide association scan for bilirubin levels in a Sardinian population 7
Seventy-five genetic loci influencing the human red blood cell 7
Caratterizzazione molecolare di eterozigoti beta-talassemici con fenotipo clinico grave 6
Post-GWAS Validation of Target Genes Associated with HbF and HbA2 Levels 6
Red cell pyruvate Kinase deficiency in Southern Sardinia 5
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 5
Relationship between neonatal screening results by HPLC and the number of ±-thalassaemia gene mutations; consequences for the cut-off value. 5
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels 5
Association of alpha globin gene quadruplication and heterozygous beta thalassemia in patients with thalassemia intermedia 5
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia 5
KLF1gene mutations cause borderline HbA2 5
Analysis of candidate SNPs for high HbF in ² thalassemia intermedia patients. 5
Delta-globin gene expression improves sickle cell disease in a humanised mouse model 5
Cholelithiasis in thalassemia major. 5
Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null mice 5
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation 5
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach 5
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 4
The effect of ß thalassemia mutations on the clinical severity of the sickle-ßthalassemia syndrome 4
Amelioration of Sardinian beta-0 thalassemia by genetic modifiers 4
Diagniosi molecolare con DHPLC in soggetti con HbA2 borderline 4
MUTATION ANALYSIS OF DELTA-GLOBIN GENE IN SARDINIA 4
Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype. 4
Analisi molecolare del difetto di piruvatochinasi 4
Delta-Globin Gene Expression Is Enhanced in vivo by Interferon Type I 4
Genetic Modifiers of Homozygous Beta Zero Thalassemia 4
VARIABILITÀ DEL GENE DELTA GLOBINICO 4
AHSP expression in Beta-Thalassemia carriers with Thalassemia Intermedia Phenotype 3
Analisi dei polimorfismi associati ad aumento di HbF in pazienti sardi con talassemia intermedia 3
AHSP PROMOTER HOMOPOLYMER IN BETA-THALASSEMIA SYNDROMES 3
MOLECULAR ANALYSIS OF ALPHA HEMOGLOBIN STABILIZING PROTEIN(AHSP) IN SARDINIAN PATIENTS WITH HOMOZYGOUS BETA°-THALASSEMIA. 3
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients. 3
Thalassemia minor, the Gilbert mutation, and the risk of gallstones. 3
I DIFETTI EMOGLOBINICI E LA LORO VALUTAZIONE DI LABORATORIO 3
Studio del gene AHSP in portatori di beta Talassemia con fenotipo di Talassemia intermedia 3
CLINICAL AND MOLECULAR ANALYSIS OF HAEMOGLOBIN H DISEASE IN SARDINIA: HAEMATOLOGICAL, OBSTETRIC AND CARDIAC ASPECTS IN PATIENTS WITH DIFFERENT GENOTYPES. 3
ANALISI DEGLI OMOPOLIMERI NEL PROMOTER DEL GENE AHSP NELLE SINDROMI TALASSEMICHE 3
Totale 176
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Categoria #
all - tutte 886
article - articoli 641
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.527
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20245 0 0 0 0 0 0 0 0 0 0 5 0
2024/2025171 2 4 51 18 96 0 0 0 0 0 0 0
Totale 176