CNR Institutional Research Information System

SOLE, GABRIELLA
 Distribuzione geografica
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Continente #
AS - Asia 93
NA - Nord America 42
EU - Europa 34
Totale 169
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Nazione #
SG - Singapore 72
US - Stati Uniti d'America 42
IT - Italia 34
CN - Cina 11
KR - Corea 10
Totale 169
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Città #
Singapore 52
Cagliari 17
Santa Clara 15
Assemini 12
Guangzhou 11
Seoul 10
Springfield 2
Boardman 1
Forest City 1
Fort Worth 1
Totale 122
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Nome #
A novel mutation in the GLC1A gene causes Juvenile Open Angle Glaucoma in four families from the Italian region of Puglia. 12
Understanding the role of IRAK-M in allergic asthma: replication in European children and functional analysis 11
Ruolo del gene IRAK-M nella suscettibilità dell asma allergico: studio mutazionale e funzionale e replica dell associazione in popolazioni Europee 6
PRF1 mutation alters immune system activation, inflammation, and risk of autoimmunity 5
Serum IgE Reactivity Profiling in an Asthma Affected Cohort 5
Mutation and functional analysis of the IRAK-M gene in asthmatic patients. 4
Rational design of new candidate compounds for multiple sclerosis treatment based on analysis of biological targets identified through genome wide association studies in Sardinia. 4
Mutation and functional analysis of the IRAK-M gene in Sardinian asthmatic patients 4
Overexpression of the Cytokine BAFF and Autoimmunity Risk 4
Autoantibodies against actin stress fibres in coeliac patients with associated hepatopathy." 3
Un caso di deficit congenito di triosofosfato-isomerasi (TPI): studio ematologico, biochimico, immunologico e genetico 3
Role of candidate regions for asthma susceptibility on Sardinian population 3
Genetic factors associated with levels of immune cell types. 3
Genetic factors regulating the levels of immune system cells in health and disease 3
Individuazione di loci di suscettibilità in un campione di famiglie con asma allergico di origine Sarda 3
System and pathway analysis of variants associated with immune cell levels 3
Disequilibrium extension analysis on the Xq13 region in Corsica 3
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy 3
Molecular and biochemical data on some Glucose-6-phosphate dehydrogenase variants from Southern Sardinia 3
IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma 3
Effects of aging and sex difference on immune-related phenotypes. 3
Identification of a gene involved in Hereditary Microcytic Anemia due to defective iron absorption in a Sardinian family 2
HLA DRB1*0301-DQA1*0501-DQB1*0201 haplotype in Sardinian patients with primary biliary cirrhosis 2
Molecular Basis of open-angle glaucoma in Italy 2
Phosphodiesterase 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function. 2
Iron overload and lysosomal stability in beta-thalassemia intermedia 2
Genome-wide search for asthma susceptibility loci in Sardinian population 2
Livelli dell'Hb A1C in soggetti G-6-PD carenti 2
Identification of a gene involved in hereditary microcytic anemia due to defective iron absorption in a Sardinian family 2
Linkage and association analyses and characteristics of the sample 2
Identificazione di IRAK-M come gene di suscettibilità per l asma persistente ad esordio precoce 2
Crown-rump length: are they different or similar after homologous vs heterologous oocyte/embryo donation? 2
Variability of Linkage Disequilibrium (LD) among Corsican populations 2
Extent of linkage disequilibrium in Sardinian population 2
Genetic heterogeneity of beta-thalassemia intermedia in Southern Sardinia 2
Generation and analysis of new mouse models for the study of immunosenescence and autoimmunity 2
Linkage Disequilibrium's extension in Corsica. Looking for genetic isolates. 2
Studies on linkage and association of asthma with the Interleukin 4-Receptor alpha chain gene (IL-4Ra) in Sardinian population 2
Complete congenital stationary night blindness maps on Xp11.4 in a sardinian family 2
Heritability and genetic mapping of hundreds of immune-related quantitative traits measured in a large Sardinian cohort. 2
Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region. 2
L'Hb F nei pazienti neoplastici. Dati preliminari 2
Glucose-6-phoshate dehydrogenase variants from Southern Sardinia: biochemical data and clinical rilevance 2
Genetic variants regulating immune cell levels in health and disease. 2
P.E.04.16 How the immune system faces seasonal threats 2
Linkage Disequilibrium extension analysis on the Xq13 region in the island of Corsica 2
A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome. 2
Genetic analysis of congenital stationary night blindness Sardinian families. 1
Analysis of the Linkage Disequilibrium (LD) extension in three sub-isolated population of Corsica. 1
AHSP expression in Beta-Thalassemia carriers with Thalassemia Intermedia Phenotype 1
Mutation in TMPRSS6, a suppressor of hepcidin gene expression, in familial iron deficiency anemia. 1
Linkage Disequilibrium extension analysis on the Xq13 region in the island of Corsica 1
Molecular pathology of Wilson disease in Mediterranean populations 1
Identificazione di un locus coinvolto in una forma ereditaria di anemia microcitica in una famiglia Sarda. 1
Esiste una predisposizione genetica per l'espansione infartuale? Valutazione dei polimorfismi genetici del sistema renina-angiotensina 1
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta(GP1BB) that impacts thrombocytopenia 1
N-Acetil-beta-D-Glucosaminidasi sierica e suo pattern isoenzimatico in corso di malattie epatiche 1
The value of some Corsican sub-populations for genetic association studies. 1
A common beta-ig-h3 gene mutation in a large cohort of Sardinian Reis Bücklers' Corneal Dystrophy patients. 1
Polimorfismi del sistema renina-angiotensina in una popolazione del Nord Sardegna: associazione fra angiotensinogeno ed ipertensione arteriosa essenziale ad insorgenza precoce. 1
Genetic mapping of autosomal dominant primary open-angle glaucoma (POAG) in Sardinia. 1
A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron. 1
Enterocyte actin autoantibody detection: a new diagnostic tool in celiac disease diagnosis: results of a multicenter study. 1
Studio del gene AHSP in portatori di beta Talassemia con fenotipo di Talassemia intermedia 1
Mutazione nel gene TMPRSS6 responsabile dell'anemia sideropenica familiare refrattaria al trattamento con ferro orale 1
Beta Globin haplotype frequencies and distribution in Sardinian and Corsican populations 1
Systematic assessment of the immune system by genetic mapping of its quantitative dimensions 1
Una nuova variante della glucosio-6-fosfato deidrogenasi: la G-6-PD Villasalto 1
Anti-actin stress fibres antibodies in coeliac disease 1
Coinvolgimento del miocardio remoto nel corso di infarto miocardico acuto con sopralivellamento del tratto ST: le alterazioni ischemiche eterozonali all'elettrocardiogramma 1
Studio delle basi genetiche delle tireopatie autoimmuni nella popolazione sarda 1
Incidenza del difetto della G-6-PD eritrocitaria, della beta- ed alfa-talassemia nella Sardegna Meridionale: risultati di tre anni di screening 1
Iron overload and lysosomal stability in beta-thalassemia intermedia 1
Totale 169
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Categoria #
all - tutte 1.374
article - articoli 829
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 20
Totale 2.223
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202440 0 0 0 0 0 0 0 0 4 1 23 12
2024/2025129 1 21 106 1 0 0 0 0 0 0 0 0
Totale 169